What is the recommended approach for pediatric Rapid Sequence Intubation (RSI)?

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Pediatric Rapid Sequence Intubation

Medication Protocol

For pediatric RSI, administer atropine pretreatment (0.01-0.02 mg/kg IV) in children 28 days to 8 years old, followed by ketamine (1-2 mg/kg IV) as the induction agent, and succinylcholine as the first-line neuromuscular blocker (dose varies by age: 1.8 mg/kg for neonates <1 month, 2.0 mg/kg for infants 1 month-1 year, 1.2 mg/kg for children 1-10 years, and 1-1.5 mg/kg for children >10 years). 1, 2

Pretreatment Phase

Atropine administration is mandatory for specific pediatric populations:

  • Give atropine 0.01-0.02 mg/kg IV (maximum 0.5 mg) to all children aged 28 days to 8 years, particularly those with septic shock, hypovolemia, or when using succinylcholine 1, 2
  • This prevents bradycardia during laryngoscopy and from succinylcholine-induced vagal stimulation 1
  • For patients with elevated intracranial pressure, consider lidocaine 1-2 mg/kg IV administered 30 seconds to 5 minutes before airway instrumentation 1, 2

Induction Agent Selection

Ketamine is the preferred first-line sedative-hypnotic agent:

  • Dose ketamine at 1-2 mg/kg IV for most pediatric RSI scenarios 1, 2
  • Alternative dosing: 3-4 mg/kg for infants <18 months; 2 mg/kg for children ≥18 months 2
  • Ketamine maintains hemodynamic stability through sympathomimetic effects, making it ideal for hemodynamically unstable patients 1, 2
  • This agent is strongly preferred over etomidate in septic shock due to adrenal suppression concerns with etomidate 3, 2

Etomidate is an alternative option with specific indications:

  • Dose etomidate at 0.2-0.4 mg/kg IV (maximum 20 mg) 1, 2
  • Use etomidate preferentially in children >2 years old with head injury, as it lowers intracranial pressure 1
  • Avoid etomidate in septic patients due to adrenal suppression risk 2
  • Etomidate has minimal hemodynamic effects but should not be used in sepsis 1

Neuromuscular Blocking Agent Selection

Succinylcholine remains the first-line paralytic:

  • Use succinylcholine for children with respiratory or cardiovascular compromise 4, 1, 2
  • Age-specific dosing is critical:
    • Neonates <1 month: 1.8 mg/kg IV 1, 2
    • Infants 1 month to 1 year: 2.0 mg/kg IV 1, 2
    • Children 1-10 years: 1.2 mg/kg IV 4, 1, 2
    • Children >10 years: 1-1.5 mg/kg IV 1, 2
  • Succinylcholine provides rapid onset and short duration, making it ideal for emergency situations 4

Rocuronium is the alternative when succinylcholine is contraindicated:

  • Dose rocuronium at 0.9-1.2 mg/kg IV 4, 1, 2
  • Use rocuronium when succinylcholine is contraindicated (hyperkalemia risk, neuromuscular disease, malignant hyperthermia history) 4
  • Sugammadex must be immediately available when using rocuronium for potential reversal in a "can't intubate, can't ventilate" scenario 4, 1, 2
  • The choice between succinylcholine and rocuronium should consider desired duration of paralysis, risk of difficult intubation, and presence of neuromuscular disease 4

Equipment and Monitoring Considerations

Videolaryngoscopy should be considered in specific scenarios:

  • Use videolaryngoscopy as first option for anticipated difficult intubation with possible mask ventilation 4
  • Consider videolaryngoscopy after failed direct laryngoscopy to increase success rates 4
  • In children with prior difficult intubation history, videolaryngoscopy can be chosen as first-line 4

Essential monitoring and preparation:

  • Personnel with advanced airway management skills must be present when administering neuromuscular blockers 2
  • Age-appropriate equipment for aspiration, oxygenation, intubation, and ventilation must be immediately available 2
  • Continuous oxygen saturation monitoring is mandatory 2

Critical Pitfalls to Avoid

Common errors that increase morbidity:

  • Failure to administer atropine in young children (<8 years), especially with succinylcholine use, significantly increases risk of clinically significant bradycardia 1, 2
  • Using succinylcholine in patients with hyperkalemia risk (crush injuries, burns >24 hours old, denervation injuries, neuromuscular disease) can cause cardiac arrest 1
  • Proceeding with rocuronium without immediately available sugammadex creates unnecessary risk in failed airway scenarios 4, 1
  • Using ketamine-only approach (without neuromuscular blocker) results in significantly lower first-pass success (61%) compared to proper RSI (90%) and higher complication rates 5
  • Attempting intubation without muscle relaxation is not recommended, as muscle relaxation significantly improves intubation conditions 4

Clinical Success Data

RSI demonstrates superior outcomes in pediatric patients:

  • RSI achieves 78% first-attempt success compared to 47% without medications and 44% with sedation alone 6
  • Overall success rate with RSI reaches 99% in pediatric emergency department intubations 6
  • True complications occur in only 1% of RSI attempts versus 5% with no medications 6
  • The majority of pediatric emergency intubations (81%) utilize RSI as the preferred method 6

References

Guideline

Pediatric Rapid Sequence Intubation Medication Regimen

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Rapid Sequence Intubation in Children

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Rapid Sequence Intubation Medication Regimen

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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