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![Dellinger et al
Dr. Dellinger consulted for Biotest (immunoglobulin concentrate available in Dr. Douglas received grants paid to his institution from Eli Lilly (PROWESS
Europe for potential use in sepsis) and AstraZeneca (anti-TNF compound Shock site), Eisai (study site), National Institutes of Health (ARDS Network),
unsuccessful in recently completed sepsis clinical trial); his institution received Accelr8 (VAP diagnostics), CCCTG (Oscillate Study), and Hospira (Dexme-
consulting income from IKARIA for new product development (IKARIA has detomidine in Alcohol Withdrawal RCT). His institution received an honorar-
inhaled nitric oxide available for off-label use in ARDS) and grant support from ium from the Society of Critical Care Medicine (Paragon ICU Improvement);
Spectral Diagnostics Inc (current endotoxin removal clinical trial), Ferring (vaso- he consulted for Eli Lilly (PROWESS Shock SC and Sepsis Genomics
pressin analog clinical trial-ongoing); as well as serving on speakers bureau for Study) in accordance with institutional policy; he received payment for pro-
Eisai (anti-endotoxin compound that failed to show benefit in clinical trial). viding expert testimony (Smith Moore Leatherwood LLP); travel/accommo-
dations reimbursed by Eli Lilly and Company (PROWESS Shock Steering
Dr. Levy received grant support from Eisai (Ocean State Clinical Coordi-
Committee) and the Society of Critical Care Medicine (Hospital Quality Alli-
nating Center to fund clinical trial [$500K]), he received honoraria from Eli
ance, Washington DC, four times per year 2009−2011); he received hono-
Lilly (lectures in India $8,000), and he has been involved with the Surviving
raria from Covidien (non-CME lecture 2010, US$500) and the University
Sepsis Campaign guideline from its beginning.
of Minnesota Center for Excellence in Critical Care CME program (2009,
Dr. Rhodes consulted for Eli Lilly with monetary compensation paid to him- 2010); he has a pending patent for a bed backrest elevation monitor.
self as well as his institution (Steering Committee for the PROWESS Shock
Dr. Jaeschke has disclosed that he has no potential conflicts of interest.
trial) and LiDCO; travel/accommodation reimbursement was received from
Eli Lilly and LiDCO; he received income for participation in review activities Dr. Osborn consulted for Sui Generis Health ($200). Her institution
such as data monitoring boards, statistical analysis from Orion, and for Eli receives grant support from the National Institutes of Health Research,
Lilly; he is an author on manuscripts describing early goal-directed therapy, Health Technology Assessment Programme-United Kingdom (trial doc-
and believes in the concept of minimally invasive hemodynamic monitoring. tor for sepsis-related RCT). Salary paid through the NIHR government
funded (nonindustry) grant. Grant awarded to chief investigator from
Dr. Annane participated on the Fresenius Kabi International Advisory Board ICNARC. She is a trial clinician for ProMISe.
(honorarium 2000€). His nonfinancial disclosures include being the princi-
pal investigator of a completed investigator-led multicenter randomized con- Dr. Nunnally received a stipend for a chapter on diabetes mellitus; he is an
trolled trial assessing the early guided benefit to risk of NIRS tissue oxygen author of editorials contesting classic tight glucose control.
saturation; he was the principal investigator of an investigator-led randomized Dr. Townsend is an advocate for healthcare quality improvement.
controlled trial of epinephrine vs norepinephrine (CATS study)–Lancet 2007; Dr. Reinhart consulted for EISAI (Steering Committee member−less then
he also is the principle investigator of an ongoing investigator-led multina- US $10,000); BRAHMS Diagnostics (less than US $10,000); and SIRS-
tional randomized controlled trial of crystalloids vs colloids (Crystal Study). Lab Jena (founding member, less than US $10,000). He received hono-
Dr. Gerlach has disclosed that he has no potential conflicts of interest; raria for lectures including service on the speakers’ bureau from Biosyn
he is an author of a review on the use of activated protein C in surgical Germany (less than €10,000) and Braun Melsungen (less than €10,000).
patients (published in the New England Journal of Medicine, 2009). He received royalties from Edwards Life Sciences for sales of central
venous oxygen catheters (~$100,000).
Dr. Opal consulted for Genzyme Transgenics (consultant on trans-
genic antithrombin $1,000), Pfizer (consultant on TLR4 inhibitor project Dr. Kleinpell received monetary compensation for providing expert testimony
$3,000), British Therapeutics (consultant on polyclonal antibody project (four depositions and one trial in the past year). Her institution receives
$1,000), and Biotest A (consultant on immunoglobul project $2,000). grants from the Agency for Healthcare Research and Quality and the Prince
His institution received grant support from Novartis (Clinical Coordinat- Foundation (4-year R01 grant, PI and 3-year foundation grant, Co-l). She
ing Center to assist in patient enrollment in a phase III trial with the use received honoraria from the Cleveland Clinic and the American Association
of Tissue Factor Pathway Inhibitor [TFPI] in severe community acquired of Critical Care Nurses for keynote speeches at conferences; she received
pneumonia [SCAP] $30,000 for 2 years), Eisai ($30,000 for 3 years), royalties from McGraw Hill (co-editor of critical care review book); travel/
Astra Zeneca ($30,000 for 1 year), Aggenix ($30,000 for 1 year), Inimex accommodations reimbursed from the American Academy of Nurse Prac-
($10,000), Eisai ($10,000), Atoxbio ($10,000), Wyeth ($20,000), Sirtris titioners, Society of Critical Care Medicine, and American Association of
(preclinical research $50,000), and Cellular Bioengineering Inc. ($500). Critical Care Nurses (one night hotel coverage at national conference).
He received honoraria from Novartis (clinical evaluation committee TFPI Dr. Angus consulted for Eli Lilly (member of the Data Safety Monitoring
study for SCAP $20,000) and Eisai ($25,000). He received travel/accom- Board, Multicenter trial of a PC for septic shock), Eisai Inc (Anti-TLR4
modations reimbursed from Sangart (data and safety monitoring $2,000), therapy for severe sepsis), and Idaho Technology (sepsis biomarkers); he
Spectral Diagnostics (data and safety monitoring $2,000), Takeda (data received grant support (investigator, long-term follow-up of phase III trial
and safety monitoring $2,000) and Canadian trials group ROS II oseltami- of an anti-TLR4 agent in severe sepsis), a consulting income (anti-TRL4
vir study (data and safety monitoring board (no money). He is also on the therapy for severe sepsis), and travel/accommodation expense reimburse-
Data Safety Monitoring Board for Tetraphase (received US $600 in 2012). ment from Eisai, Inc; he is the primary investigator for an ongoing National
Institutes of Health-funded study comparing early resuscitation strategies
Dr. Sevransky received grant support to his institution from Sirius Genom- for sepsis-induced tissue hypoperfusion.
ics Inc; he consulted for Idaho Technology ($1,500); he is the co-principal
investigator of a multicenter study evaluating the association between Dr. Deutschman has nonfinancial involvement as a coauthor of the Society
intensive care unit organizational and structural factors, including proto- of Critical Care Medicine’s Glycemic Control guidelines.
cols and in-patient mortality. He maintains that protocols serve as useful Dr. Machado reports unrestricted grant support paid to her institution for
reminders to busy clinicians to consider certain therapies in patients with Surviving Sepsis Campaign implementation in Brazil (Eli Lilly do Brasil);
sepsis or other life-threatening illness. she is the primary investigator for an ongoing study involving vasopressin.
Dr. Sprung received grants paid to his institution from Artisan Pharma Dr. Rubenfeld received grant support from nonprofit agencies or foundations
($25,000–$50,000), Eisai, Corp ($1,000–$5,000 ACCESS), Ferring including National Institutes of Health ($10 million), Robert Wood Johnson
Pharmaceuticals A/S ($5,000–$10,000), Hutchinson Technology Incorpo- Foundation ($500,000), and CIHR ($200,000). His institution received grants
rated ($1,000–$5,000), Novartis Corp (less than $1,000). His institution from for-profit companies including Advanced Lifeline System ($150,000),
receives grant support for patients enrolled in clinical studies from Eisai Cor- Siemens ($50,000), Bayer ($10,000), Byk Gulden ($15,000), AstraZen-
poration (PI. Patients enrolled in the ACCESS study $50,000–$100,000), eca ($10,000), Faron Pharmaceuticals ($5,000), and Cerus Corporation
Takeda (PI. Study terminated before patients enrolled). He received grants ($11,000). He received honoraria, consulting fees, editorship, royalties, and
paid to his institution and consulting income from Artisan Pharma/Asahi Data and Safety Monitoring Board membership fees paid to him from Bayer
Kasei Pharma America Corp ($25,000–$50,000). He consulted for Eli ($500), DHD ($1,000), Eli Lilly ($5,000), Oxford University Press ($10,000),
Lilly (Sabbatical Consulting fee $10,000–$25,000) and received honoraria Hospira ($15,000), Cerner ($5,000), Pfizer ($1,000), KCI ($7,500), Ameri-
from Eli Lilly (lecture $1,000–$5,000). He is a member of the Australia and can Association for Respiratory Care ($10,000), American Thoracic Society
New Zealand Intensive Care Society Clinical Trials Group for the NICE- ($7,500), BioMed Central ($1,000), National Institutes of Health ($1,500),
SUGAR Study (no money received); he is a council member of the Inter- and the Alberta Heritage Foundation for Medical Research ($250). He has
national Sepsis Forum (as of Oct. 2010); he has held long time research database access or other intellectual (non financial) support from Cerner.
interests in steroids in sepsis, PI of Corticus study, end-of-life decision mak- Dr. Webb consulted for AstraZeneca (anti-infectives $1,000−$5,000) and
ing and PI of Ethicus, Ethicatt, and Welpicus studies. Jansen-Cilag (anti-infectives $1,000-$5,000). He received grant support
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![Dellinger et al
Selection and Organization of Committee Members Grading of Recommendations
The selection of committee members was based on inter- We advised the authors to follow the principles of the Grading
est and expertise in specific aspects of sepsis. Co-chairs and of Recommendations Assessment, Development and Evalua-
executive committee members were appointed by the Society tion (GRADE) system to guide assessment of quality of evi-
of Critical Care Medicine and European Society of Intensive dence from high (A) to very low (D) and to determine the
Care Medicine governing bodies. Each sponsoring organiza- strength of recommendations (Tables 3 and 4). (9–11). The
tion appointed a representative who had sepsis expertise. Addi- SSC Steering Committee and individual authors collaborated
tional committee members were appointed by the co-chairs with GRADE representatives to apply the system during the
and executive committee to create continuity with the previous SSC guidelines revision process. The members of the GRADE
committees’ membership as well as to address content needs group were directly involved, either in person or via e-mail, in
for the development process. Four clinicians with experience all discussions and deliberations among the guidelines com-
in the GRADE process application (referred to in this docu- mittee members as to grading decisions.
ment as GRADE group or Evidence-Based Medicine [EBM] The GRADE system is based on a sequential assessment of
group) took part in the guidelines development. the quality of evidence, followed by assessment of the balance
The guidelines development process began with appoint- between the benefits and risks, burden, and cost, leading to
ment of group heads and assignment of committee members development and grading of a management recommendation.
to groups according to their specific expertise. Each group was Keeping the rating of quality of evidence and strength of
responsible for drafting the initial update to the 2008 edition recommendation explicitly separate constitutes a crucial and
in their assigned area (with major additional elements of infor- defining feature of the GRADE approach. This system classifies
mation incorporated into the evolving manuscript through quality of evidence as high (grade A), moderate (grade B), low
year-end 2011 and early 2012). (grade C), or very low (grade D). Randomized trials begin
With input from the EBM group, an initial group meet- as high-quality evidence but may be downgraded due to
ing was held to establish procedures for literature review and limitations in implementation, inconsistency, or imprecision of
development of tables for evidence analysis. Committees and the results, indirectness of the evidence, and possible reporting
their subgroups continued work via phone and the Internet. bias (Table 3). Examples of indirectness of the evidence
Several subsequent meetings of subgroups and key indi- include population studied, interventions used, outcomes
viduals occurred at major international meetings (nominal measured, and how these relate to the question of interest.
groups), with work continuing via teleconferences and elec- Well-done observational (nonrandomized) studies begin as
tronic-based discussions among subgroups and members low-quality evidence, but the quality level may be upgraded on
of the entire committee. Ultimately, a meeting of all group the basis of a large magnitude of effect. An example of this is
heads, executive committee members, and other key commit- the quality of evidence for early administration of antibiotics.
tee members was held to finalize the draft document for sub- References to supplemental digital content appendices of
mission to reviewers. GRADEpro Summary of Evidence Tables appear throughout
this document.
Search Techniques The GRADE system classifies recommendations as strong
A separate literature search was performed for each clearly (grade 1) or weak (grade 2). The factors influencing this deter-
defined question. The committee chairs worked with subgroup mination are presented in Table 4. The assignment of strong
heads to identify pertinent search terms that were to include, or weak is considered of greater clinical importance than a
at a minimum, sepsis, severe sepsis, septic shock, and sepsis syn- difference in letter level of quality of evidence. The commit-
drome crossed against the subgroup’s general topic area, as well tee assessed whether the desirable effects of adherence would
as appropriate key words of the specific question posed. All outweigh the undesirable effects, and the strength of a rec-
questions used in the previous guidelines publications were ommendation reflects the group’s degree of confidence in
searched, as were pertinent new questions generated by gen- that assessment. Thus, a strong recommendation in favor of
eral topic-related searches or recent trials. The authors were an intervention reflects the panel’s opinion that the desirable
specifically asked to look for existing meta-analyses related to effects of adherence to a recommendation (beneficial health
their question and search a minimum of one general database outcomes; lesser burden on staff and patients; and cost sav-
(ie, MEDLINE, EMBASE) and the Cochrane Library (both ings) will clearly outweigh the undesirable effects (harm to
The Cochrane Database of Systematic Reviews [CDSR] and health; more burden on staff and patients; and greater costs).
Database of Abstracts of Reviews of Effectiveness [DARE]). The potential drawbacks of making strong recommenda-
Other databases were optional (ACP Journal Club, Evidence- tions in the presence of low-quality evidence were taken into
Based Medicine Journal, Cochrane Registry of Controlled account. A weak recommendation in favor of an intervention
Clinical Trials, International Standard Randomized Controlled indicates the judgment that the desirable effects of adherence
Trial Registry [http://www.controlled-trials.com/isrctn/] or to a recommendation probably will outweigh the undesirable
metaRegister of Controlled Trials [http://www.controlled- effects, but the panel is not confident about these tradeoffs—
trials.com/mrct/]. Where appropriate, available evidence was either because some of the evidence is low quality (and thus
summarized in the form of evidence tables. uncertainty remains regarding the benefits and risks) or the
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Table 5. (Continued) Recommendations: Initial Resuscitation and Infection Issues
4b. mpiric combination therapy should not be administered for more than 3–5 days. De-escalation to the most appropriate single
E
therapy should be performed as soon as the susceptibility profile is known (grade 2B).
5. Duration of therapy typically 7–10 days; longer courses may be appropriate in patients who have a slow clinical response,
undrainable foci of infection, bacteremia with S. aureus; some fungal and viral infections or immunologic deficiencies, including
neutropenia (grade 2C).
6. Antiviral therapy initiated as early as possible in patients with severe sepsis or septic shock of viral origin (grade 2C).
7. Antimicrobial agents should not be used in patients with severe inflammatory states determined to be of noninfectious cause
(UG).
E. Source Control
1. A specific anatomical diagnosis of infection requiring consideration for emergent source control be sought and diagnosed or
excluded as rapidly as possible, and intervention be undertaken for source control within the first 12 hr after the diagnosis is
made, if feasible (grade 1C).
2. When infected peripancreatic necrosis is identified as a potential source of infection, definitive intervention is best delayed until
adequate demarcation of viable and nonviable tissues has occurred (grade 2B).
3. When source control in a severely septic patient is required, the effective intervention associated with the least physiologic insult
should be used (eg, percutaneous rather than surgical drainage of an abscess) (UG).
4. f intravascular access devices are a possible source of severe sepsis or septic shock, they should be removed promptly after
I
other vascular access has been established (UG).
F. Infection Prevention
1a. elective oral decontamination and selective digestive decontamination should be introduced and investigated as a method to
S
reduce the incidence of ventilator-associated pneumonia; This infection control measure can then be instituted in health care
settings and regions where this methodology is found to be effective (grade 2B).
1b. ral chlorhexidine gluconate be used as a form of oropharyngeal decontamination to reduce the risk of ventilator-associated
O
pneumonia in ICU patients with severe sepsis (grade 2B).
In mechanically ventilated patients or those with known fluid responsiveness during resuscitation, including flow and
preexisting decreased ventricular compliance, a higher target possibly volumetric indices and microcirculatory changes,
CVP of 12 to 15 mm Hg should be achieved to account for may have advantages (29–32). Available technologies allow
the impediment in filling (16). Similar consideration may be measurement of flow at the bedside (33, 34); however, the effi-
warranted in circumstances of increased abdominal pressure cacy of these monitoring techniques to influence clinical out-
(17). Elevated CVP may also be seen with preexisting clini- comes from early sepsis resuscitation remains incomplete and
cally significant pulmonary artery hypertension, making use requires further study before endorsement.
of this variable untenable for judging intravascular volume The global prevalence of severe sepsis patients initially pre-
status. Although the cause of tachycardia in septic patients senting with either hypotension with lactate ≥ 4 mmol//L, hypo-
may be multifactorial, a decrease in elevated pulse rate with tension alone, or lactate ≥ 4 mmol/L alone, is reported as 16.6%,
fluid resuscitation is often a useful marker of improving intra- 49.5%, and 5.4%, respectively (15). The mortality rate is high in
vascular filling. Published observational studies have dem- septic patients with both hypotension and lactate ≥ 4 mmol/L
onstrated an association between good clinical outcome in (46.1%) (15), and is also increased in severely septic patients
septic shock and MAP ≥ 65 mm Hg as well as Scvo2 ≥ 70% with hypotension alone (36.7%) and lactate ≥ 4 mmol/L alone
(measured in the superior vena cava, either intermittently or (30%) (15). If Scvo2 is not available, lactate normalization may
continuously [18]). Many studies support the value of early be a feasible option in the patient with severe sepsis-induced
protocolized resuscitation in severe sepsis and sepsis-induced tissue hypoperfusion. Scvo2 and lactate normalization may also
tissue hypoperfusion (19–24). Studies of patients with shock be used as a combined endpoint when both are available. Two
indicate that Svo2 runs 5% to 7% lower than Scvo2 (25). While multicenter randomized trials evaluated a resuscitation strat-
the committee recognized the controversy surrounding egy that included lactate reduction as a single target or a tar-
resuscitation targets, an early quantitative resuscitation pro- get combined with Scvo2 normalization (35, 36). The first trial
tocol using CVP and venous blood gases can be readily estab- reported that early quantitative resuscitation based on lactate
lished in both emergency department and ICU settings (26). clearance (decrease by at least 10%) was noninferior to early
Recognized limitations to static ventricular filling pressure quantitative resuscitation based on achieving Scvo2 of 70% or
estimates exist as surrogates for fluid resuscitation (27, 28), but more (35). The intention-to-treat group contained 300, but the
measurement of CVP is currently the most readily obtainable number of patients actually requiring either Scvo2 normalization
target for fluid resuscitation. Targeting dynamic measures of or lactate clearance was small (n = 30). The second trial included
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incidence of ventilator-associated pneumonia (VAP); this 3. We suggest the use of albumin in the fluid resuscitation of
infection control measure can then be instituted in health- severe sepsis and septic shock when patients require sub-
care settings and regions where this methodology is found stantial amounts of crystalloids (grade 2C).
to be effective (grade 2B).
Rationale. The absence of any clear benefit following the
1b. We suggest oral chlorhexidine gluconate (CHG) be used administration of colloid solutions compared to crystalloid
as a form of oropharyngeal decontamination to reduce the solutions, together with the expense associated with colloid
risk of VAP in ICU patients with severe sepsis (grade 2B). solutions, supports a high-grade recommendation for the use
of crystalloid solutions in the initial resuscitation of patients
Rationale. Careful infection control practices (eg, hand
with severe sepsis and septic shock.
washing, expert nursing care, catheter care, barrier precau-
Three recent multicenter RCTs evaluating 6% HES
tions, airway management, elevation of the head of the bed,
130/0.4 solutions (tetra starches) have been published. The
subglottic suctioning) should be instituted during the care of
CRYSTMAS study demonstrated no difference in mortality
septic patients as reviewed in the nursing considerations for
with HES vs. 0.9% normal saline (31% vs. 25.3%, p = 0.37)
the Surviving Sepsis Campaign (114). The role of SDD with
in the resuscitation of septic shock patients; however the
systemic antimicrobial prophylaxis and its variants (eg, SOD,
study was underpowered to detect the 6% difference in
CHG) has been a contentious issue ever since the concept was
absolute mortality observed (122). In a sicker patient
first developed more than 30 years ago. The notion of limit-
cohort, a Scandinavian multicenter study in septic patients
ing the acquisition of opportunistic, often multidrug-resistant,
(6S Trial Group) showed increased mortality rates with
healthcare-associated microorganisms has its appeal by pro-
6% HES 130/0.42 fluid resuscitation compared to Ringer’s
moting “colonization resistance” from the resident microbi-
acetate (51% vs. 43% p = 0.03) (123). The CHEST study,
ome existing along mucosal surfaces of the alimentary tract.
conducted in a heterogenous population of patients admit-
However, the efficacy of SDD, its safety, propensity to prevent
ted to intensive care (HES vs. isotonic saline, n = 7000
or promote antibiotic resistance, and cost-effectiveness remain
critically ill patients), showed no difference in 90-day mor-
debatable despite a number of favorable meta-analyses and
controlled clinical trials (115). The data indicate an overall tality between resuscitation with 6% HES with a molecular
reduction in VAP but no consistent improvement in mortality, weight of 130 kD/0.40 and isotonic saline (18% vs. 17%,
except in selected populations in some studies. Most studies p = 0.26); the need for renal replacement therapy was higher
do not specifically address the efficacy of SDD in patients who in the HES group (7.0% vs. 5.8%; relative risk [RR], 1.21;
present with sepsis, but some do (116–118). 95% confidence interval [CI], 1.00−1.45; p = 0.04) (124).
Oral CHG is relatively easy to administer, decreases risk of A meta-analysis of 56 randomized trials found no overall
nosocomial infection, and reduces the potential concern over difference in mortality between crystalloids and artificial
promotion of antimicrobial resistance by SDD regimens. This colloids (modified gelatins, HES, dextran) when used for
remains a subject of considerable debate, despite the recent initial fluid resuscitation (125). Information from 3 ran-
evidence that the incidence of antimicrobial resistance does domized trials (n = 704 patients with severe sepsis/septic
not change appreciably with current SDD regimens (119–121). shock) did not show survival benefit with use of heta-,
The grade 2B was designated for both SOD and CHG as it hexa-, or pentastarches compared to other fluids (RR, 1.15;
was felt that risk was lower with CHG and the measure better 95% CI, 0.95−1.39; random effect; I2 = 0%) (126–128).
accepted despite less published literature than with SOD. However, these solutions increased the risk of acute kidney
Supplemental Digital Content 3 (http://links.lww.com/ injury (RR, 1.60; 95% CI, 1.26−2.04; I2 = 0%) (126–128).
CCM/A615) shows a GRADEpro Summary of Evidence Table The evidence of harm observed in the 6S and CHEST stud-
for the use of topical digestive tract antibiotics and CHG for ies and the meta-analysis supports a high-level recommen-
prophylaxis against VAP. dation advising against the use of HES solutions in patients
with severe sepsis and septic shock, particularly since other
Hemodynamic Support and Adjunctive Therapy options for fluid resuscitation exist. The CRYSTAL trial,
(Table 6) another large prospective clinical trial comparing crystal-
loids and colloids, was recently completed and will provide
G. Fluid Therapy of Severe Sepsis
additional insight into HES fluid resuscitation.
1. We recommend crystalloids be used as the initial fluid of The SAFE study indicated that albumin administration
choice in the resuscitation of severe sepsis and septic shock was safe and equally as effective as 0.9% saline (129). A
(grade 1B). meta-analysis aggregated data from 17 randomized trials
2. We recommend against the use of hydroxyethyl starches (n = 1977) of albumin vs. other fluid solutions in patients
(HES) for fluid resuscitation of severe sepsis and septic with severe sepsis/septic shock (130); 279 deaths occurred
shock (grade 1B). (This recommendation is based on the among 961 albumin-treated patients vs. 343 deaths among
results of the VISEP [128], CRYSTMAS [122], 6S [123], 1.016 patients treated with other fluids, thus favor-
and CHEST [124] trials. The results of the recently com- ing albumin (odds ratio [OR], 0.82; 95% CI, 0.67−1.00;
pleted CRYSTAL trial were not considered.) I2 = 0%). When albumin-treated patients were compared
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4. We recommend an initial fluid challenge in patients is a fundamental aspect of the hemodynamic management of
with sepsis-induced tissue hypoperfusion with suspi- patients with septic shock and should ideally be achieved before
cion of hypovolemia to achieve a minimum of 30 mL/ vasopressors and inotropes are used; however, using vasopres-
kg of crystalloids (a portion of this may be albumin sors early as an emergency measure in patients with severe shock
equivalent). More rapid administration and greater is frequently necessary, as when diastolic blood pressure is too
amounts of fluid may be needed in some patients (see Ini- low. When that occurs, great effort should be directed to wean-
tial Resuscitation recommendations) (grade 1C). ing vasopressors with continuing fluid resuscitation.
2. We recommend norepinephrine as the first-choice vaso-
5. We recommend that a fluid challenge technique be applied
pressor (grade 1B).
wherein fluid administration is continued as long as there is
3. We suggest epinephrine (added to and potentially sub-
hemodynamic improvement either based on dynamic (eg,
stituted for norepinephrine) when an additional agent is
change in pulse pressure, stroke volume variation) or static
needed to maintain adequate blood pressure (grade 2B).
(eg, arterial pressure, heart rate) variables (UG).
4. Vasopressin (up to 0.03 U/min) can be added to nor-
Rationale. Dynamic tests to assess patients’ responsiveness to epinephrine with the intent of raising MAP to target or
fluid replacement have become very popular in recent years in decreasing norepinephrine dosage (UG).
the ICU (131). These tests are based on monitoring changes in 5. Low-dose vasopressin is not recommended as the single ini-
stroke volume during mechanical ventilation or after passive leg tial vasopressor for treatment of sepsis-induced hypoten-
raising in spontaneously breathing patients. A systematic review sion, and vasopressin doses higher than 0.03–0.04 U/min
(29 trials, n = 685 critically ill patients) looked at the association should be reserved for salvage therapy (failure to achieve an
between stroke volume variation, pulse pressure variation, and/ adequate MAP with other vasopressor agents) (UG).
or stroke volume variation and the change in stroke volume/ 6. We suggest dopamine as an alternative vasopressor agent to
cardiac index after a fluid or positive end-expiratory pressure norepinephrine only in highly selected patients (eg, patients
challenge (132). The diagnostic OR of fluid responsiveness was with low risk of tachyarrhythmias and absolute or relative
59.86 (14 trials, 95% CI, 23.88−150.05) and 27.34 (five trials, bradycardia) (grade 2C).
95% CI, 3.46−55.53) for the pulse pressure variation and the 7. Phenylephrine is not recommended in the treatment of sep-
stroke volume variation, respectively. Utility of pulse pressure tic shock except in the following circumstances: (a) norepi-
variation and stroke volume variation is limited in the presence nephrine is associated with serious arrhythmias, (b) cardiac
of atrial fibrillation, spontaneous breathing, and low pressure output is known to be high and blood pressure persistently
support breathing. These techniques generally require sedation. low, or (c) as salvage therapy when combined inotrope/
H. Vasopressors vasopressor drugs and low-dose vasopressin have failed to
achieve the MAP target (grade 1C).
1. We recommend that vasopressor therapy initially target a
MAP of 65 mm Hg (grade 1C). Rationale. The physiologic effects of vasopressor and com-
bined inotrope/vasopressors selection in septic shock are set out
Rationale. Vasopressor therapy is required to sustain life in an extensive number of literature entries (135–147). Table 7
and maintain perfusion in the face of life-threatening hypoten- depicts a GRADEpro Summary of Evidence Table comparing
sion, even when hypovolemia has not yet been resolved. Below dopamine and norepinephrine in the treatment of septic shock.
a threshold MAP, autoregulation in critical vascular beds can be Dopamine increases MAP and cardiac output, primarily due
lost, and perfusion can become linearly dependent on pressure. to an increase in stroke volume and heart rate. Norepinephrine
Thus, some patients may require vasopressor therapy to achieve increases MAP due to its vasoconstrictive effects, with little
a minimal perfusion pressure and maintain adequate flow (133, change in heart rate and less increase in stroke volume compared
134). The titration of norepinephrine to a MAP as low as 65 mm with dopamine. Norepinephrine is more potent than dopamine
Hg has been shown to preserve tissue perfusion (134). Note that and may be more effective at reversing hypotension in patients
the consensus definition of sepsis-induced hypotension for use with septic shock. Dopamine may be particularly useful in
of MAP in the diagnosis of severe sepsis is different (MAP patients with compromised systolic function but causes more
70 mm Hg) from the evidence-based target of 65 mm Hg used in tachycardia and may be more arrhythmogenic than norepi-
this recommendation. In any case, the optimal MAP should be nephrine (148). It may also influence the endocrine response via
individualized as it may be higher in patients with atherosclero- the hypothalamic pituitary axis and have immunosuppressive
sis and/or previous hypertension than in young patients without effects. However, information from five randomized trials (n =
cardiovascular comorbidity. For example, a MAP of 65 mm Hg 1993 patients with septic shock) comparing norepinephrine to
might be too low in a patient with severe uncontrolled hyperten- dopamine does not support the routine use of dopamine in the
sion; in a young, previously normotensive patient, a lower MAP management of septic shock (136, 149–152). Indeed, the rela-
might be adequate. Supplementing endpoints, such as blood tive risk of short-term mortality was 0.91 (95% CI, 0.84−1.00;
pressure, with assessment of regional and global perfusion, such fixed effect; I2 = 0%) in favor of norepinephrine. A recent meta-
as blood lactate concentrations, skin perfusion, mental status, analysis showed dopamine was associated with an increased risk
and urine output, is important. Adequate fluid resuscitation (RR, 1.10 [1.01−1.20]; p = 0.035); in the two trials that reported
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Table 7. Norepinephrine Compared With Dopamine in Severe Sepsis Summary of Evidence
Norepinephrine compared with dopamine in severe sepsis
Patient or population: Patients with severe sepsis
Settings: Intensive care unit
Intervention: Norepinephrine
Comparison: Dopamine
Sources: Analysis performed by Djillali Annane for Surviving Sepsis Campaign using following publications: De Backer D. N Engl J
Med 2010; 362:779–789; Marik PE. JAMA 1994; 272:1354–1357; Mathur RDAC. Indian J Crit Care Med 2007; 11:186–191;
Martin C. Chest 1993; 103:1826–1831; Patel GP. Shock 2010; 33:375–380; Ruokonen E. Crit Care Med 1993; 21:1296–1303
Illustrative Comparative Risksa
(95% CI) Quality
Relative No. of of the
Assumed Corresponding Effect Participants Evidence
Outcomes Risk Risk (95% CI) (Studies) (GRADE) Comments
Dopamine Norepinephrine
Short-term mortality Study population RR 0.91 2043 (6 studies) ⊕⊕⊕
(0.83 to 0.99) moderateb,c
530 per 1000 482 per 1000 (440 to 524)
Serious adverse events Study population RR 0.47 1931 (2 studies) ⊕⊕⊕
−Supraventricular (0.38 to 0.58) moderateb,c
arrhythmias 229 per 1000 82 per 1000 (34 to 195)
Serious adverse Study population RR 0.35 1931 (2 studies) ⊕⊕⊕
events −Ventricular (0.19 to 0.66) moderateb,c
arrhythmias 39 per 1000 15 per 1000 (8 to 27)
a
The assumed risk is the control group risk across studies. The corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group and
the relative effect of the intervention (and its 95% CI). CI = confidence interval, RR = risk ratio.
b
Strong heterogeneity in the results (I2 = 85%), however this reflects degree of effect, not direction of effect. We have decided not to lower the evidence quality.
c
Effect results in part from hypovolemic and cardiogenic shock patients in De Backer, N Engl J Med 2010. We have lowered the quality of evidence one level for
indirectness.
arrhythmias, these were more frequent with dopamine than has similar effects but is long acting (164). Studies show that
with norepinephrine (RR, 2.34 [1.46−3.77]; p = 0.001) (153). vasopressin concentrations are elevated in early septic shock, but
Although some human and animal studies suggest decrease to normal range in the majority of patients between 24
epinephrine has deleterious effects on splanchnic circulation and 48 hrs as shock continues (165). This has been called relative
and produces hyperlactatemia, no clinical evidence shows that vasopressin deficiency because in the presence of hypotension,
epinephrine results in worse outcomes, and it should be the vasopressin would be expected to be elevated. The significance
first alternative to norepinephrine. Indeed, information from of this finding is unknown. The VASST trial, an RCT comparing
4 randomized trials (n = 540) comparing norepinephrine norepinephrine alone to norepinephrine plus vasopressin at
to epinephrine found no evidence for differences in the risk 0.03 U/min, showed no difference in outcome in the intent-to-
of dying (RR, 0.96; CI, 0.77−1.21; fixed effect; I2 = 0%) (142, treat population (166). An a priori defined subgroup analysis
147, 154, 155). Epinephrine may increase aerobic lactate demonstrated that survival among patients receiving 15 µg/
production via stimulation of skeletal muscles’ β2-adrenergic min norepinephrine at the time of randomization was better
receptors and thus may prevent the use of lactate clearance to with the addition of vasopressin; however, the pretrial rationale
guide resuscitation. With its almost pure α-adrenergic effects, for this stratification was based on exploring potential benefit in
phenylephrine is the adrenergic agent least likely to produce the population requiring ≥ 15 µg/min norepinephrine. Higher
tachycardia, but it may decrease stroke volume and is therefore doses of vasopressin have been associated with cardiac, digital,
not recommended for use in the treatment of septic shock except and splanchnic ischemia and should be reserved for situations
in circumstances where norepinephrine is: a) associated with where alternative vasopressors have failed (167). Information
serious arrhythmias, or b) cardiac output is known to be high, or from seven trials (n = 963 patients with septic shock) comparing
c) as salvage therapy when other vasopressor agents have failed norepinephrine with vasopressin (or terlipressin) does not
to achieve target MAP (156). Vasopressin levels in septic shock support the routine use of vasopressin or its analog terlipressin
have been reported to be lower than anticipated for a shock state (93, 95, 97, 99, 159, 161, 164, 166, 168–170). Indeed, the relative
(157). Low doses of vasopressin may be effective in raising blood risk of dying was 1.12 (95% CI, 0.96−1.30; fixed effects; I2 = 0%).
pressure in patients, refractory to other vasopressors and may However, the risk of supraventricular arrhythmias was increased
have other potential physiologic benefits (158–163). Terlipressin with norepinephrine (RR, 7.25; 95% CI, 2.30−22.90; fixed effect;
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I2 = 0%). Cardiac output measurement targeting maintenance J. Corticosteroids
of a normal or elevated flow is desirable when these pure
1. We suggest not using intravenous hydrocortisone as a treat-
vasopressors are instituted.
ment of adult septic shock patients if adequate fluid resus-
8. We recommend that low-dose dopamine not be used for citation and vasopressor therapy are able to restore hemo-
renal protection (grade 1A). dynamic stability (see goals for Initial Resuscitation). If this
is not achievable, we suggest intravenous hydrocortisone
Rationale. A large randomized trial and meta-analysis com-
alone at a dose of 200 mg per day (grade 2C).
paring low-dose dopamine to placebo found no difference in
either primary outcomes (peak serum creatinine, need for renal Rationale. The response of septic shock patients to fluid
replacement, urine output, time to recovery of normal renal and vasopressor therapy seems to be an important factor in
function) or secondary outcomes (survival to either ICU or selection of patients for optional hydrocortisone therapy. One
hospital discharge, ICU stay, hospital stay, arrhythmias) (171, French multicenter RCT of patients in vasopressor-unrespon-
172). Thus, the available data do not support administration of sive septic shock (hypotension despite fluid resuscitation and
low doses of dopamine solely to maintain renal function. vasopressors for more than 60 mins) showed significant shock
9. We recommend that all patients requiring vasopressors have reversal and reduction of mortality rate in patients with rela-
an arterial catheter placed as soon as practical if resources tive adrenal insufficiency (defined as postadrenocorticotropic
are available (UG). hormone [ACTH] cortisol increase ≤ 9 µg/dL) (175). Two
smaller RCTs also showed significant effects on shock reversal
Rationale. In shock states, estimation of blood pressure with steroid therapy (176, 177). In contrast, a large, European
using a cuff is commonly inaccurate; use of an arterial cannula multicenter trial (CORTICUS) that enrolled patients without
provides a more appropriate and reproducible measurement sustained shock and had a lower risk of death than the French
of arterial pressure. These catheters also allow continuous trial failed to show a mortality benefit with steroid therapy
analysis so that decisions regarding therapy can be based on (178). Unlike the French trial that only enrolled shock patients
immediate and reproducible blood pressure information. with blood pressure unresponsive to vasopressor therapy, the
CORTICUS study included patients with septic shock regard-
I. Inotropic Therapy less of how the blood pressure responded to vasopressors; the
1. We recommend that a trial of dobutamine infusion up to study baseline (placebo) 28-day mortality rate was 61% and
20 μg/kg/min be administered or added to vasopressor (if 31%, respectively. The use of the ACTH test (responders and
in use) in the presence of: a) myocardial dysfunction, as nonresponders) did not predict the faster resolution of shock.
suggested by elevated cardiac filling pressures and low car- In recent years, several systematic reviews have examined the
diac output, or b) ongoing signs of hypoperfusion, despite use of low-dose hydrocortisone in septic shock with contradic-
achieving adequate intravascular volume and adequate tory results: Annane et al (179) analyzed the results of 12 stud-
MAP (grade 1C). ies and calculated a significant reduction in 28-day mortality
2. We recommend against the use of a strategy to increase car- with prolonged low-dose steroid treatment in adult septic
diac index to predetermined supranormal levels (grade 1B). shock patients (RR, 0.84; 95% CI, 0.72−0.97; p = 0.02) (180).
Rationale. Dobutamine is the first choice inotrope for patients In parallel, Sligl and colleagues (180) used a similar technique,
with measured or suspected low cardiac output in the presence of but only identified eight studies for their meta-analysis, six
adequate left ventricular filling pressure (or clinical assessment of of which had a high-level RCT design with low risk of bias
adequate fluid resuscitation) and adequate MAP. Septic patients (181). In contrast to the aforementioned review, this analysis
who remain hypotensive after fluid resuscitation may have low, revealed no statistically significant difference in mortality (RR,
normal, or increased cardiac outputs. Therefore, treatment with 1.00; 95% CI, 0.84−1.18). Both reviews, however, confirmed
a combined inotrope/vasopressor, such as norepinephrine or the improved shock reversal by using low-dose hydrocortisone
epinephrine, is recommended if cardiac output is not measured. (180, 181). A recent review on the use of steroids in adult sep-
When the capability exists for monitoring cardiac output in addi- tic shock underlined the importance of selection of studies for
tion to blood pressure, a vasopressor, such as norepinephrine, may systematic analysis (181) and identi ed only 6 high-level RCTs
fi
be used separately to target specific levels of MAP and cardiac as adequate for systematic review (175–178, 182, 183). When
output. Large prospective clinical trials, which included critically only these six studies are analyzed, we found that in “low risk”
ill ICU patients who had severe sepsis, failed to demonstrate ben- patients from three studies (ie, those with a placebo mortal-
efit from increasing oxygen delivery to supranormal targets by use ity rate of less than 50%, which represents the majority of all
of dobutamine (173, 174). These studies did not specifically tar- patients), hydrocortisone failed to show any benefit on out-
get patients with severe sepsis and did not target the first 6 hrs of come (RR, 1.06). The minority of patients from the remain-
resuscitation. If evidence of tissue hypoperfusion persists despite ing three studies, who had a placebo mortality of greater than
adequate intravascular volume and adequate MAP, a viable alter- 60%, showed a nonsignificant trend to lower mortality by using
native (other than reversing underlying insult) is to add inotropic hydrocortisone (see Supplemental Digital Content 4, http://
therapy. links.lww.com/CCM/A615, Summary of Evidence Table).
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conditions. Patients with severe sepsis and septic shock may L. Immunoglobulins
have coexisting conditions that meet indications for the use
1. We suggest not using intravenous immunoglobulins in
of erythropoietin.
adult patients with severe sepsis or septic shock (grade 2B).
3. We suggest that fresh frozen plasma not be used to correct
Rationale. One larger multicenter RCT (n = 624) (210) in
laboratory clotting abnormalities in the absence of bleeding adult patients and one large multinational RCT in infants with
or planned invasive procedures (grade 2D). neonatal sepsis (n = 3493) (211) found no benefit for intravenous
Rationale. Although clinical studies have not assessed the immunoglobulin (IVIG). (For more on this trial, see the section,
impact of transfusion of fresh frozen plasma on outcomes in Pediatric Considerations.). A meta-analysis by the Cochrane col-
critically ill patients, professional organizations have recom- laboration, which did not include this most recent RCT, iden-
mended it for coagulopathy when there is a documented defi- tified 10 polyclonal IVIG trials (n = 1430) and seven trials on
ciency of coagulation factors (increased prothrombin time, immunoglobulin (Ig) M-enriched polyclonal IVIG (n = 528)
international normalized ratio, or partial thromboplastin time) (212). Compared with placebo, IVIG resulted in a significant
and the presence of active bleeding or before surgical or invasive reduction in mortality (RR, 0.81 and 95% CI, 0.70−0.93; and RR,
procedures (200–203). In addition, transfusion of fresh frozen 0.66 and 95% CI, 0.51−0.85, respectively). Also the subgroup of
plasma usually fails to correct the prothrombin time in non- IgM-enriched IVIGs (n = 7 trials) showed a significant reduc-
bleeding patients with mild abnormalities (204, 205). No studies tion in mortality rates compared with placebo (RR, 0.66; 95%
suggest that correction of more severe coagulation abnormali- CI, 0.51−0.85). Trials with low risk of bias showed no reduction
ties benefits patients who are not bleeding. in mortality with polyclonal IVIG (RR, 0.97; 95% CI, 0.81−1.15;
five trials, n = 945). Three of these trials (210, 213, 214) used stan-
4. We recommend against antithrombin administration for dard polyclonal IVIG and two IgM-enriched IVIG (215, 216).
the treatment of severe sepsis and septic shock (grade 1B). These findings are in accordance with those of two older
Rationale. A phase III clinical trial of high-dose antithrom- meta-analyses (217, 218) from other Cochrane authors. One
bin did not demonstrate any beneficial effect on 28-day all- systematic review (217) included a total of 21 trials and showed
cause mortality in adults with severe sepsis and septic shock. a relative risk of death of 0.77 with immunoglobulin treatment
High-dose antithrombin was associated with an increased risk (95% CI, 0.68−0.88); however, the results of only high-quality
of bleeding when administered with heparin (206). Although trials (total of 763 patients) showed a relative risk of 1.02 (95%
a post hoc subgroup analysis of patients with severe sepsis and CI, 0.84−1.24). Similarly, Laupland et al (218) found a significant
reduction in mortality with the use of IVIG treatment (OR, 0.66;
high risk of death showed better survival in patients receiving
95% CI, 0.53−0.83; p 0.005). When only high-quality studies
antithrombin, this agent cannot be recommended until further
were pooled, the OR for mortality was 0.96 (95% CI, 0.71−1.3;
clinical trials are performed (207).
p = 0.78). Two meta-analyses, which used less strict criteria to
5. In patients with severe sepsis, we suggest that platelets be identify sources of bias or did not state their criteria for the
administered prophylactically when counts are ≤ 10,000/ assessment of study quality, found significant improvement in
mm3 (10 × 109/L) in the absence of apparent bleeding, patient mortality with IVIG treatment (219, 220). In contrast
as well when counts are ≤ 20,000/mm3 (20 × 109/L) if the to the most recent Cochrane review, Kreymann et al (219) clas-
patient has a significant risk of bleeding. Higher platelet sified five studies that investigated IgM-enriched preparation as
counts (≥ 50,000/mm3 [50 × 109/L]) are advised for active high-quality studies, combining studies in adults and neonates,
bleeding, surgery, or invasive procedures (grade 2D). and found an OR for mortality of 0.5 (95% CI, 0.34−0.73).
Most IVIG studies are small, some have methodological
Rationale. Guidelines for transfusion of platelets are derived flaws; the only large study (n = 624) showed no effect (210).
from consensus opinion and experience in patients with Subgroup effects between IgM-enriched and nonenriched for-
chemotherapy-induced thrombocytopenia. Patients with severe mulations reveal substantial heterogeneity. In addition, indi-
sepsis are likely to have some limitation of platelet production similar rectness and publication bias were considered in grading this
to that in chemotherapy-treated patients, but they also are likely to recommendation. The low-quality evidence led to the grading
have increased platelet consumption. Recommendations take into as a weak recommendation. The statistical information that
account the etiology of thrombocytopenia, platelet dysfunction, comes from the high-quality trials does not support a benefi-
risk of bleeding, and presence of concomitant disorders (200, 202, cial effect of polyclonal IVIG. We encourage conducting large
203, 208, 209). Factors that may increase the bleeding risk and multicenter studies to further evaluate the effectiveness of
indicate the need for a higher platelet count are frequently present other polyclonal immunoglobulin preparations given intrave-
in patients with severe sepsis. Sepsis itself is considered to be a nously in patients with severe sepsis.
risk factor for bleeding in patients with chemotherapy-induced
thrombocytopenia. Other factors considered to increase the risk of
M. Selenium
bleeding in patients with severe sepsis include temperature higher
than 38°C, recent minor hemorrhage, rapid decrease in platelet 1. We suggest not using intravenous selenium to treat severe
count, and other coagulation abnormalities (203, 208, 209). sepsis (grade 2C).
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Table 8. Recommendations: Other Supportive Therapy of Severe Sepsis
K. Blood Product Administration
1. Once tissue hypoperfusion has resolved and in the absence of extenuating circumstances, such as myocardial ischemia, severe
hypoxemia, acute hemorrhage, or ischemic heart disease, we recommend that red blood cell transfusion occur only when
hemoglobin concentration decreases to 7.0 g/dL to target a hemoglobin concentration of 7.0 –9.0 g/dL in adults (grade 1B).
2. Not using erythropoietin as a specific treatment of anemia associated with severe sepsis (grade 1B).
3. Fresh frozen plasma not be used to correct laboratory clotting abnormalities in the absence of bleeding or planned invasive
procedures (grade 2D).
4. Not using antithrombin for the treatment of severe sepsis and septic shock (grade 1B).
5. In patients with severe sepsis, administer platelets prophylactically when counts are 10,000/mm3 (10 x 109/L) in the absence
of apparent bleeding. We suggest prophylactic platelet transfusion when counts are 20,000/mm3 (20 x 109/L) if the patient
has a significant risk of bleeding. Higher platelet counts (≥50,000/mm3 [50 x 109/L]) are advised for active bleeding, surgery,
or invasive procedures (grade 2D).
L. Immunoglobulins
1. Not using intravenous immunoglobulins in adult patients with severe sepsis or septic shock (grade 2B).
M. Selenium
1. Not using intravenous selenium for the treatment of severe sepsis (grade 2C).
N. History of Recommendations Regarding Use of Recombinant Activated Protein C (rhAPC)
A history of the evolution of SSC recommendations as to rhAPC (no longer available) is provided.
O. Mechanical Ventilation of Sepsis-Induced Acute Respiratory Distress Syndrome (ARDS)
1. Target a tidal volume of 6 mL/kg predicted body weight in patients with sepsis-induced ARDS (grade 1A vs. 12 mL/kg).
2. Plateau pressures be measured in patients with ARDS and initial upper limit goal for plateau pressures in a passively inflated
lung be ≤30 cm H2O (grade 1B).
3. Positive end-expiratory pressure (PEEP) be applied to avoid alveolar collapse at end expiration (atelectotrauma) (grade 1B).
4. Strategies based on higher rather than lower levels of PEEP be used for patients with sepsis- induced moderate or severe
ARDS (grade 2C).
5. Recruitment maneuvers be used in sepsis patients with severe refractory hypoxemia (grade 2C).
6. Prone positioning be used in sepsis-induced ARDS patients with a Pao2/Fio2 ratio ≤ 100 mm Hg in facilities that have
experience with such practices (grade 2B).
7. That mechanically ventilated sepsis patients be maintained with the head of the bed elevated to 30-45 degrees to limit
aspiration risk and to prevent the development of ventilator-associated pneumonia (grade 1B).
8. That noninvasive mask ventilation (NIV) be used in that minority of sepsis-induced ARDS patients in whom the benefits of NIV
have been carefully considered and are thought to outweigh the risks (grade 2B).
9. That a weaning protocol be in place and that mechanically ventilated patients with severe sepsis undergo spontaneous
breathing trials regularly to evaluate the ability to discontinue mechanical ventilation when they satisfy the following criteria: a)
arousable; b) hemodynamically stable (without vasopressor agents); c) no new potentially serious conditions; d) low ventilatory
and end-expiratory pressure requirements; and e) low Fio2 requirements which can be met safely delivered with a face mask or
nasal cannula. If the spontaneous breathing trial is successful, consideration should be given for extubation (grade 1A).
0. Against the routine use of the pulmonary artery catheter for patients with sepsis-induced ARDS (grade 1A).
1
1. A conservative rather than liberal fluid strategy for patients with established sepsis-induced ARDS who do not have evidence of
1
tissue hypoperfusion (grade 1C).
12. In the absence of specific indications such as bronchospasm, not using beta 2-agonists for treatment of sepsis-induced ARDS (grade 1B).
P. Sedation, Analgesia, and Neuromuscular Blockade in Sepsis
1. Continuous or intermittent sedation be minimized in mechanically ventilated sepsis patients, targeting specific titration endpoints (grade 1B).
2. Neuromuscular blocking agents (NMBAs) be avoided if possible in the septic patient without ARDS due to the risk of
prolonged neuromuscular blockade following discontinuation. If NMBAs must be maintained, either intermittent bolus as
required or continuous infusion with train-of-four monitoring of the depth of blockade should be used (grade 1C).
(Continued)
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![Dellinger et al
Rationale. Although NMBAs are often administered to total dose of NMBAs and shorter intubation times) also may
critically ill patients, their role in the ICU is not well defined. exist, although this has not been studied formally.
No evidence exists that neuromuscular blockade in this patient Q. Glucose Control
population reduces mortality or major morbidity. In addition,
1. We recommend a protocolized approach to blood glucose
no studies have been published that specifically address the use
management in ICU patients with severe sepsis, commenc-
of NMBAs in septic patients.
ing insulin dosing when two consecutive blood glucose lev-
The most common indication for NMBA use in the ICU is
els are 180 mg/dL. This approach should target an upper
to facilitate mechanical ventilation (314). When appropriately
blood glucose level ≤ 180 mg/dL rather than an upper target
used, these agents may improve chest wall compliance, prevent
blood glucose ≤ 110 mg/dL (grade 1A).
respiratory dyssynchrony, and reduce peak airway pressures
2. We recommend blood glucose values be monitored every 1
(315). Muscle paralysis may also reduce oxygen consumption
to 2 hrs until glucose values and insulin infusion rates are
by decreasing the work of breathing and respiratory muscle
stable, then every 4 hrs thereafter (grade 1C).
blood flow (316). However, a randomized, placebo-controlled 3. We recommend that glucose levels obtained with point-of-
clinical trial in patients with severe sepsis demonstrated that care testing of capillary blood be interpreted with caution,
oxygen delivery, oxygen consumption, and gastric intramuco- as such measurements may not accurately estimate arterial
sal pH were not improved during deep neuromuscular block- blood or plasma glucose values (UG).
ade (317).
A recent randomized clinical trial of continuous infusions Rationale. One large RCT single-center trial in a predomi-
of cisatracurium in patients with early ARDS and a Pao2/Fio2 nantly cardiac surgical ICU demonstrated a reduction in ICU
150 mm Hg showed improved adjusted survival rates and mortality with intensive intravenous insulin (Leuven protocol)
more organ failure-free days without an increased risk in ICU- targeting blood glucose to 80 to 110 mg/dL (326). A second
acquired weakness compared with placebo-treated patients randomized trial of intensive insulin therapy using the Leuven
(318). The investigators used a high fixed dose of cisatracurium protocol enrolled medical ICU patients with an anticipated
without train-of-four monitoring, and half of the patients in the ICU length of stay of more than 3 days in three medical ICUs
placebo group received at least a single dose of NMBA. Whether and overall mortality was not reduced (327).
another NMBA would have similar effects is unknown. Although Since these studies (326, 327) and the previous Surviving
many of the patients enrolled into this trial appeared to meet Sepsis Guidelines (7) appeared, several RCTs (128, 328–332)
and meta-analyses (333–337) of intensive insulin therapy have
sepsis criteria, it is not clear whether similar results would occur
been performed. The RCTs studied mixed populations of sur-
in sepsis patients. A GRADEpro Summary of Evidence Table
gical and medical ICU patients (128, 328–332) and found that
regarding use of NMBA in ARDS appears in Supplemental
intensive insulin therapy did not significantly decrease mortality
Digital Content 5 (http://links.lww.com/CCM/A615).
(128, 328–332), whereas the NICE-SUGAR trial demonstrated
An association between NMBA use and myopathies and
an increased mortality (331). All studies (128, 326–332) reported
neuropathies has been suggested by case studies and prospec-
a much higher inci ence of severe hypoglycemia (glucose ≤ 40
d
tive observational studies in the critical care population (315,
mg/dL) (6%−29%) with intensive insulin therapy. Several meta-
319–322), but the mechanisms by which NMBAs produce or analyses confirmed that intensive insulin therapy was not associ-
contribute to myopathies and neuropathies in these patients ated with a mortality benefit in surgical, medical, or mixed ICU
are unknown. Although no studies are specific to the septic patients (333, 335, 337). The meta-analysis by Griesdale and col-
patient population, it seems clinically prudent, based on exist- leagues (334), using between-trial comparisons driven mainly by
ing knowledge, that NMBAs not be administered unless there the 2001 study by van den Berghe et al (326), found that inten-
is a clear indication for neuromuscular blockade that cannot be sive insulin therapy was beneficial in surgical ICU patients (risk
safely achieved with appropriate sedation and analgesia (315). ratio, 0.63 [0.44−0.9]), whereas the meta-analysis by Friedrich
Only one prospective RCT has compared peripheral et al (336), using within-trial comparisons, showed no benefit
nerve stimulation and standard clinical assessment in ICU for surgical patients in mixed medical-surgical ICUs (risk ratio
patients. Rudis et al (323) randomized 77 critically ill ICU 0.99 [0.82−1.11]) and no subgroup of surgical patients who ben-
patients requiring neuromuscular blockade to receive dosing efited from intensive insulin therapy. Interestingly, the RCTs that
of vecuronium based on train-of-four stimulation or on clini- reported (326, 327) compared intensive insulin therapy to high
cal assessment (control group). The peripheral nerve stimu- controls (180−200 mg/dL) (OR, 0.89 [0.73−1.09]), whereas those
lation group received less drug and recovered neuromuscular that did not demonstrate benefit (330–332) compared intensive
function and spontaneous ventilation faster than the control therapy to moderate controls (108−180 mg/dL) [OR, 1.14 (1.02
group. Nonrandomized observational studies have suggested to −1.26)]. See Supplemental Digital Content 6 (http://links.
that peripheral nerve monitoring reduces or has no effect on lww.com/CCM/A615) for details.
clinical recovery from NMBAs in the ICU (324, 325). The trigger to start an insulin protocol for blood glucose
Benefits to neuromuscular monitoring, including faster levels 180 mg/dL with an upper target blood glucose level
recovery of neuromuscular function and shorter intubation 180 mg/dL derives from the NICE-SUGAR study (331),
times, appear to exist. A potential for cost savings (reduced which used these values for initiating and stopping therapy. The
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![Dellinger et al
dose for continuous renal replacement therapy would be 20 to hemodynamically compromised patient) are dire. Therefore,
25 mL/kg/hr of effluent generation. prevention of VTE is highly desirable, especially if it can be
done safely and effectively.
Prophylaxis is generally effective. In particular, nine placebo-
S. Bicarbonate Therapy
controlled RCTs of VTE prophylaxis have been conducted in
1. We recommend against the use of sodium bicarbonate ther- general populations of acutely ill patients (381–389). All trials
apy for the purpose of improving hemodynamics or reduc- showed reduction in DVT or pulmonary embolism, a benefit
ing vasopressor requirements in patients with hypoperfu- that is also supported by meta-analyses (390, 391). Thus, the
sion-induced lactic acidemia with pH ≥ 7.15 (grade 2B). evidence strongly supports the value of VTE prophylaxis (grade
1A). The prevalence of infection/sepsis was 17% in those studies
Rationale. Although bicarbonate therapy may be useful in
in which this could be ascertained. One study investigated only
limiting tidal volume in ARDS in some situations of permissive
ICU patients only, and 52% of those enrolled had infection/
hypercapnia (see section, Mechanical Ventilation of ARDS), no
sepsis. The need to extrapolate from general, acutely ill patients
evidence supports the use of bicarbonate therapy in the treat-
to critically ill patients to septic patients downgrades the
ment of hypoperfusion-induced lactic acidemia associated with
evidence. That the effect is pronounced and the data are robust
sepsis. Two blinded, crossover RCTs that compared equimolar
somewhat mitigate against the extrapolation, leading to a grade
saline and bicarbonate in patients with lactic acidosis failed to
B determination. Because the patient’s risk of administration is
reveal any difference in hemodynamic variables or vasopressor
small, the gravity of not administering may be great, and the
requirements (378, 379). The number of patients with 7.15 pH
cost is low, the strength of the recommendation is strong (1).
in these studies was small. Bicarbonate administration has been
Deciding how to provide prophylaxis is decidedly more
associated with sodium and fluid overload, an increase in lac-
difficult. The Canadian Critical Care Trials Group compared
tate and Pco2, and a decrease in serum ionized calcium, but the
UFH (5000 IU twice daily) to LMWH (dalteparin, 5000
relevance of these variables to outcome is uncertain. The effect
IU once per day and a second placebo injection to ensure
of bicarbonate administration on hemodynamics and vasopres-
parallel-group equivalence) (392). No statistically signifi-
sor requirements at lower pH, as well as the effect on clinical
cant difference in asymptomatic DVTs was found between
outcomes at any pH, is unknown. No studies have examined the
the two groups (hazard ratio, 0.92; 95% CI, 0.68−1.23; p =
effect of bicarbonate administration on outcomes.
0.57), but the proportion of patients diagnosed with pul-
T. Deep Vein Thrombosis Prophylaxis monary embolism on CT scan, high-probability ventila-
tion perfusion scan, or autopsy was significantly lower in
1. We recommend that patients with severe sepsis receive
the LMWH group (hazard ratio, 0.51; 95% CI, 0.30−0.88;
daily pharmacoprophylaxis against venous thromboembo-
p = 0.01).The study did not account for the use of other forms
lism (VTE) (grade 1B). We recommend that this be accom-
of LMWH. These data suggest that LMWH (dalteparin) is
plished with daily subcutaneous low-molecular weight
the treatment of choice over UFH administered twice daily
heparin (LMWH) (grade 1B versus unfractionated heparin
in critically ill patients. Also, because the study included sep-
[UFH] twice daily and grade 2C versus UFH given thrice
tic patients, the evidence supporting the use of dalteparin over
daily). If creatinine clearance is 30 mL/min, we recom-
twice daily UFH in critically ill, and perhaps septic, patients is
mend use of dalteparin (grade 1A) or another form of
strong. Similarly, a meta-analysis of acutely ill, general medical
LMWH that has a low degree of renal metabolism (grade
patients comparing UFH twice and thrice daily demonstrated
2C) or UFH (grade 1A).
that the latter regimen was more effective at preventing VTE,
2. We suggest that patients with severe sepsis be treated with
but twice daily dosing produced less bleeding (393). Both criti-
a combination of pharmacologic therapy and intermit-
cally ill and septic patients were included in these analyses, but
tent pneumatic compression devices whenever possible
their numbers are unclear. Nonetheless, the quality of evidence
(grade 2C).
supporting the use of three times daily, as opposed to twice
3. We recommend that septic patients who have a contraindica-
daily, UFH dosing in preventing VTE in acutely ill medial c
tion to heparin use (eg, thrombocytopenia, severe coagulopathy,
patients is high (A). However, comparing LMWH to twice daily
active bleeding, recent intracerebral hemorrhage) not receive
UFH, or twice daily UFH to three times daily UFH, in sepsis
pharmacoprophylaxis (grade 1B). Rather we suggest they
requires extrapolation, downgrading the data. No data exist on
receive mechanical prophylactic treatment, such as graduated
direct comparison of LMWH to UFH administered three times
compression stockings or intermittent compression devices
daily, nor are there any studies directly comparing twice daily
(grade 2C), unless contraindicated. When the risk decreases, we
and thrice daily UFH dosing in septic or critically ill patients.
suggest starting pharmacoprophylaxis (grade 2C).
Therefore, it is not possible to state that LMWH is superior to
Rationale. ICU patients are at risk for deep vein thrombosis three times daily UFH or that three times daily dosing is supe-
(DVT) (380). It is logical that patients with severe sepsis would rior to twice daily administration in sepsis. This downgrades
be at a similar or higher risk than the general ICU population. the quality of the evidence and therefore the recommendation.
The consequences of VTE in the setting of sepsis (increased Douketis et al (394) conducted a study of 120 critically
risk of potentially fatal pulmonary emboli in an already ill patients with acute kidney injury (creatinine clearance
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![Special Article
30 mL/min) who received VTE prophylaxis with dalteparin Both old and new meta-analyses show prophylaxis-induced
5000 IU daily for between 4 and 14 days and had at least one reduction in clinically significant upper GI bleeding, which we
trough anti-factor Xa level measured. None of the patients consider significant even in the absence of proven mortality
had bio-accumulation (trough anti-factor Xa level lower than benefit (409–411). The benefit of prevention of upper GI
0.06 IU/mL). The incidence of major bleeding was somewhat bleeding must be weighed against the potential (unproven)
higher than in trials of other agents, but most other studies effect of increased stomach pH on a greater incidence of VAP
did not involve critically ill patients, in whom the bleeding risk and C. difficile infection (409, 412, 413). (See Supplemental
is higher. Further, bleeding did not correlate with detectable Digital Content 7 and 8 [http://links.lww.com/CCM/
trough levels (394). Therefore, we recommend that dalteparin A615], Summary of Evidence Tables for effects of treatments
can be administered to critically ill patients with acute renal on specific outcomes.) In an exploratory hypothesis, we
failure (A). Data on other LMWHs are lacking. Consequently, considered (as did the authors of the meta-analysis) (411) the
these forms should probably be avoided or, if used, anti-factor possibility of less benefit and more harm in prophylaxis among
Xa levels should be monitored (grade 2C). UFH is not renally patients receiving enteral nutrition but decided to provide one
cleared and is safe (grade 1A). recommendation while lowering the quality of evidence. The
Mechanical methods (intermittent compression devices and balance of benefits and risks may thus depend on the individual
graduated compression stockings) are recommended when patient’s characteristics as well as on the local epidemiology of
anticoagulation is contraindicated (395–397). A meta-analysis VAP and C. difficile infections. The rationale for considering
of 11 studies, including six RCTs, published in the Cochrane only suppression of acid production (and not sucralfate) is
Library concluded that the combination of pharmacologic and based on the study of 1,200 patients by Cook et al comparing
mechanical prophylaxis was superior to either modality alone H2 blockers and sucralfate (414). More recent meta-analyses
in preventing DVT and was better than compression alone provide low-quality evidence suggesting more effective GI
in preventing pulmonary embolism (398). This analysis did bleeding protection with the use of proton pump inhibitors
than with H2RA (415–417). Patients should be periodically
not focus on sepsis or critically ill patients but included stud-
evaluated for the continued need for prophylaxis.
ies of prophylaxis after orthopedic, pelvic, and cardiac surgery.
In addition, the type of pharmacologic prophylaxis varied,
V. Nutrition
including UFH, LMWH, aspirin, and warfarin. Nonetheless,
the minimal risk associated with compression devices lead 1. We suggest administering oral or enteral (if necessary) feed-
us to recommend combination therapy in most cases. In ings, as tolerated, rather than either complete fasting or pro-
very-high-risk patients, LMWH is preferred over UFH (392, vision of only intravenous glucose within the first 48 hrs
399–401). Patients receiving heparin should be monitored for after a diagnosis of severe sepsis/septic shock (grade 2C).
development of heparin-induced thrombocytopenia. These 2. We suggest avoiding mandatory full caloric feeding in the
recommendations are consistent with those developed by the first week, but rather suggest low-dose feeding (eg, up to
American College of Chest Physicians (402). 500 kcal per day), advancing only as tolerated (grade 2B).
3. We suggest using intravenous glucose and enteral nutrition
U. Stress Ulcer Prophylaxis rather than total parenteral nutrition (TPN) alone or paren-
teral nutrition in conjunction with enteral feeding in the first 7
1. We recommend that stress ulcer prophylaxis using H2 blocker days after a diagnosis of severe sepsis/septic shock (grade 2B).
or proton pump inhibitor be given to patients with severe 4. We suggest using nutrition with no specific immunomodulat-
sepsis/septic shock who have bleeding risk factors (grade 1B). ing supplementation in patients with severe sepsis (grade 2C).
2. When stress ulcer prophylaxis is used, we suggest the use of
proton pump inhibitors rather than H2 receptor antagonists Rationale. Early enteral nutrition has theoretical advan-
(H2RA) (grade 2C). tages in the integrity of gut mucosa and prevention of bacterial
3. We suggest that patients without risk factors should not translocation and organ dysfunction, but also concerning is the
receive prophylaxis (grade 2B). risk of ischemia, mainly in hemodynamically unstable patients.
Unfortunately, no clinical trial has specifically addressed
Rationale. Although no study has been performed specifi- early feeding in septic patients. Studies on different subpopula-
cally in patients with severe sepsis, trials confirming the benefit tions of critically ill patients, mostly surgical patients, are not
of stress ulcer prophylaxis in reducing upper gastrointestinal consistent, with great variability in the intervention and con-
(GI) bleeding in general ICU populations included 20% to 25% trol groups; all are of low methodological quality (418–427)
of patients with sepsis (403–406). This benefit should be appli- and none was individually powered for mortality, with very
cable to patients with severe sepsis and septic shock. In addition, low mortality rates (418–420, 423, 426). Authors of previously
the risk factors for GI bleeding (eg, coagulopathy, mechanical published meta-analyses of optimal nutrition strategies for the
ventilation for at least 48 hrs, possibly hypotension) are fre- critically ill all reported that the studies they included had high
quently present in patients with severe sepsis and septic shock heterogeneity and low quality(418–430). Although no consis-
(407, 408). Patients without these risk factors are unlikely (0.2%; tent effect on mortality was observed, there was evidence of
95% CI, 0.02−0.5) to have clinically important bleeding (407). benefit from some early enteral feeding on secondary outcomes,
Critical Care Medicine www.ccmjournal.org 611](https://image.slidesharecdn.com/ssc-guidelines-130311115623-phpapp02/75/Ssc-guidelines-32-2048.jpg)
![Dellinger et al
donated time of committee members over the last 2 years; 18. Varpula M, Tallgren M, Saukkonen K, et al: Hemodynamic variables
related to outcome in septic shock. Intensive Care Med 2005;
the sponsoring organizations that worked with us toward the
31:1066–1071
reality of a consensus document across so many disciplines, 19. Kortgen A, Niederprüm P, Bauer M: Implementation of an evidence-
specialties, and continents; and those that contribute in so based “standard operating procedure” and outcome in septic shock.
many ways to create the new science to move us forward in Crit Care Med 2006; 34:943–949
treating this potentially devastating disease: the funders of 20. Sebat F, Johnson D, Musthafa AA, et al: A multidisciplinary community
hospital program for early and rapid resuscitation of shock in non-
research, the investigators, the subjects, and those associated trauma patients. Chest 2005; 127:1729–1743
with the evidence publishing bodies. Finally, we thank 21. Shapiro NI, Howell MD, Talmor D, et al: Implementation and out-
Deborah McBride for the incredible editorial support provided comes of the Multiple Urgent Sepsis Therapies (MUST) protocol. Crit
persistently over months that brought the manuscript to life Care Med 2006; 34:1025–1032
and finalization. 22. Micek ST, Roubinian N, Heuring T, et al: Before-after study of a stan-
dardized hospital order set for the management of septic shock. Crit
Care Med 2006; 34:2707–2713
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![Special Article
Appendix C
ARDSnet Ventilator Management
Assist control mode—volume ventilation
Reduce tidal volume to 6 mL/kg lean body weight
eep plateau pressure 30 cm H2O
K
–Reduce tidal volume as low as 4 mL/kg predicted body weight to limit plateau pressure
Maintain Sao2/Spo2 between 88% and 95%
Anticipated PEEP settings at various Fio2 requirements
Fio2 0.3 0.4 0.4 0.5 0.5 0.6 0.7 0.7 0.7 0.8 0.9 0.9 0.9 1.0
PEEP
5 5 8 8 10 10 10 12 14 14 14 16 18 20-24
Predicted Body Weight Calculation
Male— 50 + 2.3 [height (inches) – 60] or 50 + 0.91 [height (cm) – 152.4]
Female—45.5 + 2.3 [height (inches) – 60] or 45.5 + 0.91 [height (cm) – 152.4]
Sao2 = arterial oxygen saturation, PEEP = positive end-expiratory pressure, Spo2 = oxygen saturation on pulse oximetry. Adapted from Acute Respiratory
Distress Syndrome Network. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory
distress syndrome.
N Engl J Med 2000; 342:1301–1308.
Appendix D
Summary of Ventilator Procedures in the Higher PEEP Groups of the ALVEOLI Trial
Procedure Value
Ventilator mode Volume assist/control
Tidal volume goal 6 mL/kg of predicted body weight
Plateau pressure goal ≤ 30 cm H2O
Ventilator rate and pH goal 6–35, adjusted to achieve arterial pH ≥ 7.30 if possible
Inspiration expiration time 1:1−1:3
Oxygenation goal
Pao2 55−80 mm Hg
Spo2 88%−95%
Weaning Weaning attempted by means of pressure support when level of arterial oxygenation
acceptable with PEEP 8 cm H2O and Fio2 0.40
Allowable combinations of PEEP and Fio2a
Higher PEEP group (after protocol changed to use higher levels of PEEP)
Fio2 0.3 0.3 0.4 0.4 0.5 0.5 0.5–0.8 0.8 0.9 1
PEEP 12 14 14 16 16 18 20 22 22 22–24
Note: Complete ventilator procedures and eligibility criteria can be found at www.ardsnet.org.
Spo2 = oxyhemoglobin saturation as measured by pulse oximetry, Fio2 = fraction of inspired oxygen, PEEP = positive end-expiratory pressure.
a
In both study groups (lower and higher PEEP), additional increases in PEEP to 34 cm H2O were allowed but not required after Fio2 had been
increased to 1.0, according to the protocol.
Adapted from Brower RG, Lanken PN, MacIntyre N, et al: Higher vs. lower positive end-expiratory pressures in patients with the acute respiratory
distress syndrome.
N Engl J Med. 2004; 351(4):327–336.
Critical Care Medicine www.ccmjournal.org 637](https://image.slidesharecdn.com/ssc-guidelines-130311115623-phpapp02/75/Ssc-guidelines-58-2048.jpg)
Ssc guidelines
- 1. Special Articles Surviving SepsisCampaign: International Guidelines for Management of Severe Sepsis and Septic Shock: 2012 R. Phillip Dellinger, MD1; Mitchell M. Levy, MD2; Andrew Rhodes, MB BS3; Djillali Annane, MD4; Herwig Gerlach, MD, PhD5; Steven M. Opal, MD6; Jonathan E. Sevransky, MD7; Charles L. Sprung, MD8; Ivor S. Douglas, MD9; Roman Jaeschke, MD10; Tiffany M. Osborn, MD, MPH11; Mark E. Nunnally, MD12; Sean R. Townsend, MD13; Konrad Reinhart, MD14; Ruth M. Kleinpell, PhD, RN-CS15; Derek C. Angus, MD, MPH16; Clifford S. Deutschman, MD, MS17; Flavia R. Machado, MD, PhD18; Gordon D. Rubenfeld, MD19; Steven A. Webb, MB BS, PhD20; Richard J. Beale, MB BS21; Jean-Louis Vincent, MD, PhD22; Rui Moreno, MD, PhD23; and the Surviving Sepsis Campaign Guidelines Committee including the Pediatric Subgroup* Objective: To provide an update to the “Surviving Sepsis Cam- Methods: The authors were advised to follow the principles of the paign Guidelines for Management of Severe Sepsis and Septic Grading of Recommendations Assessment, Development and Shock,” last published in 2008. Evaluation (GRADE) system to guide assessment of quality of evi- Design: A consensus committee of 68 international experts rep- dence from high (A) to very low (D) and to determine the strength resenting 30 international organizations was convened. Nominal of recom endations as strong (1) or weak (2). The potential draw- m groups were assembled at key international meetings (for those backs of making strong recommendations in the presence of low- committee members attending the conference). A formal con- quality evidence were emphasized. Some recommendations were flict of interest policy was developed at the onset of the process ungraded (UG). Recommendations were classified into three and enforced throughout. The entire guidelines process was groups: 1) those directly targeting severe sepsis; 2) those targeting conducted independent of any industry funding. A stand-alone general care of the critically ill patient and considered high priority in meeting was held for all subgroup heads, co- and vice-chairs, severe sepsis; and 3) pediatric considerations. and selected individuals. Teleconferences and electronic-based Results: Key recommendations and suggestions, listed by cat- discussion among subgroups and among the entire committee egory, include: early quantitative resuscitation of the septic served as an integral part of the development. patient during the first 6 hrs after recognition (1C); blood ultures c 1 Cooper University Hospital, Camden, New Jersey. 20 Royal Perth Hospital, Perth, Western Australia. 2 Warren Alpert Medical School of Brown University, Providence, Rhode 21 Guy’s and St. Thomas’ Hospital Trust, London, United Kingdom. Island. 22 Erasme University Hospital, Brussels, Belgium. 3 St. George’s Hospital, London, United Kingdom. 23 UCINC, Hospital de São José, Centro Hospitalar de Lisboa Central, 4 Hôpital Raymond Poincaré, Garches, France. E.P.E., Lisbon, Portugal. 5 Vivantes-Klinikum Neukölln, Berlin, Germany. * embers of the 2012 SSC Guidelines Committee and Pediatric Sub- M 6 Memorial Hospital of Rhode Island, Pawtucket, Rhode Island. group are listed in Appendix A at the end of this article. 7 Emory University Hospital, Atlanta, Georgia. Supplemental digital content is available for this article. Direct URL cita- 8 Hadassah Hebrew University Medical Center, Jerusalem, Israel. tions appear in the printed text and are provided in the HTML and PDF ver- 9 Denver Health Medical Center, Denver, Colorado. sions of this on the journal’s Web site (http://journals.lww.com/ccmjournal). 10 McMaster University, Hamilton, Ontario, Canada. 11 Barnes-Jewish Hospital, St. Louis, Missouri. Complete author and committee disclosures are listed in Supplemental 12 University of Chicago Medical Center, Chicago, Illinois. Digital Content 1 (http://links.lww.com/CCM/A615). 13 California Pacific Medical Center, San Francisco, California. This article is being simultaneously published in Critical Care Medicine 14 Friedrich Schiller University Jena, Jena, Germany. and Intensive Care Medicine. 15 Rush University Medical Center, Chicago, Illinois. For additional information regarding this article, contact R.P. Dellinger 16 University of Pittsburgh, Pittsburgh, Pennsylvania. ([email protected]). 17 Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania. Copyright © 2013 by the Society of Critical Care Medicine and the Euro- 18 Federal University of Sao Paulo, Sao Paulo, Brazil. pean Society of Intensive Care Medicine 19 Sunnybrook Health Sciences Center, Toronto, Ontario, Canada. DOI: 10.1097/CCM.0b013e31827e83af 580 www.ccmjournal.org February 2013 • Volume 41 • Number 2
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Special Article before antibiotictherapy (1C); imaging studies performed unless contraindicated (1B); a conservative fluid strategy for promptly to confirm a potential source of infection (UG); admin- patients with established ARDS who do not have evidence of istration of broad-spectrum antimicrobials therapy within 1 hr of tissue hypoperfusion (1C); protocols for weaning and seda- recognition of septic shock (1B) and severe sepsis without sep- tion (1A); minimizing use of either intermittent bolus sedation tic shock (1C) as the goal of therapy; reassessment of antimi- or continuous infusion sedation targeting specific titration crobial therapy daily for de-escalation, when appropriate (1B); endpoints (1B); avoidance of neuromuscular blockers if pos- infection source control with attention to the balance of risks and sible in the septic patient without ARDS (1C); a short course benefits of the chosen method within 12 hrs of diagnosis (1C); of neuromuscular blocker (no longer than 48 hrs) for patients initial fluid resuscitation with crystalloid (1B) and consideration with early ARDS and a Pao2/Fio2 150 mm Hg (2C); a proto- of the addition of albumin in patients who continue to require colized approach to blood glucose management commencing substantial amounts of crystalloid to maintain adequate mean insulin dosing when two consecutive blood glucose levels are arterial pressure (2C) and the avoidance of hetastarch formula- 180 mg/dL, targeting an upper blood glucose ≤ 180 mg/dL tions (1C); initial fluid challenge in patients with sepsis-induced (1A); equivalency of continuous veno-venous hemofiltration or tissue hypoperfusion and suspicion of hypovolemia to achieve a intermittent hemodialysis (2B); prophylaxis for deep vein throm- minimum of 30 mL/kg of crystalloids (more rapid administration bosis (1B); use of stress ulcer prophylaxis to prevent upper and greater amounts of fluid may be needed in some patients) gastrointestinal bleeding in patients with bleeding risk factors (1C); fluid challenge technique continued as long as hemody- (1B); oral or enteral (if necessary) feedings, as tolerated, rather namic improvement, as based on either dynamic or static vari- than either complete fasting or provision of only intravenous ables (UG); norepinephrine as the first-choice vasopressor to glucose within the first 48 hrs after a diagnosis of severe sep- maintain mean arterial pressure ≥ 65 mm Hg (1B); epinephrine sis/septic shock (2C); and addressing goals of care, including when an additional agent is needed to maintain adequate blood treatment plans and end-of-life planning (as appropriate) (1B), pressure (2B); vasopressin (0.03 U/min) can be added to nor- as early as feasible, but within 72 hrs of intensive care unit epinephrine to either raise mean arterial pressure to target or admission (2C). Recommendations specific to pediatric severe to decrease norepinephrine dose but should not be used as sepsis include: therapy with face mask oxygen, high flow nasal the initial vasopressor (UG); dopamine is not recommended cannula oxygen, or nasopharyngeal continuous PEEP in the except in highly selected circumstances (2C); dobutamine presence of respiratory distress and hypoxemia (2C), use of infusion administered or added to vasopressor in the presence physical examination therapeutic endpoints such as capillary of a) myocardial dysfunction as suggested by elevated cardiac refill (2C); for septic shock associated with hypovolemia, the filling pressures and low cardiac output, or b) ongoing signs use of crystalloids or albumin to deliver a bolus of 20 mL/kg of hypoperfusion despite achieving adequate intravascular vol- of crystalloids (or albumin equivalent) over 5 to 10 mins (2C); ume and adequate mean arterial pressure (1C); avoiding use more common use of inotropes and vasodilators for low cardiac of intravenous hydrocortisone in adult septic shock patients if output septic shock associated with elevated systemic vascular adequate fluid resuscitation and vasopressor therapy are able resistance (2C); and use of hydrocortisone only in children with to restore hemodynamic stability (2C); hemoglobin target of suspected or proven “absolute”‘ adrenal insufficiency (2C). 7–9 g/dL in the absence of tissue hypoperfusion, ischemic Conclusions: Strong agreement existed among a large cohort coronary artery disease, or acute hemorrhage (1B); low tidal of international experts regarding many level 1 recommenda- volume (1A) and limitation of inspiratory plateau pressure (1B) tions for the best care of patients with severe sepsis. Although for acute respiratory distress syndrome (ARDS); application of a significant number of aspects of care have relatively weak at least a minimal amount of positive end-expiratory pressure support, evidence-based recommendations regarding the (PEEP) in ARDS (1B); higher rather than lower level of PEEP acute management of sepsis and septic shock are the founda- for patients with sepsis-induced moderate or severe ARDS tion of improved outcomes for this important group of critically (2C); recruitment maneuvers in sepsis patients with severe ill patients. (Crit Care Med 2013; 41:580–637) refractory hypoxemia due to ARDS (2C); prone positioning in Key Words: evidence-based medicine; Grading of Recommendations sepsis-induced ARDS patients with a Pao2/Fio2 ratio of ≤ 100 Assessment, Development and Evaluation criteria; guidelines; mm Hg in facilities that have experience with such practices infection; sepsis; sepsis bundles; sepsis syndrome; septic shock; (2C); head-of-bed elevation in mechanically ventilated patients severe sepsis; Surviving Sepsis Campaign Sponsoring organizations: American Association of Critical-Care America, Indian Society of Critical Care Medicine, International Pan Nurses, American College of Chest Physicians, American College Arabian Critical Care Medicine Society, Japanese Association for Acute of Emergency Physicians, American Thoracic Society, Asia Pacific Medicine, Japanese Society of Intensive Care Medicine, Pediatric Acute Association of Critical Care Medicine, Australian and New Zealand Lung Injury and Sepsis Investigators, Society for Academic Emergency Intensive Care Society, Brazilian Society of Critical Care, Canadian Medicine, Society of Critical Care Medicine, Society of Hospital Critical Care Society, Chinese Society of Critical Care Medicine, Medicine, Surgical Infection Society, World Federation of Critical Chinese Society of Critical Care Medicine−China Medical Association, Emirates Intensive Care Society, European Respiratory Society, Care Nurses, World Federation of Pediatric Intensive and Critical Care European Society of Clinical Microbiology and Infectious Diseases, Societies; World Federation of Societies of Intensive and Critical Care European Society of Intensive Care Medicine, European Society of Medicine. Participation and endorsement: The German Sepsis Society Pediatric and Neonatal Intensive Care, Infectious Diseases Society of and the Latin American Sepsis Institute. Critical Care Medicine www.ccmjournal.org 581
- 3. Dellinger et al Dr.Dellinger consulted for Biotest (immunoglobulin concentrate available in Dr. Douglas received grants paid to his institution from Eli Lilly (PROWESS Europe for potential use in sepsis) and AstraZeneca (anti-TNF compound Shock site), Eisai (study site), National Institutes of Health (ARDS Network), unsuccessful in recently completed sepsis clinical trial); his institution received Accelr8 (VAP diagnostics), CCCTG (Oscillate Study), and Hospira (Dexme- consulting income from IKARIA for new product development (IKARIA has detomidine in Alcohol Withdrawal RCT). His institution received an honorar- inhaled nitric oxide available for off-label use in ARDS) and grant support from ium from the Society of Critical Care Medicine (Paragon ICU Improvement); Spectral Diagnostics Inc (current endotoxin removal clinical trial), Ferring (vaso- he consulted for Eli Lilly (PROWESS Shock SC and Sepsis Genomics pressin analog clinical trial-ongoing); as well as serving on speakers bureau for Study) in accordance with institutional policy; he received payment for pro- Eisai (anti-endotoxin compound that failed to show benefit in clinical trial). viding expert testimony (Smith Moore Leatherwood LLP); travel/accommo- dations reimbursed by Eli Lilly and Company (PROWESS Shock Steering Dr. Levy received grant support from Eisai (Ocean State Clinical Coordi- Committee) and the Society of Critical Care Medicine (Hospital Quality Alli- nating Center to fund clinical trial [$500K]), he received honoraria from Eli ance, Washington DC, four times per year 2009−2011); he received hono- Lilly (lectures in India $8,000), and he has been involved with the Surviving raria from Covidien (non-CME lecture 2010, US$500) and the University Sepsis Campaign guideline from its beginning. of Minnesota Center for Excellence in Critical Care CME program (2009, Dr. Rhodes consulted for Eli Lilly with monetary compensation paid to him- 2010); he has a pending patent for a bed backrest elevation monitor. self as well as his institution (Steering Committee for the PROWESS Shock Dr. Jaeschke has disclosed that he has no potential conflicts of interest. trial) and LiDCO; travel/accommodation reimbursement was received from Eli Lilly and LiDCO; he received income for participation in review activities Dr. Osborn consulted for Sui Generis Health ($200). Her institution such as data monitoring boards, statistical analysis from Orion, and for Eli receives grant support from the National Institutes of Health Research, Lilly; he is an author on manuscripts describing early goal-directed therapy, Health Technology Assessment Programme-United Kingdom (trial doc- and believes in the concept of minimally invasive hemodynamic monitoring. tor for sepsis-related RCT). Salary paid through the NIHR government funded (nonindustry) grant. Grant awarded to chief investigator from Dr. Annane participated on the Fresenius Kabi International Advisory Board ICNARC. She is a trial clinician for ProMISe. (honorarium 2000€). His nonfinancial disclosures include being the princi- pal investigator of a completed investigator-led multicenter randomized con- Dr. Nunnally received a stipend for a chapter on diabetes mellitus; he is an trolled trial assessing the early guided benefit to risk of NIRS tissue oxygen author of editorials contesting classic tight glucose control. saturation; he was the principal investigator of an investigator-led randomized Dr. Townsend is an advocate for healthcare quality improvement. controlled trial of epinephrine vs norepinephrine (CATS study)–Lancet 2007; Dr. Reinhart consulted for EISAI (Steering Committee member−less then he also is the principle investigator of an ongoing investigator-led multina- US $10,000); BRAHMS Diagnostics (less than US $10,000); and SIRS- tional randomized controlled trial of crystalloids vs colloids (Crystal Study). Lab Jena (founding member, less than US $10,000). He received hono- Dr. Gerlach has disclosed that he has no potential conflicts of interest; raria for lectures including service on the speakers’ bureau from Biosyn he is an author of a review on the use of activated protein C in surgical Germany (less than €10,000) and Braun Melsungen (less than €10,000). patients (published in the New England Journal of Medicine, 2009). He received royalties from Edwards Life Sciences for sales of central venous oxygen catheters (~$100,000). Dr. Opal consulted for Genzyme Transgenics (consultant on trans- genic antithrombin $1,000), Pfizer (consultant on TLR4 inhibitor project Dr. Kleinpell received monetary compensation for providing expert testimony $3,000), British Therapeutics (consultant on polyclonal antibody project (four depositions and one trial in the past year). Her institution receives $1,000), and Biotest A (consultant on immunoglobul project $2,000). grants from the Agency for Healthcare Research and Quality and the Prince His institution received grant support from Novartis (Clinical Coordinat- Foundation (4-year R01 grant, PI and 3-year foundation grant, Co-l). She ing Center to assist in patient enrollment in a phase III trial with the use received honoraria from the Cleveland Clinic and the American Association of Tissue Factor Pathway Inhibitor [TFPI] in severe community acquired of Critical Care Nurses for keynote speeches at conferences; she received pneumonia [SCAP] $30,000 for 2 years), Eisai ($30,000 for 3 years), royalties from McGraw Hill (co-editor of critical care review book); travel/ Astra Zeneca ($30,000 for 1 year), Aggenix ($30,000 for 1 year), Inimex accommodations reimbursed from the American Academy of Nurse Prac- ($10,000), Eisai ($10,000), Atoxbio ($10,000), Wyeth ($20,000), Sirtris titioners, Society of Critical Care Medicine, and American Association of (preclinical research $50,000), and Cellular Bioengineering Inc. ($500). Critical Care Nurses (one night hotel coverage at national conference). He received honoraria from Novartis (clinical evaluation committee TFPI Dr. Angus consulted for Eli Lilly (member of the Data Safety Monitoring study for SCAP $20,000) and Eisai ($25,000). He received travel/accom- Board, Multicenter trial of a PC for septic shock), Eisai Inc (Anti-TLR4 modations reimbursed from Sangart (data and safety monitoring $2,000), therapy for severe sepsis), and Idaho Technology (sepsis biomarkers); he Spectral Diagnostics (data and safety monitoring $2,000), Takeda (data received grant support (investigator, long-term follow-up of phase III trial and safety monitoring $2,000) and Canadian trials group ROS II oseltami- of an anti-TLR4 agent in severe sepsis), a consulting income (anti-TRL4 vir study (data and safety monitoring board (no money). He is also on the therapy for severe sepsis), and travel/accommodation expense reimburse- Data Safety Monitoring Board for Tetraphase (received US $600 in 2012). ment from Eisai, Inc; he is the primary investigator for an ongoing National Institutes of Health-funded study comparing early resuscitation strategies Dr. Sevransky received grant support to his institution from Sirius Genom- for sepsis-induced tissue hypoperfusion. ics Inc; he consulted for Idaho Technology ($1,500); he is the co-principal investigator of a multicenter study evaluating the association between Dr. Deutschman has nonfinancial involvement as a coauthor of the Society intensive care unit organizational and structural factors, including proto- of Critical Care Medicine’s Glycemic Control guidelines. cols and in-patient mortality. He maintains that protocols serve as useful Dr. Machado reports unrestricted grant support paid to her institution for reminders to busy clinicians to consider certain therapies in patients with Surviving Sepsis Campaign implementation in Brazil (Eli Lilly do Brasil); sepsis or other life-threatening illness. she is the primary investigator for an ongoing study involving vasopressin. Dr. Sprung received grants paid to his institution from Artisan Pharma Dr. Rubenfeld received grant support from nonprofit agencies or foundations ($25,000–$50,000), Eisai, Corp ($1,000–$5,000 ACCESS), Ferring including National Institutes of Health ($10 million), Robert Wood Johnson Pharmaceuticals A/S ($5,000–$10,000), Hutchinson Technology Incorpo- Foundation ($500,000), and CIHR ($200,000). His institution received grants rated ($1,000–$5,000), Novartis Corp (less than $1,000). His institution from for-profit companies including Advanced Lifeline System ($150,000), receives grant support for patients enrolled in clinical studies from Eisai Cor- Siemens ($50,000), Bayer ($10,000), Byk Gulden ($15,000), AstraZen- poration (PI. Patients enrolled in the ACCESS study $50,000–$100,000), eca ($10,000), Faron Pharmaceuticals ($5,000), and Cerus Corporation Takeda (PI. Study terminated before patients enrolled). He received grants ($11,000). He received honoraria, consulting fees, editorship, royalties, and paid to his institution and consulting income from Artisan Pharma/Asahi Data and Safety Monitoring Board membership fees paid to him from Bayer Kasei Pharma America Corp ($25,000–$50,000). He consulted for Eli ($500), DHD ($1,000), Eli Lilly ($5,000), Oxford University Press ($10,000), Lilly (Sabbatical Consulting fee $10,000–$25,000) and received honoraria Hospira ($15,000), Cerner ($5,000), Pfizer ($1,000), KCI ($7,500), Ameri- from Eli Lilly (lecture $1,000–$5,000). He is a member of the Australia and can Association for Respiratory Care ($10,000), American Thoracic Society New Zealand Intensive Care Society Clinical Trials Group for the NICE- ($7,500), BioMed Central ($1,000), National Institutes of Health ($1,500), SUGAR Study (no money received); he is a council member of the Inter- and the Alberta Heritage Foundation for Medical Research ($250). He has national Sepsis Forum (as of Oct. 2010); he has held long time research database access or other intellectual (non financial) support from Cerner. interests in steroids in sepsis, PI of Corticus study, end-of-life decision mak- Dr. Webb consulted for AstraZeneca (anti-infectives $1,000−$5,000) and ing and PI of Ethicus, Ethicatt, and Welpicus studies. Jansen-Cilag (anti-infectives $1,000-$5,000). He received grant support 582 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 4. Special Article from aNHMRC project grant (ARISE RECT of EGDT); NHMRC proj- Eli Lilly and Company (development of educational presentations including ect grant and Fresinius-unrestricted grant (CHEST RCT of voluven vs. service on speaker’ bureaus (intensive care school hosted in department); saline); RCT of steroid vs. placebo for septic shock); NHMRC project travel/accommodations were reimbursed from bioMerieux (GeneXpert Focus grant (BLISS study of bacteria detection by PRC in septic shock) Intensive Group, France) and LiDCO (Winter Anaesthetic and Critical Care Review Care Foundation-ANZ (BLING pilot RCT of beta-lactam administration Conference), Surviving Sepsis Campaign (Publications Meeting, New York; by infusion); Hospira (SPICE programme of sedation delirium research); Care Bundles Conference, Manchester), SSC Publication Committee Meet- NHMRC Centres for Research Excellent Grant (critical illness microbi- ing and SSC Executive Committee Meeting, Nashville; SSC Meeting, Man- ology observational studies); Hospira-unrestricted grant (DAHlia RCT of chester), Novartis (Advisory Board Meeting, Zurich), Institute of Biomedical dexmedetomidine for agitated delirium). Travel/accommodations reim- Engineering (Hospital of the Future Grand Challenge Kick-Off Meeting, bursed by Jansen-Cilag ($5,000–$10,000) and AstraZeneca ($1,000- Hospital of the Future Grand Challenge Interviews EPSRC Headquarters, $5,000); he has a patent for a meningococcal vaccine. He is chair of the Swindon, Philips (Kick-Off Meeting, Boeblingen, Germany; MET Conference, ANZICS Clinical Trials Group and is an investigator in trials of EGDT, PCR Cohenhagen), Covidien (Adult Monitoring Advisory Board Meeting, Frank- for determining bacterial load and a steroid in the septic shock trial. furt), Eisai (ACCESS Investigators Meeting, Barcelona). His nonfinancial dis- closures include authorship of the position statement on fluid resuscitation Dr. Beale received compensation for his participation as board member for from the ESICM task force on colloids (yet to be finalized). Eisai, Inc, Applied Physiology, bioMérieux, Covidien, SIRS-Lab, and Novartis; consulting income was paid to his institution from PriceSpective Ltd, Easton Dr. Vincent reports consulting income paid to his institution from Astellas, Associates (soluble guanylate cyclase activator in acute respiratory distress AstraZeneca, Curacyte, Eli Lilly, Eisai, Ferring, GlaxoSmithKline, Merck, and syndrome/acute lung injury adjunct therapy to supportive care and ventila- Pfizer. His institution received honoraria on his behalf from Astellas, Astra- tion strategies), Eisai (eritoran), and Phillips (Respironics); he provided expert Zeneca, Curacyte, Eli Lilly, Eisai, Ferring, Merck, and Pfizer. His institution testimony for Eli Lilly and Company (paid to his institution); honoraria received received grant support from Astellas, Curacyte, Eli Lilly, Eisai, Ferring, and (paid to his institution) from Applied Physiology (Applied Physiology PL SAB, Pfizer. His institution received payment for educational presentations from Applied Physiology SAB, Brussels, Satellite Symposium at the ISICEM, Astellas, AstraZeneca, Curacyte, Eli Lilly, Eisai, Ferring, Merck, and Pfizer. Brussels), bioMérieux (GeneXpert Focus Group, France), SIRS-Lab (SIRS- Dr. Moreno consulted for bioMerieux (expert meeting). He is a coauthor of LAB SAB Forum, Brussels and SIRS-LAB SAB, Lisbon), Eli Lilly (CHMP a paper on corticosteroids in patients with septic shock. He is the author Hearing), Eisai (eritoran through leader touch plan in Brussels), Eli Lilly of several manuscripts defining sepsis and stratification of the patient with (Lunchtime Symposium, Vienna), Covidien (adult monitoring advisory board sepsis. He is also the author of several manuscripts contesting the utility meeting, Frankfurt), Covidien (Global Advisory Board CNIBP Boulder USA), of sepsis bundles. S METHODOLOGY epsis is a systemic, deleterious host response to infection leading to severe sepsis (acute organ dysfunction second- ary to documented or suspected infection) and septic Definitions shock (severe sepsis plus hypotension not reversed with fluid Sepsis is defined as the presence (probable or documented) of resuscitation). Severe sepsis and septic shock are major health- infection together with systemic manifestations of infection. care problems, affecting millions of people around the world Severe sepsis is defined as sepsis plus sepsis-induced organ each year, killing one in four (and often more), and increasing dysfunction or tissue hypoperfusion (Tables 1 and 2) (6). in incidence (1–5). Similar to polytrauma, acute myocardial Throughout this manuscript and the performance improve- infarction, or stroke, the speed and appropriateness of therapy ment bundles, which are included, a distinction is made administered in the initial hours after severe sepsis develops between definitions and therapeutic targets or thresholds. Sep- are likely to influence outcome. sis-induced hypotension is defined as a systolic blood pressure The recommendations in this document are intended to (SBP) 90 mm Hg or mean arterial pressure (MAP) 70 mm provide guidance for the clinician caring for a patient with Hg or a SBP decrease 40 mm Hg or less than two standard severe sepsis or septic shock. Recommendations from these deviations below normal for age in the absence of other causes guidelines cannot replace the clinician’s decision-making capa- of hypotension. An example of a therapeutic target or typical bility when he or she is presented with a patient’s unique set of threshold for the reversal of hypotension is seen in the sepsis clinical variables. Most of these recommendations are appro- bundles for the use of vasopressors. In the bundles, the MAP priate for the severe sepsis patient in the ICU and non-ICU set- threshold is ≥ 65 mm Hg. The use of definition vs. threshold will tings. In fact, the committee believes that the greatest outcome be evident throughout this article. Septic shock is defined as improvement can be made through education and process sepsis-induced hypotension persisting despite adequate fluid change for those caring for severe sepsis patients in the non- resuscitation. Sepsis-induced tissue hypoperfusion is defined ICU setting and across the spectrum of acute care. Resource as infection-induced hypotension, elevated lactate, or oliguria. limitations in some institutions and countries may prevent physicians from accomplishing particular recommendations. History of the Guidelines Thus, these recommendations are intended to be best practice These clinical practice guidelines are a revision of the 2008 (the committee considers this a goal for clinical practice) and SSC guidelines for the management of severe sepsis and septic not created to represent standard of care. The Surviving Sepsis shock (7). The initial SSC guidelines were published in 2004 Campaign (SSC) Guidelines Committee hopes that over time, (8) and incorporated the evidence available through the end particularly through education programs and formal audit of 2003. The 2008 publication analyzed evidence available and feedback performance improvement initiatives, the guide- through the end of 2007. The most current iteration is based lines will influence bedside healthcare practitioner behavior on updated literature search incorporated into the evolving that will reduce the burden of sepsis worldwide. manuscript through fall 2012. Critical Care Medicine www.ccmjournal.org 583
- 5. Dellinger et al Selectionand Organization of Committee Members Grading of Recommendations The selection of committee members was based on inter- We advised the authors to follow the principles of the Grading est and expertise in specific aspects of sepsis. Co-chairs and of Recommendations Assessment, Development and Evalua- executive committee members were appointed by the Society tion (GRADE) system to guide assessment of quality of evi- of Critical Care Medicine and European Society of Intensive dence from high (A) to very low (D) and to determine the Care Medicine governing bodies. Each sponsoring organiza- strength of recommendations (Tables 3 and 4). (9–11). The tion appointed a representative who had sepsis expertise. Addi- SSC Steering Committee and individual authors collaborated tional committee members were appointed by the co-chairs with GRADE representatives to apply the system during the and executive committee to create continuity with the previous SSC guidelines revision process. The members of the GRADE committees’ membership as well as to address content needs group were directly involved, either in person or via e-mail, in for the development process. Four clinicians with experience all discussions and deliberations among the guidelines com- in the GRADE process application (referred to in this docu- mittee members as to grading decisions. ment as GRADE group or Evidence-Based Medicine [EBM] The GRADE system is based on a sequential assessment of group) took part in the guidelines development. the quality of evidence, followed by assessment of the balance The guidelines development process began with appoint- between the benefits and risks, burden, and cost, leading to ment of group heads and assignment of committee members development and grading of a management recommendation. to groups according to their specific expertise. Each group was Keeping the rating of quality of evidence and strength of responsible for drafting the initial update to the 2008 edition recommendation explicitly separate constitutes a crucial and in their assigned area (with major additional elements of infor- defining feature of the GRADE approach. This system classifies mation incorporated into the evolving manuscript through quality of evidence as high (grade A), moderate (grade B), low year-end 2011 and early 2012). (grade C), or very low (grade D). Randomized trials begin With input from the EBM group, an initial group meet- as high-quality evidence but may be downgraded due to ing was held to establish procedures for literature review and limitations in implementation, inconsistency, or imprecision of development of tables for evidence analysis. Committees and the results, indirectness of the evidence, and possible reporting their subgroups continued work via phone and the Internet. bias (Table 3). Examples of indirectness of the evidence Several subsequent meetings of subgroups and key indi- include population studied, interventions used, outcomes viduals occurred at major international meetings (nominal measured, and how these relate to the question of interest. groups), with work continuing via teleconferences and elec- Well-done observational (nonrandomized) studies begin as tronic-based discussions among subgroups and members low-quality evidence, but the quality level may be upgraded on of the entire committee. Ultimately, a meeting of all group the basis of a large magnitude of effect. An example of this is heads, executive committee members, and other key commit- the quality of evidence for early administration of antibiotics. tee members was held to finalize the draft document for sub- References to supplemental digital content appendices of mission to reviewers. GRADEpro Summary of Evidence Tables appear throughout this document. Search Techniques The GRADE system classifies recommendations as strong A separate literature search was performed for each clearly (grade 1) or weak (grade 2). The factors influencing this deter- defined question. The committee chairs worked with subgroup mination are presented in Table 4. The assignment of strong heads to identify pertinent search terms that were to include, or weak is considered of greater clinical importance than a at a minimum, sepsis, severe sepsis, septic shock, and sepsis syn- difference in letter level of quality of evidence. The commit- drome crossed against the subgroup’s general topic area, as well tee assessed whether the desirable effects of adherence would as appropriate key words of the specific question posed. All outweigh the undesirable effects, and the strength of a rec- questions used in the previous guidelines publications were ommendation reflects the group’s degree of confidence in searched, as were pertinent new questions generated by gen- that assessment. Thus, a strong recommendation in favor of eral topic-related searches or recent trials. The authors were an intervention reflects the panel’s opinion that the desirable specifically asked to look for existing meta-analyses related to effects of adherence to a recommendation (beneficial health their question and search a minimum of one general database outcomes; lesser burden on staff and patients; and cost sav- (ie, MEDLINE, EMBASE) and the Cochrane Library (both ings) will clearly outweigh the undesirable effects (harm to The Cochrane Database of Systematic Reviews [CDSR] and health; more burden on staff and patients; and greater costs). Database of Abstracts of Reviews of Effectiveness [DARE]). The potential drawbacks of making strong recommenda- Other databases were optional (ACP Journal Club, Evidence- tions in the presence of low-quality evidence were taken into Based Medicine Journal, Cochrane Registry of Controlled account. A weak recommendation in favor of an intervention Clinical Trials, International Standard Randomized Controlled indicates the judgment that the desirable effects of adherence Trial Registry [http://www.controlled-trials.com/isrctn/] or to a recommendation probably will outweigh the undesirable metaRegister of Controlled Trials [http://www.controlled- effects, but the panel is not confident about these tradeoffs— trials.com/mrct/]. Where appropriate, available evidence was either because some of the evidence is low quality (and thus summarized in the form of evidence tables. uncertainty remains regarding the benefits and risks) or the 584 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 6. Special Article Table 1. Diagnostic Criteria for Sepsis Infection, documented or suspected, and some of the following: General variables Fever ( 38.3°C) Hypothermia (core temperature 36°C) Heart rate 90/min–1 or more than two sd above the normal value for age Tachypnea Altered mental status Significant edema or positive fluid balance ( 20 mL/kg over 24 hr) Hyperglycemia (plasma glucose 140 mg/dL or 7.7 mmol/L) in the absence of diabetes Inflammatory variables Leukocytosis (WBC count 12,000 µL–1) Leukopenia (WBC count 4000 µL–1) Normal WBC count with greater than 10% immature forms Plasma C-reactive protein more than two sd above the normal value Plasma procalcitonin more than two sd above the normal value Hemodynamic variables Arterial hypotension (SBP 90 mm Hg, MAP 70 mm Hg, or an SBP decrease 40 mm Hg in adults or less than two sd below normal for age) Organ dysfunction variables Arterial hypoxemia (Pao2/Fio2 300) Acute oliguria (urine output 0.5 mL/kg/hr for at least 2 hrs despite adequate fluid resuscitation) Creatinine increase 0.5 mg/dL or 44.2 µmol/L Coagulation abnormalities (INR 1.5 or aPTT 60 s) Ileus (absent bowel sounds) Thrombocytopenia (platelet count 100,000 µL–1) Hyperbilirubinemia (plasma total bilirubin 4 mg/dL or 70 µmol/L) Tissue perfusion variables Hyperlactatemia ( 1 mmol/L) Decreased capillary refill or mottling WBC = white blood cell; SBP = systolic blood pressure; MAP = mean arterial pressure; INR = international normalized ratio; aPTT = activated partial thromboplastin time. Diagnostic criteria for sepsis in the pediatric population are signs and symptoms of inflammation plus infection with hyper- or hypothermia (rectal temperature 38.5° or 35°C), tachycardia (may be absent in hypothermic patients), and at least one of the following indications of altered organ function: altered mental status, hypoxemia, increased serum lactate level, or bounding pulses. Adapted from Levy MM, Fink MP, Marshall JC, et al: 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference. Crit Care Med 2003; 31: 1250–1256. benefits and downsides are closely balanced. A strong recom- The implications of calling a recommendation strong mendation is worded as “we recommend” and a weak recom- are that most well-informed patients would accept that mendation as “we suggest.” intervention and that most clinicians should use it in most Throughout the document are a number of statements situations. Circumstances may exist in which a strong rec- that either follow graded recommendations or are listed as ommendation cannot or should not be followed for an stand-alone numbered statements followed by “ungraded” individual because of that patient’s preferences or clinical in parentheses (UG). In the opinion of the committee, characteristics that make the recommendation less applica- these recommendations were not conducive for the GRADE ble. A strong recommendation does not automatically imply process. standard of care. For example, the strong recommendation Critical Care Medicine www.ccmjournal.org 585
- 7. Dellinger et al Table2. Severe Sepsis Severe sepsis definition = sepsis-induced tissue hypoperfusion or organ dysfunction (any of the following thought to be due to the infection) Sepsis-induced hypotension Lactate above upper limits laboratory normal Urine output 0.5 mL/kg/hr for more than 2 hrs despite adequate fluid resuscitation Acute lung injury with Pao2/Fio2 250 in the absence of pneumonia as infection source Acute lung injury with Pao2/Fio2 200 in the presence of pneumonia as infection source Creatinine 2.0 mg/dL (176.8 µmol/L) Bilirubin 2 mg/dL (34.2 µmol/L) Platelet count 100,000 µL Coagulopathy (international normalized ratio 1.5) Adapted from Levy MM, Fink MP, Marshall JC, et al: 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference. Crit Care Med 2003; 31: 1250–1256. for administering antibiotics within 1 hr of the diagnosis were available for advice throughout the process. Subgroups of severe sepsis, as well as the recommendation for achiev- agreed electronically on draft proposals that were then ing a central venous pressure (CVP) of 8 mm Hg and a cen- presented for general discussion among subgroup heads, the tral venous oxygen saturation (Scvo2) of 70% in the first 6 SSC Steering Committee (two co-chairs, two co-vice chairs, hrs of resuscitation of sepsis-induced tissue hypoperfusion, and an at-large committee member), and several selected key although deemed desirable, are not yet standards of care as committee members who met in July 2011 in Chicago. The verified by practice data. results of that discussion were incorporated into the next Significant education of committee members on the version of recommendations and again discussed with the GRADE approach built on the process conducted during 2008 whole group using electronic mail. Draft recommendations efforts. Several members of the committee were trained in were distributed to the entire committee and finalized during the use of GRADEpro software, allowing more formal use of an additional nominal group meeting in Berlin in October the GRADE system (12). Rules were distributed concerning 2011. Deliberations and decisions were then recirculated to the assessing the body of evidence, and GRADE representatives entire committee for approval. At the discretion of the chairs Table 3. Determination of the Quality of Evidence Underlying methodology A (high) RCTs B (moderate) Downgraded RCTs or upgraded observational studies C (low) Well-done observational studies with control RCTs D (very low) Downgraded controlled studies or expert opinion based on other evidence Factors that may decrease the strength of evidence 1. Poor quality of planning and implementation of available RCTs, suggesting high likelihood of bias 2. Inconsistency of results, including problems with subgroup analyses 3. Indirectness of evidence (differing population, intervention, control, outcomes, comparison) 4. Imprecision of results 5. High likelihood of reporting bias Main factors that may increase the strength of evidence 1. Large magnitude of effect (direct evidence, relative risk 2 with no plausible confounders) 2. Very large magnitude of effect with relative risk 5 and no threats to validity (by two levels) 3. Dose-response gradient RCT = randomized controlled trial. 586 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 8. Special Article Table 4. Factors Determining Strong vs. Weak Recommendation What Should be Considered Recommended Process High or moderate evidence The higher the quality of evidence, the more likely a strong recommendation. (Is there high or moderate quality evidence?) Certainty about the balance of benefits vs. The larger the difference between the desirable and undesirable consequences and harms and burdens (Is there certainty?) the certainty around that difference, the more likely a strong recommendation. The smaller the net benefit and the lower the certainty for that benefit, the more likely a weak recommendation. Certainty in or similar values The more certainty or similarity in values and preferences, the more likely a strong (Is there certainty or similarity?) recommendation. Resource implications The lower the cost of an intervention compared to the alternative and other costs related to (Are resources worth expected benefits?) the decision–ie, fewer resources consumed–the more likely a strong recommendation. and following discussion, competing proposals for wording they had the least COI. They were required to work within of recommendations or assigning strength of evidence were their group with full disclosure when a topic for which they resolved by formal voting within subgroups and at nominal had relevant COI was discussed, and they were not allowed group meetings. The manuscript was edited for style and form to serve as group head. At the time of final approval of the by the writing committee with final approval by subgroup document, an update of the COI statement was required. No heads and then by the entire committee. To satisfy peer review additional COI issues were reported that required further during the final stages of manuscript approval for publication, adjudication. several recommendations were edited with approval of the SSC executive committee group head for that recommendation and MANAGEMENT OF SEVERE SEPSIS the EBM lead. Initial Resuscitation and Infection Issues (Table 5) Conflict of Interest Policy A. Initial Resuscitation Since the inception of the SSC guidelines in 2004, no members 1. We recommend the protocolized, quantitative resuscitation of of the committee represented industry; there was no industry patients with sepsis- induced tissue hypoperfusion (defined in input into guidelines development; and no industry represen- this document as hypotension persisting after initial fluid chal- tatives were present at any of the meetings. Industry awareness lenge or blood lactate concentration ≥ 4 mmol/L). This proto- or comment on the recommendations was not allowed. No col should be initiated as soon as hypoperfusion is recognized member of the guidelines committee received honoraria for and should not be delayed pending ICU admission. During the any role in the 2004, 2008, or 2012 guidelines process. first 6 hrs of resuscitation, the goals of initial resuscitation of A detailed description of the disclosure process and all sepsis-induced hypoperfusion should include all of the follow- author disclosures appear in Supplemental Digital Content 1 ing as a part of a treatment protocol (grade 1C): in the supplemental materials to this document. Appendix B a) CVP 8–12 mm Hg shows a flowchart of the COI disclosure process. Committee b) MAP ≥ 65 mm Hg members who were judged to have either financial or nonfi- c) Urine output ≥ 0.5 mL·kg·hr nancial/academic competing interests were recused during the d) uperior vena cava oxygenation saturation (Scvo2) or S closed discussion session and voting session on that topic. Full mixed venous oxygen saturation (Svo2) 70% or 65%, disclosure and transparency of all committee members’ poten- respectively. tial conflicts were sought. 2. We suggest targeting resuscitation to normalize lactate in On initial review, 68 financial conflict of interest (COI) patients with elevated lactate levels as a marker of tissue disclosures and 54 nonfinancial disclosures were submitted hypoperfusion (grade 2C). by committee members. Declared COI disclosures from 19 members were determined by the COI subcommittee to be Rationale. In a randomized, controlled, single-center study, not relevant to the guidelines content process. Nine who early quantitative resuscitation improved survival for emer- were determined to have COI (financial and nonfinancial) gency department patients presenting with septic shock (13). were adjudicated by group reassignment and requirement Resuscitation targeting the physiologic goals expressed in rec- to adhere to SSC COI policy regarding discussion or voting ommendation 1 (above) for the initial 6-hr period was associ- at any committee meetings where content germane to their ated with a 15.9% absolute reduction in 28-day mortality rate. COI was discussed. Nine were judged as having conflicts This strategy, termed early goal-directed therapy, was evalu- that could not be resolved solely by reassignment. One of ated in a multicenter trial of 314 patients with severe sepsis in these individuals was asked to step down from the commit- eight Chinese centers (14). This trial reported a 17.7% absolute tee. The other eight were assigned to the groups in which reduction in 28-day mortality (survival rates, 75.2% vs. 57.5%, Critical Care Medicine www.ccmjournal.org 587
- 9. Dellinger et al p= 0.001). A large number of other observational studies using generally can be relied upon as supporting positive response to similar forms of early quantitative resuscitation in comparable fluid loading. Either intermittent or continuous measurements patient populations have shown significant mortality reduction of oxygen saturation were judged to be acceptable. During compared to the institutions’ historical controls (Supplemental the first 6 hrs of resuscitation, if Scvo2 less than 70% or Svo2 Digital Content 2, http://links.lww.com/CCM/A615). Phase III equivalent of less than 65% persists with what is judged to be of the SSC activities, the international performance improve- adequate intravascular volume repletion in the presence of ment program, showed that the mortality of septic patients persisting tissue hypoperfusion, then dobutamine infusion (to a presenting with both hypotension and lactate ≥ 4 mmol/L was maximum of 20 μg/kg/min) or transfusion of packed red blood 46.1%, similar to the 46.6% mortality found in the first trial cited cells to achieve a hematocrit of greater than or equal to 30% in above (15). As part of performance improvement programs, attempts to achieve the Scvo2 or Svo2 goal are options. The strong some hospitals have lowered the lactate threshold for triggering recommendation for achieving a CVP of 8 mm Hg and an Scvo2 quantitative resuscitation in the patient with severe sepsis, but of 70% in the first 6 hrs of resuscitation of sepsis-induced tissue these thresholds have not been subjected to randomized trials. hypoperfusion, although deemed desirable, are not yet the The consensus panel judged use of CVP and Svo2 targets standard of care as verified by practice data. The publication to be recommended physiologic targets for resuscitation. of the initial results of the international SSC performance Although there are limitations to CVP as a marker of improvement program demonstrated that adherence to CVP intravascular volume status and response to fluids, a low CVP and Scvo2 targets for initial resuscitation was low (15). Table 5. Recommendations: Initial Resuscitation and Infection Issues A. Initial Resuscitation 1. rotocolized, quantitative resuscitation of patients with sepsis- induced tissue hypoperfusion (defined in this document as hypotension P persisting after initial fluid challenge or blood lactate concentration ≥ 4 mmol/L). Goals during the first 6 hrs of resuscitation: a) Central venous pressure 8–12 mm Hg b) Mean arterial pressure (MAP) ≥ 65 mm Hg c) Urine output ≥ 0.5 mL/kg/hr d) Central venous (superior vena cava) or mixed venous oxygen saturation 70% or 65%, respectively (grade 1C). 2. In patients with elevated lactate levels targeting resuscitation to normalize lactate (grade 2C). B. Screening for Sepsis and Performance Improvement 1. outine screening of potentially infected seriously ill patients for severe sepsis to allow earlier implementation of therapy (grade 1C). R 2. Hospital–based performance improvement efforts in severe sepsis (UG). C. Diagnosis 1. ultures as clinically appropriate before antimicrobial therapy if no significant delay ( 45 mins) in the start of antimicrobial(s) (grade C 1C). At least 2 sets of blood cultures (both aerobic and anaerobic bottles) be obtained before antimicrobial therapy with at least 1 drawn percutaneously and 1 drawn through each vascular access device, unless the device was recently (48 hrs) inserted (grade 1C). 2. se of the 1,3 beta-D-glucan assay (grade 2B), mannan and anti-mannan antibody assays (2C), if available and invasive U candidiasis is in differential diagnosis of cause of infection. 3. Imaging studies performed promptly to confirm a potential source of infection (UG). D. Antimicrobial Therapy 1. dministration of effective intravenous antimicrobials within the first hour of recognition of septic shock (grade 1B) and severe A sepsis without septic shock (grade 1C) as the goal of therapy. 2a. nitial empiric anti-infective therapy of one or more drugs that have activity against all likely pathogens (bacterial and/or fungal or I viral) and that penetrate in adequate concentrations into tissues presumed to be the source of sepsis (grade 1B). 2b. Antimicrobial regimen should be reassessed daily for potential deescalation (grade 1B). 3. se of low procalcitonin levels or similar biomarkers to assist the clinician in the discontinuation of empiric antibiotics in patients U who initially appeared septic, but have no subsequent evidence of infection (grade 2C). 4a. Combination empirical therapy for neutropenic patients with severe sepsis (grade 2B) and for patients with difficult-to-treat, multidrug- resistant bacterial pathogens such as Acinetobacter and Pseudomonas spp. (grade 2B). For patients with severe infections associated with respiratory failure and septic shock, combination therapy with an extended spectrum beta-lactam and either an aminoglycoside or a fluoroquinolone is for P. aeruginosa bacteremia (grade 2B). A combination of beta-lactam and macrolide for patients with septic shock from bacteremic Streptococcus pneumoniae infections (grade 2B). (Continued) 588 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 10. Special Article Table 5. (Continued)Recommendations: Initial Resuscitation and Infection Issues 4b. mpiric combination therapy should not be administered for more than 3–5 days. De-escalation to the most appropriate single E therapy should be performed as soon as the susceptibility profile is known (grade 2B). 5. Duration of therapy typically 7–10 days; longer courses may be appropriate in patients who have a slow clinical response, undrainable foci of infection, bacteremia with S. aureus; some fungal and viral infections or immunologic deficiencies, including neutropenia (grade 2C). 6. Antiviral therapy initiated as early as possible in patients with severe sepsis or septic shock of viral origin (grade 2C). 7. Antimicrobial agents should not be used in patients with severe inflammatory states determined to be of noninfectious cause (UG). E. Source Control 1. A specific anatomical diagnosis of infection requiring consideration for emergent source control be sought and diagnosed or excluded as rapidly as possible, and intervention be undertaken for source control within the first 12 hr after the diagnosis is made, if feasible (grade 1C). 2. When infected peripancreatic necrosis is identified as a potential source of infection, definitive intervention is best delayed until adequate demarcation of viable and nonviable tissues has occurred (grade 2B). 3. When source control in a severely septic patient is required, the effective intervention associated with the least physiologic insult should be used (eg, percutaneous rather than surgical drainage of an abscess) (UG). 4. f intravascular access devices are a possible source of severe sepsis or septic shock, they should be removed promptly after I other vascular access has been established (UG). F. Infection Prevention 1a. elective oral decontamination and selective digestive decontamination should be introduced and investigated as a method to S reduce the incidence of ventilator-associated pneumonia; This infection control measure can then be instituted in health care settings and regions where this methodology is found to be effective (grade 2B). 1b. ral chlorhexidine gluconate be used as a form of oropharyngeal decontamination to reduce the risk of ventilator-associated O pneumonia in ICU patients with severe sepsis (grade 2B). In mechanically ventilated patients or those with known fluid responsiveness during resuscitation, including flow and preexisting decreased ventricular compliance, a higher target possibly volumetric indices and microcirculatory changes, CVP of 12 to 15 mm Hg should be achieved to account for may have advantages (29–32). Available technologies allow the impediment in filling (16). Similar consideration may be measurement of flow at the bedside (33, 34); however, the effi- warranted in circumstances of increased abdominal pressure cacy of these monitoring techniques to influence clinical out- (17). Elevated CVP may also be seen with preexisting clini- comes from early sepsis resuscitation remains incomplete and cally significant pulmonary artery hypertension, making use requires further study before endorsement. of this variable untenable for judging intravascular volume The global prevalence of severe sepsis patients initially pre- status. Although the cause of tachycardia in septic patients senting with either hypotension with lactate ≥ 4 mmol//L, hypo- may be multifactorial, a decrease in elevated pulse rate with tension alone, or lactate ≥ 4 mmol/L alone, is reported as 16.6%, fluid resuscitation is often a useful marker of improving intra- 49.5%, and 5.4%, respectively (15). The mortality rate is high in vascular filling. Published observational studies have dem- septic patients with both hypotension and lactate ≥ 4 mmol/L onstrated an association between good clinical outcome in (46.1%) (15), and is also increased in severely septic patients septic shock and MAP ≥ 65 mm Hg as well as Scvo2 ≥ 70% with hypotension alone (36.7%) and lactate ≥ 4 mmol/L alone (measured in the superior vena cava, either intermittently or (30%) (15). If Scvo2 is not available, lactate normalization may continuously [18]). Many studies support the value of early be a feasible option in the patient with severe sepsis-induced protocolized resuscitation in severe sepsis and sepsis-induced tissue hypoperfusion. Scvo2 and lactate normalization may also tissue hypoperfusion (19–24). Studies of patients with shock be used as a combined endpoint when both are available. Two indicate that Svo2 runs 5% to 7% lower than Scvo2 (25). While multicenter randomized trials evaluated a resuscitation strat- the committee recognized the controversy surrounding egy that included lactate reduction as a single target or a tar- resuscitation targets, an early quantitative resuscitation pro- get combined with Scvo2 normalization (35, 36). The first trial tocol using CVP and venous blood gases can be readily estab- reported that early quantitative resuscitation based on lactate lished in both emergency department and ICU settings (26). clearance (decrease by at least 10%) was noninferior to early Recognized limitations to static ventricular filling pressure quantitative resuscitation based on achieving Scvo2 of 70% or estimates exist as surrogates for fluid resuscitation (27, 28), but more (35). The intention-to-treat group contained 300, but the measurement of CVP is currently the most readily obtainable number of patients actually requiring either Scvo2 normalization target for fluid resuscitation. Targeting dynamic measures of or lactate clearance was small (n = 30). The second trial included Critical Care Medicine www.ccmjournal.org 589
- 11. Dellinger et al 348patients with lactate levels ≥ 3 mmol/L (36). The strategy in 32,000 patient charts gathered from 239 hospitals in 17 countries this trial was based on a greater than or equal to 20% decrease through September 2011 as part of phase III of the campaign in lactate levels per 2 hrs of the first 8 hrs in addition to Scvo2 informed the revision of the bundles in conjunction with the target achievement, and was associated with a 9.6% absolute 2012 guidelines. As a result, for the 2012 version, the management reduction in mortality (p = 0.067; adjusted hazard ratio, 0.61; bundle was dropped and the resuscitation bundle was broken into 95% CI, 0.43−0.87; p = 0.006). two parts and modified as shown in Figure 1. For performance B. Screening for Sepsis and Performance improvement quality indicators, resuscitation target thresholds Improvement are not considered. However, recommended targets from the guidelines are included with the bundles for reference purposes. 1. We recommend routine screening of potentially infected seriously ill patients for severe sepsis to increase the early C. Diagnosis identification of sepsis and allow implementation of early 1. We recommend obtaining appropriate cultures before anti- sepsis therapy (grade 1C). microbial therapy is initiated if such cultures do not cause sig- Rationale. The early identification of sepsis and imple- nificant delay ( 45 minutes) in the start of antimicrobial(s) mentation of early evidence-based therapies have been doc- administration (grade 1C). To optimize identification of caus- umented to improve outcomes and decrease sepsis-related ative organisms, we recommend obtaining at least two sets of mortality (15). Reducing the time to diagnosis of severe sepsis blood cultures (both aerobic and anaerobic bottles) before is thought to be a critical component of reducing mortality antimicrobial therapy, with at least one drawn percutaneously from sepsis-related multiple organ dysfunction (35). Lack of and one drawn through each vascular access device, unless early recognition is a major obstacle to sepsis bundle initiation. the device was recently ( 48 hours) inserted. These blood Sepsis screening tools have been developed to monitor ICU cultures can be drawn at the same time if they are obtained patients (37–41), and their implementation has been associ- from different sites. Cultures of other sites (preferably quan- ated with decreased sepsis-related mortality (15). titative where appropriate), such as urine, cerebrospinal fluid, wounds, respiratory secretions, or other body fluids that may 2. Performance improvement efforts in severe sepsis should be be the source of infection, should also be obtained before used to improve patient outcomes (UG). antimicrobial therapy if doing so does not cause significant Rationale. Performance improvement efforts in sepsis have delay in antibiotic administration (grade 1C). been associated with improved patient outcomes (19, 42–46). Improvement in care through increasing compliance with sep- Rationale. Although sampling should not delay timely sis quality indicators is the goal of a severe sepsis performance administration of antimicrobial agents in patients with severe improvement program (47). Sepsis management requires a mul- sepsis (eg, lumbar puncture in suspected meningitis), obtain- tidisciplinary team (physicians, nurses, pharmacy, respiratory, ing appropriate cultures before administration of antimicrobials dieticians, and administration) and multispecialty collaboration is essential to confirm infection and the responsible pathogens, (medicine, surgery, and emergency medicine) to maximize the and to allow de-escalation of antimicrobial therapy after receipt chance for success. Evaluation of process change requires consis- of the susceptibility profile. Samples can be refrigerated or fro- tent education, protocol development and implementation, data zen if processing cannot be performed immediately. Because collection, measurement of indicators, and feedback to facilitate rapid sterilization of blood cultures can occur within a few the continuous performance improvement. Ongoing educational hours after the first antimicrobial dose, obtaining those cultures sessions provide feedback on indicator compliance and can help before therapy is essential if the causative organism is to be iden- identify areas for additional improvement efforts. In addition to tified. Two or more blood cultures are recommended (51). In traditional continuing medical education efforts to introduce patients with indwelling catheters (for more than 48 hrs), at least guidelines into clinical practice, knowledge translation efforts one blood culture should be drawn through each lumen of each have recently been introduced as a means to promote the use of vascular access device (if feasible, especially for vascular devices high-quality evidence in changing behavior (48). Protocol imple- with signs of inflammation, catheter dysfunction, or indicators mentation associated with education and performance feedback of thrombus formation). Obtaining blood cultures peripherally has been shown to change clinician behavior and is associated and through a vascular access device is an important strategy. If with improved outcomes and cost-effectiveness in severe sepsis the same organism is recovered from both cultures, the likeli- (19, 23, 24, 49). In partnership with the Institute for Healthcare hood that the organism is causing the severe sepsis is enhanced. Improvement, phase III of the Surviving Sepsis Campaign targeted In addition, if equivalent volumes of blood drawn for cul- the implementation of a core set (“bundle”) of recommendations ture and the vascular access device is positive much earlier than in hospital environments where change in behavior and clinical the peripheral blood culture (ie, more than 2 hrs earlier), the impact were measured (50). The SSC guidelines and bundles can data support the concept that the vascular access device is the be used as the basis of a sepsis performance improvement program. source of the infection (36, 51, 52). Quantitative cultures of Application of the SSC sepsis bundles led to sustained, catheter and peripheral blood may also be useful for determin- continuous quality improvement in sepsis care and was associated ing whether the catheter is the source of infection. The volume with reduced mortality (15). Analysis of the data from nearly of blood drawn with the culture tube should be ≥ 10 mL (53). 590 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 12. Special Article Rationale. The diagnosis of SURVIVING SEPSIS CAMPAIGN BUNDLES systemic fungal infection (usu- TO BE COMPLETED WITHIN 3 HOURS: ally candidiasis) in the critically 1) Measure lactate level ill patient can be challenging, 2) Obtain blood cultures prior to administration of antibiotics 3) Administer broad spectrum antibiotics and rapid diagnostic methodolo- 4) Administer 30 mL/kg crystalloid for hypotension or lactate 4mmol/L gies, such as antigen and antibody detection assays, can be helpful in TO BE COMPLETED WITHIN 6 HOURS: 5) Apply vasopressors (for hypotension that does not respond to initial fluid resuscitation) detecting candidiasis in the ICU to maintain a mean arterial pressure (MAP) ≥ 65 mm Hg patient. These suggested tests have 6) In the event of persistent arterial hypotension despite volume resuscitation (septic shown positive results significantly shock) or initial lactate 4 mmol/L (36 mg/dL): - Measure central venous pressure (CVP)* earlier than standard culture meth- - Measure central venous oxygen saturation (ScvO2)* ods (62–67), but false-positive 7) Remeasure lactate if initial lactate was elevated* reactions can occur with coloni- *Targets for quantitative resuscitation included in the guidelines are CVP of ≥8 mm Hg, zation alone, and their diagnostic ScvO2 of 70%, and normalization of lactate. utility in managing fungal infec- tion in the ICU needs additional Figure 1. Surviving Sepsis Campaign Care Bundles. study (65). Quantitative (or semiquantitative) cultures of respiratory tract 3. We recommend that imaging studies be performed secretions are often recommended for the diagnosis of venti- promptly in attempts to confirm a potential source of infec- lator-associated pneumonia (54), but their diagnostic value tion. Potential sources of infection should be sampled as remains unclear (55). they are identified and in consideration of patient risk for The Gram stain can be useful, in particular for respiratory transport and invasive procedures (eg, careful coordination tract specimens, to determine if inflammatory cells are pres- and aggressive monitoring if the decision is made to trans- ent (greater than five polymorphonuclear leukocytes/high- port for a CT-guided needle aspiration). Bedside studies, powered field and less than ten squamous cells/low-powered such as ultrasound, may avoid patient transport (UG). field) and if culture results will be informative of lower respi- Rationale. Diagnostic studies may identify a source of ratory pathogens. Rapid influenza antigen testing during peri- infection that requires removal of a foreign body or drainage to ods of increased influenza activity in the community is also maximize the likelihood of a satisfactory response to therapy. recommended. A focused history can provide vital informa- Even in the most organized and well-staffed healthcare facili- tion about potential risk factors for infection and likely patho- ties, however, transport of patients can be dangerous, as can gens at specific tissue sites. The potential role of biomarkers be placing patients in outside-unit imaging devices that are for diagnosis of infection in patients presenting with severe difficult to access and monitor. Balancing risk and benefit is sepsis remains undefined. The utility of procalcitonin levels or therefore mandatory in those settings. other biomarkers (such as C-reactive protein) to discriminate the acute inflammatory pattern of sepsis from other causes of D. Antimicrobial Therapy generalized inflammation (eg, postoperative, other forms of 1. The administration of effective intravenous antimicrobials shock) has not been demonstrated. No recommendation can within the first hour of recognition of septic shock (grade be given for the use of these markers to distinguish between 1B) and severe sepsis without septic shock (grade 1C) severe infection and other acute inflammatory states (56–58). should be the goal of therapy. Remark: Although the weight In the near future, rapid, non-culture-based diagnostic meth- of the evidence supports prompt administration of antibi- ods (polymerase chain reaction, mass spectroscopy, microar- otics following the recognition of severe sepsis and septic rays) might be helpful for a quicker identification of pathogens shock, the feasibility with which clinicians may achieve this and major antimicrobial resistance determinants (59). These ideal state has not been scientifically evaluated. methodologies could be particularly useful for difficult-to-cul- ture pathogens or in clinical situations where empiric antimi- Rationale. Establishing vascular access and initiating crobial agents have been administered before culture samples aggressive fluid resuscitation are the first priorities when were been obtained. Clinical experience remains limited, and managing patients with severe sepsis or septic shock. Prompt more clinical studies are needed before recommending these infusion of antimicrobial agents should also be a priority and non-culture molecular methods as a replacement for standard may require additional vascular access ports (68, 69). In the presence of septic shock, each hour delay in achieving admin- blood culture methods (60, 61). istration of effective antibiotics is associated with a measurable 2. We suggest the use of the 1,3 β-d-glucan assay (grade 2B), increase in mortality in a number of studies (15, 68, 70–72). mannan and anti-mannan antibody assays (grade 2C) Overall, the preponderance of data support giving antibiot- when invasive candidiasis is in the differential diagnosis of ics as soon as possible in patients with severe sepsis with or infection. without septic shock (15, 68, 70–77). The administration of Critical Care Medicine www.ccmjournal.org 591
- 13. Dellinger et al antimicrobialagents with a spectrum of activity likely to treat of amphotericin B) should be tailored to the local pattern of the responsible pathogen(s) effectively within 1 hr of the diag- the most prevalent Candida species and any recent exposure nosis of severe sepsis and septic shock. Practical considerations, to antifungal drugs (78). Recent Infectious Diseases Society for example challenges with clinicians’ early identification of of America (IDSA) guidelines recommend either fluconazole patients or operational complexities in the drug delivery chain, or an echinocandin. Empiric use of an echinocandin is pre- represent unstudied variables that may impact achieving this ferred in most patients with severe illness, especially in those goal. Future trials should endeavor to provide an evidence base patients who have recently been treated with antifungal agents, in this regard. This should be the target goal when managing or if Candida glabrata infection is suspected from earlier cul- patients with septic shock, whether they are located within the ture data. Knowledge of local resistance patterns to antifungal hospital ward, the emergency department, or the ICU. The agents should guide drug selection until fungal susceptibility strong recommendation for administering antibiotics within 1 test results, if available, are performed. Risk factors for candi- hr of the diagnosis of severe sepsis and septic shock, although demia, such as immunosuppressed or neutropenic state, prior judged to be desirable, is not yet the standard of care as verified intense antibiotic therapy, or colonization in multiple sites, by published practice data (15). should also be considered when choosing initial therapy. If antimicrobial agents cannot be mixed and delivered promptly Because patients with severe sepsis or septic shock have little from the pharmacy, establishing a supply of premixed antibiotics margin for error in the choice of therapy, the initial selection for such urgent situations is an appropriate strategy for ensuring of antimicrobial therapy should be broad enough to cover all prompt administration. Many antibiotics will not remain stable if likely pathogens. Antibiotic choices should be guided by local premixed in a solution. This risk must be taken into consideration prevalence patterns of bacterial pathogens and susceptibility in institutions that rely on premixed solutions for rapid availabil- data. Ample evidence exists that failure to initiate appropriate ity of antibiotics. In choosing the antimicrobial regimen, clinicians therapy (ie, therapy with activity against the pathogen that is should be aware that some antimicrobial agents have the advan- subsequently identified as the causative agent) correlates with tage of bolus administration, while others require a lengthy infu- increased morbidity and mortality in patients with severe sep- sion. Thus, if vascular access is limited and many different agents sis or septic shock (68, 71, 79, 80). Recent exposure to anti- must be infused, bolus drugs may offer an advantage. microbials (within last 3 months) should be considered in the choice of an empiric antibacterial regimen. Patients with 2a. We recommend that initial empiric anti-infective therapy severe sepsis or septic shock warrant broad-spectrum therapy include one or more drugs that have activity against all until the causative organism and its antimicrobial susceptibili- likely pathogens (bacterial and/or fungal or viral) and that ties are defined. Although a global restriction of antibiotics is penetrate in adequate concentrations into the tissues pre- an important strategy to reduce the development of antimi- sumed to be the source of sepsis (grade 1B). crobial resistance and to reduce cost, it is not an appropri- Rationale. The choice of empirical antimicrobial therapy ate strategy in the initial therapy for this patient population. depends on complex issues related to the patient’s history, However, as soon as the causative pathogen has been identi- including drug intolerances, recent receipt of antibiotics (previ- fied, de-escalation should be performed by selecting the most ous 3 months), underlying disease, the clinical syndrome, and appropriate antimicrobial agent that covers the pathogen susceptibility patterns of pathogens in the community and hos- and is safe and cost-effective. Collaboration with antimicro- pital, and that previously have been documented to colonize bial stewardship programs, where they exist, is encouraged to or infect the patient. The most common pathogens that cause ensure appropriate choices and rapid availability of effective septic shock in hospitalized patients are Gram-positive bac- antimicrobials for treating septic patients. All patients should teria, followed by Gram-negative and mixed bacterial micro- receive a full loading dose of each agent. Patients with sepsis organisms. Candidiasis, toxic shock syndromes, and an array often have abnormal and vacillating renal or hepatic function, of uncommon pathogens should be considered in selected or may have abnormally high volumes of distribution due to patients. An especially wide range of potential pathogens exists aggressive fluid resuscitation, requiring dose adjustment. Drug for neutropenic patients. Recently used anti-nfective agents i serum concentration monitoring can be useful in an ICU set- should generally be avoided. When choosing empirical therapy, ting for those drugs that can be measured promptly. Significant clinicians should be cognizant of the virulence and growing expertise is required to ensure that serum concentrations max- prevalence of oxacillin (methicillin)-esistant Staphylococcus r imize efficacy and minimize toxicity (81, 82). aureus, and resistance to broad-spectrum beta-lactams and car- 2b. The antimicrobial regimen should be reassessed daily for bapenem among Gram-negative bacilli in some communities potential de-escalation to prevent the development of resis- and healthcare settings. Within regions in which the prevalence tance, to reduce toxicity, and to reduce costs (grade 1B). of such drug-resistant organisms is significant, empiric therapy adequate to cover these pathogens is warranted. Rationale. Once the causative pathogen has been identified, Clinicians should also consider whether candidemia is a the most appropriate antimicrobial agent that covers the pathogen likely pathogen when choosing initial therapy. When deemed and is safe and cost-effective should be selected. On occasion, warranted, the selection of empirical antifungal therapy (eg, an continued use of specific combinations of antimicrobials echinocandin, triazoles such as fluconazole, or a formulation might be indicated even after susceptibility testing is available 592 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 14. Special Article (eg, Pseudomonasspp. only susceptible to aminoglycosides; would include aminoglycoside monotherapy, which should enterococcal endocarditis; Acinetobacter spp. infections susceptible be generally avoided, particularly for P. aeruginosa sepsis, only to polymyxins). Decisions on definitive antibiotic choices and for selected forms of endocarditis, where prolonged should be based on the type of pathogen, patient characteristics, courses of combinations of antibiotics are warranted. and favored hospital treatment regimens. Narrowing the spectrum of antimicrobial coverage and Rationale. A propensity-matched analysis, meta-analysis, reducing the duration of antimicrobial therapy will reduce the and meta-regression analysis, along with additional observa- likelihood that the patient will develop superinfection with tional studies, have demonstrated that combination therapy other pathogenic or resistant organisms, such as Candida spe- produces a superior clinical outcome in severely ill, septic cies, Clostridium difficile, or vancomycin-resistant Enterococcus patients with a high risk of death (86–90). In light of the faecium. However, the desire to minimize superinfections and increasing frequency of resistance to antimicrobial agents other complications should not take precedence over giving an in many parts of the world, broad-spectrum coverage gen- adequate course of therapy to cure the infection that caused erally requires the initial use of combinations of antimi- the severe sepsis or septic shock. crobial agents. Combination therapy used in this context connotes at least two different classes of antibiotics (usually 3. We suggest the use of low procalcitonin levels or similar a beta-lactam agent with a macrolide, fluoroquinolone, or biomarkers to assist the clinician in the discontinuation aminoglycoside for select patients). A controlled trial sug- of empiric antibiotics in patients who appeared septic, but gested, however, that when using a carbapenem as empiric have no subsequent evidence of infection (grade 2C). therapy in a population at low risk for infection with resis- Rationale. This suggestion is predicated on the preponder- tant microorganisms, the addition of a fluoroquinolone ance of the published literature relating to the use of procalcito- does not improve outcomes of patients (85). A number of nin as a tool to discontinue unnecessary antimicrobials (58, 83). other recent observational studies and some small, pro- However, clinical experience with this strategy is limited and the spective trials support initial combination therapy for potential for harm remains a concern (83). No evidence demon- selected patients with specific pathogens (eg, pneumococ- strates that this practice reduces the prevalence of antimicrobial cal sepsis, multidrug-resistant Gram-negative pathogens) resistance or the risk of antibiotic-related diarrhea from C. dif- (91–93), but evidence from adequately powered, random- ficile. One recent study failed to show any benefit of daily procal- ized clinical trials is not available to support combination citonin measurement in early antibiotic therapy or survival (84). over monotherapy other than in septic patients at high risk 4a. Empiric therapy should attempt to provide antimicrobial of death. In some clinical scenarios, combination therapies activity against the most likely pathogens based upon each are biologically plausible and are likely clinically useful even patient’s presenting illness and local patterns of infection. if evidence has not demonstrated improved clinical outcome We suggest combination empiric therapy for neutropenic (89, 90, 94, 95). Combination therapy for suspected or known patients with severe sepsis (grade 2B) and for patients with Pseudomonas aeruginosa or other multidrug-resistant Gram- difficult-to-treat, multidrug-resistant bacterial pathogens negative pathogens, pending susceptibility results, increases such as Acinetobacter and Pseudomonas spp. (grade 2B). the likelihood that at least one drug is effective against that For selected patients with severe infections associated with strain and positively affects outcome (88, 96). respiratory failure and septic shock, combination therapy 5. We suggest that the duration of therapy typically be 7 to 10 with an extended spectrum beta-lactam and either an ami- days if clinically indicated; longer courses may be appropri- noglycoside or a fluoroquinolone is suggested for P. aeru- ginosa bacteremia (grade 2B). Similarly, a more complex ate in patients who have a slow clinical response, undrain- combination of beta-lactam and a macrolide is suggested able foci of infection, bacteremia with S. aureus; some fungal for patients with septic shock from bacteremic Streptococ- and viral infections, or immunologic deficiencies, including cus pneumoniae infections (grade 2B). neutropenia (grade 2C). Rationale. Complex combinations might be needed in set- Rationale. Although patient factors may influence the length tings where highly antibiotic-resistant pathogens are preva- of antibiotic therapy, in general, a duration of 7-10 days (in the lent, with such regimens incorporating carbapenems, colistin, absence of source control issues) is adequate. Thus, decisions to rifampin, or other agents. However, a recent controlled trial continue, narrow, or stop antimicrobial therapy must be made suggested that adding a fluoroquinolone to a carbapenem as on the basis of clinician judgment and clinical information. Cli- empiric therapy did not improve outcome in a population at nicians should be cognizant of blood cultures being negative in low risk for infection with resistant microorganisms (85). a significant percentage of cases of severe sepsis or septic shock, 4b. We suggest that combination therapy, when used empirically despite the fact that many of these cases are very likely caused in patients with severe sepsis, should not be administered by bacteria or fungi. Clinicians should be cognizant that blood for longer than 3 to 5 days. De-escalation to the most appro- cultures will be negative in a significant percentage of cases of priate single-agent therapy should be performed as soon as severe sepsis or septic shock, despite many of these cases are the susceptibility profile is known (grade 2B). Exceptions very likely caused by bacteria or fungi. Critical Care Medicine www.ccmjournal.org 593
- 15. Dellinger et al 6. We suggest that antiviral therapy be initiated as early as pos- excluded as rapidly as possible, and intervention be under- sible in patients with severe sepsis or septic shock of viral taken for source control within the first 12 hr after the diag- origin (grade 2C). nosis is made, if feasible (grade 1C). 2. We suggest that when infected peripancreatic necrosis is Rationale. Recommendations for antiviral treatment identified as a potential source of infection, definitive inter- include the use of: a) early antiviral treatment of suspected vention is best delayed until adequate demarcation of viable or confirmed influenza among persons with severe influenza and nonviable tissues has occurred (grade 2B). (eg, those who have severe, complicated, or progressive illness 3. When source control in a severely septic patient is required, or who require hospitalization); b) early antiviral treatment the effective intervention associated with the least physi- of suspected or confirmed influenza among persons at higher risk for influenza complications; and c) therapy with a ologic insult should be used (eg, percutaneous rather than neuraminidase inhibitor (oseltamivir or zanamivir) for persons surgical drainage of an abscess) (UG). with influenza caused by 2009 H1N1 virus, influenza A (H3N2) 4. If intravascular access devices are a possible source virus, or influenza B virus, or when the influenza virus type or of severe sepsis or septic shock, they should be influenza A virus subtype is unknown (97, 98). Susceptibility removed promptly after other vascular access has been to antivirals is highly variable in a rapidly evolving virus such established (UG). as influenza, and therapeutic decisions must be guided by Rationale. The principles of source control in the manage- updated information regarding the most active, strain-specific, ment of sepsis include a rapid diagnosis of the specific site of antiviral agents during influenza epidemics (99, 100). infection and identification of a focus of infection amenable The role of cytomegalovirus (CMV) and other herpesviruses to source control measures (specifically the drainage of an as significant pathogens in septic patients, especially those not abscess, debridement of infected necrotic tissue, removal of a known to be severely immunocompromised, remains unclear. potentially infected device, and definitive control of a source Active CMV viremia is common (15%−35%) in critically ill of ongoing microbial contamination) (105). Foci of infec- patients; the presence of CMV in the bloodstream has been tion readily amenable to source control measures include an repeatedly found to be a poor prognostic indicator (101, 102). intra-abdominal abscess or gastrointestinal perforation, chol- What is not known is whether CMV simply is a marker of dis- angitis or pyelonephritis, intestinal ischemia or necrotizing ease severity or if the virus actually contributes to organ injury soft tissue infection, and other deep space infection, such as and death in septic patients (103). No treatment recommen- an empyema or septic arthritis. Such infectious foci should dations can be given based on the current level of evidence. be controlled as soon as possible following successful initial In those patients with severe primary or generalized varicella- resuscitation (106–108), and intravascular access devices zoster virus infections, and in rare patients with disseminated that are potentially the source of severe sepsis or septic shock herpes simplex infections, antiviral agents such as acyclovir should be removed promptly after establishing other sites for can be highly effective when initiated early in the course of vascular access (109, 110). infection (104). A randomized, controlled trial (RCT) comparing early 7. We recommend that antimicrobial agents not be used in to delayed surgical intervention for peripancreatic necro- patients with severe inflammatory states determined to be sis showed better outcomes with a delayed approach (111). of noninfectious cause (UG). Moreover, a randomized surgical study found that a mini- mally invasive, step-up approach was better tolerated by Rationale. When infection is found not to be present, patients and had a lower mortality than open necrosectomy antimicrobial therapy should be stopped promptly to mini- in necrotizing pancreatitis (112), although areas of uncer- mize the likelihood that the patient will become infected tainty exist, such as definitive documentation of infection and with an antimicrobial-resistant pathogen or will develop a appropriate length of delay. The selection of optimal source drug-related adverse effect. Although it is important to stop control methods must weigh the benefits and risks of the unnecessary antibiotics early, clinicians should be cogni- specific intervention as well as risks of transfer (113). Source zant that blood cultures will be negative in more than 50% control interventions may cause further complications, such of cases of severe sepsis or septic shock if the patients are as bleeding, fistulas, or inadvertent organ injury. Surgical receiving empiric antimicrobial therapy; yet many of these intervention should be considered when other interventional cases are very likely caused by bacteria or fungi. Thus, the approaches are inadequate or when diagnostic uncertainty decisions to continue, narrow, or stop antimicrobial therapy persists despite radiologic evaluation. Specific clinical situa- must be made on the basis of clinician judgment and clinical tions require consideration of available choices, the patient’s information. preferences, and the clinician’s expertise. E. Source Control F. Infection Prevention 1. We recommend that a specific anatomical diagnosis of infection requiring consideration for emergent source con- 1a. We suggest that selective oral decontamination (SOD) trol (eg, necrotizing soft tissue infection, peritonitis, chol- and selective digestive decontamination (SDD) should angitis, intestinal infarction) be sought and diagnosed or be introduced and investigated as a method to reduce the 594 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 16. Special Article incidence of ventilator-associated pneumonia (VAP); this 3. We suggest the use of albumin in the fluid resuscitation of infection control measure can then be instituted in health- severe sepsis and septic shock when patients require sub- care settings and regions where this methodology is found stantial amounts of crystalloids (grade 2C). to be effective (grade 2B). Rationale. The absence of any clear benefit following the 1b. We suggest oral chlorhexidine gluconate (CHG) be used administration of colloid solutions compared to crystalloid as a form of oropharyngeal decontamination to reduce the solutions, together with the expense associated with colloid risk of VAP in ICU patients with severe sepsis (grade 2B). solutions, supports a high-grade recommendation for the use of crystalloid solutions in the initial resuscitation of patients Rationale. Careful infection control practices (eg, hand with severe sepsis and septic shock. washing, expert nursing care, catheter care, barrier precau- Three recent multicenter RCTs evaluating 6% HES tions, airway management, elevation of the head of the bed, 130/0.4 solutions (tetra starches) have been published. The subglottic suctioning) should be instituted during the care of CRYSTMAS study demonstrated no difference in mortality septic patients as reviewed in the nursing considerations for with HES vs. 0.9% normal saline (31% vs. 25.3%, p = 0.37) the Surviving Sepsis Campaign (114). The role of SDD with in the resuscitation of septic shock patients; however the systemic antimicrobial prophylaxis and its variants (eg, SOD, study was underpowered to detect the 6% difference in CHG) has been a contentious issue ever since the concept was absolute mortality observed (122). In a sicker patient first developed more than 30 years ago. The notion of limit- cohort, a Scandinavian multicenter study in septic patients ing the acquisition of opportunistic, often multidrug-resistant, (6S Trial Group) showed increased mortality rates with healthcare-associated microorganisms has its appeal by pro- 6% HES 130/0.42 fluid resuscitation compared to Ringer’s moting “colonization resistance” from the resident microbi- acetate (51% vs. 43% p = 0.03) (123). The CHEST study, ome existing along mucosal surfaces of the alimentary tract. conducted in a heterogenous population of patients admit- However, the efficacy of SDD, its safety, propensity to prevent ted to intensive care (HES vs. isotonic saline, n = 7000 or promote antibiotic resistance, and cost-effectiveness remain critically ill patients), showed no difference in 90-day mor- debatable despite a number of favorable meta-analyses and controlled clinical trials (115). The data indicate an overall tality between resuscitation with 6% HES with a molecular reduction in VAP but no consistent improvement in mortality, weight of 130 kD/0.40 and isotonic saline (18% vs. 17%, except in selected populations in some studies. Most studies p = 0.26); the need for renal replacement therapy was higher do not specifically address the efficacy of SDD in patients who in the HES group (7.0% vs. 5.8%; relative risk [RR], 1.21; present with sepsis, but some do (116–118). 95% confidence interval [CI], 1.00−1.45; p = 0.04) (124). Oral CHG is relatively easy to administer, decreases risk of A meta-analysis of 56 randomized trials found no overall nosocomial infection, and reduces the potential concern over difference in mortality between crystalloids and artificial promotion of antimicrobial resistance by SDD regimens. This colloids (modified gelatins, HES, dextran) when used for remains a subject of considerable debate, despite the recent initial fluid resuscitation (125). Information from 3 ran- evidence that the incidence of antimicrobial resistance does domized trials (n = 704 patients with severe sepsis/septic not change appreciably with current SDD regimens (119–121). shock) did not show survival benefit with use of heta-, The grade 2B was designated for both SOD and CHG as it hexa-, or pentastarches compared to other fluids (RR, 1.15; was felt that risk was lower with CHG and the measure better 95% CI, 0.95−1.39; random effect; I2 = 0%) (126–128). accepted despite less published literature than with SOD. However, these solutions increased the risk of acute kidney Supplemental Digital Content 3 (http://links.lww.com/ injury (RR, 1.60; 95% CI, 1.26−2.04; I2 = 0%) (126–128). CCM/A615) shows a GRADEpro Summary of Evidence Table The evidence of harm observed in the 6S and CHEST stud- for the use of topical digestive tract antibiotics and CHG for ies and the meta-analysis supports a high-level recommen- prophylaxis against VAP. dation advising against the use of HES solutions in patients with severe sepsis and septic shock, particularly since other Hemodynamic Support and Adjunctive Therapy options for fluid resuscitation exist. The CRYSTAL trial, (Table 6) another large prospective clinical trial comparing crystal- loids and colloids, was recently completed and will provide G. Fluid Therapy of Severe Sepsis additional insight into HES fluid resuscitation. 1. We recommend crystalloids be used as the initial fluid of The SAFE study indicated that albumin administration choice in the resuscitation of severe sepsis and septic shock was safe and equally as effective as 0.9% saline (129). A (grade 1B). meta-analysis aggregated data from 17 randomized trials 2. We recommend against the use of hydroxyethyl starches (n = 1977) of albumin vs. other fluid solutions in patients (HES) for fluid resuscitation of severe sepsis and septic with severe sepsis/septic shock (130); 279 deaths occurred shock (grade 1B). (This recommendation is based on the among 961 albumin-treated patients vs. 343 deaths among results of the VISEP [128], CRYSTMAS [122], 6S [123], 1.016 patients treated with other fluids, thus favor- and CHEST [124] trials. The results of the recently com- ing albumin (odds ratio [OR], 0.82; 95% CI, 0.67−1.00; pleted CRYSTAL trial were not considered.) I2 = 0%). When albumin-treated patients were compared Critical Care Medicine www.ccmjournal.org 595
- 17. Dellinger et al Table6. Recommendations: Hemodynamic Support and Adjunctive Therapy G. Fluid Therapy of Severe Sepsis 1. Crystalloids as the initial fluid of choice in the resuscitation of severe sepsis and septic shock (grade 1B). 2. Against the use of hydroxyethyl starches for fluid resuscitation of severe sepsis and septic shock (grade 1B). 3. Albumin in the fluid resuscitation of severe sepsis and septic shock when patients require substantial amounts of crystalloids (grade 2C). 4. Initial fluid challenge in patients with sepsis-induced tissue hypoperfusion with suspicion of hypovolemia to achieve a minimum of 30 mL/kg of crystalloids (a portion of this may be albumin equivalent). More rapid administration and greater amounts of fluid may be needed in some patients (grade 1C). 5. Fluid challenge technique be applied wherein fluid administration is continued as long as there is hemodynamic improvement either based on dynamic (eg, change in pulse pressure, stroke volume variation) or static (eg, arterial pressure, heart rate) variables (UG). H. Vasopressors 1. Vasopressor therapy initially to target a mean arterial pressure (MAP) of 65 mm Hg (grade 1C). 2. Norepinephrine as the first choice vasopressor (grade 1B). 3. Epinephrine (added to and potentially substituted for norepinephrine) when an additional agent is needed to maintain adequate blood pressure (grade 2B). 4. Vasopressin 0.03 units/minute can be added to norepinephrine (NE) with intent of either raising MAP or decreasing NE dosage (UG). 5. Low dose vasopressin is not recommended as the single initial vasopressor for treatment of sepsis-induced hypotension and vasopressin doses higher than 0.03-0.04 units/minute should be reserved for salvage therapy (failure to achieve adequate MAP with other vasopressor agents) (UG). 6. Dopamine as an alternative vasopressor agent to norepinephrine only in highly selected patients (eg, patients with low risk of tachyarrhythmias and absolute or relative bradycardia) (grade 2C). 7. Phenylephrine is not recommended in the treatment of septic shock except in circumstances where (a) norepinephrine is associated with serious arrhythmias, (b) cardiac output is known to be high and blood pressure persistently low or (c) as salvage therapy when combined inotrope/vasopressor drugs and low dose vasopressin have failed to achieve MAP target (grade 1C). 8. Low-dose dopamine should not be used for renal protection (grade 1A). 9. All patients requiring vasopressors have an arterial catheter placed as soon as practical if resources are available (UG). I. Inotropic Therapy 1. A trial of dobutamine infusion up to 20 micrograms/kg/min be administered or added to vasopressor (if in use) in the presence of (a) myocardial dysfunction as suggested by elevated cardiac filling pressures and low cardiac output, or (b) ongoing signs of hypoperfusion, despite achieving adequate intravascular volume and adequate MAP (grade 1C). 2. Not using a strategy to increase cardiac index to predetermined supranormal levels (grade 1B). J. Corticosteroids 1. Not using intravenous hydrocortisone to treat adult septic shock patients if adequate fluid resuscitation and vasopressor therapy are able to restore hemodynamic stability (see goals for Initial Resuscitation). In case this is not achievable, we suggest intravenous hydrocortisone alone at a dose of 200 mg per day (grade 2C). 2. Not using the ACTH stimulation test to identify adults with septic shock who should receive hydrocortisone (grade 2B). 3. In treated patients hydrocortisone tapered when vasopressors are no longer required (grade 2D). 4. Corticosteroids not be administered for the treatment of sepsis in the absence of shock (grade 1D). 5. When hydrocortisone is given, use continuous flow (grade 2D). with those receiving crystalloids (seven trials, n = 1441), the reduction in 28-day mortality (from 26.3% to 24.1%), but OR of dying was significantly reduced for albumin-treated did not achieve statistical significance. These data support patients (OR, 0.78; 95% CI, 0.62−0.99; I2 = 0%). A multi- a low-level recommendation regarding the use of albumin center randomized trial (n = 794) in patients with septic in patients with sepsis and septic shock (personal com- shock compared intravenous albumin (20 20%) every g, munication from J.P. Mira and as presented at the 32nd 8 hrs for 3 days to intravenous saline solution (130); International ISICEM Congress 2012, Brussels and the 25th albumin therapy was associated with 2.2% absolute ESICM Annual Congress 2012, Lisbon). 596 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 18. Special Article 4. We recommendan initial fluid challenge in patients is a fundamental aspect of the hemodynamic management of with sepsis-induced tissue hypoperfusion with suspi- patients with septic shock and should ideally be achieved before cion of hypovolemia to achieve a minimum of 30 mL/ vasopressors and inotropes are used; however, using vasopres- kg of crystalloids (a portion of this may be albumin sors early as an emergency measure in patients with severe shock equivalent). More rapid administration and greater is frequently necessary, as when diastolic blood pressure is too amounts of fluid may be needed in some patients (see Ini- low. When that occurs, great effort should be directed to wean- tial Resuscitation recommendations) (grade 1C). ing vasopressors with continuing fluid resuscitation. 2. We recommend norepinephrine as the first-choice vaso- 5. We recommend that a fluid challenge technique be applied pressor (grade 1B). wherein fluid administration is continued as long as there is 3. We suggest epinephrine (added to and potentially sub- hemodynamic improvement either based on dynamic (eg, stituted for norepinephrine) when an additional agent is change in pulse pressure, stroke volume variation) or static needed to maintain adequate blood pressure (grade 2B). (eg, arterial pressure, heart rate) variables (UG). 4. Vasopressin (up to 0.03 U/min) can be added to nor- Rationale. Dynamic tests to assess patients’ responsiveness to epinephrine with the intent of raising MAP to target or fluid replacement have become very popular in recent years in decreasing norepinephrine dosage (UG). the ICU (131). These tests are based on monitoring changes in 5. Low-dose vasopressin is not recommended as the single ini- stroke volume during mechanical ventilation or after passive leg tial vasopressor for treatment of sepsis-induced hypoten- raising in spontaneously breathing patients. A systematic review sion, and vasopressin doses higher than 0.03–0.04 U/min (29 trials, n = 685 critically ill patients) looked at the association should be reserved for salvage therapy (failure to achieve an between stroke volume variation, pulse pressure variation, and/ adequate MAP with other vasopressor agents) (UG). or stroke volume variation and the change in stroke volume/ 6. We suggest dopamine as an alternative vasopressor agent to cardiac index after a fluid or positive end-expiratory pressure norepinephrine only in highly selected patients (eg, patients challenge (132). The diagnostic OR of fluid responsiveness was with low risk of tachyarrhythmias and absolute or relative 59.86 (14 trials, 95% CI, 23.88−150.05) and 27.34 (five trials, bradycardia) (grade 2C). 95% CI, 3.46−55.53) for the pulse pressure variation and the 7. Phenylephrine is not recommended in the treatment of sep- stroke volume variation, respectively. Utility of pulse pressure tic shock except in the following circumstances: (a) norepi- variation and stroke volume variation is limited in the presence nephrine is associated with serious arrhythmias, (b) cardiac of atrial fibrillation, spontaneous breathing, and low pressure output is known to be high and blood pressure persistently support breathing. These techniques generally require sedation. low, or (c) as salvage therapy when combined inotrope/ H. Vasopressors vasopressor drugs and low-dose vasopressin have failed to achieve the MAP target (grade 1C). 1. We recommend that vasopressor therapy initially target a MAP of 65 mm Hg (grade 1C). Rationale. The physiologic effects of vasopressor and com- bined inotrope/vasopressors selection in septic shock are set out Rationale. Vasopressor therapy is required to sustain life in an extensive number of literature entries (135–147). Table 7 and maintain perfusion in the face of life-threatening hypoten- depicts a GRADEpro Summary of Evidence Table comparing sion, even when hypovolemia has not yet been resolved. Below dopamine and norepinephrine in the treatment of septic shock. a threshold MAP, autoregulation in critical vascular beds can be Dopamine increases MAP and cardiac output, primarily due lost, and perfusion can become linearly dependent on pressure. to an increase in stroke volume and heart rate. Norepinephrine Thus, some patients may require vasopressor therapy to achieve increases MAP due to its vasoconstrictive effects, with little a minimal perfusion pressure and maintain adequate flow (133, change in heart rate and less increase in stroke volume compared 134). The titration of norepinephrine to a MAP as low as 65 mm with dopamine. Norepinephrine is more potent than dopamine Hg has been shown to preserve tissue perfusion (134). Note that and may be more effective at reversing hypotension in patients the consensus definition of sepsis-induced hypotension for use with septic shock. Dopamine may be particularly useful in of MAP in the diagnosis of severe sepsis is different (MAP patients with compromised systolic function but causes more 70 mm Hg) from the evidence-based target of 65 mm Hg used in tachycardia and may be more arrhythmogenic than norepi- this recommendation. In any case, the optimal MAP should be nephrine (148). It may also influence the endocrine response via individualized as it may be higher in patients with atherosclero- the hypothalamic pituitary axis and have immunosuppressive sis and/or previous hypertension than in young patients without effects. However, information from five randomized trials (n = cardiovascular comorbidity. For example, a MAP of 65 mm Hg 1993 patients with septic shock) comparing norepinephrine to might be too low in a patient with severe uncontrolled hyperten- dopamine does not support the routine use of dopamine in the sion; in a young, previously normotensive patient, a lower MAP management of septic shock (136, 149–152). Indeed, the rela- might be adequate. Supplementing endpoints, such as blood tive risk of short-term mortality was 0.91 (95% CI, 0.84−1.00; pressure, with assessment of regional and global perfusion, such fixed effect; I2 = 0%) in favor of norepinephrine. A recent meta- as blood lactate concentrations, skin perfusion, mental status, analysis showed dopamine was associated with an increased risk and urine output, is important. Adequate fluid resuscitation (RR, 1.10 [1.01−1.20]; p = 0.035); in the two trials that reported Critical Care Medicine www.ccmjournal.org 597
- 19. Dellinger et al Table7. Norepinephrine Compared With Dopamine in Severe Sepsis Summary of Evidence Norepinephrine compared with dopamine in severe sepsis Patient or population: Patients with severe sepsis Settings: Intensive care unit Intervention: Norepinephrine Comparison: Dopamine Sources: Analysis performed by Djillali Annane for Surviving Sepsis Campaign using following publications: De Backer D. N Engl J Med 2010; 362:779–789; Marik PE. JAMA 1994; 272:1354–1357; Mathur RDAC. Indian J Crit Care Med 2007; 11:186–191; Martin C. Chest 1993; 103:1826–1831; Patel GP. Shock 2010; 33:375–380; Ruokonen E. Crit Care Med 1993; 21:1296–1303 Illustrative Comparative Risksa (95% CI) Quality Relative No. of of the Assumed Corresponding Effect Participants Evidence Outcomes Risk Risk (95% CI) (Studies) (GRADE) Comments Dopamine Norepinephrine Short-term mortality Study population RR 0.91 2043 (6 studies) ⊕⊕⊕ (0.83 to 0.99) moderateb,c 530 per 1000 482 per 1000 (440 to 524) Serious adverse events Study population RR 0.47 1931 (2 studies) ⊕⊕⊕ −Supraventricular (0.38 to 0.58) moderateb,c arrhythmias 229 per 1000 82 per 1000 (34 to 195) Serious adverse Study population RR 0.35 1931 (2 studies) ⊕⊕⊕ events −Ventricular (0.19 to 0.66) moderateb,c arrhythmias 39 per 1000 15 per 1000 (8 to 27) a The assumed risk is the control group risk across studies. The corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI = confidence interval, RR = risk ratio. b Strong heterogeneity in the results (I2 = 85%), however this reflects degree of effect, not direction of effect. We have decided not to lower the evidence quality. c Effect results in part from hypovolemic and cardiogenic shock patients in De Backer, N Engl J Med 2010. We have lowered the quality of evidence one level for indirectness. arrhythmias, these were more frequent with dopamine than has similar effects but is long acting (164). Studies show that with norepinephrine (RR, 2.34 [1.46−3.77]; p = 0.001) (153). vasopressin concentrations are elevated in early septic shock, but Although some human and animal studies suggest decrease to normal range in the majority of patients between 24 epinephrine has deleterious effects on splanchnic circulation and 48 hrs as shock continues (165). This has been called relative and produces hyperlactatemia, no clinical evidence shows that vasopressin deficiency because in the presence of hypotension, epinephrine results in worse outcomes, and it should be the vasopressin would be expected to be elevated. The significance first alternative to norepinephrine. Indeed, information from of this finding is unknown. The VASST trial, an RCT comparing 4 randomized trials (n = 540) comparing norepinephrine norepinephrine alone to norepinephrine plus vasopressin at to epinephrine found no evidence for differences in the risk 0.03 U/min, showed no difference in outcome in the intent-to- of dying (RR, 0.96; CI, 0.77−1.21; fixed effect; I2 = 0%) (142, treat population (166). An a priori defined subgroup analysis 147, 154, 155). Epinephrine may increase aerobic lactate demonstrated that survival among patients receiving 15 µg/ production via stimulation of skeletal muscles’ β2-adrenergic min norepinephrine at the time of randomization was better receptors and thus may prevent the use of lactate clearance to with the addition of vasopressin; however, the pretrial rationale guide resuscitation. With its almost pure α-adrenergic effects, for this stratification was based on exploring potential benefit in phenylephrine is the adrenergic agent least likely to produce the population requiring ≥ 15 µg/min norepinephrine. Higher tachycardia, but it may decrease stroke volume and is therefore doses of vasopressin have been associated with cardiac, digital, not recommended for use in the treatment of septic shock except and splanchnic ischemia and should be reserved for situations in circumstances where norepinephrine is: a) associated with where alternative vasopressors have failed (167). Information serious arrhythmias, or b) cardiac output is known to be high, or from seven trials (n = 963 patients with septic shock) comparing c) as salvage therapy when other vasopressor agents have failed norepinephrine with vasopressin (or terlipressin) does not to achieve target MAP (156). Vasopressin levels in septic shock support the routine use of vasopressin or its analog terlipressin have been reported to be lower than anticipated for a shock state (93, 95, 97, 99, 159, 161, 164, 166, 168–170). Indeed, the relative (157). Low doses of vasopressin may be effective in raising blood risk of dying was 1.12 (95% CI, 0.96−1.30; fixed effects; I2 = 0%). pressure in patients, refractory to other vasopressors and may However, the risk of supraventricular arrhythmias was increased have other potential physiologic benefits (158–163). Terlipressin with norepinephrine (RR, 7.25; 95% CI, 2.30−22.90; fixed effect; 598 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 20. Special Article I2 =0%). Cardiac output measurement targeting maintenance J. Corticosteroids of a normal or elevated flow is desirable when these pure 1. We suggest not using intravenous hydrocortisone as a treat- vasopressors are instituted. ment of adult septic shock patients if adequate fluid resus- 8. We recommend that low-dose dopamine not be used for citation and vasopressor therapy are able to restore hemo- renal protection (grade 1A). dynamic stability (see goals for Initial Resuscitation). If this is not achievable, we suggest intravenous hydrocortisone Rationale. A large randomized trial and meta-analysis com- alone at a dose of 200 mg per day (grade 2C). paring low-dose dopamine to placebo found no difference in either primary outcomes (peak serum creatinine, need for renal Rationale. The response of septic shock patients to fluid replacement, urine output, time to recovery of normal renal and vasopressor therapy seems to be an important factor in function) or secondary outcomes (survival to either ICU or selection of patients for optional hydrocortisone therapy. One hospital discharge, ICU stay, hospital stay, arrhythmias) (171, French multicenter RCT of patients in vasopressor-unrespon- 172). Thus, the available data do not support administration of sive septic shock (hypotension despite fluid resuscitation and low doses of dopamine solely to maintain renal function. vasopressors for more than 60 mins) showed significant shock 9. We recommend that all patients requiring vasopressors have reversal and reduction of mortality rate in patients with rela- an arterial catheter placed as soon as practical if resources tive adrenal insufficiency (defined as postadrenocorticotropic are available (UG). hormone [ACTH] cortisol increase ≤ 9 µg/dL) (175). Two smaller RCTs also showed significant effects on shock reversal Rationale. In shock states, estimation of blood pressure with steroid therapy (176, 177). In contrast, a large, European using a cuff is commonly inaccurate; use of an arterial cannula multicenter trial (CORTICUS) that enrolled patients without provides a more appropriate and reproducible measurement sustained shock and had a lower risk of death than the French of arterial pressure. These catheters also allow continuous trial failed to show a mortality benefit with steroid therapy analysis so that decisions regarding therapy can be based on (178). Unlike the French trial that only enrolled shock patients immediate and reproducible blood pressure information. with blood pressure unresponsive to vasopressor therapy, the CORTICUS study included patients with septic shock regard- I. Inotropic Therapy less of how the blood pressure responded to vasopressors; the 1. We recommend that a trial of dobutamine infusion up to study baseline (placebo) 28-day mortality rate was 61% and 20 μg/kg/min be administered or added to vasopressor (if 31%, respectively. The use of the ACTH test (responders and in use) in the presence of: a) myocardial dysfunction, as nonresponders) did not predict the faster resolution of shock. suggested by elevated cardiac filling pressures and low car- In recent years, several systematic reviews have examined the diac output, or b) ongoing signs of hypoperfusion, despite use of low-dose hydrocortisone in septic shock with contradic- achieving adequate intravascular volume and adequate tory results: Annane et al (179) analyzed the results of 12 stud- MAP (grade 1C). ies and calculated a significant reduction in 28-day mortality 2. We recommend against the use of a strategy to increase car- with prolonged low-dose steroid treatment in adult septic diac index to predetermined supranormal levels (grade 1B). shock patients (RR, 0.84; 95% CI, 0.72−0.97; p = 0.02) (180). Rationale. Dobutamine is the first choice inotrope for patients In parallel, Sligl and colleagues (180) used a similar technique, with measured or suspected low cardiac output in the presence of but only identified eight studies for their meta-analysis, six adequate left ventricular filling pressure (or clinical assessment of of which had a high-level RCT design with low risk of bias adequate fluid resuscitation) and adequate MAP. Septic patients (181). In contrast to the aforementioned review, this analysis who remain hypotensive after fluid resuscitation may have low, revealed no statistically significant difference in mortality (RR, normal, or increased cardiac outputs. Therefore, treatment with 1.00; 95% CI, 0.84−1.18). Both reviews, however, confirmed a combined inotrope/vasopressor, such as norepinephrine or the improved shock reversal by using low-dose hydrocortisone epinephrine, is recommended if cardiac output is not measured. (180, 181). A recent review on the use of steroids in adult sep- When the capability exists for monitoring cardiac output in addi- tic shock underlined the importance of selection of studies for tion to blood pressure, a vasopressor, such as norepinephrine, may systematic analysis (181) and identi ed only 6 high-level RCTs fi be used separately to target specific levels of MAP and cardiac as adequate for systematic review (175–178, 182, 183). When output. Large prospective clinical trials, which included critically only these six studies are analyzed, we found that in “low risk” ill ICU patients who had severe sepsis, failed to demonstrate ben- patients from three studies (ie, those with a placebo mortal- efit from increasing oxygen delivery to supranormal targets by use ity rate of less than 50%, which represents the majority of all of dobutamine (173, 174). These studies did not specifically tar- patients), hydrocortisone failed to show any benefit on out- get patients with severe sepsis and did not target the first 6 hrs of come (RR, 1.06). The minority of patients from the remain- resuscitation. If evidence of tissue hypoperfusion persists despite ing three studies, who had a placebo mortality of greater than adequate intravascular volume and adequate MAP, a viable alter- 60%, showed a nonsignificant trend to lower mortality by using native (other than reversing underlying insult) is to add inotropic hydrocortisone (see Supplemental Digital Content 4, http:// therapy. links.lww.com/CCM/A615, Summary of Evidence Table). Critical Care Medicine www.ccmjournal.org 599
- 21. Dellinger et al 2. We suggest not using the ACTH stimulation test to identify Rationale. Several randomized trials on the use of low-dose the subset of adults with septic shock who should receive hydrocortisone in septic shock patients revealed a significant hydrocortisone (grade 2B). increase of hyperglycemia and hypernatremia (175) as side effects. A small prospective study demonstrated that repeti- Rationale. In one study, the observation of a potential inter- tive bolus application of hydrocortisone leads to a significant action between steroid use and ACTH test was not statistically increase in blood glucose; this peak effect was not detectable significant (175). Furthermore, no evidence of this distinc- during continuous infusion. Furthermore, considerable inter- tion was observed between responders and nonresponders in a individual variability was seen in this blood glucose peak after recent multicenter trial (178). Random cortisol levels may still the hydrocortisone bolus (192). Although an association of be useful for absolute adrenal insufficiency; however, for septic hyperglycemia and hypernatremia with patient outcome mea- shock patients who suffer from relative adrenal insufficiency (no sures could not be shown, good practice includes strategies for adequate stress response), random cortisol levels have not been avoidance and/or detection of these side effects. demonstrated to be useful. Cortisol immunoassays may over- or underestimate the actual cortisol level, affecting the assignment of patients to responders or nonresponders (184). Although the SUPPORTIVE THERAPY OF SEVERE SEPSIS clinical significance is not clear, it is now recognized that etomi- (TABLE 8) date, when used for induction for intubation, will suppress the K. Blood Product Administration hypothalamic-pituitary-adrenal axis (185, 186). Moreover, a subanalysis of the CORTICUS trial (178) revealed that the use 1. Once tissue hypoperfusion has resolved and in the absence of etomidate before application of low-dose steroids was associ- of extenuating circumstances, such as myocardial ischemia, ated with an increased 28-day mortality rate (187). An inappro- severe hypoxemia, acute hemorrhage, or ischemic coronary priately low random cortisol level ( 18 μg/dL) in a patient with artery disease, we recommend that red blood cell transfu- shock would be considered an indication for steroid therapy sion occur when the hemoglobin concentration decreases along traditional adrenal insufficiency guidelines. to 7.0 g/dL to target a hemoglobin concentration of 7.0 to 9.0 g/dL in adults (grade 1B). 3. We suggest that clinicians taper the treated patient from steroid therapy when vasopressors are no longer required Rationale. Although the optimum hemoglobin concentra- (grade 2D). tion for patients with severe sepsis has not been specifically investigated, the Transfusion Requirements in Critical Care Rationale. There has been no comparative study between a trial suggested that a hemoglobin level of 7 to 9 g/dL, compared fixed-duration and clinically guided regimen or between taper- with 10 to 12 g/dL, was not associated with increased mortality ing and abrupt cessation of steroids. Three RCTs used a fixed- in critically ill adults (193). No significant differences in 30-day duration protocol for treatment (175, 177, 178), and therapy was mortality rates were observed between treatment groups in the decreased after shock resolution in two RCTs (176, 182). In four subgroup of patients with severe infections and septic shock studies, steroids were tapered over several days (176–178, 182), (22.8% and 29.7%, respectively; p = 0.36), and steroids were withdrawn abruptly in two RCTs (175, 183). Although less applicable to septic patients, results of a ran- One crossover study showed hemodynamic and immunologic domized trial in patients undergoing cardiac surgery with car- rebound effects after abrupt cessation of corticosteroids (188). diopulmonary bypass support a restrictive transfusion strategy Furthermore, a study revealed that there is no difference in out- using a threshold hematocrit of 24% (hemoglobin ≈8 g/ come of septic shock patients if low-dose hydrocortisone is used dL) as equivalent to a transfusion threshold of hematocrit of for 3 or 7 days; hence, no recommendation can be given with 30% (hemoglobin ≈10 g/dL) (194). Red blood cell transfu- regard to the optimal duration of hydrocortisone therapy (189). sion in septic patients increases oxygen delivery but does not 4. We recommend that corticosteroids not be administered for usually increase oxygen consumption (195–197). The trans- the treatment of sepsis in the absence of shock (grade 1D). fusion threshold of 7 g/dL contrasts with early goal-directed resuscitation protocols that use a target hematocrit of 30% in Rationale. Steroids may be indicated in the presence of a patients with low Scvo2 during the first 6 hrs of resuscitation of history of steroid therapy or adrenal dysfunction, but whether septic shock (13). low-dose steroids have a preventive potency in reducing the incidence of severe sepsis and septic shock in critically ill 2. We recommend not using erythropoietin as a specific treat- patients cannot be answered. A preliminary study of stress- ment of anemia associated with severe sepsis (grade 1B). dose level steroids in community-acquired pneumonia showed Rationale. No specific information regarding erythro- improved outcome measures in a small population (190), and poietin use in septic patients is available, but clinical trials a recent confirmatory RCT revealed reduced hospital length of of erythropoietin administration in critically ill patients stay without affecting mortality (191). show some decrease in red cell transfusion requirement 5. When low-dose hydrocortisone is given, we suggest using with no effect on clinical outcome (198, 199). The effect continuous infusion rather than repetitive bolus injec- of erythropoietin in severe sepsis and septic shock would tions (grade 2D). not be expected to be more beneficial than in other critical 600 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 22. Special Article conditions. Patientswith severe sepsis and septic shock may L. Immunoglobulins have coexisting conditions that meet indications for the use 1. We suggest not using intravenous immunoglobulins in of erythropoietin. adult patients with severe sepsis or septic shock (grade 2B). 3. We suggest that fresh frozen plasma not be used to correct Rationale. One larger multicenter RCT (n = 624) (210) in laboratory clotting abnormalities in the absence of bleeding adult patients and one large multinational RCT in infants with or planned invasive procedures (grade 2D). neonatal sepsis (n = 3493) (211) found no benefit for intravenous Rationale. Although clinical studies have not assessed the immunoglobulin (IVIG). (For more on this trial, see the section, impact of transfusion of fresh frozen plasma on outcomes in Pediatric Considerations.). A meta-analysis by the Cochrane col- critically ill patients, professional organizations have recom- laboration, which did not include this most recent RCT, iden- mended it for coagulopathy when there is a documented defi- tified 10 polyclonal IVIG trials (n = 1430) and seven trials on ciency of coagulation factors (increased prothrombin time, immunoglobulin (Ig) M-enriched polyclonal IVIG (n = 528) international normalized ratio, or partial thromboplastin time) (212). Compared with placebo, IVIG resulted in a significant and the presence of active bleeding or before surgical or invasive reduction in mortality (RR, 0.81 and 95% CI, 0.70−0.93; and RR, procedures (200–203). In addition, transfusion of fresh frozen 0.66 and 95% CI, 0.51−0.85, respectively). Also the subgroup of plasma usually fails to correct the prothrombin time in non- IgM-enriched IVIGs (n = 7 trials) showed a significant reduc- bleeding patients with mild abnormalities (204, 205). No studies tion in mortality rates compared with placebo (RR, 0.66; 95% suggest that correction of more severe coagulation abnormali- CI, 0.51−0.85). Trials with low risk of bias showed no reduction ties benefits patients who are not bleeding. in mortality with polyclonal IVIG (RR, 0.97; 95% CI, 0.81−1.15; five trials, n = 945). Three of these trials (210, 213, 214) used stan- 4. We recommend against antithrombin administration for dard polyclonal IVIG and two IgM-enriched IVIG (215, 216). the treatment of severe sepsis and septic shock (grade 1B). These findings are in accordance with those of two older Rationale. A phase III clinical trial of high-dose antithrom- meta-analyses (217, 218) from other Cochrane authors. One bin did not demonstrate any beneficial effect on 28-day all- systematic review (217) included a total of 21 trials and showed cause mortality in adults with severe sepsis and septic shock. a relative risk of death of 0.77 with immunoglobulin treatment High-dose antithrombin was associated with an increased risk (95% CI, 0.68−0.88); however, the results of only high-quality of bleeding when administered with heparin (206). Although trials (total of 763 patients) showed a relative risk of 1.02 (95% a post hoc subgroup analysis of patients with severe sepsis and CI, 0.84−1.24). Similarly, Laupland et al (218) found a significant reduction in mortality with the use of IVIG treatment (OR, 0.66; high risk of death showed better survival in patients receiving 95% CI, 0.53−0.83; p 0.005). When only high-quality studies antithrombin, this agent cannot be recommended until further were pooled, the OR for mortality was 0.96 (95% CI, 0.71−1.3; clinical trials are performed (207). p = 0.78). Two meta-analyses, which used less strict criteria to 5. In patients with severe sepsis, we suggest that platelets be identify sources of bias or did not state their criteria for the administered prophylactically when counts are ≤ 10,000/ assessment of study quality, found significant improvement in mm3 (10 × 109/L) in the absence of apparent bleeding, patient mortality with IVIG treatment (219, 220). In contrast as well when counts are ≤ 20,000/mm3 (20 × 109/L) if the to the most recent Cochrane review, Kreymann et al (219) clas- patient has a significant risk of bleeding. Higher platelet sified five studies that investigated IgM-enriched preparation as counts (≥ 50,000/mm3 [50 × 109/L]) are advised for active high-quality studies, combining studies in adults and neonates, bleeding, surgery, or invasive procedures (grade 2D). and found an OR for mortality of 0.5 (95% CI, 0.34−0.73). Most IVIG studies are small, some have methodological Rationale. Guidelines for transfusion of platelets are derived flaws; the only large study (n = 624) showed no effect (210). from consensus opinion and experience in patients with Subgroup effects between IgM-enriched and nonenriched for- chemotherapy-induced thrombocytopenia. Patients with severe mulations reveal substantial heterogeneity. In addition, indi- sepsis are likely to have some limitation of platelet production similar rectness and publication bias were considered in grading this to that in chemotherapy-treated patients, but they also are likely to recommendation. The low-quality evidence led to the grading have increased platelet consumption. Recommendations take into as a weak recommendation. The statistical information that account the etiology of thrombocytopenia, platelet dysfunction, comes from the high-quality trials does not support a benefi- risk of bleeding, and presence of concomitant disorders (200, 202, cial effect of polyclonal IVIG. We encourage conducting large 203, 208, 209). Factors that may increase the bleeding risk and multicenter studies to further evaluate the effectiveness of indicate the need for a higher platelet count are frequently present other polyclonal immunoglobulin preparations given intrave- in patients with severe sepsis. Sepsis itself is considered to be a nously in patients with severe sepsis. risk factor for bleeding in patients with chemotherapy-induced thrombocytopenia. Other factors considered to increase the risk of M. Selenium bleeding in patients with severe sepsis include temperature higher than 38°C, recent minor hemorrhage, rapid decrease in platelet 1. We suggest not using intravenous selenium to treat severe count, and other coagulation abnormalities (203, 208, 209). sepsis (grade 2C). Critical Care Medicine www.ccmjournal.org 601
- 23. Dellinger et al Table8. Recommendations: Other Supportive Therapy of Severe Sepsis K. Blood Product Administration 1. Once tissue hypoperfusion has resolved and in the absence of extenuating circumstances, such as myocardial ischemia, severe hypoxemia, acute hemorrhage, or ischemic heart disease, we recommend that red blood cell transfusion occur only when hemoglobin concentration decreases to 7.0 g/dL to target a hemoglobin concentration of 7.0 –9.0 g/dL in adults (grade 1B). 2. Not using erythropoietin as a specific treatment of anemia associated with severe sepsis (grade 1B). 3. Fresh frozen plasma not be used to correct laboratory clotting abnormalities in the absence of bleeding or planned invasive procedures (grade 2D). 4. Not using antithrombin for the treatment of severe sepsis and septic shock (grade 1B). 5. In patients with severe sepsis, administer platelets prophylactically when counts are 10,000/mm3 (10 x 109/L) in the absence of apparent bleeding. We suggest prophylactic platelet transfusion when counts are 20,000/mm3 (20 x 109/L) if the patient has a significant risk of bleeding. Higher platelet counts (≥50,000/mm3 [50 x 109/L]) are advised for active bleeding, surgery, or invasive procedures (grade 2D). L. Immunoglobulins 1. Not using intravenous immunoglobulins in adult patients with severe sepsis or septic shock (grade 2B). M. Selenium 1. Not using intravenous selenium for the treatment of severe sepsis (grade 2C). N. History of Recommendations Regarding Use of Recombinant Activated Protein C (rhAPC) A history of the evolution of SSC recommendations as to rhAPC (no longer available) is provided. O. Mechanical Ventilation of Sepsis-Induced Acute Respiratory Distress Syndrome (ARDS) 1. Target a tidal volume of 6 mL/kg predicted body weight in patients with sepsis-induced ARDS (grade 1A vs. 12 mL/kg). 2. Plateau pressures be measured in patients with ARDS and initial upper limit goal for plateau pressures in a passively inflated lung be ≤30 cm H2O (grade 1B). 3. Positive end-expiratory pressure (PEEP) be applied to avoid alveolar collapse at end expiration (atelectotrauma) (grade 1B). 4. Strategies based on higher rather than lower levels of PEEP be used for patients with sepsis- induced moderate or severe ARDS (grade 2C). 5. Recruitment maneuvers be used in sepsis patients with severe refractory hypoxemia (grade 2C). 6. Prone positioning be used in sepsis-induced ARDS patients with a Pao2/Fio2 ratio ≤ 100 mm Hg in facilities that have experience with such practices (grade 2B). 7. That mechanically ventilated sepsis patients be maintained with the head of the bed elevated to 30-45 degrees to limit aspiration risk and to prevent the development of ventilator-associated pneumonia (grade 1B). 8. That noninvasive mask ventilation (NIV) be used in that minority of sepsis-induced ARDS patients in whom the benefits of NIV have been carefully considered and are thought to outweigh the risks (grade 2B). 9. That a weaning protocol be in place and that mechanically ventilated patients with severe sepsis undergo spontaneous breathing trials regularly to evaluate the ability to discontinue mechanical ventilation when they satisfy the following criteria: a) arousable; b) hemodynamically stable (without vasopressor agents); c) no new potentially serious conditions; d) low ventilatory and end-expiratory pressure requirements; and e) low Fio2 requirements which can be met safely delivered with a face mask or nasal cannula. If the spontaneous breathing trial is successful, consideration should be given for extubation (grade 1A). 0. Against the routine use of the pulmonary artery catheter for patients with sepsis-induced ARDS (grade 1A). 1 1. A conservative rather than liberal fluid strategy for patients with established sepsis-induced ARDS who do not have evidence of 1 tissue hypoperfusion (grade 1C). 12. In the absence of specific indications such as bronchospasm, not using beta 2-agonists for treatment of sepsis-induced ARDS (grade 1B). P. Sedation, Analgesia, and Neuromuscular Blockade in Sepsis 1. Continuous or intermittent sedation be minimized in mechanically ventilated sepsis patients, targeting specific titration endpoints (grade 1B). 2. Neuromuscular blocking agents (NMBAs) be avoided if possible in the septic patient without ARDS due to the risk of prolonged neuromuscular blockade following discontinuation. If NMBAs must be maintained, either intermittent bolus as required or continuous infusion with train-of-four monitoring of the depth of blockade should be used (grade 1C). (Continued) 602 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 24. Special Article Table 8. (Continued)Recommendations: Other Supportive Therapy of Severe Sepsis 3. A short course of NMBA of not greater than 48 hours for patients with early sepsis-induced ARDS and a Pao2/Fio2 150 mm Hg (grade 2C). Q. Glucose Control 1. A protocolized approach to blood glucose management in ICU patients with severe sepsis commencing insulin dosing when 2 consecutive blood glucose levels are 180 mg/dL. This protocolized approach should target an upper blood glucose ≤180 mg/dL rather than an upper target blood glucose ≤ 110 mg/dL (grade 1A). 2. Blood glucose values be monitored every 1–2 hrs until glucose values and insulin infusion rates are stable and then every 4 hrs thereafter (grade 1C). 3. Glucose levels obtained with point-of-care testing of capillary blood be interpreted with caution, as such measurements may not accurately estimate arterial blood or plasma glucose values (UG). R. Renal Replacement Therapy 1. Continuous renal replacement therapies and intermittent hemodialysis are equivalent in patients with severe sepsis and acute renal failure (grade 2B). 2. Use continuous therapies to facilitate management of fluid balance in hemodynamically unstable septic patients (grade 2D). S. Bicarbonate Therapy 1. Not using sodium bicarbonate therapy for the purpose of improving hemodynamics or reducing vasopressor requirements in patients with hypoperfusion-induced lactic acidemia with pH ≥7.15 (grade 2B). T. Deep Vein Thrombosis Prophylaxis 1. Patients with severe sepsis receive daily pharmacoprophylaxis against venous thromboembolism (VTE) (grade 1B). This should be accomplished with daily subcutaneous low-molecular weight heparin (LMWH) (grade 1B versus twice daily UFH, grade 2C versus three times daily UFH). If creatinine clearance is 30 mL/min, use dalteparin (grade 1A) or another form of LMWH that has a low degree of renal metabolism (grade 2C) or UFH (grade 1A). 2. Patients with severe sepsis be treated with a combination of pharmacologic therapy and intermittent pneumatic compression devices whenever possible (grade 2C). 3. Septic patients who have a contraindication for heparin use (eg, thrombocytopenia, severe coagulopathy, active bleeding, recent intracerebral hemorrhage) not receive pharmacoprophylaxis (grade 1B), but receive mechanical prophylactic treatment, such as graduated compression stockings or intermittent compression devices (grade 2C), unless contraindicated. When the risk decreases start pharmacoprophylaxis (grade 2C). U. Stress Ulcer Prophylaxis 1. Stress ulcer prophylaxis using H2 blocker or proton pump inhibitor be given to patients with severe sepsis/septic shock who have bleeding risk factors (grade 1B). 2. When stress ulcer prophylaxis is used, proton pump inhibitors rather than H2RA (grade 2D) 3. Patients without risk factors do not receive prophylaxis (grade 2B). V. Nutrition 1. Administer oral or enteral (if necessary) feedings, as tolerated, rather than either complete fasting or provision of only intravenous glucose within the first 48 hours after a diagnosis of severe sepsis/septic shock (grade 2C). 2. Avoid mandatory full caloric feeding in the first week but rather suggest low dose feeding (eg, up to 500 calories per day), advancing only as tolerated (grade 2B). 3. Use intravenous glucose and enteral nutrition rather than total parenteral nutrition (TPN) alone or parenteral nutrition in conjunction with enteral feeding in the first 7 days after a diagnosis of severe sepsis/septic shock (grade 2B). 4. Use nutrition with no specific immunomodulating supplementation rather than nutrition providing specific immunomodulating supplementation in patients with severe sepsis (grade 2C). W. Setting Goals of Care 1. Discuss goals of care and prognosis with patients and families (grade 1B). 2. Incorporate goals of care into treatment and end-of-life care planning, utilizing palliative care principles where appropriate (grade 1B). 3. Address goals of care as early as feasible, but no later than within 72 hours of ICU admission (grade 2C). Critical Care Medicine www.ccmjournal.org 603
- 25. Dellinger et al Rationale. Selenium was administered in the hope that it guidelines recommended use of rhAPC in line with the prod- could correct the known reduction of selenium concentration uct labeling instructions required by the U.S. and European in sepsis patients and provide a pharmacologic effect through regulatory authorities with a grade B quality of evidence (7, 8). an antioxidant defense. Although some RCTs are available, By the time of publication of the 2008 SSC guidelines, addi- the evidence on the use of intravenous selenium is still very tional studies of rhAPC in severe sepsis (as required by regula- weak. Only one large clinical trial has examined the effect on tory agencies) had shown it ineffective in less severely ill patients mortality rates, and no significant impact was reported on the with severe sepsis as well as in children (229, 230). The 2008 SSC intent-to-treat population with severe systemic inflammatory recommendations reflected these findings, and the strength of response syndrome, sepsis, or septic shock (OR, 0.66; 95% CI, the rhAPC recommendation was downgraded to a suggestion 0.39−1.10; p = 0.109) (221). Overall, there was a trend toward for use in adult patients with a clinical assessment of high risk of a concentration-dependent reduction in mortality; no differ- death, most of whom will have Acute Physiology and Chronic ences in secondary outcomes or adverse events were detected. Health Evaluation (APACHE) II scores ≥ 25 or multiple organ Finally, no comment on standardization of sepsis management failure (grade 2C; quality of evidence was also downgraded from was included in this study, which recruited 249 patients over a 2004, from B to C) (7). The 2008 guidelines also recommended period of 6 years (1999–2004) (221). against use of rhAPC in low-risk adult patients, most of whom A French RCT in a small population revealed no effect on will have APACHE II scores ≤ 20 or single organ failures (grade primary (shock reversal) or secondary (days on mechanical ven- 1A), and against use in all pediatric patients (grade 1B). tilation, ICU mortality) endpoints (222). Another small RCT The results of the PROWESS SHOCK trial (1,696 patients) revealed less early VAP in the selenium group (p = 0.04), but no were released in late 2011, showing no benefit of rhAPC in patients difference in late VAP or secondary outcomes such as ICU or with septic shock (mortality 26.4% for rhAPC, 24.2% placebo) hospital mortality (223). This is in accordance with two RCTs with a relative risk of 1.09 and a p value of 0.31 (231). The drug that resulted in reduced number of infectious episodes (224) or was withdrawn from the market and is no longer available, negat- increase in glutathione peroxidase concentrations (225); neither ing any need for an SSC recommendation regarding its use. study, however, showed a beneficial effect on secondary out- come measures (renal replacement, ICU mortality) (224, 225). O. Mechanical Ventilation of Sepsis-Induced Acute A more recent large RCT tried to determine if the addition of Respiratory Distress Syndrome relatively low doses of supplemental selenium (glutamine was 1. We recommend that clinicians target a tidal volume of also tested in a two-factorial design) to parenteral nutrition in 6 mL/kg predicted body weight in patients with sepsis- critically ill patients reduces infections and improves outcome induced acute respiratory distress syndrome (ARDS) (grade (226). Selenium supplementation did not significantly affect the 1A vs. 12 mL/kg). development of a new infection (OR, 0.81; 95% CI, 0.57−1.15), 2. We recommend that plateau pressures be measured in and the 6-month mortality rate was not unaffected (OR, 0.89; patients with ARDS and that the initial upper limit goal for 95% CI, 0.62−1.29). In addition, length of stay, days of anti- plateau pressures in a passively inflated lung be ≤ 30 cm H2O biotic use, and modified Sequential Organ Failure Assessment (grade 1B). score were not significantly affected by selenium (227). In addition to the lack of evidence, the questions of optimal Rationale. Of note, studies used to determine recommen- dosing and application mode remain unanswered. Reported dations in this section enrolled patients using criteria from the high-dose regimens have involved a loading dose followed by American-European Consensus Criteria Definition for Acute an infusion, while animal trials suggest that bolus dosing could Lung Injury (ALI) and ARDS (232). For this document, we be more effective (227); this, however, has not been tested in have used the updated Berlin definition and used the terms humans. These unsolved problems require additional trials, and mild, moderate, and severe ARDS (Pao2/Fio2 ≤300, ≤200, and we encourage conducting large multicenter studies to further ≤100 mm Hg, respectively) for the syndromes previously evaluate the effectiveness of intravenous selenium in patients known as ALI and ARDS (233). Several multicenter random- with severe sepsis. This recommendation does not exclude the ized trials have been performed in patients with established use of low-dose selenium as part of the standard minerals and ARDS to evaluate the effects of limiting inspiratory pressure oligo-elements used during total parenteral nutrition. through moderation of tidal volume (234–238). These studies showed differing results that may have been caused by differ- N. History of Recommendations Regarding Use of ences in airway pressures in the treatment and control groups Recombinant Activated Protein C (233, 234, 239). Several meta-analyses suggest decreased mor- Recombinant human activated protein C (rhAPC) was tality in patients with a pressure- and volume-limited strategy approved for use in adult patients in a number of countries for established ARDS (240, 241). in 2001 following the PROWESS (Recombinant Human Acti- The largest trial of a volume- and pressure-limited strategy vated Protein C Worldwide Evaluation in Severe Sepsis) trial, showed an absolute 9% decrease in all-cause mortality in patients which enrolled 1,690 severe sepsis patients and showed a sig- with ARDS ventilated with tidal volumes of 6 mL/kg compared nificant reduction in mortality (24.7%) with rhAPC com- with 12 mL/kg of predicted body weight (PBW), and aiming for pared with placebo (30.8%, p = 0.005) (228). The 2004 SSC a plateau pressure ≤ 30 cm H2O (233). The use of lung-protective 604 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 26. Special Article strategies forpatients with ARDS is supported by clinical trials Rationale. Raising PEEP in ARDS keeps lung units open to and has been widely accepted, but the precise choice of tidal vol- participate in gas exchange. This will increase Pao2 when PEEP ume for an individual patient with ARDS may require adjust- is applied through either an endotracheal tube or a face mask ment for such factors as the plateau pressure achieved, the level (252–254). In animal experiments, avoidance of end-expira- of positive end-expiratory pressure chosen, the compliance of the tory alveolar collapse helps minimize ventilator-induced lung thoracoabdominal compartment, and the vigor of the patient’s injury when relatively high plateau pressures are in use. Three breathing effort. Patients with profound metabolic acidosis, high large multicenter trials using higher vs. lower levels of PEEP in obligate minute ventilations, or short stature may require addi- conjunction with low tidal volumes did not uncover benefit or tional manipulation of tidal volumes. Some clinicians believe harm (255–257). A meta-analysis using individual patient data it may be safe to ventilate with tidal volumes 6 mL/kg PBW showed no benefit in all patients with ARDS; however, patients as long as the plateau pressure can be maintained ≤ 30 cm H2O with moderate or severe ARDS (Pao2/Fio2 ratio ≤ 200 mm Hg) (242, 243). The validity of this ceiling value will depend on the had decreased mortality with the use of higher PEEP, whereas patient’s effort, as those who are actively breathing generate those with mild ARDS did not (258). Two options are recom- higher transalveolar pressures for a given plateau pressure than mended for PEEP titration. One option is to titrate PEEP (and tidal volume) according to bedside measurements of thoraco- patients who are passively inflated. Conversely, patients with very pulmonary compliance with the objective of obtaining the best stiff chest walls may require plateau pressures 30 H2O to cm compliance, reflecting a favorable balance of lung recruitment meet vital clinical objectives. A retrospective study suggested that and overdistension (259). The second option is to titrate PEEP tidal volumes should be lowered even with plateau pressures ≤ based on severity of oxygenation deficit and guided by the Fio2 30 cm H2O (244) as lower plateau pressures were associated with required to maintain adequate oxygenation (234, 255, 256). A decreased in-hospital mortality (245). PEEP 5 cm H2O is usually required to avoid lung collapse (260). High tidal volumes that are coupled with high plateau pres- The ARDSNet standard PEEP strategy is shown in Appendix C. sures should be avoided in ARDS. Clinicians should use as a The higher PEEP strategy recommended for ARDS is shown in starting point the objective of reducing tidal volume over 1 to Appendix D and comes from the ALVEOLI trial (257). 2 hrs from its initial value toward the goal of a “low” tidal vol- ume (≈6 mL/kg PBW) achieved in conjunction with an end- 5. We suggest recruitment maneuvers in sepsis patients with inspiratory plateau pressure ≤ 30 cm H2O. If the plateau pressure severe refractory hypoxemia due to ARDS (grade 2C). remains 30 cm H2O after reduction of tidal volume to 6 mL/kg 6. We suggest prone positioning in sepsis-induced ARDS PBW, tidal volume may be reduced further to as low as 4 mL/kg patients with a Pao2/Fio2 ratio ≤ 100 mm Hg in facilities that PBW per protocol. (Appendix C provides ARDSNet ventilator have experience with such practices (grade 2B). management and formulas to calculate PBW.) Using volume- Rationale. Many strategies exist for treating refractory and pressure-limited ventilation may lead to hypercapnia with hypoxemia in patients with severe ARDS (261). Temporarily maximum tolerated set respiratory rates. In such cases, hyper- raising transpulmonary pressure may facilitate opening atel- capnia that is otherwise not contraindicated (eg, high intracra- ectatic alveoli to permit gas exchange (260), but could also nial pressure) and appears to be tolerated should be allowed. overdistend aerated lung units leading to ventilator-induced Sodium bicarbonate or tromethamine (THAM) infusion may be lung injury and temporary hypotension. The application of considered in selected patients to facilitate use of limited ventila- transient sustained use of continuous positive airway pressure tor conditions that result in permissive hypercapnia (246, 247). appears to improve oxygenation in patients initially, but these A number of observational trials in mechanically venti- effects can be transient (262). Although selected patients with lated patients have demonstrated a decreased risk of devel- severe hypoxemia may benefit from recruitment maneuvers in oping ARDS when smaller trial volumes are used (248–251). conjunction with higher levels of PEEP, little evidence supports Accordingly, high tidal volumes and plateau pressures should the routine use in all ARDS patients (262). Blood pressure and be avoided in mechanically ventilated patients at risk for devel- oxygenation should be monitored and recruitment maneuvers oping ARDS, including those with sepsis. discontinued if deterioration in these variables is observed. No single mode of ventilation (pressure control, volume Several small studies and one large study in patients with control) has consistently been shown to be advantageous when hypoxemic respiratory failure or ARDS have shown that most compared with any other that respects the same principles of patients respond to the prone position with improved oxygen- lung protection. ation (263–266). None of the individual trials of prone posi- 3. We recommend that positive end-expiratory pressure tioning in patients with ARDS or hypoxemic respiratory failure (PEEP) be applied to avoid alveolar collapse at end expira- demonstrated a mortality benefit (267–270). One meta-analy- sis suggested potential benefits for prone positioning in patients tion (atelectotrauma) (grade 1B). with profound hypoxemia and Pao2/Fio2 ratio ≤ 100 mm Hg, but 4. We suggest strategies based on higher rather than lower lev- not in those with less severe hypoxemia (270). Prone position- els of PEEP for patients with sepsis-induced moderate to ing may be associated with potentially life-threatening com- severe ARDS (grade 2C). plications, including accidental dislodging of the endotracheal Critical Care Medicine www.ccmjournal.org 605
- 27. Dellinger et al andchest tubes; these complications occur more frequently in following criteria: a) arousable; b) hemodynamically stable patients in the prone compared with supine position (270). (without vasopressor agents); c) no new potentially serious Other methods to treat refractory hypoxemia, including conditions; d) low ventilatory and end-expiratory pressure high-frequency oscillatory ventilation, airway pressure release requirements; and e) low Fio2 requirements which can be ventilation, and extracorporeal membrane oxygenation (271), safely delivered with a face mask or nasal cannula. If the may be considered as rescue therapies in centers with expertise spontaneous breathing trial is successful, extubation should and experience with their use (261, 271–274). Inhaled nitric be considered (grade 1A). oxide does not improve mortality rates in patients with ARDS Rationale. Spontaneous breathing trial options include a and should not be routinely used (275). low level of pressure support, continuous positive airway pres- 7. We recommend that mechanically ventilated sepsis patients sure (≈5 cm H2O), or a use of a T-piece. Studies demonstrated be maintained with the head of the bed elevated between that daily spontaneous breathing trials in appropriately selected 30 and 45 degrees to limit aspiration risk and to prevent the patients reduce the duration of mechanical ventilation (282, development of VAP (grade 1B). 283). These breathing trials should be conducted in conjunction Rationale. The semi-recumbent position has been demon- with a spontaneous awakening trial (284). Successful comple- strated to decrease the incidence of VAP (276). Enteral feeding tion of spontaneous breathing trials leads to a high likelihood of increased the risk of developing VAP; 50% of the patients who successful early discontinuation of mechanical ventilation. were fed enterally in the supine position developed VAP com- 10. We recommend against the routine use of the pulmonary pared with 9% of those fed in the semi-recumbent position artery catheter for patients with sepsis-induced ARDS (276). However, the bed position was monitored only once a (grade 1A). day, and patients who did not achieve the desired bed eleva- tion were not included in the analysis (276). One study did not Rationale. Although insertion of a pulmonary artery (PA) show a difference in incidence of VAP between patients main- catheter may provide useful information on a patient’s volume tained in supine and semi-recumbent positions (277); patients status and cardiac function, these benefits may be confounded assigned to the semi-recumbent group did not consistently by differences in the interpretation of results (285–287), lack achieve the desired head of the bed elevation, and the head of of correlation of PA occlusion pressures with clinical response bed elevation in the supine group approached that of the semi- (288), and an absence of a proven strategy to use catheter recumbent group by day 7 (277). When necessary, patients results to improve patient outcomes (173). Two multicenter may be laid flat for procedures, hemodynamic measurements, randomized trials, one in patients with shock or ARDS (289) and during episodes of hypotension. Patients should not be fed and the other in those with only ARDS (290), failed to show enterally while supine. benefit with the routine use of PA catheters in ARDS. In addi- 8. We suggest that noninvasive mask ventilation (NIV) be tion, other studies in different types of critically ill patients used in that minority of sepsis-induced ARDS patients in have failed to show definitive benefit with routine use of the whom the benefits of NIV have been carefully considered PA catheter (291–293). Well-selected patients remain appropri- and are thought to outweigh the risks (grade 2B). ate candidates for PA catheter insertion only when the answers to important management decisions depend on information Rationale. Obviating the need for airway intubation con- solely obtainable from direct measurements made within the fers multiple advantages: better communication, lower inci- PA (292, 294). dence of infection, and reduced requirements for sedation. Two RCTs in patients with acute respiratory failure demon- 11. We recommend a conservative fluid strategy for patients strated improved outcome with the use of NIV when it can be with established sepsis-induced ARDS who do not have used successfully (278, 279). Unfortunately, only a small per- evidence of tissue hypoperfusion (grade 1C). centage of sepsis patients with life-threatening hypoxemia can Rationale. Mechanisms for the development of pulmo- be managed in this way (280, 281). nary edema in patients with ARDS include increased capillary NIV should be considered in patients with sepsis-induced permeability, increased hydrostatic pressure, and decreased ARDS if they are responsive to relatively low levels of pressure oncotic pressure (295). Small prospective studies in patients support and PEEP with stable hemodynamics, can be made with critical illness and ARDS have suggested that low weight comfortable, and are easily arousable; if they are able to protect gain is associated with improved oxygenation (296) and fewer the airway and spontaneously clear the airway of secretions; days of mechanical ventilation (297, 298). A fluid-conservative and if they are anticipated to recover rapidly from the precipi- strategy to minimize fluid infusion and weight gain in patients tating insult (280, 281). A low threshold for airway intubation with ARDS, based on either a central venous catheter (CVP should be maintained. 4 mm Hg) or a PA catheter (pulmonary artery wedge pressure 9. We recommend that a weaning protocol be in place and that 8 mm Hg), along with clinical variables to guide treatment, mechanically ventilated patients with severe sepsis undergo led to fewer days of mechanical ventilation and reduced length spontaneous breathing trials regularly to evaluate the ability of ICU stay without altering the incidence of renal failure or to discontinue mechanical ventilation when they satisfy the mortality rates (299). This strategy was only used in patients 606 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 28. Special Article with establishedARDS, some of whom had shock present dur- preferentially had significantly more days without ventilation, ing the ICU stay, and active attempts to reduce fluid volume shorter stay in ICU and hospital, than patients who received were conducted only outside periods of shock. sedation (propofol and midazolam) in addition to morphine (307). However, agitated delirium was more frequently detected 12. In the absence of specific indications such as bronchospasm, in the intervention group. Although not specifically studied we recommend against the use of β2-agonists for treatment in patients with sepsis, the administration of intermittent of patients with sepsis-induced ARDS (grade 1B). sedation, daily sedative interruption, and systematic titration Rationale. Patients with sepsis-induced ARDS often develop to a predefined endpoint have been demonstrated to decrease increased vascular permeability. Preclinical and early clinical data the duration of mechanical ventilation (284, 305, 308, 309). suggest that β-adrenergic agonists may speed resorption of alveo- Patients receiving neuromuscular blocking agents (NMBAs) lar edema (300). Two randomized clinical trials studied the effect must be individually assessed regarding discontinuation of of β-agonists in patients with ARDS (301, 302). In one, a com- sedative drugs because the neuromuscular blockade must first parison of aerosolized albuterol and placebo in 282 patients with be reversed. The use of intermittent vs. continuous methods ARDS, the trial was stopped for futility (301). Patients receiv- for the delivery of sedation in critically ill patients has been ing albuterol had higher heart rates on day 2, and a trend was examined in an observational study of mechanically ventilated detected toward decreased ventilator-free days (days alive and off patients that showed that patients receiving continuous the ventilator). The rates of death before discharge were 23.0% in sedation had significantly longer durations of mechanical the albuterol group vs. 17.7% in placebo-treated patients. More ventilation and ICU and hospital lengths of stay (310). than half of the patients enrolled in this trial had pulmonary or Clinical trials have evaluated daily interruption of continu- nonpulmonary sepsis as the cause of the ARDS (301). ous sedative infusions. A prospective, randomized controlled The use of intravenous salbutamol was tested in the trial in 128 mechanically ventilated adults receiving continu- BALTI-2 trial (302). Three hundred twenty-six patients with ous intravenous sedation demonstrated that a daily interrup- ARDS, 251 of whom had pulmonary or nonpulmonary sepsis tion in the continuous sedative infusion until the patient was as cause, were randomized to intravenous salbutatmol, 15 μg/ awake decreased the duration of mechanical ventilation and kg of ideal body weight, or placebo for up to 7 days. Patients ICU length of stay (283). Although the patients did receive treated with salbutamol had increased 28-day mortality rates continuous sedative infusions in this study, the daily inter- (34% vs. 23%; RR, 1.4; 95% CI, 1.03−2.08) leading to early ter- ruption and awakening allowed for titration of sedation, in mination of the trial (302). effect making the dosing intermittent. In addition, a paired Beta-2 agonists may have specific indications, such as treat- spontaneous awakening trial combined with a spontaneous ment of bronchospasm and hyperkalemia. In the absence of breathing trial decreased the duration of mechanical venti- these conditions, we recommend against the routine use of lation, length of ICU and hospital stay, and 1-year mortality β-agonists, either in intravenous or aerosolized form, for the (284). More recently, a multicenter randomized trial compared treat ent of patients with sepsis-induced ARDS. m protocolized sedation with protocolized sedation plus daily P. Sedation, Analgesia, and Neuromuscular Blockade sedation interruption in 423 critically ill mechanically venti- in Sepsis lated medical and surgical patients (311). There were no dif- 1. We recommend that either continuous or intermittent ferences in duration of mechanical ventilation or lengths of sedation be minimized in mechanically ventilated sepsis stay between the groups; and daily interruption was associated patients, targeting specific titration endpoints (grade 1B). with higher daily opioid and benzodiazepines doses, as well as higher nurse workload. Additionally, a randomized prospec- Rationale. A growing body of evidence indicates that limiting tive blinded observational study demonstrated that although the use of sedation in critically ill ventilated patients can myocardial ischemia is common in critically ill ventilated reduce the duration of mechanical ventilation and ICU and patients, daily sedative interruption is not associated with an hospital lengths of stay (303–305). While studies limiting increased occurrence of myocardial ischemia (312). Regardless sedation have been performed in a wide range of critically ill of sedation approach, early physical rehabilitation should be a patients, there is little reason to assume that septic patients goal (313). will not derive benefit from this approach (305). The use of protocols for sedation is one method to limit sedation use, and 2. We recommend that NMBAs be avoided if possible in the a randomized, controlled clinical trial found that protocolized septic patient without ARDS due to the risk of prolonged sedation compared with usual care reduced duration of neuromuscular blockade following discontinuation. If mechanical ventilation, lengths of stay, and tracheostomy NMBAs must be maintained, either intermittent bolus as rates (305). Avoidance of sedation is another strategy. A required or continuous infusion with train-of-four moni- recent observational study of 250 critically ill patients suggests toring of the depth of blockade should be used (grade 1C). that deep sedation is common in mechanically ventilated 3. We suggest a short course of an NMBA (≤ 48 hours) for patients (306). A randomized, controlled clinical trial found patients with early, sepsis-induced ARDS and Pao2/Fio2 that patients treated with intravenous morphine boluses 150 mm Hg (grace 2C). Critical Care Medicine www.ccmjournal.org 607
- 29. Dellinger et al Rationale. Although NMBAs are often administered to total dose of NMBAs and shorter intubation times) also may critically ill patients, their role in the ICU is not well defined. exist, although this has not been studied formally. No evidence exists that neuromuscular blockade in this patient Q. Glucose Control population reduces mortality or major morbidity. In addition, 1. We recommend a protocolized approach to blood glucose no studies have been published that specifically address the use management in ICU patients with severe sepsis, commenc- of NMBAs in septic patients. ing insulin dosing when two consecutive blood glucose lev- The most common indication for NMBA use in the ICU is els are 180 mg/dL. This approach should target an upper to facilitate mechanical ventilation (314). When appropriately blood glucose level ≤ 180 mg/dL rather than an upper target used, these agents may improve chest wall compliance, prevent blood glucose ≤ 110 mg/dL (grade 1A). respiratory dyssynchrony, and reduce peak airway pressures 2. We recommend blood glucose values be monitored every 1 (315). Muscle paralysis may also reduce oxygen consumption to 2 hrs until glucose values and insulin infusion rates are by decreasing the work of breathing and respiratory muscle stable, then every 4 hrs thereafter (grade 1C). blood flow (316). However, a randomized, placebo-controlled 3. We recommend that glucose levels obtained with point-of- clinical trial in patients with severe sepsis demonstrated that care testing of capillary blood be interpreted with caution, oxygen delivery, oxygen consumption, and gastric intramuco- as such measurements may not accurately estimate arterial sal pH were not improved during deep neuromuscular block- blood or plasma glucose values (UG). ade (317). A recent randomized clinical trial of continuous infusions Rationale. One large RCT single-center trial in a predomi- of cisatracurium in patients with early ARDS and a Pao2/Fio2 nantly cardiac surgical ICU demonstrated a reduction in ICU 150 mm Hg showed improved adjusted survival rates and mortality with intensive intravenous insulin (Leuven protocol) more organ failure-free days without an increased risk in ICU- targeting blood glucose to 80 to 110 mg/dL (326). A second acquired weakness compared with placebo-treated patients randomized trial of intensive insulin therapy using the Leuven (318). The investigators used a high fixed dose of cisatracurium protocol enrolled medical ICU patients with an anticipated without train-of-four monitoring, and half of the patients in the ICU length of stay of more than 3 days in three medical ICUs placebo group received at least a single dose of NMBA. Whether and overall mortality was not reduced (327). another NMBA would have similar effects is unknown. Although Since these studies (326, 327) and the previous Surviving many of the patients enrolled into this trial appeared to meet Sepsis Guidelines (7) appeared, several RCTs (128, 328–332) and meta-analyses (333–337) of intensive insulin therapy have sepsis criteria, it is not clear whether similar results would occur been performed. The RCTs studied mixed populations of sur- in sepsis patients. A GRADEpro Summary of Evidence Table gical and medical ICU patients (128, 328–332) and found that regarding use of NMBA in ARDS appears in Supplemental intensive insulin therapy did not significantly decrease mortality Digital Content 5 (http://links.lww.com/CCM/A615). (128, 328–332), whereas the NICE-SUGAR trial demonstrated An association between NMBA use and myopathies and an increased mortality (331). All studies (128, 326–332) reported neuropathies has been suggested by case studies and prospec- a much higher inci ence of severe hypoglycemia (glucose ≤ 40 d tive observational studies in the critical care population (315, mg/dL) (6%−29%) with intensive insulin therapy. Several meta- 319–322), but the mechanisms by which NMBAs produce or analyses confirmed that intensive insulin therapy was not associ- contribute to myopathies and neuropathies in these patients ated with a mortality benefit in surgical, medical, or mixed ICU are unknown. Although no studies are specific to the septic patients (333, 335, 337). The meta-analysis by Griesdale and col- patient population, it seems clinically prudent, based on exist- leagues (334), using between-trial comparisons driven mainly by ing knowledge, that NMBAs not be administered unless there the 2001 study by van den Berghe et al (326), found that inten- is a clear indication for neuromuscular blockade that cannot be sive insulin therapy was beneficial in surgical ICU patients (risk safely achieved with appropriate sedation and analgesia (315). ratio, 0.63 [0.44−0.9]), whereas the meta-analysis by Friedrich Only one prospective RCT has compared peripheral et al (336), using within-trial comparisons, showed no benefit nerve stimulation and standard clinical assessment in ICU for surgical patients in mixed medical-surgical ICUs (risk ratio patients. Rudis et al (323) randomized 77 critically ill ICU 0.99 [0.82−1.11]) and no subgroup of surgical patients who ben- patients requiring neuromuscular blockade to receive dosing efited from intensive insulin therapy. Interestingly, the RCTs that of vecuronium based on train-of-four stimulation or on clini- reported (326, 327) compared intensive insulin therapy to high cal assessment (control group). The peripheral nerve stimu- controls (180−200 mg/dL) (OR, 0.89 [0.73−1.09]), whereas those lation group received less drug and recovered neuromuscular that did not demonstrate benefit (330–332) compared intensive function and spontaneous ventilation faster than the control therapy to moderate controls (108−180 mg/dL) [OR, 1.14 (1.02 group. Nonrandomized observational studies have suggested to −1.26)]. See Supplemental Digital Content 6 (http://links. that peripheral nerve monitoring reduces or has no effect on lww.com/CCM/A615) for details. clinical recovery from NMBAs in the ICU (324, 325). The trigger to start an insulin protocol for blood glucose Benefits to neuromuscular monitoring, including faster levels 180 mg/dL with an upper target blood glucose level recovery of neuromuscular function and shorter intubation 180 mg/dL derives from the NICE-SUGAR study (331), times, appear to exist. A potential for cost savings (reduced which used these values for initiating and stopping therapy. The 608 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 30. Special Article NICE-SUGAR trialis the largest, most compelling study to date severe sepsis and acute renal failure because they achieve on glucose control in ICU patients given its inclusion of multi- similar short-term survival rates (grade 2B). ple ICUs and hospitals and a general patient population. Several 2. We suggest the use of continuous therapies to facilitate medical organizations, including the American Association management of fluid balance in hemodynamically unstable of Clinical Endocrinologists, American Diabetes Association, septic patients (grade 2D). American Heart Association, American College of Physicians, and Society of Critical Care Medicine, have published consensus Rationale. Although numerous nonrandomized studies have statements for glycemic control of hospitalized patients (338– reported a nonsignificant trend toward improved survival using 341). These statements usually targeted glucose levels between continuous methods (357–364), two meta-analyses (365, 366) 140 and 180 mg/dL. As there is no evidence that targets between reported the absence of significant difference in hospital mor- 140 and 180 mg/dL are different from targets of 110 to 140 mg/ tality between patients who receive continuous and intermittent dL, the recommendations use an upper target blood glucose renal replacement therapies. This absence of apparent benefit of ≤ 180 mg/dL without a lower target other than hypoglycemia. one modality over the other persists even when the analysis is Treatment should avoid hyperglycemia ( 180 mg/dL), hypogly- restricted to RCT studies (366). To date, five prospective RCTs cemia, and wide swings in glucose levels. The continuation of have been published (367–371); four found no significant dif- insulin infusions, especially with the cessation of nutrition, has ference in mortality (368–371), whereas one found significantly been identified as a risk factor for hypoglycemia (332). Balanced higher mortality in the continuous treatment group (367), but nutrition may be associated with a reduced risk of hypoglyce- imbalanced randomization had led to a higher baseline severity mia (342). Several studies have suggested that the variability in of illness in this group. When a multivariable model was used glucose levels over time is an important determinant of mortal- to adjust for severity of illness, no difference in mortality was ity (343–345). Hyperglycemia and glucose variability seem to be apparent between the groups (367). Most studies comparing unassociated with increased mortality rates in diabetic patients modes of renal replacement in the critically ill have included compared to nondiabetic patients (346, 347). a small number of patients and some major weaknesses (ie, Several factors may affect the accuracy and reproducibil- randomization failure, modifications of therapeutic protocol ity of point-of-care testing of blood capillary blood glucose, during the study period, combination of different types of con- including the type and model of the device used, user expertise, tinuous renal replacement therapies, small number of hetero- and patient factors, including hematocrit (false elevation with geneous groups of enrollees). The most recent and largest RCT anemia), Pao2, and drugs (348). Plasma glucose values by cap- (371) enrolled 360 patients and found no significant difference illary point-of-care testing have been found to be inaccurate in survival between the continuous and intermittent groups. with frequent false elevations (349, 350) over the range of glu- Moreover, no evidence supports the use of continuous therapies cose levels (350), but especially in the hypoglycemic (349, 351) in sepsis independent of renal replacement needs. and hyperglycemic ranges (351) and in hypotensive patients No evidence supports a better tolerance with continu- (352) or patients receiving catecholamines (353). A review of ous treatments regarding the hemodynamic tolerance of each 12 published insulin infusion protocols for critically ill patients method. Two prospective studies (369, 372) have reported a bet- showed wide variability in dose recommendations and variable ter hemodynamic tolerance with continuous treatment, with no glucose control (354). This lack of consensus about optimal improvement in regional perfusion (372) and no survival ben- dosing of intravenous insulin may reflect variability in patient efit (369). Four other prospective studies did not find any sig- factors (severity of illness, surgical vs. medical settings), or prac- nificant difference in mean arterial pressure or drop in systolic tice patterns (eg, approaches to feeding, intravenous dextrose) pressure between the two methods (368, 370, 371, 373). Two in the environments in which these protocols were developed studies reported a significant improvement in goal achievement and tested. Alternatively, some protocols may be more effec- with continuous methods (367, 369) regarding fluid balance tive than others, conclusion supported by the wide variability management. In summary, the evidence is insufficient to draw in hypoglycemia rates reported with protocols (128, 326–333). strong conclusions regarding the mode of replacement therapy Thus, the use of established insulin protocols is important not for acute renal failure in septic patients. only for clinical care but also for the conduct of clinical trials The effect of dose of continuous renal replacement on out- to avoid hypoglycemia, adverse events, and premature termina- comes in patients with acute renal failure has shown mixed tion of trials before the efficacy signal, if any, can be determined. results (374, 375). None of these trials was conducted specifi- Several studies have suggested that computer-based algorithms cally in patients with sepsis. Although the weight of evidence result in tighter glycemic control with a reduced risk of hypo- suggests that higher doses of renal replacement may be associ- glycemia (355, 356). Further study of validated, safe, and effec- ated with improved outcomes, these results may not be general- tive protocols for controlling blood glucose concentrations and izable. Two large multicenter randomized trials comparing the variability in the severe sepsis population is needed. dose of renal replacement (Acute Renal Failure Trial Network R. Renal Replacement Therapy in the United States and RENAL Renal Replacement Therapy 1. We suggest that continuous renal replacement therapies and Study in Australia and New Zealand) failed to show benefit of intermittent hemodialysis are equivalent in patients with more aggressive renal replacement dosing. (376, 377). A typical Critical Care Medicine www.ccmjournal.org 609
- 31. Dellinger et al dosefor continuous renal replacement therapy would be 20 to hemodynamically compromised patient) are dire. Therefore, 25 mL/kg/hr of effluent generation. prevention of VTE is highly desirable, especially if it can be done safely and effectively. Prophylaxis is generally effective. In particular, nine placebo- S. Bicarbonate Therapy controlled RCTs of VTE prophylaxis have been conducted in 1. We recommend against the use of sodium bicarbonate ther- general populations of acutely ill patients (381–389). All trials apy for the purpose of improving hemodynamics or reduc- showed reduction in DVT or pulmonary embolism, a benefit ing vasopressor requirements in patients with hypoperfu- that is also supported by meta-analyses (390, 391). Thus, the sion-induced lactic acidemia with pH ≥ 7.15 (grade 2B). evidence strongly supports the value of VTE prophylaxis (grade 1A). The prevalence of infection/sepsis was 17% in those studies Rationale. Although bicarbonate therapy may be useful in in which this could be ascertained. One study investigated only limiting tidal volume in ARDS in some situations of permissive ICU patients only, and 52% of those enrolled had infection/ hypercapnia (see section, Mechanical Ventilation of ARDS), no sepsis. The need to extrapolate from general, acutely ill patients evidence supports the use of bicarbonate therapy in the treat- to critically ill patients to septic patients downgrades the ment of hypoperfusion-induced lactic acidemia associated with evidence. That the effect is pronounced and the data are robust sepsis. Two blinded, crossover RCTs that compared equimolar somewhat mitigate against the extrapolation, leading to a grade saline and bicarbonate in patients with lactic acidosis failed to B determination. Because the patient’s risk of administration is reveal any difference in hemodynamic variables or vasopressor small, the gravity of not administering may be great, and the requirements (378, 379). The number of patients with 7.15 pH cost is low, the strength of the recommendation is strong (1). in these studies was small. Bicarbonate administration has been Deciding how to provide prophylaxis is decidedly more associated with sodium and fluid overload, an increase in lac- difficult. The Canadian Critical Care Trials Group compared tate and Pco2, and a decrease in serum ionized calcium, but the UFH (5000 IU twice daily) to LMWH (dalteparin, 5000 relevance of these variables to outcome is uncertain. The effect IU once per day and a second placebo injection to ensure of bicarbonate administration on hemodynamics and vasopres- parallel-group equivalence) (392). No statistically signifi- sor requirements at lower pH, as well as the effect on clinical cant difference in asymptomatic DVTs was found between outcomes at any pH, is unknown. No studies have examined the the two groups (hazard ratio, 0.92; 95% CI, 0.68−1.23; p = effect of bicarbonate administration on outcomes. 0.57), but the proportion of patients diagnosed with pul- T. Deep Vein Thrombosis Prophylaxis monary embolism on CT scan, high-probability ventila- tion perfusion scan, or autopsy was significantly lower in 1. We recommend that patients with severe sepsis receive the LMWH group (hazard ratio, 0.51; 95% CI, 0.30−0.88; daily pharmacoprophylaxis against venous thromboembo- p = 0.01).The study did not account for the use of other forms lism (VTE) (grade 1B). We recommend that this be accom- of LMWH. These data suggest that LMWH (dalteparin) is plished with daily subcutaneous low-molecular weight the treatment of choice over UFH administered twice daily heparin (LMWH) (grade 1B versus unfractionated heparin in critically ill patients. Also, because the study included sep- [UFH] twice daily and grade 2C versus UFH given thrice tic patients, the evidence supporting the use of dalteparin over daily). If creatinine clearance is 30 mL/min, we recom- twice daily UFH in critically ill, and perhaps septic, patients is mend use of dalteparin (grade 1A) or another form of strong. Similarly, a meta-analysis of acutely ill, general medical LMWH that has a low degree of renal metabolism (grade patients comparing UFH twice and thrice daily demonstrated 2C) or UFH (grade 1A). that the latter regimen was more effective at preventing VTE, 2. We suggest that patients with severe sepsis be treated with but twice daily dosing produced less bleeding (393). Both criti- a combination of pharmacologic therapy and intermit- cally ill and septic patients were included in these analyses, but tent pneumatic compression devices whenever possible their numbers are unclear. Nonetheless, the quality of evidence (grade 2C). supporting the use of three times daily, as opposed to twice 3. We recommend that septic patients who have a contraindica- daily, UFH dosing in preventing VTE in acutely ill medial c tion to heparin use (eg, thrombocytopenia, severe coagulopathy, patients is high (A). However, comparing LMWH to twice daily active bleeding, recent intracerebral hemorrhage) not receive UFH, or twice daily UFH to three times daily UFH, in sepsis pharmacoprophylaxis (grade 1B). Rather we suggest they requires extrapolation, downgrading the data. No data exist on receive mechanical prophylactic treatment, such as graduated direct comparison of LMWH to UFH administered three times compression stockings or intermittent compression devices daily, nor are there any studies directly comparing twice daily (grade 2C), unless contraindicated. When the risk decreases, we and thrice daily UFH dosing in septic or critically ill patients. suggest starting pharmacoprophylaxis (grade 2C). Therefore, it is not possible to state that LMWH is superior to Rationale. ICU patients are at risk for deep vein thrombosis three times daily UFH or that three times daily dosing is supe- (DVT) (380). It is logical that patients with severe sepsis would rior to twice daily administration in sepsis. This downgrades be at a similar or higher risk than the general ICU population. the quality of the evidence and therefore the recommendation. The consequences of VTE in the setting of sepsis (increased Douketis et al (394) conducted a study of 120 critically risk of potentially fatal pulmonary emboli in an already ill patients with acute kidney injury (creatinine clearance 610 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 32. Special Article 30 mL/min) who received VTE prophylaxis with dalteparin Both old and new meta-analyses show prophylaxis-induced 5000 IU daily for between 4 and 14 days and had at least one reduction in clinically significant upper GI bleeding, which we trough anti-factor Xa level measured. None of the patients consider significant even in the absence of proven mortality had bio-accumulation (trough anti-factor Xa level lower than benefit (409–411). The benefit of prevention of upper GI 0.06 IU/mL). The incidence of major bleeding was somewhat bleeding must be weighed against the potential (unproven) higher than in trials of other agents, but most other studies effect of increased stomach pH on a greater incidence of VAP did not involve critically ill patients, in whom the bleeding risk and C. difficile infection (409, 412, 413). (See Supplemental is higher. Further, bleeding did not correlate with detectable Digital Content 7 and 8 [http://links.lww.com/CCM/ trough levels (394). Therefore, we recommend that dalteparin A615], Summary of Evidence Tables for effects of treatments can be administered to critically ill patients with acute renal on specific outcomes.) In an exploratory hypothesis, we failure (A). Data on other LMWHs are lacking. Consequently, considered (as did the authors of the meta-analysis) (411) the these forms should probably be avoided or, if used, anti-factor possibility of less benefit and more harm in prophylaxis among Xa levels should be monitored (grade 2C). UFH is not renally patients receiving enteral nutrition but decided to provide one cleared and is safe (grade 1A). recommendation while lowering the quality of evidence. The Mechanical methods (intermittent compression devices and balance of benefits and risks may thus depend on the individual graduated compression stockings) are recommended when patient’s characteristics as well as on the local epidemiology of anticoagulation is contraindicated (395–397). A meta-analysis VAP and C. difficile infections. The rationale for considering of 11 studies, including six RCTs, published in the Cochrane only suppression of acid production (and not sucralfate) is Library concluded that the combination of pharmacologic and based on the study of 1,200 patients by Cook et al comparing mechanical prophylaxis was superior to either modality alone H2 blockers and sucralfate (414). More recent meta-analyses in preventing DVT and was better than compression alone provide low-quality evidence suggesting more effective GI in preventing pulmonary embolism (398). This analysis did bleeding protection with the use of proton pump inhibitors than with H2RA (415–417). Patients should be periodically not focus on sepsis or critically ill patients but included stud- evaluated for the continued need for prophylaxis. ies of prophylaxis after orthopedic, pelvic, and cardiac surgery. In addition, the type of pharmacologic prophylaxis varied, V. Nutrition including UFH, LMWH, aspirin, and warfarin. Nonetheless, the minimal risk associated with compression devices lead 1. We suggest administering oral or enteral (if necessary) feed- us to recommend combination therapy in most cases. In ings, as tolerated, rather than either complete fasting or pro- very-high-risk patients, LMWH is preferred over UFH (392, vision of only intravenous glucose within the first 48 hrs 399–401). Patients receiving heparin should be monitored for after a diagnosis of severe sepsis/septic shock (grade 2C). development of heparin-induced thrombocytopenia. These 2. We suggest avoiding mandatory full caloric feeding in the recommendations are consistent with those developed by the first week, but rather suggest low-dose feeding (eg, up to American College of Chest Physicians (402). 500 kcal per day), advancing only as tolerated (grade 2B). 3. We suggest using intravenous glucose and enteral nutrition U. Stress Ulcer Prophylaxis rather than total parenteral nutrition (TPN) alone or paren- teral nutrition in conjunction with enteral feeding in the first 7 1. We recommend that stress ulcer prophylaxis using H2 blocker days after a diagnosis of severe sepsis/septic shock (grade 2B). or proton pump inhibitor be given to patients with severe 4. We suggest using nutrition with no specific immunomodulat- sepsis/septic shock who have bleeding risk factors (grade 1B). ing supplementation in patients with severe sepsis (grade 2C). 2. When stress ulcer prophylaxis is used, we suggest the use of proton pump inhibitors rather than H2 receptor antagonists Rationale. Early enteral nutrition has theoretical advan- (H2RA) (grade 2C). tages in the integrity of gut mucosa and prevention of bacterial 3. We suggest that patients without risk factors should not translocation and organ dysfunction, but also concerning is the receive prophylaxis (grade 2B). risk of ischemia, mainly in hemodynamically unstable patients. Unfortunately, no clinical trial has specifically addressed Rationale. Although no study has been performed specifi- early feeding in septic patients. Studies on different subpopula- cally in patients with severe sepsis, trials confirming the benefit tions of critically ill patients, mostly surgical patients, are not of stress ulcer prophylaxis in reducing upper gastrointestinal consistent, with great variability in the intervention and con- (GI) bleeding in general ICU populations included 20% to 25% trol groups; all are of low methodological quality (418–427) of patients with sepsis (403–406). This benefit should be appli- and none was individually powered for mortality, with very cable to patients with severe sepsis and septic shock. In addition, low mortality rates (418–420, 423, 426). Authors of previously the risk factors for GI bleeding (eg, coagulopathy, mechanical published meta-analyses of optimal nutrition strategies for the ventilation for at least 48 hrs, possibly hypotension) are fre- critically ill all reported that the studies they included had high quently present in patients with severe sepsis and septic shock heterogeneity and low quality(418–430). Although no consis- (407, 408). Patients without these risk factors are unlikely (0.2%; tent effect on mortality was observed, there was evidence of 95% CI, 0.02−0.5) to have clinically important bleeding (407). benefit from some early enteral feeding on secondary outcomes, Critical Care Medicine www.ccmjournal.org 611
- 33. Dellinger et al suchas reduced incidence of infectious complications (418, in treatment effects across subgroups, including the sepsis sub- 422, 426, 427–430), reduced length of mechanical ventilation jects. Therefore, no studies suggest the superiority of TPN over (421, 427), and reduced ICU (421, 427) and hospital stays (428). enteral alone in the first 24 hrs. In fact, there is a suggestion that No evidence of harm was demonstrated in any of those studies. enteral nutrition may in fact be superior to TPN vis-à-vis infec- Therefore, there is insufficient evidence to issue a strong recom- tious complications and possibly requirement for intensive care mendation, but the suggestion of benefit and absence of harm and organ support. supports a suggestion that some enteral feeding is warranted. Immune system function can be modified through altera- Studies comparing full caloric early enteral feeding to lower tions in the supply of certain nutrients, such as arginine, gluta- targets in the critically ill have produced inconclusive results. mine, or omega-3 fatty acids. Numerous studies have assessed In four studies, no effect on mortality was seen (431–434); one whether use of these agents as nutritional supplements can reported fewer infectious complications (431), and the others affect the course of critical illness, but few specifically addressed reported increased diarrhea and gastric residuals (433, 434) their early use in sepsis. Four meta-analyses evaluated immune- and increased incidence of infectious complications with full enhancing nutrition and found no difference in mortality, nei- caloric feeding (432). In another study, mortality was greater ther in surgical nor medical patients (445–448). However, they with higher feeding, but differences in feeding strategies were analyzed all studies together, regardless of the immunocompo- modest and the sample size was small (435). Therefore, evidence nent used, which could have compromised their conclusions. is insufficient to support an early target of full caloric intake Other individual studies analyzed diets with a mix of arginine, and, indeed, some possibility of harm exists. Underfeeding glutamine, antioxidants, and/or omega-3 with negative results (60%−70% of target) or trophic feeding (upper limit of 500 (449, 450) including a small study in septic patients showing a kcal) is probably a better nutritional strategy in the first week of nonsignificant increase in ICU mortality (451, 452). severe sepsis/septic shock. This upper limit for trophic feeding Arginine. is a somewhat arbitrary number, but based in part on the fact Arginine availability is reduced in sepsis, which can lead that the two recent studies used a range of 240−480 kcal (433, to reduced nitric oxide synthesis, loss of microcirculatory 434). Underfeeding/trophic feeding strategies did not exclude regulation, and enhanced production of superoxide and advancing diet as tolerated in those who improved quickly. peroxynitrite. However, arginine supplementation could lead Some form of parenteral nutrition has been compared to to unwanted vasodilation and hypotension (452, 453). Human alternative feeding strategies (eg, fasting or enteral nutrition) trials of l-arginine supplementation have generally been small in well over 50 studies, although only one exclusively studied and reported variable effects on mortality (454–457). The sepsis (436), and eight meta-analyses have been published only study in septic patients showed improved survival, but (429, 437–443). Two of the meta-analyses summarize com- had limitations in study design (455). Other studies suggested parisons of parenteral nutrition vs. fasting or intravenous glu- no benefit (449, 454, 455) or possible harm (455) in the cose (437, 438), and six look at parenteral vs. enteral nutrition subgroup of septic patients. Some authors found improvement (429, 439–443), two of which attempted to explore the effect in secondary outcomes in septic patients, such as reduced of early enteral nutrition (441, 442). Recently, a study much infectious complications (454, 455) and length of hospital larger than most earlier nutrition trials compared ICU patients stay (454), but the relevance of these findings in the face of randomized to early use of parenteral nutrition to augment potential harm is unclear. enteral feeding vs. enteral feeding with only late initiation of parenteral nutrition if necessary (444). Glutamine. No direct evidence supports the benefits or harm of paren- Glutamine levels are also reduced during critical illness. teral nutrition in the first 48 hrs in sepsis. Rather, the evidence Exogenous supplementation can improve gut mucosal atrophy is generated predominantly from surgical, burn, and trauma and permeability, possibly leading to reduced bacterial trans- patients. None of the meta-analyses reports a mortality ben- location. Other potential benefits are enhanced immune cell efit with parenteral nutrition, except one suggesting paren- function, decreased pro-inflammatory cytokine production, teral nutrition may be better than late introduction of enteral and higher levels of glutathione and antioxidative capacity nutrition (442). Several suggested that parenteral nutrition (452, 453). However, the clinical significance of these findings had higher infectious complications compared both to fast- is not clearly established. ing or intravenous glucose and to enteral nutrition (429, 431, Although a previous meta-analysis showed mortality reduc- 438, 439, 442). Enteral feeding was associated with a higher tion (428), four other meta-analyses did not (458–462). Other rate of enteral complications (eg, diarrhea) than parenteral small studies not included in those meta-analyses had similar nutrition (438). The use of parenteral nutrition to supple- results (463, 464). Three recent well-designed studies also failed ment enteral feeding was also analyzed by Dhaliwal et al (440), to show a mortality benefit in the primary analyses (227, 465, who also reported no benefit. The trial by Casaer et al (444) 466), but again, none focused specifically on septic patients. reported that early initiation of parenteral nutrition led to lon- Two small studies on septic patients showed no benefit in mor- ger hospital and ICU stays, longer duration of organ support, tality rates (467, 468) but a significant reduction in infectious and higher incidence of ICU-acquired infection. One-fifth of compliations (467) and a faster recovery of organ dysfunc- c patients had sepsis and there was no evidence of heterogeneity tion (468). Some previous individual studies and meta-analyses 612 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 34. Special Article showed positivesecondary outcomes, such as reduction in infec- in the ICU highlight the importance of incorporating goals tious morbidty (461, 462, 465) and organ dysfunction (462). i of care along with the prognosis into treatment plans (484). Beneficial effects were found mostly in trials using parenteral Additionally, discussing the prognosis for achieving the goals rather than enteral glutamine. However, recent and well-sized of care and level of certainty of prognosis has been identified studies could not demonstrate a reduction of infectious compli- as an important component of surrogate decision-making cations (227) or organ dysfunction (465, 466), even with paren- in the ICU (485, 486). However, variations exist in the use teral glutamine. An ongoing trial (REDOXS) of 1,200 patients of advanced care planning and integration of palliative and will test both enteral and parenteral glutamine and antioxidant end-of-life care in the ICU, which can lead to conflicts that supplementation in critically ill, mechanically ventilated patients may threaten overall quality of care (487, 488). The use of (469). Although no clear benefit could be demonstrated in clini- proactive family care conferences to identify advanced direc- cal trials with supplemental glutamine, there is no sign of harm. tives and treatment goals within 72 hrs of ICU admission The omega-3 fatty acids eicosapentaenoic acid (EPA) and promotes communication and understanding between the gamma-linolenic acid (GLA) are eicosanoid precursors. The patient’s family and the care team; improves family satisfac- prostaglandins, leukotrienes, and thromboxanes produced from tion; decreases stress, anxiety, and depression in surviving EPA/GLA are less potent than their arachidonic acid-derived relatives; facilitates end-of-life decision making; and short- equivalents, reducing the pro-inflammatory impact on the ens length of stay for patients who die in the ICU (489–494). immune response (452, 453). Three early studies were sum- Clinical practice guidelines for support of the ICU patient marized in a meta-analysis that reported a significant mortal- and family pro ote: early and repeated care conferencing to m ity reduction, increased ventilator-free days, and reduced risk of reduce family stress and improve consistency in communica- new organ dysfunction (470). However, only one study was in tion; open flexible visita ion; family presence during clinical t septic patients (471), none was individually powered for mortal- rounds and resuscitation; and attention to cultural and spiri- ity (472, 473), and all three used a diet with high omega-6 lipid tual support (495). Additionally, the integration of advanced content in the control group, which is not the usual standard of care planning and palliative care focused on pain manage- care in the criti ally ill. The authors who first reported reduced c ment, symptom control, and family support has been shown mortality in sepsis (471) conducted a follow-up multicenter to improve symptom management and patient com ort, and f study and again found improvement in nonmortality outcomes, to improve family communication (484, 490, 496). though notably with no demonstrable effect on mortality (474). Other studies using enteral (475–477) or parenteral (478–480) PEDIATRIC CONSIDERATIONS IN SEVERE fish oil failed to confirm these findings in general critical illness SEPSIS (TABLE 9) or acute lung injury. Thus, no large, reproducible findings sug- While sepsis in children is a major cause of death in industrialized gest a clear benefit in the use of immunomodulating nutritional countries with state-of-the-art ICUs, the overall mortality from supplements in sepsis, though larger trials are ongoing. severe sepsis is much lower than that in adults, estimated at about 2% to 10% (497–499). The hospital mortality rate for severe sepsis W. Setting Goals of Care is 2% in previously healthy children and 8% in chronically ill chil 1. We recommend that goals of care and prognosis be dis- dren in the United States (497). Definitions of sepsis, severe sepsis, cussed with patients and families (grade 1B). septic shock, and multiple organ dysfunction/failure syndromes 2. We recommend that the goals of care be incorporated into are similar to adult definitions but depend on age-specific heart treatment and end-of-life care planning, utilizing palliative rate, respiratory rate, and white blood cell count cutoff values care principles where appropriate (grade 1B). (500, 501). This document provides recommendations only for 3. We suggest that goals of care be addressed as early as feasible, term newborns and children in the industrialized resource-rich but no later than within 72 hrs of ICU admission (grade 2C). setting with full access to mechanical ventilation ICUs. Rationale. The majority of ICU patients receive full A. Initial Resuscitation support with aggressive, life-sustaining treatments. Many patients with multiple organ system failure or severe neu- 1. We suggest starting with oxygen administered by face mask rologic injuries will not survive or will have a poor quality or, if needed and available, high-flow nasal cannula oxy- gen or nasopharyngeal continuous positive airway pressure of life. Decisions to provide less-aggressive life-sustaining (CPAP) for respiratory distress and hypoxemia. Peripheral treatments or to withdraw life-sustaining treatments in these intravenous access or intraosseous access can be used for fluid patients may be in the patient’s best interest and may be what resuscitation and inotrope infusion when a central line is not patients and their families desire (481). Physicians have dif- available. If mechanical ventilation is required, then cardio- ferent end-of-life practices based on their region of practice, vascular instability during intubation is less likely after appro- culture, and religion (482). Although the outcome of inten- priate cardiovascular resuscitation (grade 2C). sive care treatment in critically ill patients may be difficult to prognosticate accurately, establishing realistic treat ent m Rationale. Due to low functional residual capacity, young goals is important in promoting patient-centered care in the infants and neonates with severe sepsis may require early intu- ICU (483). Models for structuring initiatives to enhance care bation; however, during intubation and mechanical ventilation, Critical Care Medicine www.ccmjournal.org 613
- 35. Dellinger et al Table9. Recommendations: Special Considerations in Pediatrics A. Initial Resuscitation 1. For respiratory distress and hypoxemia start with face mask oxygen or if needed and available, high flow nasal cannula oxygen or nasopharyngeal CPAP (NP CPAP). For improved circulation, peripheral intravenous access or intraosseus access can be used for fluid resuscitation and inotrope infusion when a central line is not available. If mechanical ventilation is required then cardiovascular instability during intubation is less likely after appropriate cardiovascular resuscitation (grade 2C). 2. Initial therapeutic end points of resuscitation of septic shock: capillary refill of ≤2 secs, normal blood pressure for age, normal pulses with no differential between peripheral and central pulses, warm extremities, urine output 1 mL·kg-1·hr-1, and normal mental status. Scvo2 saturation ≥70% and cardiac index between 3.3 and 6.0 L/min/m2 should be targeted thereafter (grade 2C). 3. Follow American College of Critical Care Medicine-Pediatric Life Support ( ACCM-PALS) guidelines for the management of septic shock (grade 1C). 4. Evaluate for and reverse pneumothorax, pericardial tamponade, or endocrine emergencies in patients with refractory shock (grade 1C). B. Antibiotics and Source Control 1. Empiric antibiotics be administered within 1 hr of the identification of severe sepsis. Blood cultures should be obtained before administering antibiotics when possible but this should not delay administration of antibiotics. The empiric drug choice should be changed as epidemic and endemic ecologies dictate (eg H1N1, MRSA, chloroquine resistant malaria, penicillin-resistant pneumococci, recent ICU stay, neutropenia ) (grade 1D). 2. Clindamycin and anti-toxin therapies for toxic shock syndromes with refractory hypotension (grade 2D). 3. Early and aggressive source control (grade 1D). 4. Clostridium difficile colitis should be treated with enteral antibiotics if tolerated. Oral vancomycin is preferred for severe disease (grade 1A). C. Fluid Resuscitation 1. In the industrialized world with access to inotropes and mechanical ventilation, initial resuscitation of hypovolemic shock begins with infusion of isotonic crystalloids or albumin with boluses of up to 20 mL/kg crystalloids (or albumin equivalent ) over 5–10 minutes, titrated to reversing hypotension, increasing urine output, and attaining normal capillary refill, peripheral pulses, and level of consciousness without inducing hepatomegaly or rales. If hepatomegaly or rales exist then inotropic support should be implemented, not fluid resuscitation. In non-hypotensive children with severe hemolytic anemia (severe malaria or sickle cell crises) blood transfusion is considered superior to crystalloid or albumin bolusing (grade 2C). D. Inotropes/Vasopressors/Vasodilators 1. Begin peripheral inotropic support until central venous access can be attained in children who are not responsive to fluid resuscitation (grade 2C). 2. Patients with low cardiac output and elevated systemic vascular resistance states with normal blood pressure be given vasodilator therapies in addition to inotropes (grade 2C). E. Extracorporeal Membrane Oxygenation (ECMO) 1. Consider ECMO for refractory pediatric septic shock and respiratory failure (grade 2C). F. Corticosteroids 1. Timely hydrocortisone therapy in children with fluid refractory, catecholamine resistant shock and suspected or proven absolute (classic) adrenal insufficiency (grade 1A). G. Protein C and Activated Protein Concentrate No recommendation as no longer available. H. Blood Products and Plasma Therapies 1. Similar hemoglobin targets in children as in adults. During resuscitation of low superior vena cava oxygen saturation shock ( 70%), hemoglobin levels of 10 g/dL are targeted. After stabilization and recovery from shock and hypoxemia then a lower target 7.0 g/dL can be considered reasonable (grade 1B). 2. Similar platelet transfusion targets in children as in adults (grade 2C). 3. Use plasma therapies in children to correct sepsis-induced thrombotic purpura disorders, including progressive disseminated intravascular coagulation, secondary thrombotic microangiopathy, and thrombotic thrombocytopenic purpura (grade 2C). I. Mechanical Ventilation. 1 Lung-protective strategies during mechanical ventilation (grade 2C) (Continued) 614 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 36. Special Article Table 9. (continued)Recommendations: Special Considerations in Pediatrics J. Sedation/Analgesia/Drug Toxicities 1. We recommend use of sedation with a sedation goal in critically ill mechanically ventilated patients with sepsis (grade 1D). 2. Monitor drug toxicity labs because drug metabolism is reduced during severe sepsis, putting children at greater risk of adverse drug-related events (grade 1C). K. Glycemic Control 1. Control hyperglycemia using a similar target as in adults ≤ 180 mg/dL. Glucose infusion should accompany insulin therapy in newborns and children because some hyperglycemic children make no insulin whereas others are insulin resistant (grade 2C). L. Diuretics and Renal Replacement Therapy 1. Use diuretics to reverse fluid overload when shock has resolved, and if unsuccessful then continuous venovenous hemofiltration (CVVH) or intermittent dialysis to prevent 10% total body weight fluid overload (grade 2C). M. Deep Vein Thrombosis (DVT) Prophylaxis N o recommendation on the use of DVT prophylaxis in prepubertal children with severe sepsis. N. Stress Ulcer(SU) Prophylaxis No recommendation on the use of SU prophylaxis in prepubertal children with severe sepsis. O. Nutrition 1. Enteral nutrition given to children who can be fed enterally, and parenteral feeding in those who cannot (grade 2C). increased intrathoracic pressure can reduce venous return and 4. We recommend evaluating for and reversing pneumotho- lead to worsening shock if the patient is not volume loaded. In rax, pericardial tamponade, or endocrine emergencies in those who desaturate despite administration of face mask oxy- patients with refractory shock (grade 1C). gen, high-flow nasal cannula oxygen or nasopharyngeal CPAP can be used to increase functional residual capacity and reduce Rationale. Endocrine emergencies include hypoadrenal- the work of breathing, allowing for establishment of intrave- ism and hypothyroidism. In select patients, intra-abdominal nous or intraosseous access for fluid resuscitation and periph- hypertension may also need to be considered (513–515). eral inotrope delivery (502, 503). Drugs used for sedation have important side effects in these patients. For example, etomidate B. Antibiotics and Source Control is associated with increased mortality in children with menin- gococcal sepsis because of adrenal suppression effect (504, 505). 1. We recommend that empiric antimicrobials be adminis- Because attainment of central access is more difficult in chil- tered within 1 hr of the identification of severe sepsis. Blood dren than adults, reliance on peripheral or intraosseous access cultures should be obtained before administering antibiot- can be substituted until and unless central access is available. ics when possible, but this should not delay initiation of antibiotics. The empiric drug choice should be changed as 2. We suggest that the initial therapeutic endpoints of resuscita- epidemic and endemic ecologies dictate (eg, H1N1, meth- tion of septic shock be capillary refill of ≤ 2 s, normal blood icillin-resistant S. aureus, chloroquine-resistant malaria, pressure for age, normal pulses with no differential between penicillin-resistant pneumococci, recent ICU stay, neutro- peripheral and central pulses, warm extremities, urine output penia) (grade 1D). 1 mL/kg/hr, and normal mental status. Thereafter, Scvo2 saturation greater than or equal to 70% and cardiac index Rationale. Vascular access and blood drawing is more dif- between 3.3 and 6.0 L/min/m2 should be targeted (grade 2C). ficult in newborns and children. Antimicrobials can be given Rationale. Adult guidelines recommend lactate clearance as intramuscularly or orally (if tolerated) until intravenous line well, but children commonly have normal lactate levels with access is available (516–519). septic shock. Because of the many modalities used to measure 2. We suggest the use of clindamycin and antitoxin therapies Scvo2 and cardiac index, the specific choice is left to the practi- for toxic shock syndromes with refractory hypotension tioner’s discretion (506–512). (grade 2D). 3. We recommend following the American College of Critical Rationale. Children are more prone to toxic shock than Care Medicine-Pediatric Advanced Life Support guidelines adults because of their lack of circulating antibodies to toxins. for the management of septic shock (grade 1C). Children with severe sepsis and erythroderma and suspected Rationale. The recommended guidelines are summarized toxic shock should be treated with clindamycin to reduce in Figure 2 (510–512). toxin production. The role of IVIG in toxic shock syndrome Critical Care Medicine www.ccmjournal.org 615
- 37. Dellinger et al Figure2. Algorithm for time sensitive, goal-directed stepwise management of hemodynamic support in infants and children. Reproduced from Brierley J, Carcillo J, Choong K, et al: Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock: 2007 update from the Ameri- can College of Critical Care Medicine. Crit Care Med 2009; 37:666–688. is unclear, but it may be considered in refractory toxic shock Rationale. Débridement and source control is paramount in syndrome (520–527). severe sepsis and septic shock. Conditions requiring débridement 3. We recommend early and aggressive infection source con- or drainage include necrotizing pneumonia, necrotizing fasciitis, trol (grade 1D). gangrenous myonecrosis, empyema, and abscesses. Perforated 616 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 38. Special Article viscus requiresrepair and peritoneal washout. Delay in use of an resuscitation can require 40 to 60 mL/kg or more; however, if appropriate antibiotic, inadequate source control, and failure to these signs are present, then fluid administration should be remove infected devices are associated with increased mortality ceased and diuretics should be given. Inotrope infusions and in a synergistic manner (528–538). mechanical ventilation are commonly required for children with fluid-refractory shock. 4. C. difficile colitis should be treated with enteral antibiotics if tolerated. Oral vancomycin is preferred for severe disease (grade 1A). D. Inotropes/Vasopressors/Vasodilators Rationale. In adults, metronidazole is a first choice; however, 1. We suggest beginning peripheral inotropic support until response to treatment with C. difficile can be best with enteral central venous access can be attained in children who are vancomycin. In very severe cases where diverting ileostomy or not responsive to fluid resuscitation (grade 2C). colectomy is performed, parenteral treatment should be con- sidered until clinical improvement is ascertained (539–541). Rationale. Cohort studies show that delay in the use of inotropic therapies is associated with major increases in C. Fluid Resuscitation mortality risk (553, 554). This delay is often related to dif- ficulty in attaining central access. In the initial resuscitation 1. In the industrialized world with access to inotropes and phase, inotrope/vasopressor therapy may be required to sus- mechanical ventilation, we suggest that initial resuscita- tain perfusion pressure, even when hypovolemia has not yet tion of hypovolemic shock begin with infusion of isotonic been resolved. Children with severe sepsis can present with crystalloids or albumin, with boluses of up to 20 mL/kg low cardiac output and high systemic vascular resistance, for crystalloids (or albumin equivalent) over 5 to 10 mins. high cardiac output and low systemic vascular resistance, These should be titrated to reversing hypotension, increas- or low cardiac output and low systemic vascular resistance ing urine output, and attaining normal capillary refill, shock (555). A child may move from one hemodynamic peripheral pulses and level of consciousness without induc- state to another. Vasopressor or inotrope therapy should be ing hepatomegaly or rales. If hepatomegaly or rales develop, used according to the hemodynamic state (555). Dopamine- inotropic support should be implemented, not fluid resus- refractory shock may reverse with epinephrine or norepi- citation. In children with severe hemolytic anemia (severe nephrine infusion. In the case of extremely low systemic malaria or sickle cell crises) who are not hypotensive, blood vascular resistance despite the use of norepinephrine, the use transfusion is considered superior to crystalloid or albumin of vasopressin and terlipressin has been described in a num- bolusing (grade 2C). ber of case reports, yet evidence to support this in pediat- Rationale. Three RCTs compared the use of colloid to ric sepsis, as well as safety data, are still lacking. Indeed, two crystalloid resuscitation in children with hypovolemic dengue RCTs showed no benefit in outcome with use of vasopres- shock with near 100% survival in all treatment arms (542– sin or terlipressin in children (556–559). Interestingly, while 544). In the industrialized world, two before-and-after studies vaso ressin levels are reduced in adults with septic shock, p observed 10-fold reductions in mortality when children with such levels seem to vary extensively in children. When vaso- purpura/meningococcal septic shock were treated with fluid pressors are used for refractory hypotension, the addition of boluses, inotropes, and mechanical ventilation in the com- inotropes is commonly needed to maintain adequate cardiac munity emergency department (545, 546). In one random- output (510, 511, 555). ized trial, septic shock mortality was reduced (40% to 12%) 2. We suggest that patients with low cardiac output and elevated when increased fluid boluses, blood, and inotropes were given systemic vascular resistance states with normal blood pres- to attain a Scvo2 monitoring goal of greater than 70% (511). sure be given vasodilator therapies in addition to inotropes A quality improvement study achieved a reduction in severe (grade 2C). sepsis mortality (from 4.0% to 2.4%) with the deliv ry of fluid e boluses and antibiotics in the first hour in a pediatric emer- Rationale. The choice of vasoactive agent is initially gency department to reverse clinical signs of shock (547). determined by the clinical examination; however, for the Children normally have a lower blood pressure than adults, child with invasive monitoring in place and demonstration and a fall in blood pressure can be prevented by vasoconstric- of a persistent low cardiac output state with high systemic tion and increasing heart rate. Therefore, blood pressure alone vascular resistance and normal blood pressure despite fluid is not a reliable endpoint for assessing the adequacy of resus- resuscitation and inotropic support, vasodilator therapy citation. However, once hypotension occurs, cardiovascular can reverse shock. Type III phosphodiesterase inhibitors collapse may soon follow. Thus, fluid resuscitation is recom- (amrinone, milrinone, enoximone) and the calcium sensitizer mended for both normotensive and hypotensive children in levosimendan can be helpful because they overcome receptor hypovolemic shock (542–554). Because hepatomegaly and/or desensitization. Other important vasodilators include rales occur in children who are fluid overloaded, these find- nitrosovasodilators, prostacyclin, and fenoldopam. In two ings can be helpful signs of hypervolemia. In the absence of RCTs, pentoxifylline reduced mortality from severe sepsis in these signs, large fluid deficits can exist, and initial volume newborns (510, 560–569). Critical Care Medicine www.ccmjournal.org 617
- 39. Dellinger et al E.Extracorporeal Membrane Oxygenation in nosocomial sepsis and lacked clear evidence of equivalence in outcomes with the restrictive strategy (584, 585). Blood 1. We suggest ECMO in children with refractory septic shock transfusion is recommended by the World Health Organization or with refractory respiratory failure associated with sepsis for severe anemia, hemoglobin value 5 g/dL, and acidosis. An (grade 2C). RCT of early goal-directed therapy for pediatric septic shock Rationale. ECMO may be used to support children and using the threshold hemoglobin of 10 g/dL for patients with neonates with septic shock or sepsis-associated respiratory a Svco2 saturation less than 70% in the first 72 hrs of pediatric failure (570, 571). The survival of septic patients supported ICU admission showed improved survival in the multimodal with ECMO is 73% for newborns and 39% for older chil- intervention arm (511). dren, and is highest in those receiving venovenous ECMO (572). Forty-one percent of children with a diagnosis of sep- 2. We suggest similar platelet transfusion targets in children as sis requiring ECMO for respiratory failure survive to hospital in adults (grade 2C). discharge (573). Venoarterial ECMO is useful in children with 3. We suggest the use of plasma therapies in children to cor- refractory septic shock (574), with one center reporting 74% rect sepsis-induced thrombotic purpura disorders, includ- survival to hospital discharge using central cannulation via ing progressive disseminated intravascular coagulation, sternotomy (575). ECMO has been used successfully in criti- secondary thrombotic microangiopathy, and thrombotic cally ill H1N1 pediatric patients with refractory respiratory thrombocytopenic purpura (grade 2C). failure (576, 577). Rationale. We give plasma to reverse thrombotic micro- angiopathies in children with thrombocytopenia-associated F. Corticosteroids multiple organ failure and progressive purpura because fresh 1. We suggest timely hydrocortisone therapy in children with frozen plasma contains protein C, antithrombin III, and other fluid-refractory, catecholamine-resistant shock and sus- anticoagulant proteins. Rapid resuscitation of shock reverses pected or proven absolute (classic) adrenal insufficiency most disseminated intravascular coagulation; however, pur- (grade 1A). pura progresses in some children in part due to critical consumption of antithrombotic proteins (eg, protein C, anti- Rationale. Approximately 25% of children with septic thrombin III, ADAMTS 13). Plasma is infused with the goal shock have absolute adrenal insufficiency. Patients at risk for of correcting prolonged prothrombin/partial thromboplastin absolute adrenal insufficiency include children with severe times and halting purpura. Large volumes of plasma require septic shock and purpura, those who have previously received concomitant use of diuretics, continuous renal replacement steroid therapies for chronic illness, and children with pitu- therapy, or plasma exchange to prevent greater than 10% fluid itary or adrenal abnormalities. Initial treatment is hydrocorti- overload (586–611). sone infusion given at stress doses (50 mg/m2/24 hr); however, infusions up to 50 mg/kg/d may be required to reverse shock in I. Mechanical Ventilation the short-term. Death from absolute adrenal insufficiency and septic shock occurs within 8 hrs of presentation. Obtaining 1. We suggest providing lung-protective strategies during a serum cortisol level at the time empiric hydrocortisone is mechanical ventilation (grade 2C). administered may be helpful (578–583). Rationale. Some patients with ARDS will require increased PEEP to attain functional residual capacity and maintain oxy- G. Protein C and Activated Protein Concentrate genation, and peak pressures above 30 to 35 cm H2O to attain See section, History of Recommendations Regarding Use of effective tidal volumes of 6 to 8 mL/kg with adequate CO2 Recombinant Activated Protein C. removal. In these patients, physicians generally transition from conventional pressure control ventilation to pressure release H. Blood Products and Plasma Therapies ventilation (airway pressure release ventilation) or to high-fre- 1. We suggest similar hemoglobin targets in children as in quency oscillatory ventilation. These modes maintain oxygen- adults. During resuscitation of low superior vena cava oxy- ation with higher mean airway pressures using an “open” lung gen saturation shock ( 70%), hemoglobin levels of 10 g/ ventilation strategy. To be effective, these modes can require dL are targeted. After stabilization and recovery from shock a mean airway pressure 5 cm H2O higher than that used with and hypoxemia, then a lower target 7.0 g/dL can be con- conventional ventilation. This can reduce venous return lead- sidered reasonable (grade 1B). ing to greater need for fluid resuscitation and vasopressor requirements (612–616). Rationale. The optimal hemoglobin for a critically ill child with severe sepsis is not known. A recent multicenter trial J. Sedation/Analgesia/Drug Toxicities reported no difference in mortality in hemodynamically stable critically ill children managed with a transfusion threshold of 7 g/ 1. We recommend use of sedation with a sedation goal in dL compared with those managed with a transfusion threshold critically ill mechanically ventilated patients with sepsis of 9.5 g/dL; however, the severe sepsis subgroup had an increase (grade 1D). 618 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 40. Special Article Rationale. Although there are no data supporting any par- fluid overload before continuous venovenous hemofiltration ticular drugs or regimens, propofol should not be used for had better survival (629–631), long-term sedation in children younger than 3 years because of the reported association with fatal metabolic acidosis. The M. DVT Prophylaxis use of etomidate and/or dexmedetomidine during septic shock 1. We make no graded recommendations on the use of DVT should be discouraged, or at least considered carefully, because prophylaxis in prepubertal children with severe sepsis. these drugs inhibit the adrenal axis and the sympathetic ner- vous system, respectively, both of which are needed for hemo- Rationale. Most DVTs in young children are associated dynamic stability (617–620). with central venous catheters. Heparin-bonded catheters may decrease the risk of catheter-associated DVT. No data exist on 2. We recommend monitoring drug toxicity labs because the efficacy of UFH or LMWH prophylaxis to prevent catheter- drug metabolism is reduced during severe sepsis, put- related DVT in children in the ICU (632, 633). ting children at greater risk of adverse drug-related events (grade 1C). N. Stress Ulcer Prophylaxis Rationale. Children with severe sepsis have reduced drug 1. We make no graded recommendations on stress ulcer metabolism (621). prophylaxis. Rationale. Studies have shown that clinically important GI K. Glycemic Control bleeding in children occurs at rates similar to those of adults. 1. We suggest controlling hyperglycemia using a similar target Stress ulcer prophylaxis is commonly used in children who are as in adults (≤ 180 mg/dL). Glucose infusion should accom- mechanically ventilated, usually with H2 blockers or proton pany insulin therapy in newborns and children (grade 2C). pump inhibitors, although its effect is not known (634, 635). Rationale. In general, infants are at risk for developing O. Nutrition hypoglycemia when they depend on intravenous fluids. This means that a glucose intake of 4 to 6 mg/kg/min or mainte- 1. Enteral nutrition should be used in children who can toler- nance fluid intake with dextrose 10% normal saline con- ate it, parenteral feeding in those who cannot (grade 2C). taining solution is advised (6−8 mg/kg/min in newborns). Rationale. Dextrose 10% (always with sodium-containing Associations have been reported between hyperglycemia solution in children) at maintenance rate provides the glu- and an increased risk of death and longer length of stay. A cose delivery requirements for newborns and children (636). retrospective pediatric ICU study reported associations of Patients with sepsis have increased glucose delivery needs hyperglycemia, hypoglycemia, and glucose variability with which can be met by this regimen. Specific measurement of increased length of stay and mortality rates. An RCT of strict caloric requirements are thought to be best attained using a glycemic control compared to moderate control using insulin metabolic cart as they are generally less in the critically ill child in a pediatric ICU population found a reduction in mortal- than in the healthy child. ity with an increase in hypoglycemia. Insulin therapy should only be conducted with frequent glucose monitoring in view of the risks for hypoglycemia which can be greater in new- SUMMARY AND FUTURE DIRECTIONS borns and children due to a) relative lack of glycogen stores Although this document is static, the optimum treatment of and muscle mass for gluconeogenesis, and b) the heterogeneity severe sepsis and septic shock is a dynamic and evolving pro- of the population with some excreting no endogenous insu- cess. Additional evidence that has appeared since the publica- lin and others demonstrating high insulin levels and insulin tion of the 2008 guidelines allows more certainty with which resistance (622–628). we make severe sepsis recommendations; however, further programmatic clinical research in sepsis is essential to optimize L. Diuretics and Renal Replacement Therapy these evidence-based medicine recommendations. New interventions will be proven and established inter- 1. We suggest the use of diuretics to reverse fluid overload ventions may need modification. This publication represents when shock has resolved and if unsuccessful, then continu- an ongoing process. The Surviving Sepsis Campaign and the ous venovenous hemofiltration or intermittent dialysis to consensus committee members are committed to updating the prevent greater than 10% total body weight fluid overload guidelines regularly as new interventions are tested and results (grade 2C). published. Rationale. A retrospective study of children with meningo- coccemia showed an associated mortality risk when children ACKNOWLEDGMENT received too little or too much fluid resuscitation (549, 553). The revision process was funded through a grant from the A retrospective study of 113 critically ill children with multiple Gordon and Betty Irene Moore Foundation. We would also organ dysfunction syndrome reported that patients with less like to acknowledge the dedication and untold hours of Critical Care Medicine www.ccmjournal.org 619
- 41. Dellinger et al donatedtime of committee members over the last 2 years; 18. Varpula M, Tallgren M, Saukkonen K, et al: Hemodynamic variables related to outcome in septic shock. Intensive Care Med 2005; the sponsoring organizations that worked with us toward the 31:1066–1071 reality of a consensus document across so many disciplines, 19. Kortgen A, Niederprüm P, Bauer M: Implementation of an evidence- specialties, and continents; and those that contribute in so based “standard operating procedure” and outcome in septic shock. many ways to create the new science to move us forward in Crit Care Med 2006; 34:943–949 treating this potentially devastating disease: the funders of 20. Sebat F, Johnson D, Musthafa AA, et al: A multidisciplinary community hospital program for early and rapid resuscitation of shock in non- research, the investigators, the subjects, and those associated trauma patients. Chest 2005; 127:1729–1743 with the evidence publishing bodies. Finally, we thank 21. Shapiro NI, Howell MD, Talmor D, et al: Implementation and out- Deborah McBride for the incredible editorial support provided comes of the Multiple Urgent Sepsis Therapies (MUST) protocol. Crit persistently over months that brought the manuscript to life Care Med 2006; 34:1025–1032 and finalization. 22. Micek ST, Roubinian N, Heuring T, et al: Before-after study of a stan- dardized hospital order set for the management of septic shock. Crit Care Med 2006; 34:2707–2713 REFERENCES 23. Nguyen HB, Corbett SW, Steele R, et al: Implementation of a bundle 1. Angus DC, Linde-Zwirble WT, Lidicker J, et al: Epidemiology of severe of quality indicators for the early management of severe sepsis and sepsis in the United States: Analysis of incidence, outcome, and septic shock is associated with decreased mortality. Crit Care Med associated costs of care. Crit Care Med 2001; 29:1303–1310 2007; 35:1105–1112 2. Dellinger RP: Cardiovascular management of septic shock. Crit Care 24. 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Garcia Branco R, Tasker RC, Ramos Garcia PC, et al: Glycemic nificant upper gastrointestinal bleeding acquired in a pediatric inten- control and insulin therapy in sepsis and critical illness. J Pediatr sive care unit. Pediatr Crit Care Med 2001; 2:294–298 (Rio J) 2007; 83(5 Suppl):S128–S136 6 36. Sheridan RL, Yu YM, Prelack K, et al: Maximal parenteral glucose 6 27. Verhoeven JJ, den Brinker M, Hokken-Koelega AC, et al: Pathophysi- oxidation in hypermetabolic young children: A stable isotope study. ological aspects of hyperglycemia in children with meningococcal JPEN J Parenter Enteral Nutr 1998; 22:212–216 APPENDIX A Intensive Care; 4Indian Society of Critical Care Medicine; 2012 Surviving Sepsis Campaign Guidelines 5 Chinese Society of Critical Care Medicine; 6Japanese Association Committee for Acute Medicine; 7American Association of Critical-Care R. Phillip Dellinger, (Co-Chair); Rui Moreno (Co-Chair); Nurses, 8Japanese Society of Intensive Care Medicine; 9Society of Leanne Aitken,1 Hussain Al Rahma,2 Derek C. Angus, Dijillali Hospital Medicine; 10World Federation of Societies of Intensive Annane, Richard J. Beale, Gordon R. Bernard, Paolo Biban,3 and Critical Care Medicine; 11Society of Academic Emergency Julian F. Bion, Thierry Calandra, Joseph A. Carcillo, Terry P. Medicine; 12European Society of Clinical Microbiology Clemmer, Clifford S. Deutschman, J.V. Divatia,4 Ivor S. Doug- and Infectious Diseases; 13Asia Pacific Association of Critical las, Bin Du,5 Seitaro Fujishima, Satoshi Gando,6 Herwig Ger- Care Medicine; 14Society of Critical Care Medicine; 15Latin lach, Caryl Goodyear-Bruch,7 Gordon Guyatt, Jan A. Hazelzet, American Sepsis Institute; 16Canadian Critical Care Society; Hiroyuki Hirasawa,8 Steven M. Hollenberg, Judith Jacobi, 17 Surgical Infection Society; 18Infectious Diseases Society of Roman Jaeschke, Ian Jenkins,9 Edgar Jimenez,10 Alan E. Jones,11 America; 19American College of Emergency Physicians; 20Chinese Robert M. Kacmarek, Winfried Kern,12 Ruth M. Kleinpell,1 Society of Critical Care-China Medical Association; 21German Shin Ok Koh,13 Joji Kotani, Mitchell Levy,14 Flavia Machado,15 Sepsis Society; 22Brazilian Society of Critical Care (AMIB); John Marini, John C. Marshall, Henry Masur, Sangeeta Mehta, 23 European Society of Intensive Care Medicine; 24American John Muscedere,16 Lena M. Napolitano,17 Mark E. Nunnally, Thoracic Society; 25International Pan Arab Critical Care Medicine Steven M. Opal,18 Tiffany M. Osborn,19 Margaret M. Parker, Society; 26Pediatric Acute Lung Injury and Sepsis Investigators; Joseph E. Parrrillo, Haibo Qiu,20 Adrienne G. Randolph, 27 American College of Chest Physicians; 28Australian and New Konrad Reinhart,21 Jordi Rello, Ederlon Resende,22 Andrew Zealand Intensive Care Society; 29European Respiratory Society; Rhodes,23 Emanuel P. Rivers, Gordon D. Rubenfeld,24 Christa World Federation of Pediatric Intensive and Critical Care Societies. A. Schorr, Jonathan E. Sevransky, Khalid Shukri,25 Eliezer Silva, Mark D. Soth, Charles L. Sprung, Ann E. Thompson,26 Sean R. Townsend, Jeffery S. Vender,27 Jean-Louis Vincent, Steve A. Pediatric Subgroup Webb,28 Tobias Welte,29 Janice L. Zimmerman. Jan A. Hazelzet, Adrienne G. Randolph, Margaret M. Parker, 1 World Federation of Critical Care Nurses; 2Emirates Intensive Ann E. Thompson, Paolo Biban, Alan Duncan, Cristina Mangia, Care Society; 3European Society of Pediatric and Neonatal Niranjan Kissoon, and Joseph A. Carcillo (Head). Critical Care Medicine www.ccmjournal.org 635
- 57. Dellinger et al AppendixB Conflict of Interest Process 636 www.ccmjournal.org February 2013 • Volume 41 • Number 2
- 58. Special Article Appendix C ARDSnetVentilator Management Assist control mode—volume ventilation Reduce tidal volume to 6 mL/kg lean body weight eep plateau pressure 30 cm H2O K –Reduce tidal volume as low as 4 mL/kg predicted body weight to limit plateau pressure Maintain Sao2/Spo2 between 88% and 95% Anticipated PEEP settings at various Fio2 requirements Fio2 0.3 0.4 0.4 0.5 0.5 0.6 0.7 0.7 0.7 0.8 0.9 0.9 0.9 1.0 PEEP 5 5 8 8 10 10 10 12 14 14 14 16 18 20-24 Predicted Body Weight Calculation Male— 50 + 2.3 [height (inches) – 60] or 50 + 0.91 [height (cm) – 152.4] Female—45.5 + 2.3 [height (inches) – 60] or 45.5 + 0.91 [height (cm) – 152.4] Sao2 = arterial oxygen saturation, PEEP = positive end-expiratory pressure, Spo2 = oxygen saturation on pulse oximetry. Adapted from Acute Respiratory Distress Syndrome Network. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med 2000; 342:1301–1308. Appendix D Summary of Ventilator Procedures in the Higher PEEP Groups of the ALVEOLI Trial Procedure Value Ventilator mode Volume assist/control Tidal volume goal 6 mL/kg of predicted body weight Plateau pressure goal ≤ 30 cm H2O Ventilator rate and pH goal 6–35, adjusted to achieve arterial pH ≥ 7.30 if possible Inspiration expiration time 1:1−1:3 Oxygenation goal Pao2 55−80 mm Hg Spo2 88%−95% Weaning Weaning attempted by means of pressure support when level of arterial oxygenation acceptable with PEEP 8 cm H2O and Fio2 0.40 Allowable combinations of PEEP and Fio2a Higher PEEP group (after protocol changed to use higher levels of PEEP) Fio2 0.3 0.3 0.4 0.4 0.5 0.5 0.5–0.8 0.8 0.9 1 PEEP 12 14 14 16 16 18 20 22 22 22–24 Note: Complete ventilator procedures and eligibility criteria can be found at www.ardsnet.org. Spo2 = oxyhemoglobin saturation as measured by pulse oximetry, Fio2 = fraction of inspired oxygen, PEEP = positive end-expiratory pressure. a In both study groups (lower and higher PEEP), additional increases in PEEP to 34 cm H2O were allowed but not required after Fio2 had been increased to 1.0, according to the protocol. Adapted from Brower RG, Lanken PN, MacIntyre N, et al: Higher vs. lower positive end-expiratory pressures in patients with the acute respiratory distress syndrome. N Engl J Med. 2004; 351(4):327–336. Critical Care Medicine www.ccmjournal.org 637