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Use of continuous positive airway pressure (CPAP) in acute viral bronchiolitis: A systematic review

✍ Scribed by Matthew Donlan; Patricia S. Fontela; Pramod S. Puligandla


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
518 KB
Volume
46
Category
Article
ISSN
8755-6863

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✦ Synopsis


Abstract

Introduction

Continuous positive airway pressure (CPAP), used either alone or associated with heliox (CPAP‐He), has become a popular therapeutic option for bronchiolitis. This systematic review assesses the impact of CPAP on endotracheal intubation, carbon dioxide pressure (PCO~2~) and respiratory distress in patients with bronchiolitis.

Methods

Systematic search including studies that used CPAP or CPAP‐He in infants with bronchiolitis admitted to a PICU. Data analysis included descriptive statistics and the GRADE system.

Results

Five CPAP (one crossover randomized controlled trial [RCT] and four before–after studies) and three CPAP‐He (one quasi‐RCT and two before–after) studies were included. CPAP was reported to reduce PCO~2~ (−6.9 to −11.7 mmHg, respectively, P < 0.015), respiratory rate (−12 to −16 breaths/min after 2 hr, P < 0.01) and the modified Wood clinical asthma score (mWCAS, −2.2 points after 1 hr, P < 0.01). CPAP‐He studies observed decreases in PCO~2~ (−9.7 mmHg, P < 0.05), mWCAS (−2.12 points, P < 0.001), and respiratory rate (−8 to −13.7 breaths/min, P < 0.05) after 1 hr of treatment. Endotracheal intubation rates ranged from 0–12.5% (CPAP‐He) to 17–27% (CPAP). After applying the GRADE system, the quality of evidence for a beneficial effect of CPAP and CPAP‐He was classified as low.

Conclusions

The evidence supporting the use of CPAP to reduce PCO~2~ and respiratory distress in bronchiolitis is of low methodological quality, and there is no conclusive evidence that CPAP reduces the need for intubation. No definitive conclusions could be drawn about the CPAP‐He effect. Further research using higher quality methodology is needed to clarify the beneficial role of these interventions. Pediatr. Pulmonol. 2011; 46:736–746. © 2011 Wiley‐Liss, Inc.


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