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Published on: April 7, 2021
Hemodynamic changes in child acute respiratory distress syndrome with airway pressure release ventilation: a case
Atsushi Kawaguchi1,2,3, Gonzalo Garcia Guerra1, Jonathan P Duff1
1Department of Pediatrics, Pediatric Critical Care Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, Canada.
Insights
Airway pressure release ventilation (APRV) can be safely used in pediatric acute respiratory distress syndrome (ARDS) patients. This study found no significant hemodynamic compromise or side effects in children receiving APRV.
Area of Science:
- Pediatric Critical Care Medicine
- Respiratory Physiology
- Mechanical Ventilation
Background:
- Airway pressure release ventilation (APRV) is a common mechanical ventilation strategy in adult intensive care units.
- Limited data exists regarding the application and safety of APRV in pediatric patients.
Purpose of the Study:
- To evaluate the safety and efficacy of APRV in pediatric patients diagnosed with acute respiratory distress syndrome (ARDS).
Main Methods:
- Retrospective review of pediatric patients with ARDS who received APRV for at least 12 hours between 2007 and 2009.
- Analysis of demographic data, ventilation duration, blood gas parameters, and hemodynamic parameters.
Main Results:
- Thirteen pediatric ARDS patients were included, with a mean weight of 18.2 kg and age of 68 months.
- APRV was used for a median of 4 days (range 1-10 days).
- No significant changes in blood gas or hemodynamic parameters (mean arterial blood pressure, central venous pressure, heart rate) were observed during APRV use.
Conclusions:
- APRV can be safely administered to pediatric patients with ARDS.
- The use of APRV in this cohort did not result in significant hemodynamic compromise or adverse effects.
Background:
Airway pressure release ventilation (APRV) is widely used in adult critical care settings. However, information on the use of APRV in the pediatric population is limited.
Methods:
All patients admitted to the medical-surgical pediatric intensive care unit with a diagnosis of acute respiratory distress syndrome (ARDS) who received APRV for at least 12 h between 2007 and 2009 were reviewed.
Results:
Thirteen patients with a variety of etiologies of ARDS were included, with a mean weight of 18.2 ± 15.0 kg, a mean age of 68 ± 57 months and a predicted mortality (based on Pediatric Index of Mortality version 2) of 23.9 ± 13.8%. Patients were placed on APRV for a median of 4 days (range 1-10 days). There was no change in blood gas parameters after 1 h or 12 h of APRV when compared with pre-APRV. There was no statistical difference in hemodynamic parameters, including mean arterial blood pressure, central venous blood pressure and heart rate, while the patients were on APRV.
Conclusion:
APRV could be safely used in pediatric ARDS patients, without significant hemodynamic compromise or side effects.
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