Nebulized Fluticasone for Preventing Postextubation Stridor in Intubated Children: A Randomized, Double-Blind

Pharsai Prasertsan1, Duangjai Nakju, Rojjanee Lertbunrian

  • 11Division of Pediatric Critical Care, Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. 2Department of Nursing, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Insights

Nebulized fluticasone propionate did not prevent postextubation stridor in children. However, it may benefit emergently intubated patients, potentially by reducing stridor severity.

Area of Science:

  • Pediatric Critical Care Medicine
  • Respiratory Medicine
  • Pharmacology

Background:

  • Postextubation stridor is a common complication in children following mechanical ventilation.
  • Effective prevention strategies are crucial to reduce respiratory distress and improve patient outcomes.

Purpose of the Study:

  • To assess the efficacy of a single dose of nebulized fluticasone propionate in preventing postextubation stridor in pediatric patients.
  • To evaluate the impact of nebulized fluticasone propionate on stridor severity and the need for noninvasive ventilation.

Main Methods:

  • A double-blind, placebo-controlled randomized clinical trial was conducted in a pediatric intensive care unit (PICU).
  • 147 children aged 1 month to 15 years undergoing mechanical ventilation received either nebulized fluticasone propionate (1,000 µg) or normal saline immediately after extubation.
  • Patients were monitored for 6 hours post-extubation, with vital signs and modified Westley scores assessed. The primary outcome was the incidence of postextubation stridor.

Main Results:

  • No significant difference in the prevalence of postextubation stridor was observed between the fluticasone and placebo groups (16% vs 18%, p = 0.797).
  • In a subgroup of emergently intubated children, the fluticasone group experienced a longer delay in initiating noninvasive ventilation (p = 0.044).
  • The modified Westley scores, indicating stridor severity, were significantly lower in the fluticasone group at 30 and 60 minutes post-extubation (p = 0.04 and p = 0.02, respectively).

Conclusions:

  • A single dose of nebulized fluticasone propionate (1,000 µg) is not effective in reducing the overall incidence of postextubation stridor in children.
  • Nebulized fluticasone propionate may offer benefits in emergently intubated children, potentially by mitigating stridor severity.
  • Further research is warranted to explore the role of fluticasone propionate in specific pediatric populations requiring mechanical ventilation.
Abstract

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