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Guidelines for Elective Pediatric Fiberoptic Intubation
Published on: January 17, 2011
Propofol Infusion Is a Feasible Bridge to Extubation in General Pediatric Intensive Care Unit
Utpal S Bhalala1,2, Abhishek Patel1,2, Malarvizhi Thangavelu1
1The Children's Hospital of San Antonio, San Antonio, TX, United States.
Insights
Propofol infusion is a feasible bridge to extubation in critically ill children requiring mechanical ventilation. This short-term use showed a high success rate with minimal adverse effects like hypotension or lactic acidosis.
Area of Science:
- Pediatric Critical Care Medicine
- Anesthesiology
- Pharmacology
Background:
- Literature on propofol as a bridge to extubation in critically ill children is limited.
- Existing studies primarily focus on pediatric patients with burns or congenital cardiac disease.
- The feasibility in broader pediatric intensive care unit (PICU) populations remains underexplored.
Purpose of the Study:
- To evaluate the feasibility of propofol infusion as a bridge to extubation in mechanically ventilated, critically ill children.
- To assess extubation success rates and identify potential adverse effects associated with short-term propofol use.
- To contribute to the understanding of propofol's role in weaning from mechanical ventilation in diverse pediatric critical care scenarios.
Main Methods:
- Retrospective chart review of pediatric patients (<21 years) in a tertiary care PICU.
- Inclusion criteria: mechanical ventilation (MV) for ≥48 hours, ≥2 sedative infusions, and propofol infusion (4-24 hours) during anticipated extubation.
- Primary outcome: extubation success (no re-intubation within 24 hours). Secondary outcomes: hemodynamic instability and lactic acidosis during propofol infusion.
Main Results:
- Thirty-five critically ill, mechanically ventilated children were evaluated.
- Extubation success rate was high, with only one patient (2.9%) requiring re-intubation within 24 hours.
- Twenty percent of patients experienced a transient drop in mean arterial pressure (>10%), but none developed lactic acidosis or needed inotropes/fluids.
Conclusions:
- Short-term propofol infusion (<12 hours) is a feasible bridge to extubation in critically ill, mechanically ventilated pediatric patients.
- The study demonstrated a high success rate for extubation with propofol.
- No significant adverse events such as profound hypotension or lactic acidosis were observed during propofol infusion.
Abstract:
Objective: The current literature on propofol infusion as a bridge to extubation in critically ill children is limited to children with burns and congenital cardiac disease. We hypothesize that propofol infusion is a feasible bridge to extubation in mechanically ventilated, critically ill children. Design: Retrospective chart review. Setting: Pediatric intensive care unit of a tertiary care teaching hospital. Patients: Children < 21 years, admitted to our Pediatric intensive care unit (PICU), requiring mechanical ventilation (MV) for at least 48 h and at least two sedative infusions and who received propofol infusion for 4 to 24 h during anticipated extubation from January 2014 to May 2017. Interventions: None. Measurements and Main Results: We assessed extubation success as primary outcome. We defined extubation success as no re-intubation within 24 h after extubation. We also assessed for occurrence of adverse effects of propofol infusion (1) hemodynamic instability [more than 10% change from pre-propofol baseline heart rate (HR) and mean arterial pressure (MAP) measured 4 h before and during propofol infusion, need for any inotrope and/or fluid bolus] and (2) occurrence of lactic acidosis in absence of any documented sepsis. We compared hemodynamic parameters before and during infusion using Wilcoxon Rank Sum Test (significant p-value ≤ 0.05). We evaluated 35 critically ill, mechanically ventilated children. The median age, weight and duration of MV were 3.8 (IQR: 1.25-10.5) years, 12 (IQR: 6-16.2) kilograms and 111 (IQR: 78-212) h, respectively. Of the 35 patients, 15 (43%) were post-surgical (10 general and 5 cardiac) and the remaining 20 (57%) were non-surgical respiratory failure cases. The median (IQR) propofol infusion dose and duration were 64.7 (53.2-81.1) mcg/kg/min and 7.8 h respectively. Only one patient got re-intubated within 24 h of extubation and was later diagnosed with vascular ring. During propofol infusion, 7/35 (20%) patients exhibited transient drop in MAP > 10% from baseline, but none had lactic acidosis or required an inotrope or fluid bolus. Conclusions: In critically ill, mechanically ventilated patients, propofol infusion used over a short duration (<12 h) was found to be a feasible bridge to extubation. No patient had significant hypotension or lactic acidosis during the infusion.
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