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Neonatal Sepsis

Neonatal sepsis is a major cause of mortality amongst the neonate. This material explained in details the organisms commonly implicated and how to preventive measures.

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0% found this document useful (0 votes)
23 views33 pages

Neonatal Sepsis

Neonatal sepsis is a major cause of mortality amongst the neonate. This material explained in details the organisms commonly implicated and how to preventive measures.

Uploaded by

okerekehenry98
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd

ILOH, KENECHUKWU

NEONATAL
SEPSIS
Introduction
• Neonatal sepsis refers to an infection involving bloodstream in
newborn infants less than 28 days old.
• It is divided into 2 groups based on the time of presentation after
birth:
• early-onset sepsis (EOS)
• late-onset sepsis (LOS).
• EOS refers to sepsis in neonates at or before 72 hours of life
• LOS is defined as sepsis occurring at or after 72 hours of life
Introduction…

• Newborn infants have immature


immune systems
• Have just been colonised with
bacteria during their recent
delivery.
• They are therefore prone to
infections which are likely to cross
barriers, for example
• between the lungs and blood,
• the gut and blood and
meninges.
Introduction…

• Many newborn infections can be


prevented by
• good hygiene at the time of
birth,
• early and exclusive
breastfeeding,
• appropriate umbilical cord care,
• appropriate eye care,
• using KMC and
• avoiding separation of the
mother and infant.
• Common systemic bacterial infections
in young infants include
• sepsis,
• pneumonia,
• urinary tract infection,
Introduction • and meningitis
… • and all these may present alike.
• Sepsis is a clinical syndrome of
systemic illness accompanied by
septicaemia (bacteria in the blood).
• It is also called bacteraemia.
EARLY ONSET NEONATAL SEPSIS:
INFECTION IN FIRST 72 HOURS OF LIFE

a) Risk factors for EO infection


Preterm births
Suspected or confirmed rupture of
membranes for >18 hrs
Intrapartum fever >38°C
confirmed/ suspected chorioamnionitis
Mother given parenteral antibiotics for
confirmed or suspected invasive
bacterial infection (such as septicaemia)
at any time during labour, or in the 48 hr
periods before and after the birth
Suspected or confirmed infection in a
co-twin
Very low birth weight
Invasive group B streptococcal infection
in a previous baby
Maternal group B streptococcal
colonisation, bacteriuria or infection
during pregnancy
Clinical indicators suggestive of EOS Sepsis

• Signs of sepsis can be very non-specific, and they include:


Fever
o Temperature of 38 °C on one occasion
o Temperature > 37.5 °C on two occasions separated by at least one hour
o If the Infant has a fever > 37.5°C but less than 38 °C and looks well,
unwrap the infant put in the coolest part of the room – DO NOT give
paracetamol.

• Recheck the temperature in 4 hours if the fever is >38 °C treat as


neonatal sepsis
Clinical indicators suggestive
of EOS Sepsis…

 Hypothermia
• Temperature <36.5 °C

 Shock
o Cold hands and feet
o Capillary refill time >3secs
o Tachycardic
 Unexplained excessive bleeding,
thrombocytopenia or abnormal
coagulation
 Oliguria persisting aged >24 hr
 Hypo/ hyperglycaemia
 Metabolic acidosis (Base excess ≥10)
Clinical indicators suggestive of EOS Sepsis…

 Respiratory distress
o Tachypnoeic (Respiratory Rate > 60/min)
o Chest indrawing
o Tracheal Tug
o Sternal recession
o Head bobbing
o Nasal flaring
o Grunting
o Cyanosis or Sp02 <90% on air

 Apnoeas and slow breathing
o No breaths for 20 seconds; especially in a
term baby or previously well preterm baby
• Respiratory rate <20/min
Clinical indicators suggestive of EOS Sepsis…

 Gastrointestinal
o Abdominal distension
o Bilious vomiting
o Bilious aspirates from NGT
 Feeding difficulties (e.g. inability
to suck and poor suck)

 Neurological
o Lethargy or not waking for feeds
o Reduced activity
o Seizures
o Abnormal posture i.e. opisthotonus
o Floppy
Clinical indicators
suggestive of EOS
Sepsis…

• Jaundice
• Yellow skin, sclera
or mucous
membranes
Clinical indicators suggestive of EOS
Sepsis…

a) Clinical features of Meningitis


• Meningitis is inflammation of the meninges.
• Symptoms and Signs
Suspect meningitis in a newborn with sepsis or if they present with
the following clinical symptoms or signs:
Drowsy, lethargy or unconscious
Persistent irritability
High pitched cry
Apnoeic episode
Convulsion
Bulging fontanelle
Note: Infants often do not have neck stiffness
A lumbar puncture must be done once meningitis is suspected
Figure 21.1: Showing bulging fontanelle
Table 21.1: Red flag signs
Red flag signs and clinical indicators suggestive of neonatal infection

Systemic antibiotics given to mother for suspected bacterial infection during labour or within 48
hr either side of birth
Suspected or confirmed infection in a co-twin
Respiratory distress starting >4 hr after birth
Seizures
Signs of shock
Need for mechanical ventilation in a term baby
Suspected or confirmed rupture of membranes for >18 hr
confirmed/ suspected chorioamnionitis
Lethargy, altered behaviour or responsiveness
Feed intolerance (e.g. abdominal distension, vomiting, excessive gastric aspirates)

Unexplained excessive bleeding, thrombocytopenia or abnormal coagulation


Actions if red flag signs are present

1.If there is any red flag sign, take samples for


investigations for complete sepsis work- up and
start antibiotics.
2.If there are no red flag signs but there are 2 or
more other risk factors or clinical indicators take
samples for investigations for complete sepsis
work-up and start antibiotics.
1. If there are no red flag signs or clinical indicators but there is 1 risk
factor, use clinical judgement and consider withholding antibiotics.
However, take samples for investigations including complete sepsis
work-up, and be guided by the laboratory investigation results.
2. Monitor baby for clinical indicators of possible infection. Monitoring
should be done at 1 hr, 2hr and then 2-hrly for 10 hrs.
3. If further clinical concerns, perform investigations including blood
cultures and start antibiotics.
Figure 21.2: Peri-umbilical flare in umbilical sepsis
Investigations before starting antibiotics

Blood culture
Lumbar puncture for CSF
analysis maintaining asepsis
if thought safe to do, but do
not delay antibiotics for LP
Measure C-Reactive Protein
at presentation and 18–24 hr
after.
Complete blood count and
micro ESR
Procalcitonin
• Take swabs when there is local
infection
a) Choice of antibiotics
Use Penicillin and an
aminoglycoside (gentamicin
or amikacin) as first choice for
empirical treatment of
neonatal sepsis. (local
antibiotics susceptibility
pattern should also be a
guide)
Second line can be
cefotaxime (or ceftazidime)
and amikacin
• Review antibiotics treatment based
on culture results
Investigations during antibiotic
treatment

CRP: If possible, measure before


starting antibiotics and 18–24
hrs after the first CRP test
Consider LP if:
o positive blood culture
o CRP >10 mg/L
baby does not respond
satisfactorily to antibiotics
• Procalcitonin can be done if available
• Review treatment at 36 hrs
 Stop antibiotics if laboratory results and
clinical examination are not suggestive
of sepsis.
If positive blood culture or clinical
suggestion of infection treat for 7 -
10 days

Continue treatment beyond 10


Usual duration days if:
of treatment
obaby not fully recovered or
oExpert microbiological advice
based on blood culture result.
Meningitis

If meningitis suspected but Gram stain is uninformative, use


ampicillin, gentamycin and cefotaxime
Review treatment decisions taking CSF results into account
If CSF Gram stain suggests GBS, give benzylpenicillin 100
mg/kg 12-hrly and gentamicin 5 mg/kg/day
If CSF culture confirms GBS, continue benzylpenicillin for at
least 14 days and gentamicin for 5 days
If CSF culture or Gram stain confirms Gram-negative
infection, review antibiotics based on culture result.
• This refers to infection after first 72
hrs of life. Common organism
implicated in LOS include
coagulase-negative staphylococci
(CoNS), Klebsiella, Serratia,
LATE ONSET Enterobacter, Pseudomonas, E. coli
NEONATAL and Acinetobacter).
SEPSIS (LOS) A.Risk factors
 Risk factors include need for
invasive interventions e.g.
prolonged ventilation, central
venous access and parenteral
nutrition, prolonged hospital
stay.

Clinical features
 Can be vague and non-specific
 Respiratory distress
 Apnoea/ bradycardia
 Cyanosis or poor colour
 Poor perfusion (CRT >3 sec; toe-core temperature gap >2°C; mottling)
 Hypotension
 Tachycardia
 Temperature instability (high or low)
 Glucose instability
 Hypotonia
 Irritability
 Lethargy/ inactivity
 Poor feeding and poor suck
 Jaundice
 Seizures
 Vomiting
 Abdominal distension
• Look for:
 Systemic signs of sepsis such as tachycardia, poor
perfusion, reduced tone, reduced activity, lethargy,
unsettled and crying/moaning

 Tachypnoea and intercostal and/or subcostal recession

 Bulging of the fontanelle suggesting raised intracranial


Clinical Signs pressure

 Abdominal distension and tenderness


 auscultate for bowel sounds; reduced or abse nt
with infection (as a result of paralytic ileus) or NEC

 inspect stool for visible blood


 petechiae, bleeding diathesis

 Septic spots in eyes, umbilicus, nails and skin


 Reluctance to move or tenderness in joints and limbs
 Swabs for culture
o Swab any suspicious lesion
(e.g. skin, umbilicus or nails)
 Blood cultures
o Asepsis for sample
collection is very
important to reduce risk
of culturing CoNS skin
contaminants
 Full blood count
o A neutrophil count <2 or
>15x109/L
o Platelet count of <100
x109/L
o Toxic granulation in
neutrophils [or if
Investigations (Aim to perform measured, an
immature:total (I:T)
before starting antibiotics) neutrophil ratio >
0.2]
Investigations  Clotting profile
o If evidence of bleeding
diathesis or in severe
infection/ septicaemia
 CRP
o Acute phase protein
synthesised in the
liver in response to
inflammatory
cytokines
o Generally, a delay of
24 hr between onset
of symptoms and
rise in serum CRP
o Mini-ESR
o Procalcitonin
 Urine microscopy, culture and sensitivity
o Clean-catch or supra-pubic aspiration (SPA). Use
ultrasound scan to check urine in bladder before SPA.
o Do not send urine collected in a bag for bacterial
culture.

Investigations  Lumbar puncture (LP)


o If baby unstable, deranged clotting or
thrombocytopenia (inform the managing consultant)
(Aim to perform o Send CSF for urgent Gram-stain and culture (MC&S),
protein and glucose
before starting o PCR for bacteria and viruses if available
o In critically ill baby, consider PCR for HSV, especially
antibiotics) •
in term babies

 Others
o Chest X-ray
o If abdominal distension noted, abdominal X-ray
 Documentation
o Always document symptoms and signs of infection
at the time of taking blood culture, CSF cultures and
abdominal radiographs
 Do not use oral antibiotics to treat
infection in babies
 Consult local microbiology department
for current recommendations. These
may differ between units according to
local resident flora
Empirical •
b) Antibiotics Late onset sepsis
treatment  If decision made to give antibiotics,
aim to start immediately.
 First line: empirical flucloxacillin and
gentamicin unless microbiology
isolates dictate otherwise
 Second line: vancomycin + gentamicin
or amikacin
 Third line: meropenem +/-
vancomycin
PREVENTION OF SEPSIS

 Health workers in the neonatal unit to be bare below elbow,


wear short sleeves
 Remove jewellery including wedding rings, watches, bracelets
 Strict hand washing with liquid soap and strict hand hygiene
(refer to section on hand washing) starting from the entrance
of the SCBU
 Minimize frequency of opening incubator doors or touching
any part of baby’s cots
 Do not lean on incubators or other patient equipment
 Wear apron and sterile gloves when
carrying out any procedure on a baby
e.g. heel prick, re-siting IV cannula
 Health workers MUST not wear same
pair of gloves for feeding and vitals of
more than one baby. Use washed hands.
 Initiate enteral feeds with maternal
PREVENTION breast milk within 24 hr of birth
 Aim to initiate skin -skin with mother
OF SEPSIS /KMC within 24 hours of birth for all
babies
 Institute buccal colostrum swabbing
within 6hours of birth for the ill small
newborns if breastfeeds not yet feasible
 Remove all IV cannulae for the baby once
no more needed
 Do not use phones in the neonatal unit
Thank
you

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