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Fluid & Elect. Pedy. DAVA - Copy-2

The document discusses fluid and electrolyte management in pediatric surgical patients, emphasizing the importance of understanding their unique physiological needs. It covers fluid compartments, management strategies for hydration, and the significance of monitoring electrolyte levels to prevent imbalances. Specific clinical scenarios and perioperative care guidelines are also outlined to ensure optimal patient outcomes.

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David Admas
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0% found this document useful (0 votes)
17 views53 pages

Fluid & Elect. Pedy. DAVA - Copy-2

The document discusses fluid and electrolyte management in pediatric surgical patients, emphasizing the importance of understanding their unique physiological needs. It covers fluid compartments, management strategies for hydration, and the significance of monitoring electrolyte levels to prevent imbalances. Specific clinical scenarios and perioperative care guidelines are also outlined to ensure optimal patient outcomes.

Uploaded by

David Admas
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
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Fluid and Electrolyte Mgt in

Pediatric Surgical Patients


Moderator: Dr. Maru
(consultant pediatric surgeon)
Presenter: Dawit. A (GSR III)
Aug. 2021
SPHMMC
Outline

• Introduction
• Fluid and electrolyte homeostasis
• Fluid management
• Electrolyte management
• Acid-base disorders
• References

2
Introduction
• Understanding fluid & electrolyte physiology and mgt of
pediatric surgical patients is very important ... !
• “children are not little adults”
• The margin between dehydration and fluid overload is
small. So it needs meticulous attention to their
hydration status.
• Surgical conditions that predisposes patients to
dehydration.
• IHPS, Gastroschisis, Short-gut syndrome, Congenital
diaphragmatic hernia and associated PHT
3
Fluid compartments
• TBW; in 2 main compartments
‘ECF & ICF’.
• TBW as a % of body wgt & its
ECF/ICF ratio vary with age, sex &
fat content.
• Fetus at 12 wks’; ~ 94% of
body wgt
• Infants at;
• full term; ~ 80% of body wgt
• 1st wk; ~ 75% of body wgt
• 1 year; ~ 60 – 65% of body
wgt 4
5
Electrolyte composition

• The serum
concentration of an
electrolyte, w/c is
measured clinically,
doesn’t always
reflect the body
content.
• Example; K and
Ca

6
Fluid and electrolyte homeostasis

• The ICF & ECF are in osmotic equilibrium. Clinically,


the primary process is usually a change in the
osmolality of ECF (Plasma Osmolality).
Osmolality = 2 × [Na] + [glucose]/18 + [BUN]/2.8
• The plasma osmolality is tightly regulated within 285–
295 mOsm/kg. Osmoreceptors in the hypothalamus
sense the plasma osmolality and regulate; ADH and
RAAS.
• Na balance is considered the main regulator of volume
status. The most important determinant of renal Na
excretion is the volume status. 7
Fluid and electrolyte
homeostasis in Sources of water loss
newborn’s; factors … !
• Gestational age • Sensible water loss;
• Physiologic diuresis (renal)
• Immaturity of neonatal • Insensible water loss;
kidney • Skin (70%); excess in
• Insensible water losses; preterm & LBW infants
Factors: GA, radiant for 2 reasons .. !
warmers, fever, ↑ RR. • RT(30%); ~ ½ of
• Inability to independently insensible losses in term
access H2O. infants
• Other fluid losses; stool, 8
Fluid management
• In pediatric surgical patients, fluid administration is
necessary
• to maintain adequate tissue perfusion and cellular
metabolism,
• to acutely replete GI, renal, blood losses and
• to compensate for insensible losses.
• The 3 phases of pediatric fluid Mgt;
• Deficit Rx; Mgt of fluid losses that occur before
patients presentation
• Maintenance Rx; those needed for neutral water
balance 9
Deficit therapy

• Estimate the severity of dehydration; Mild, Moderate, Severe


• Determine the type of fluid deficit; Isotonic, Hypotonic,
Hypertonic
• Restoration of deficit; restoration of CVS, CNS, & renal
perfusion.
• Severe dehydration; give 10-20 mL/kg NS IV bolus (20-40
mL/kg for pts with low UOP due prerenal causes). Repeat as
needed. Reevaluate Q 15-30min. Once stable, the remaining
deficit corrected slowly (over ~1-2 days).
• Moderate and mild dehydration; PO or IV
• Monitoring; by frequent assessment of fluid status … !
10
• The ideal type of for resuscitation remains unclear;
• Crystalloid (NS, LR) vs Colloids (albumin, dextran); Both
are widely used in the fluid resuscitation of critically ill
children. No evidence suggested that resuscitation with
colloids has mortality benefit … !
• NS vs RL; the most commonly used for resuscitation.
• Hypertonic (3%) saline is effective in the mgt of Burns,
Seizures due to severe hyponatremia and elevated ICP (in
TBI)

11
Maintenance therapy
• Maintenance therapy; replacing the losses under ordinary
conditions (sensible and insensible losses). Urinary losses; ~ 2/3rd
of total MF.
• MF requirements are calculated based on the lean body weight.
• 1st wk of life;

• Then after; Holliday and Segar formula (100-50-20 rule and/or


4-2-1 rule)
12
MF requirement; 1st week of life (in
mL/kg/day)
• The recommended initial IV fluid: D10W. (4-6 ml/kg/min).
• Term babies and babies with birth wgt > 1500 grams.
• Day 1: 60-70 ml/kg/day D10W. Day 2-7: increase by 15-20 ml/kg/day till a
max. of 150 ml/kg/day. Add Na after 48 hrs of age & K? (2/3rd D10W + 1/3rd
NS).
• Preterm babies and babies with birth wgt 1000-1500 grams.
• Day 1: 80 ml/kg/day D10W. Day 2-7: increased by 10-15 ml/kg/day till a max.
of 150 ml/kg/day. Add Na after 48 hrs of age & K? (2/3rd D10W + 1/3rd NS)
• If the neonate is: Febrile, Under radiant warmer, Under
phototherapy.
• Add 10-30ml/kg/day on top of MF

13
Maintenance requirement; > 7th day
• For infants >32 wks or >1.5 kg wgt GA, For neonates
>1 wk of age; For children > 2 months of age and
beyond, the daily fluid requirements can be calculated
using Holliday and Segar formula
•Body
The weight
recommended
Fluid initial IV fluidper
requirement is day
NS/RL.

0-10 kg 100 mL/kg/day


Or (4 mL/kg/hr)
11-20kg 1000 mL/day + 50 mL/kg/day for each kg b/n
11 - 20 kg
Or (40 mL/hr + 2 mL/kg/hr for each kg b/n 11 -
20 kg)
>20kg 1500 mL/day + 20 mL/kg/day for each kg b/n 14
Replacement therapy

• Replacement therapy; part of perioperative care.


• Blood losses; replace max. ABL with crystalloid in a 3:1
ratio.
• Allowable blood loss … !
• 3rd space losses; fluid replacement based on anticipated
amt of fluid loss;
• Superficial and minor surgeries (e.g. hernia operation); 1-
2ml/kg/hr
• Intrathoracic surgery; 4-7 mL/kg/hr
• Abdominal surgery; elective bowel resection; 6-10 mL/kg/hr,
Emergency surgeries; 15-20 mL/kg/hr, Laparotomy for NEC; 15
50 mL/kg/hr.
Specific clinical scenarios

• Pyloric stenosis;
• In cases of clinical dehydration, rehydration before
surgery. Defer the surgery until the child is adequately
rehydrated.
• MF ~ 1.5×. Slow resuscitation … ! Then When UOP is
adequate, add 10-20 mEq/L of KCl.
• Abdominal wall defects; Gastroschisis VS
Omphalocele
• Eviscerated bowel covered with moist nonadherent
sponges & plastic bag.
• Initial resuscitation; 10 - 20ml/kg bolus NS/LR + MF (~
2.5×). Additional fluid until UOP is established. Ongoing16
Perioperative care
• Preoperatively; In general, preoperative IV fluid is
seldom necessary.
• Assess the patient hydration status
• Recommended preop. NPO times; 2 hrs clear liquids, 4
hrs breast milk, 6 hrs non-human milk or infant formula,
8 hrs solid food.
• Intraoperatively; give calculated fluid (NS/RL); MF +
anticipated 3rd space loss + Estimated blood loss +
Insensible losses.
• Postoperatively;
• Early oral intake; to avoid dehydration. If delayed give 17
fluid.
Electrolyte management
• Electrolytes account for ~ 95% of the solute molecules
in body water. It is usually gained and lost in a
relatively equal amount to maintain balance.
• For infants receiving IV fluids, these electrolytes
generally are not given during the first 48 hours after
birth because of the relatively volume-expanded state,
and normal isotonic losses during the first days of life.
• Urine flow should be adequate before potassium is
added.

18
19
• Depending on the volume, electrolyte losses from
gastric or ileostomy drainage can be large, with
electrolyte composition:
• Because the
constituents of these
losses often
substantially differ
from the composition of
MF; it is recommended
to replace large-volume
stoma or other fluid
losses with a
physiologic equivalent
fluid.
20
• Gastric …
Normal daily electrolyte requirements
Normal serum RR
• Sodium = 136-145 mEq/L
(136-145 mmol/L)
• Potassium = 3.5-5.0
mEq/L (3.5-5.0 mmol/L)
• Magnesium = 1.8-3.0
mg/dl (0.8-1.2 mmol/L)
• Calcium = 8.5-10.5 mg/dl
(2.2-2.6 mmol/L)
• Phosphorus = 3.0-4.5
mg/dl (1.0-1.4 mmol/L)
• Chloride = 98-106 mEq/L
(98-106 mmol/L)

• Generally maintenance requirements for Na, K, & Cl is


~2-3 mEq/kg/day. 21
Electrolyte disturbance

• Electrolyte imbalances could be caused by:


• Abnormal losses (vomiting/diarrhea)
• Disproportionate IV supplementation
• Disease states: renal diseases
• Common electrolyte disturbances;
• Sodium
• Potassium
• Calcium
• Magnesium
22
Sodium
Hyponatremia
• Sodium is unique among electrolytes because water
balance, not Na balance, usually determines its
concentration. RR: 136-145 mEq/L
• Hyponatremia; Na <135 mEq/L. (Mild 130–135, Mod. 125–
129, Sev. <125)
• Hyponatremia can be classified based on serum
osmolality and volume states (extracellular fluid
volume).
• Hypertonic hyponatremia (high serum osmolality);
23
Hyperglycaemia, mannitol
• Causes; of Hypotonic hyponatremia
• Hypovolemic; RF with high UOP, Diuretics, Addison
disease, Cerebral salt wasting syndrome, Diarrhea,
Burn, 3rd space loss (peritonitis, ascites).
• Euvolemic; SIADH, Iatrogenic excess adm. of hypotonic
fluids.
• Hypervolemic; RF with low UOP, CHF, Cirrhosis, NS
• Symptoms; depends on mainly the onset
hyponatremia.
• Acute drops vs Gradually drop
• N, V, muscle weakness, lethargy, headache 24
Mgt
Hyponatremia
• Treatment ranges from fluid restriction (asymptomatic)
to hypertonic saline administration (severe cases).
• Na deficit=(desired Na-measured Na) x TBW (TBW = 0.6
x Wgt in Kg)
• Acute, Severe symp. hyponatremia, ICP; Give 5
mL/kg 3% NS (bolus);
• ↑ serum Na by 1–2 mEq/L/hr, until an ↑ of 4–6 mEq/L
has been reached within 6 hrs. No recommended max.
correction rate in the first 24 hrs
• Chronic hyponatremia; Give 5 mL/kg of 3% NaCl
(infusion);
• ↑ serum Na by no > 0.5 mEq/L/hr, until an ↑ of 4–6 25
mEq/L has been reached within 24 hrs with max.
Hypernatremia

• Serum Na >145 mEq/L. Serum osmolality is always


increased.
• Causes;
• Water deficit; hypovolemic hypernatremia (hypotonic
fluid loss) or Euvolemic hypernatremia (pure water
deficit).
• Diarrhea, Excessive sweating, Dehydration, Insufficient
water intake/poor feeding in newborn’s; DI (central or
nephrogenic).
• Sodium excess; hypervolemic hypernatremia
26
• Symptoms; Acute Vs Chronic hypernatremia.
• Acute hypernatremia; Excessive thirst, decreased
salivation, dry sticky mucous membrane,
• Irritability, restlessness, weakness, lethargy, muscular
twitching, fever, a high pitched cry, tachypnea, low BP
• With Na >160 mEq/L; intracranial hemorrhage
(confusion, seizures coma)
• Chronic hypernatremia; Sxs are usually less severe
and nonspecific, due cerebral adaption to chronic
hypernatremia.
27
Mgt
Hypernatremia
• Replacing free water deficit (FWD) with sterile water
PO or D5W IV.
• FWD (L) = ((measured Na/desired Na)-1) x TBW (L)
• In hypovolemic pts restore hypovolemia with isotonic
solutions (NS) before correcting hypernatremia.
• Acute hypernatremia; replace FWD within < 24 hrs.
• ↓ serum Na+ by no > 1–2 mEq/L/hr. Max. 15 mEq/L/day; to
prevent cerebral edema.
• Chronic hypernatremia; replace FWD over 48-72
hours. 28
Potassium
Hypokalemia
• Potassium is an important electrolyte in maintaining
RMP of excitable tissues (heart and skeletal muscles).
RR: 3.5–5 mEq/L.
• Hypokalemia; K+ < 3.5 (Mild: 3.0-3.5; Mod: 2.5-2.9;
Sev. <2.5)
• Causes;
• GI losses; Diarrhea, Vomitting ... !
• Renal losses: RTA type I, Genetic tubular disorders
(Bartter & Gitelman syndrome), Diuretics,
Glucocorticoids, Hyperaldosteronism,
29
Hypercortisolism, Hypomagnesemia.
• Symptoms; rarely seen with K+ levels >3.0 mEq/L.
• Muscle weakness; progress from lower extremities to the
trunk, upper extremities ultimately leading to paralysis and
respiratory failure.
• Others; cramps, fasciculations, rhabdomyolysis, ileus.
• Cardiac arrhythmia; premature atrial and ventricular
beats, and ventricular fibrillation, worsens digitalis-induced
arrhythmias.
• ECG changes; T wave flattening, ST depression, QT
prolongation, U waves, "torsades de pointes".
30
Mgt
Hypokalemia
• Severe hypokalemia, acute setting, high risk of recurrence:
• High-dose IV KCl (max. 0.3 mEq/kg/hr or max. of 10mEq/L through
peripheral line; or 0.5-1 mEq/kg/hr or max. of 40mEq/L through a
central line)
• Appropriate monitoring in ICU
• Moderate hypokalemia: Oral or IV repletion.
• Mild hypokalemia: Rx underlying conditions (GI fluid losses),
dietary K+ intake, Oral supplementation (2 - 4 mEq/kg/day)
• In refractory hypokalemia think of concurrent
hypomagnesemia.
31
Hyperkalemia

• Serum K+ > 5.5 mEq/L.


• Causes:
• Excessive K+ intake (iatrogenic IV overload, blood
transfusion), rapid cell death (exercise, massive
trauma, rhabdomyolysis), hemolytic crisis, tumor
lysis syndrome.
• Prolonged diarrhea (metabolic acidosis), DM, RF.
• Rarer causes; congenital adrenal hyperplasia,
adrenal insufficiency, medications (K+sparing
diuretics).
32

• Symptoms; The heart and skeletal muscle are
especially vulnerable to hyperkalemia, due to the role
of K+ in membrane polarization.
• Muscle weakness or paralysis; paresthesia and tingling.
• Cardiac conduction abnormalities; ECG changes:
• Peaked T waves, shortened QT interval (mild)
• PR prolongation, flattened P wave, wide QRS complex
• BBB, ventricular fibrillation and asystole (in severe cases)
• Hyperkalemia should be considered in the setting of
cardiac arrest of unknown etiology in a child.
33
Mgt
Hyperkalemia
• Cardiac membrane stabilization; 10% Ca gluconate
• 100 mg/kg IV over 5-10 mins. Rpeate after 5 mins if ECG
changes persist.
• Intracellular K+ shifting; Short acting insulin ±
glucose, SABA
• RI 0.05 IU/kg IV + D10W 2ml/kg load; then 0.1 IU/kg/hr + 2-
4 ml/kg/hr).
• Nebulized albuterol (10 mg); as an adjunct to insulin
• Enhanced K+ elimination; Na polystyrene sulfonate
“kayexalate”, Na bicarbonate (1-2 mEq/kg IV over 5-10
minutes), Loop diuretics, Hemodialysis 34
Calcium
Hypocalcemia
• Ca is the most abundant mineral in the body. Relatively
common … !
• Hypocalcemia; total < 8.5 mg/dl or ionized/free < 4.65 mg/dl.
• Causes;
• 24-48 hrs: asphexia, maternal hyperparathyroidism,
anticonvulsant Rx, DM
• 1st wk postnatal: Hypoparathyroidism (autoimmune, congenital),
hyperphosphatemia, Hypomagnesemia, Vit. D deficiency
(malnutrition & malabsorbtion, lack of sunlight exposure, RF)
• Others; multiple blood transfusion, Acute necrotizing pancreatitis
• Factitious hypocalcemia … !
35
• Symptoms; in the acute situations; due increased
muscular excitability: tetany + Chvostek’s sign +
Trousseau’s sign.
• Mild and/or chronic hypocalcemia; mild NM irritability;
• Muscle twitches and cramping, tingling around
mouth or fingers (paresthesia)
• Apnea, irritability, lethargy, feeding intolerance, abd.
distention
• Severe and/or symptomatic hypocalcemia;
• Carpal/pedal spasms.
• Seizure, hyperreflexia, jitteriness, laryngospasm, 36
Mgt
Hypocalcemia
• Severe or symptomatic hypocalcemia (serum Ca < 7.5 mg/dl)
• Patients should be placed on an ECG monitor as
arrythmias or cardiac arrest can occur during calcium
replacement.
• IV Ca (10% Ca gluconate or 10% CaCl2); 1 mL/kg/dose
over 5-10 mins. Once seizure subsides Ca replaced in 200-
500 mg/kg/day as a continues infusion or in 4 divided
doses.
• Mild and/or chronic hypocalcemia (7.6-8.4 mg/dl)
• Oral Ca supplementation (Ca citrate, Ca gluconate).
• Treat underlying cause.
37
Hypercalcemia
• Hypercalcemia; total > 10.5 mg/dL or ionized > 5.25
mg/dl. Mild (10.5-12), moderate (12-15), severe (>15).
It is very uncommon … !
• Causes; iatrogenic (vitamin D overdose, deficient
dietary PO4 intake); inborn error of metabolisms; less
common causes (tertiary hyperparathyroidism,
hypercalcemia of malignancy), diuretic therapy.
• Symptoms; mostly asymptomatic but can present with
GI Sxs (N, V, poor feeding), failure to thrive,
dehydration, lethargy, hypotonia, psychological &
emotional Sxs (confusion, delirium, emotional changes,38
Mgt
Hypercalcemia
• Focus on treating underlying cause; by eliminating
possible causes such as thiazide diuretics and
hypervitaminosis
• Serum PO4 should be checked and corrected first.
• Increase urinary excretion: Hydration with NS 10-20
mL/kg bolus ± Lasix
• Decrease intestinal absorption: Increased dietary PO4
• Decrease bone resorption; calcitonin or bisphosphonates.
• Dialysis; in severe cases.

39
Magnesium
Hypomagnesemia
• Hypomagnesemia; serum Mg < 1.5 mg/dl. It is unusual … !
• Causes; may be GI or renal losses, dietary deficiency,
chronic diuretic use.
• Symptoms; often reflective of associated electrolyte
abnormalities (hypocalcemia & hypokalemia). Anorexia,
weakness, lethargy, tremor.
• ECG changes; T wave flattening, long QT syndrome and "torsades
de pointes," esp. in conjunction with hypokalemia, VF.
• Treatment; Oral or IV Mg adminstration.
• Oral (1st line Rx); 6-15 mg/day of elemental Mg in 4 divided doses.
• IV; 0.2-0.4 mEq/kg/dose slowly over every 4-6 hrs (if symptomatic).
40
Hypermagnesemia
• Hypermagnesemia; serum Mg > 3 mg/dL.
• Causes; usually 2° to maternal Mg Rx (for pre-
eclampsia, preterm labor)
• Symptoms; usually appear at Mg level > 4.5 mg/dl.
Hypermagnesemia inhibits acetylcholine release at the
NMJ
• Hypotonia, weakness, hyporeflexia, hypotension,
apnea and vasodilatation with marked flushing.
Paralysis in severe cases.
• Treatment; Usually supportive until Mg level
41
gradually falls.
Acid-base disorders
• Acid-base disorders are a group of conditions
characterized by changes in the concentration of H+ or
HCO3-, which lead to changes in the arterial blood pH
(acidosis or alkalosis and have a respiratory or
metabolic origin)
• Acidosis caused by a primary ↓ in HCO3- conc.; metabolic
acidosis
• Alkalosis caused by a primary ↑ in HCO3- conc.; metabolic
alkalosis
• Acidosis caused by a primary ↑ in PCO2; respiratory
acidosis 42
ABG analysis interpretation

1. Blood pH (RR: 7.35-7.45); pH < 7.35: acidosis; pH > 7.45:


alkalosis
2. PaCO2 level (RR: 33–45 mm Hg)
• pH and PaCO2 change in the opposite direction: respiratory
disorders
• pH and PaCO2 change in the same direction: metabolic
disorders. In metabolic acidosis, anion gap calculation helps
to reach to a precise diagnosis.
3. HCO3- level (RR: 22–28 mEq/L): Low, Normal, High
4. Mixed acid-base disorder if:
• pCO2 or HCO3- is abnormal and pH is normal
• pCO2 and HCO3- shift towards acidosis or alkalosis 43
ABG
analysis
interpreta
tion

44
Compensatory response

• The lungs play a compensatory role in the cases of metabolic acidosis


and alkalosis
• In metabolic acidosis, hyperventilation occurs to blow off excess CO2
and thus carbonic acid, although this cannot completely compensate for
the acidosis.
• In metabolic alkalosis, hypoventilation occurs to retain CO2 and thus
carbonic acid, although this cannot completely compensate for the
alkalosis.
45
Respiratory acidosis

• Alveolar hypoventilation → ↑ CO2 retention → ↑ PaCO2


• Renal compensation: Increased excretion of H+ and
NH4+ and increased reabsorption of HCO3–.
• Acute respiratory acidosis: Renal compensation has
not yet occurred (intracellular fluid buffering only).
Each 10 mmHg ↑ in Paco2 leads to a 1 mEq/L ↑ in
HCO3– and a 0.08 ↓ in pH.
• Chronic respiratory acidosis: Renal compensation
has occurred. Each 10 mmHg ↑ in Paco2 leads to a 3.5
mEq/L ↑ in HCO3– and a 0.03 ↓ in pH.
46
• Causes;
• Decreased CO2 exchange; Airway obstruction, COPD,
asthma, ARDS, acute lung diseases (pneumonia,
Pulmonary edema, empyma, PTX);
• Respiratory muscle weakness; MG, GBS, ALS, and MS
• CNS respiratory center depression (due to inhibition
of the medullary respiratory center); Narcotic over
dose, opiates, sedatives, and anesthetics
• Treatment; treat the underlying cause, adequate
ventilation (O2 administration), treatment of secondary
change
47
Respiratory alkalosis

• Alveolar hyperventilation (↑ RR) → ↑ CO2 washout → ↓


PCO2
• Renal compensation: Decreased excretion of H+ and
NH4+, decreased reabsorption of HCO3–.
• Acute respiratory alkalosis: Renal compensation has
not yet occurred (intracellular fluid buffering only). Each
10 mmHg ↓ in Paco2 leads to a 2 mEq/L ↓ in HCO3 – and
a 0.08 ↑ in pH.
• Chronic respiratory alkalosis: Renal compensation has
occurred. Each 10 mmHg ↓ in Paco2 leads to a 5 mEq/L
↓ in HCO3– and a 0.03 ↑ in pH.
48
• Causes;
• Fever, pulmonary embolism (PE), high altitude (due
to hypoxemia and increased ventilation rate)
• Pain or anxiety, salicylate toxicity, pregnancy,
cirrhosis (due to direct stimulation of the medullary
respiratory center).
• Others; CHF, Sepsis, Hypothalamic lesion
• Treatment; treat the underlying cause, direct
treatment of the hyperventilation as needed, Sedation

49
Metabolic acidosis

• Loss of HCO3- Or Increased production/ingestion of H+


• Causes;
• Normal anion gap; GI loss of HCO3- (Diarrhea, GI
fistula, intestinal stoma), RTA. HARD-ASS
• Increased anion gap; Lactic acidosis (most common
causes), DKA, Renal insufficiency, Exogenous organic
acids. MUDPILES.
• Treatment; treat the underlying cause, Restore adequate
tissue perfusion with volume resuscitation, Na bicarbonate
… !, Correct electrolyte disturbance.
50
Metabolic alkalosis

• Loss of H+ Or Increased production/ingestion of HCO3-


• Causes;
• Chloride responsive; Persistent vomiting, Pyloric
stenosis, GOO, Prolonged gastric suction, Diuretics
• Chloride resistant; Hyperaldosteronism, Cushing
syndrome, Genetic tubular disorders (Bartter & Gitelman
syndrome), Cystic fibrosis
• Treatment; treat the underlying cause, volume
replacement with isotonic saline), Acetazolamide (for
bicarbonate excess), Correct electrolyte disturbance (K+
administration once adequate OUP is ensured).
51
References

• Ashcraft pediatric surgery 5th edition.


• Nelsone pediatrics 20th edition.
• NICU Guideline TAH, AAU; 2021
• UpToDate; 23rd

52
Thanks … !

53

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