Skip to main navigation Skip to search Skip to main content

Ketamine sedation for pediatric gastroenterology procedures

  • Steven M. Green
  • , Marquelle Klooster
  • , Troy Harris
  • , Elizabeth L. Lynch
  • , Steven G. Rothrock

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Background: Although the dissociative sedative ketamine is used commonly for pediatric procedural sedation in other settings, the safety of this agent in pediatric gastroenterology is not well-studied. A 5-year experience with ketamine sedation for pediatric gastroenterology procedures was reviewed to document the safety profile of this agent and to identify predictors of laryngospasm during esophagogastroduodenoscopy (EGD). Methods: The study was a retrospective consecutive case series of children receiving ketamine administered by pediatric gastroenterologists skilled in basic airway management to facilitate pediatric gastrointestinal procedures during a 5-year period. Patient's records were reviewed to determine indication, dosage, adverse effects, drugs, inadequate sedation, and recovery time for each sedation. A multiple logistic regression analysis was performed to identify predictors of laryngospasm during EGD. Outcome measures were descriptive features of sedation, including adverse effects and predictors of laryngospasm during EGD. Results: During the study period pediatric gastroenterologists administered ketamine 636 times, primarily for EGD (86%) and primarily by the intravenous route (98%). The median loading dose and total dose were 1.00 mg/kg and 1.34 mg/kg, respectively. Inadequate sedation was noted in seven (1.1%) procedures. Adverse effects included transient laryngospasm (8.2%), emesis (4.1%), recovery agitation (2.4%), partial airway obstruction (1.3%), apnea and respiratory depression (0.5%), and excessive salivation (0.3%). There were no adverse outcomes attributable to ketamine. Nearly half (46%) the subjects had severe underlying illness (American Society of Anesthesiologists [ASA] class ≥3). All instances of laryngospasm occurred during EGD (9.5% incidence), and the only independent predictor of laryngospasm in this sample was decreasing age. The incidence of laryngospasm was 13.9% in preschool-aged (≤6 years) children and was 3.6% in school-aged (>6 years) children (difference 10.3%, 95% confidence intervals 5.5-14.9%). No dose relationship was noted with laryngospasm, and the risk did not increase with underlying illness. Conclusion: Pediatric gastroenterologists skilled in ketamine administration and basic airway management can effectively administer this drug to facilitate gastrointestinal procedures. Transient laryngospasm occurred in 9.5% of children receiving ketamine for EGD, and its incidence was greater in preschool than in school-aged children. © 2001 Lippincott Williams & Wilkins, Inc.
    Original languageEnglish
    Pages (from-to)26-33
    Number of pages8
    JournalJournal of Pediatric Gastroenterology and Nutrition
    Volume32
    Issue number1
    DOIs
    StatePublished - Jan 2001

    ASJC Scopus Subject Areas

    • Pediatrics, Perinatology, and Child Health
    • Gastroenterology

    Keywords

    • Child
    • Dissociative sedation
    • Endoscopy
    • Gastroenterology
    • Ketamine
    • Injections, Intravenous
    • Ketamine/administration & dosage
    • Age Factors
    • Gastroenterology/methods
    • Humans
    • Child, Preschool
    • Infant
    • Anesthetics, Dissociative/administration & dosage
    • Laryngismus/epidemiology
    • Adolescent
    • Adult
    • Retrospective Studies
    • Safety
    • Outcome Assessment, Health Care

    Cite this