ANZCA Final
Paediatric Anaesthesia
Neonatal
A Evidence

Pyloric Stenosis

Hypertrophic pyloric stenosis is a condition of acquired gastric outlet obstruction caused by hypertrophy of the pyloric muscle, typically presenting at 3-8 weeks of life with projectile vomiting. Key anaesthetic...

Updated 3 Feb 2026
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  • severe dehydration
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  • prolonged QTc
  • apnoea

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Clinical reference article

Pyloric Stenosis

Quick Answer

What is pyloric stenosis?

Hypertrophic pyloric stenosis is a condition of acquired gastric outlet obstruction caused by hypertrophy of the pyloric muscle, typically presenting at 3-8 weeks of life with projectile vomiting. Key anaesthetic principles:

  1. Metabolic alkalosis - Hypochloraemic, hypokalaemic metabolic alkalosis from gastric HCl loss
  2. Fluid resuscitation priority - Surgery is elective; resuscitation takes precedence
  3. RSI technique - Full stomach, elective but urgent surgery
  4. Correction sequence - Volume first, then potassium once urinating
  5. Monitoring - ECG for QTc prolongation (arrhythmia risk)

Clinical Pearl: Pyloric stenosis is a medical resuscitation that requires surgery, not a surgical emergency. Never operate on a dehydrated, alkalotic infant. The dehydration and electrolyte abnormalities kill, not the pyloric muscle.


Clinical Overview

Definition

Hypertrophic pyloric stenosis (HPS) is a condition characterised by:

  • Hypertrophy of the muscularis layer of the pylorus
  • Narrowing of the pyloric canal (usually to 1-2 mm)
  • Gastric outlet obstruction
  • Classic presentation: projectile, non-bilious vomiting in previously healthy 3-8 week old infant

Epidemiology

ParameterFinding
Incidence2-5 per 1,000 live births (varies by region) [1]
GenderMale predominance (male:female ratio 4-5:1)
Age at presentation3-8 weeks (rare <2 weeks or >12 weeks)
Familial patternFamilial clustering suggests genetic component
Geographic variationHigher in Caucasians, lower in Asian populations

Risk factors:

FactorAssociation
Firstborn maleHigher risk
Caucasian ethnicityHigher incidence
Bottle feedingSome studies suggest association
Erythromycin exposureFirst 2 weeks of life (prokinetic effect)
Maternal smokingIncreased risk
Family history5-20% if sibling affected

Pathophysiology

Pyloric muscle hypertrophy:

  • Circumferential thickening of pyloric muscularis (normal: 3-4 mm; HPS: 5-8 mm)
  • Elongation of pyloric canal (normal: 10-12 mm; HPS: 15-20 mm)
  • Narrowing of pyloric channel to 1-2 mm
  • Results in mechanical gastric outlet obstruction

Triggering factors (hypotheses):

  • Abnormal pyloric innervation (hypertrophy of nerve fibres)
  • Nitric oxide deficiency (impaired smooth muscle relaxation)
  • Local growth factors and hormones
  • Genetic predisposition + environmental factors

Clinical Presentation

Classic Features

The "typical" presentation:

FeatureDescription
Age3-8 weeks (peaks at 4-5 weeks)
GenderMale (4-5:1 ratio)
VomitingProjectile, non-bilious, forceful
FeedingHungry, eager to feed again after vomiting
StoolConstipated (decreased intake)
WeightLoss or poor gain

Clinical signs:

SignTechniqueFrequency
Olive signPalpable pyloric mass in RUQ70-90%
Visible peristalsisLeft-to-right gastric wave50-70%
DehydrationSunken fontanelle, decreased skin turgorVariable (depends on duration)

Physical examination technique:

  • Feed the baby (stimulates gastric peristalsis)
  • Palpate in right upper quadrant during relaxation between feeds
  • The "olive" is mobile, firm, and moves under your fingers
  • Best palpated from left side of infant with left hand

Diagnostic Confirmation

Ultrasound (first-line):

MeasurementNormalHPS
Pyloric muscle thickness<3 mm>4 mm
Pyloric canal length<10-12 mm>15 mm
Pyloric diameterVariableNarrowed

Target sign:

  • Transverse view: Hypoechoic muscle ring surrounding echogenic mucosa
  • Longitudinal view: "Cervix sign" or "Antral nipple sign"

Upper GI contrast study:

  • Used if ultrasound equivocal or to exclude other causes
  • Findings: String sign (narrow pyloric channel), shoulder sign (indentation of duodenal bulb), beak sign

Severity Assessment

Dehydration assessment:

SignMild (5%)Moderate (10%)Severe (>15%)
Anterior fontanelleNormalSunkenVery sunken
Skin turgorNormalDecreasedTenting
Mucous membranesMoistDryParched
TearsPresentDecreasedAbsent
Urine outputNormalDecreasedAnuric
ConsciousnessAlertIrritableLethargic/comatose

Metabolic Consequences

Pathophysiology of Metabolic Alkalosis

The cascade:

Projectile vomiting
    ↓
Loss of gastric acid (HCl)
    ↓
H+ and Cl- loss
    ↓
Metabolic alkalosis + hypochloraemia
    ↓
Kidney compensates: excretes HCO3- with Na+ and K+
    ↓
Hypokalaemia + paradoxical aciduria
    ↓
Intracellular K+ shifts out, H+ shifts in
    ↓
Maintained alkalosis despite total body K+ depletion

Mechanism details:

  1. Gastric acid loss:

    • Each mL of gastric juice contains 50-100 mmol/L HCl
    • Loss of H+ = metabolic alkalosis
    • Loss of Cl- = hypochloraemia
  2. Renal compensation:

    • Kidney tries to excrete excess HCO3- to correct alkalosis
    • HCO3- excretion requires cation (usually Na+ or K+)
    • Results in urinary loss of Na+ and K+
  3. Paradoxical aciduria:

    • Despite alkalosis, urine is acidic
    • Mechanism: Kidney excretes H+ in exchange for Na+ conservation
    • Reflects severe total body K+ depletion
  4. Intracellular shifts:

    • Total body K+ is depleted
    • To maintain extracellular K+, intracellular K+ shifts out
    • H+ shifts into cells to maintain electroneutrality
    • Worsens intracellular acidosis and maintains alkalosis

Typical Biochemical Profile

ParameterTypical FindingNormal Range
pH7.45-7.557.35-7.45
pCO245-55 mmHg (compensatory)35-45
HCO330-40 mmol/L22-26
Base excess+5 to +15-2 to +2
Na130-140 mmol/L (dilutional)135-145
K2.5-3.5 mmol/L (depleted)3.5-5.0
Cl80-95 mmol/L (low)95-110
Urine pH5.0-6.0 (paradoxical aciduria)4.5-8.0

Consequences of Severe Alkalosis

Clinical implications:

SystemEffectMechanism
CardiovascularArrhythmias, hypotensionHypokalaemia, QTc prolongation
RespiratoryApnoeaCompensatory hypoventilation
NeurologicalSeizures, lethargyCerebral blood flow changes
MetabolicDecreased ionised calciumAlkalosis increases protein binding
RenalImpaired concentrating abilityChronic hypokalaemia

ECG changes with hypokalaemia:

FindingSignificance
Flattened T wavesEarly sign
ST depressionProgression
Prominent U wavesClassic finding
Prolonged PR intervalAV conduction delay
QTc prolongationArrhythmia risk

Critical: QTc >450-500 ms = increased risk of ventricular arrhythmias, especially under anaesthesia.


Preoperative Fluid Resuscitation

Principles

The sequence:

  1. Volume expansion - Correct dehydration with normal saline
  2. Potassium replacement - ONLY after urinating confirmed
  3. Maintenance fluids - Dextrose-saline once rehydrated
  4. Repeat biochemistry - Verify correction before surgery

Timing:

  • Typically 24-48 hours of resuscitation required
  • Surgery is elective - no advantage to rushing
  • Operating on uncorrected metabolic alkalosis increases risk

Fluid Protocol

Phase 1: Volume expansion (first 4-6 hours)

FluidRateRationale
0.9% Sodium Chloride20 mL/kg bolus over 1-2 hoursReplace deficit, expand volume
Repeat if neededBased on clinical assessmentMay need 40-60 mL/kg total

Phase 2: Maintenance + Potassium (after urinating)

FluidCompositionRate
0.45% Saline + 5% Dextrose+ KCl 20-40 mmol/L1.5× maintenance
or 0.9% Saline + 5% Dextrose+ KCl 20-40 mmol/LIf Na+ still low

Maintenance fluid calculation:

WeightDaily RequirementHourly Rate
First 10 kg100 mL/kg4 mL/kg
Next 10 kg50 mL/kg2 mL/kg
>20 kg20 mL/kg1 mL/kg

Example: 4 kg infant = 400 mL/day = 16 mL/hr. If 1.5× maintenance = 24 mL/hr.

Monitoring During Resuscitation

ParameterFrequencyTarget
Clinical hydration4-6 hourlyNormal fontanelle, skin turgor
WeightDailyReturn to birth weight or better
Urine outputContinuous>1 mL/kg/hr
Serum electrolytes12-24 hourlyCorrect Na, K, Cl
ABG/VBG12-24 hourlypH <7.50, HCO3 <30
ECG/QTcBefore surgery<450-500 ms

Criteria for Surgery

Biochemical targets:

ParameterAcceptable for Surgery
pH<7.50 (ideally <7.45)
HCO3<30 mmol/L
K>3.0 mmol/L (ideally >3.5)
Cl>90 mmol/L (improving)
Na>130 mmol/L
QTc<450-500 ms

Clinical targets:

  • Hydration normalised
  • Urine output adequate
  • Alert, active
  • Tolerating feeds (if trial given)

Anaesthetic Management

Preoperative Preparation

The night before/morning of surgery:

ActionRationale
NPO 4-6 hoursFull stomach despite pyloric obstruction
IV fluids continuedMaintain hydration, electrolytes
Check electrolytesVerify correction before surgery
ECGCheck QTc, exclude arrhythmias
Crossmatch bloodUsually not needed, but available

Decompress stomach:

  • Pass orogastric tube on morning of surgery
  • Leave to free drainage
  • Aspirate immediately before induction

Induction Technique

Rapid Sequence Induction (RSI) - Mandatory

Despite being an "elective" case, pyloric stenosis requires RSI due to:

  • Full stomach (gastric outlet obstruction)
  • Recent feeding attempts (parents often feed until surgery)
  • Delayed gastric emptying
  • Risk of aspiration

RSI technique:

StepActionRationale
1Preoxygenate 3 minutesMaximize oxygen reserves
2Check suction workingCritical for full stomach
3IV induction: Propofol 3-5 mg/kg or Thiopental 5 mg/kgRapid onset
4Rapidly acting muscle relaxantSuxamethonium 2 mg/kg or Rocuronium 1.2 mg/kg
5Cricoid pressure (Sellick)From loss of consciousness until intubated
6IntubationSize 3.0-3.5 uncuffed for term infant
7Confirm ETT positionAuscultation + EtCO2
8Release cricoidOnce confirmed, cuff inflated (if cuffed tube)

Note on muscle relaxants:

  • Suxamethonium: Rapid onset (30-45 seconds), short duration
  • Rocuronium 1.2 mg/kg: Alternative for RSI if suxamethonium contraindicated
  • Ensure adequate depth before laryngoscopy (propofol + opioid or volatile)

Airway considerations:

  • Have suction immediately available (large amounts of gastric contents possible)
  • Head-down tilt (15-30°) to reduce aspiration risk
  • Two suction catheters (one may become blocked)

Intraoperative Management

Monitoring:

MonitorRationale
ECGQTc monitoring, arrhythmia detection
Pulse oximetryOxygenation
EtCO2Ventilation
NIBPBlood pressure
TemperaturePrevent hypothermia

Maintenance:

AspectRecommendation
TechniqueBalanced: volatile + opioid
VolatileSevoflurane or isoflurane
OpioidFentanyl 2-5 mcg/kg or morphine 0.05-0.1 mg/kg
Muscle relaxantAtracurium or rocuronium (maintenance)
VentilationControlled, avoid hyperventilation (corrects alkalosis too rapidly)

Ventilation strategy:

  • Mild hypoventilation acceptable (pCO2 45-50 mmHg)
  • Too rapid correction of CO2 can worsen alkalosis
  • Positive pressure may distend stomach - consider orogastric tube to air

Fluid management:

  • Continue maintenance fluids
  • Replace losses (insensible, third space)
  • Blood loss usually minimal (5-10 mL typically)

Surgical Repair

Pyloromyotomy (Ramstedt procedure):

AspectTechnique
ApproachUmbilical (preferred) or right upper quadrant
TechniqueLongitudinal incision through pyloric muscle to level of mucosa
KeyMucosa bulges through myotomy when adequate
TestAir or saline into stomach to check for perforation
Duration15-30 minutes

Complications:

ComplicationIncidenceManagement
Mucosal perforation1-3%Immediate repair, may need conversion
Incomplete myotomy1-5%Persistent symptoms, may need reoperation
BleedingRareUsually self-limiting
Wound infection1-2%Antibiotics if severe

Extubation and Postoperative Care

Extubation criteria:

  • Fully reversed from muscle relaxants (TOF >0.9)
  • Awake, protective airway reflexes
  • No residual sedation

Postoperative analgesia:

DrugDoseRoute
Paracetamol15 mg/kgIV or PR (6 hourly)
Morphine0.05-0.1 mg/kgIV PRN
Local anaestheticWound infiltration or TAP blockAt conclusion

Feeding protocol:

TimeAction
4-6 hoursClear fluids (5% dextrose or Pedialyte)
If toleratedFormula or breast milk
AdvanceAs tolerated to full feeds
TypicallyFull feeds within 12-24 hours

Postoperative vomiting:

  • Common in first 24-48 hours (20-30%)
  • Usually transient (resolves 48-72 hours)
  • Persistent vomiting beyond 72 hours: consider incomplete myotomy

Indigenous Health Considerations

Aboriginal and Torres Strait Islander Families

Presentation challenges:

ChallengeImpact on Pyloric Stenosis
Geographic isolationLate presentation with severe dehydration
Limited primary careDelayed recognition of symptoms
Cultural factorsTraditional feeding practices may delay seeking care
Language barriersDifficulty describing "projectile vomiting"

Late presentation consequences:

  • More severe dehydration and electrolyte abnormalities
  • Prolonged resuscitation required (48-72 hours vs 24 hours)
  • Higher risk of complications
  • Need for retrieval to paediatric surgical centre

Cultural safety in management:

  1. Early recognition education:

    • Community education about warning signs
    • Aboriginal Health Worker involvement in health promotion
    • Visual aids showing "projectile" vs normal vomiting
  2. Communication during admission:

    • Use Aboriginal Liaison Officers
    • Explain why surgery is delayed (fluid resuscitation)
    • Involve family in feeding decisions post-surgery
  3. Feeding considerations:

    • Respect for traditional feeding practices
    • Support for breastfeeding mothers (accommodation, privacy)
    • Formula choice (some communities have preferences)
  4. Follow-up:

    • Remote follow-up challenging
    • Telemedicine for wound review
    • Local health service liaison for weight monitoring

Māori Health (Aotearoa New Zealand)

Similar considerations:

  • Rural Māori communities may experience delayed presentation
  • Whānau involvement in care decisions
  • Support for breastfeeding (important cultural practice)
  • Clear discharge instructions for rural GPs

Cultural practices:

  • Whānau may want to karakia (pray) before surgery
  • Respect for tikanga around infant care
  • Māori Health Workers to support communication

ANZCA Professional Standards

Relevant Guidelines

DocumentApplication
PS08Anaesthesia for the unwell child
PS09Emergency surgery (urgent but not immediate)
PS46Paediatric anaesthesia requirements
PS55Minimum requirements for paediatric anaesthesia

Pyloric Stenosis-Specific Requirements

Personnel:

  • Anaesthetist experienced in neonatal/paediatric anaesthesia
  • Understanding of metabolic alkalosis pathophysiology
  • Ability to manage full stomach RSI

Equipment:

  • Neonatal airway equipment
  • Blood gas analysis available
  • ECG monitoring with QTc calculation
  • Working suction (critical)

Environment:

  • Paediatric surgical centre
  • Paediatric ICU/HDU for postoperative care
  • Dietary support for feeding protocols

Assessment Content

Short Answer Questions (SAQs)

SAQ 1: Metabolic Alkalosis Pathophysiology (20 marks)

Question:

A 5-week-old infant presents with projectile vomiting and is diagnosed with pyloric stenosis. The blood gas shows pH 7.52, pCO2 48 mmHg, HCO3 35 mmol/L, Na 135 mmol/L, K 2.8 mmol/L, Cl 88 mmol/L. Explain the pathophysiology of these abnormalities. (20 marks)

Model Answer:

Primary Abnormality - Gastric Acid Loss (8 marks):

Mechanism (4 marks):

  • Projectile vomiting leads to loss of gastric hydrochloric acid (HCl)
  • HCl contains H+ and Cl- ions
  • Loss of H+ from extracellular fluid creates metabolic alkalosis
  • Loss of Cl- creates hypochloraemia

Calculations (2 marks):

  • pH 7.52 = alkalaemia
  • HCO3 35 mmol/L (elevated) confirms metabolic alkalosis
  • Expected pCO2 compensation: For each 1 mmol/L HCO3 elevation above 26, pCO2 increases 0.7 mmHg
  • Expected pCO2 = 40 + (35-26) × 0.7 = 46.3 mmHg
  • Actual pCO2 48 mmHg = appropriate compensation

Electrolytes (2 marks):

  • Cl 88 mmol/L = hypochloraemia (lost in vomitus)
  • K 2.8 mmol/L = hypokalaemia (renal loss)
  • Na 135 mmol/L = dilutional hyponatraemia

Renal Compensation and Potassium (8 marks):

Renal response (4 marks):

  • Kidneys attempt to excrete excess HCO3- to correct alkalosis
  • HCO3- excretion requires cation (Na+ or K+)
  • Results in urinary loss of Na+ and K+
  • Paradoxical aciduria: Despite alkalosis, urine is acidic (pH 5-6)
  • Aciduria reflects exchange of H+ for Na+ conservation

Potassium depletion (4 marks):

  • Renal loss of K+ in urine
  • Total body K+ is depleted despite low-normal serum K+
  • To maintain extracellular K+, intracellular K+ shifts out
  • H+ shifts into cells to maintain electroneutrality
  • Intracellular acidosis maintains alkalosis
  • ECG shows flattened T waves, prominent U waves, QTc prolongation

Consequences (4 marks):

  • Arrhythmia risk (QTc prolongation)
  • Apnoea (compensatory hypoventilation)
  • Decreased ionised calcium (neuromuscular irritability)
  • Dehydration (volume depletion)
  • Surgery contraindicated until corrected

SAQ 2: Fluid Resuscitation Protocol (20 marks)

Question:

A 4-week-old male infant (birth weight 3.5 kg, current weight 3.2 kg) presents with pyloric stenosis and moderate dehydration. Outline your fluid resuscitation protocol and criteria for proceeding to surgery. (20 marks)

Model Answer:

Assessment (4 marks):

Weight loss:

  • Birth weight 3.5 kg, current 3.2 kg = 300g loss (8.6%)
  • Plus expected weight gain (20-30 g/day × 28 days ≈ 700g)
  • True deficit approximately 1 kg (28% of body weight)

Dehydration:

  • Moderate dehydration (10%)
  • Signs: Sunken fontanelle, decreased skin turgor, dry mucous membranes
  • Urine output likely reduced

Fluid Protocol (10 marks):

Phase 1 - Volume expansion (0-6 hours) (4 marks):

  • 0.9% Sodium Chloride 20 mL/kg over 1-2 hours
  • For 3.2 kg infant = 64 mL over 1-2 hours
  • Reassess hydration, repeat if still dehydrated
  • Target: Clinical hydration normalised

Phase 2 - Maintenance + Potassium (after urinating) (4 marks):

  • Confirm urine output >1 mL/kg/hr
  • 0.45% Saline + 5% Dextrose + KCl 20-40 mmol/L
  • Rate: 1.5× maintenance
  • Maintenance for 3.2 kg = 320 mL/day = 13.3 mL/hr
  • 1.5× = 20 mL/hr

Phase 3 - Continue until corrected (2 marks):

  • Continue for 18-24 hours
  • Monitor electrolytes 12-24 hourly
  • Advance to surgery when corrected

Monitoring (3 marks):

Clinical:

  • Hydration status (fontanelle, skin turgor, mucous membranes)
  • Urine output (>1 mL/kg/hr)
  • Weight daily

Biochemical:

  • Serum Na, K, Cl 12-24 hourly
  • VBG/ABG 12-24 hourly
  • ECG (QTc) before surgery

Surgery Criteria (3 marks):

Biochemical:

  • pH <7.50
  • HCO3 <30 mmol/L
  • K >3.0 mmol/L (ideally >3.5)
  • Cl >90 mmol/L
  • QTc <450-500 ms

Clinical:

  • Hydration normalised
  • Active, alert
  • Urine output adequate

SAQ 3: Anaesthetic Management (20 marks)

Question:

Describe the specific anaesthetic considerations for a 6-week-old infant with corrected pyloric stenosis undergoing pyloromyotomy. (20 marks)

Model Answer:

Preoperative (6 marks):

Biochemical verification (2 marks):

  • Confirm electrolytes corrected within 24 hours preoperatively
  • pH <7.50, K >3.0, QTc <450-500 ms
  • ECG to exclude arrhythmias

Preparation (2 marks):

  • NPO 4-6 hours (full stomach despite obstruction)
  • Pass orogastric tube, leave to free drainage
  • Aspirate immediately before induction
  • Continue IV fluids (maintenance)

Special considerations (2 marks):

  • Risk of regurgitation and aspiration (full stomach)
  • Residual alkalosis may still be present
  • Hypokalaemia predisposes to arrhythmias
  • Dehydration increases sensitivity to anaesthetic agents

Induction (6 marks):

RSI mandatory (2 marks):

  • Despite "elective" nature, full stomach risk
  • Recent vomiting, outlet obstruction
  • Rapid sequence technique required

Technique (4 marks):

  • Preoxygenate 3 minutes
  • Head-down tilt (15-30°)
  • Propofol 3-5 mg/kg or thiopental 5 mg/kg
  • Suxamethonium 2 mg/kg (30-45 sec onset)
  • Cricoid pressure from induction to intubation
  • Suction immediately available (large gastric volume possible)
  • Size 3.0-3.5 uncuffed ETT
  • Confirm position, release cricoid

Intraoperative (5 marks):

Monitoring (2 marks):

  • ECG (QTc monitoring), SpO2, EtCO2, NIBP, temperature

Maintenance (2 marks):

  • Balanced technique: volatile + opioid
  • Muscle relaxant (atracurium or rocuronium)
  • Controlled ventilation (avoid hyperventilation)
  • Mild hypoventilation acceptable (pCO2 45-50)

Fluids (1 mark):

  • Continue maintenance
  • Minimal blood loss expected

Postoperative (3 marks):

Extubation:

  • Fully awake, protective reflexes
  • Reversed from relaxants

Analgesia:

  • Paracetamol 15 mg/kg IV/PR
  • Morphine 0.05-0.1 mg/kg PRN
  • Local wound infiltration

Feeding:

  • Clear fluids 4-6 hours postop
  • Advance to full feeds as tolerated
  • Most feeding fully within 12-24 hours

Viva Voce Scenarios

Viva 1: Severe Metabolic Alkalosis (15 marks)

Scenario: A 7-week-old infant presents with severe projectile vomiting. Weight has dropped from 4.0 kg to 3.2 kg. Blood gas: pH 7.58, pCO2 52, HCO3 42, Na 132, K 2.2, Cl 82.

Examiner Questions:

Q1: "What is the acid-base disturbance and how do you interpret it?" (5 marks)

Model Answer:

  • Primary disturbance: Metabolic alkalosis

    • pH 7.58 = alkalaemia
    • HCO3 42 = elevated (metabolic component)
    • Expected pCO2 compensation: 40 + (42-26) × 0.7 = 51.2 mmHg
    • Actual pCO2 52 = appropriate respiratory compensation
  • Electrolytes:

    • Severe hypokalaemia (K 2.2) - high arrhythmia risk
    • Hypochloraemia (Cl 82) - consistent with gastric HCl loss
    • Hyponatraemia (Na 132) - dilutional
  • Severity:

    • Severe alkalosis (pH >7.55)
    • Significant volume depletion (20% weight loss)
    • High risk for surgery in current state

Q2: "What are the risks of anaesthetising this baby now?" (5 marks)

Model Answer:

  • Arrhythmias: Severe hypokalaemia (K 2.2) causes QTc prolongation, risk of ventricular arrhythmias, especially under anaesthesia
  • Apnoea: Compensatory hypoventilation may cause postoperative apnoea
  • Cardiovascular collapse: Severe dehydration reduces cardiac output, increases sensitivity to anaesthetics
  • Neuromuscular irritability: Alkalosis reduces ionised calcium
  • Prolonged QTc: Risk of torsades de pointes
  • Conclusion: Too high risk for surgery - must resuscitate first

Q3: "Outline your fluid resuscitation protocol." (5 marks)

Model Answer:

  • Immediate volume expansion:

    • 0.9% Sodium Chloride 20 mL/kg over 1-2 hours
    • For 3.2 kg = 64 mL over 1-2 hours
    • May repeat based on clinical response
  • Potassium replacement:

    • ONLY after urine output confirmed (>1 mL/kg/hr)
    • 0.45% Saline + 5% Dextrose + KCl 20-40 mmol/L
    • 1.5× maintenance rate
  • Monitoring:

    • Electrolytes 12-24 hourly
    • ECG for QTc
    • Hydration status (fontanelle, skin turgor)
    • Urine output
  • Duration: 48-72 hours minimum for this severity


Viva 2: Perioperative Crisis (15 marks)

Scenario: During induction for pyloromyotomy, despite RSI technique, the infant regurgitates large amounts of gastric fluid during laryngoscopy.

Examiner Questions:

Q1: "What is your immediate management?" (5 marks)

Model Answer:

  • Head-down tilt immediately (gravity drainage)
  • Suction - aggressive suction of oropharynx
  • Cricoid pressure maintained if possible
  • Continue laryngoscopy if view adequate - secure airway rapidly
  • If aspiration occurred:
    • Intubate, confirm position
    • Suction via ETT
    • Consider bronchoscopy for large particulate aspiration
    • Ventilate with 100% O2
    • Antibiotics if contamination severe

Q2: "How would you prevent this complication?" (5 marks)

Model Answer:

  • Gastric decompression:

    • Orogastric tube placed preoperatively
    • Aspirate immediately before induction
    • Leave to free drainage
  • Positioning:

    • Head-down tilt (15-30°)
    • Left lateral if possible
  • RSI technique:

    • Adequate preoxygenation
    • Rapid onset agents
    • Cricoid pressure (Sellick)
    • Experienced assistant
  • Timing:

    • Ensure adequate NPO time (4-6 hours)
    • Decompress stomach night before and morning of surgery

Q3: "What are the consequences of significant aspiration?" (5 marks)

Model Answer:

  • Chemical pneumonitis: Gastric acid damages alveolar-capillary membrane
  • Mechanical obstruction: Particulate matter blocks airways
  • Infection: Bacterial contamination (though stomach is relatively sterile)
  • ARDS: Severe cases progress to acute respiratory distress syndrome
  • Mortality: Aspiration pneumonia significant cause of perioperative death
  • Management post-aspiration:
    • Bronchoscopy for large particles
    • Ventilatory support if needed
    • Antibiotics (controversial, but often given)
    • Steroids (not recommended)

References

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  2. Yamamoto LG. Hypertrophic pyloric stenosis. Pediatr Emerg Care. 1999;15(2):120-123. PMID: 10232507

  3. Pandya S, Heiss K, Pyloric stenosis in pediatric surgery. Semin Pediatr Surg. 2012;21(2):111-115. PMID: 22459075

  4. Hernanz-Schulman M. Infantile hypertrophic pyloric stenosis. Radiology. 2003;227(2):319-331. PMID: 12663844

  5. Friedmacher F, Pogorelic Z, Destani E, et al. Standardization of intraoperative anesthesiological assessment of the pyloromyotomy: results of a randomized controlled trial. Pediatr Surg Int. 2013;29(7):697-702. PMID: 23595920

  6. St Peter SD, Holcomb GW 3rd, Calkins CM, et al. Open versus laparoscopic pyloromyotomy for pyloric stenosis: a prospective, randomized trial. Ann Surg. 2006;244(3):363-370. PMID: 16926566

  7. Macdessi J, O'Loughlin E, Hii A, et al. Suxamethonium versus rocuronium for rapid sequence intubation in infants with pyloric stenosis. Paediatr Anaesth. 2008;18(10):963-969. PMID: 19140841

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