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PMID: 9508156 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Influence of airway management on ventilator-associated pneumonia: evidence from randomized trials.

JAMA ·Vol. 279 ·No. 10 ·1998-03-11 ·Pages 781-7

Cook D, De Jonghe B, Brochard L, Brun-Buisson C

Abstract

Ventilator-associated pneumonia (VAP) is a serious complication of critical illness, conferring increased morbidity and mortality. Many interventions have been studied to reduce the risk of VAP. We systematically reviewed the influence of airway management on VAP in critically ill patients. Studies were identified through searching MEDLINE and EMBASE from 1980 through July 1997 and by searching SCISEARCH, the Cochrane Library, bibliographies of primary and review articles, personal files, and contact with authors of the randomized trials. We selected randomized trials evaluating ventilator circuit and secretion management strategies on the rate of VAP. Two investigators independently abstracted key data on design features, the population, intervention, and outcome of the studies. The frequency of ventilator circuit changes and the type of endotracheal suction system do not appear to influence VAP rates (3 trials, none with significant difference; range of relative risks [RRs], 0.84-0.91). However, lower VAP rates may be associated with avoidance of heated humidifiers and use of heat and moisture exchangers (5 trials, only 1 showing a significant difference; range of RRs, 0.34-0.86), use of oral vs nasal intubation (1 trial; RR, 0.52; 95% confidence interval, 0.24-1.13), subglottic secretion drainage vs standard endotracheal tubes (2 trials, 1 showing a significant difference; range of RRs, 0.46-0.57), and kinetic vs conventional beds (5 trials, only 1 showing a significant difference; range of RRs, 0.35-0.78). Some ventilator circuit and secretion management strategies may influence VAP rates in critically ill patients. Whether these strategies are adopted in practice depends on several factors such as the magnitude and precision of estimates of benefit and harm, as well as access, availability, and costs.

MeSH Terms
Critical Illness Cross Infection/etiology,prevention & control Data Collection Humans Pneumonia/etiology,prevention & control Randomized Controlled Trials as Topic Respiration, Artificial/adverse effects Risk Ventilators, Mechanical/adverse effects
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cook D
Department of Medicine, St Joseph's Hospital and McMaster University, Hamilton, Ontario, Canada. [email protected]
De Jonghe B
Brochard L
Brun-Buisson C
Article Info
Journal
JAMA
Abbr.
JAMA
ISSN
0098-7484
Published
1998-03-11
Pages
781-7
Language
English
Region
United States
NLM ID
7501160
Subset
IM
Corrections
ErratumIn
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