Background Critically ill patients who require mechanical ventilationare at risk for ventilator-associated pneumonia. Current dataare conflicting as to the optimal diagnostic approach in patientswho have suspected ventilator-associated pneumonia.
Methods In a multicenter trial, we randomly assigned immunocompetentadults who were receiving mechanical ventilation and who hadsuspected ventilator-associated pneumonia after 4 days in theintensive care unit (ICU) to undergo either bronchoalveolarlavage with quantitative culture of the bronchoalveolar-lavagefluid or endotracheal aspiration with nonquantitative cultureof the aspirate. Patients known to be colonized or infectedwith pseudomonas species or methicillin-resistant Staphylococcusaureus were excluded. Empirical antibiotic therapy was initiatedin all patients until culture results were available, at whichpoint a protocol of targeted therapy was used for discontinuingor reducing the dose or number of antibiotics, or for resumingantibiotic therapy to treat a preenrollment condition if theculture was negative.
Results We enrolled 740 patients in 28 ICUs in Canada and theUnited States. There was no significant difference in the primaryoutcome (28-day mortality rate) between the bronchoalveolar-lavagegroup and the endotracheal-aspiration group (18.9% and 18.4%,respectively; P=0.94). The bronchoalveolar-lavage group andthe endotracheal-aspiration group also had similar rates oftargeted therapy (74.2% and 74.6%, respectively; P=0.90), daysalive without antibiotics (10.4±7.5 and 10.6±7.9,P=0.86), and maximum organ-dysfunction scores (mean [±SD],8.3±3.6 and 8.6±4.0; P=0.26). The two groups didnot differ significantly in the length of stay in the ICU orhospital.
Conclusions Two diagnostic strategies for ventilator-associatedpneumonia bronchoalveolar lavage with quantitative cultureof the bronchoalveolar-lavage fluid and endotracheal aspirationwith nonquantitative culture of the aspirate are associatedwith similar clinical outcomes and similar overall use of antibiotics.(Current Controlled Trials number, ISRCTN51767272
[controlled-trials.com]
.)
Source Information
The Steering Committee (study chair, Daren Heyland, M.D., Kingston General Hospital and Queens University, Kingston, ON; Deborah Cook, M.D., St. Joseph's Hospital and McMaster University, Hamilton, ON; Peter Dodek, M.D., St. Paul's Hospital and University of British Columbia, Vancouver, BC; and John Muscedere, M.D., and Andrew Day, M.Sc., Kingston General Hospital and Queens University, Kingston, ON all in Canada) of the Canadian Critical Care Trials Group assumes responsibility for the overall content and integrity of the article.
Address reprint requests to Dr. Heyland at Angada 4, Kingston General Hospital, Kingston, ON K7L 2V7, Canada, or at dkh2{at}post.queensu.ca.
Diagnosis of Ventilator-Associated Pneumonia
Chastre J., Fagon J.-Y., Misset B., Garrouste-Orgeas M., Carlet J., Marik P. E., Baram M., Heyland D., Cook D., Muscedere J., the Canadian Critical Care Trials Group
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