Erschienen in:
01.07.2009 | Original
Bacterial ventilator-associated pneumonia: bronchoalveolar lavage results are not influenced by dilution
verfasst von:
Olivier Baldesi, Fabrice Michel, Christophe Guervilly, Nathalie Embriaco, Aliocha Granfond, Bernard La Scola, Henri Portugal, Laurent Papazian
Erschienen in:
Intensive Care Medicine
|
Ausgabe 7/2009
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Abstract
Objective
This study was designed to determine if bronchoalveolar lavage (BAL) quantitative culture results can be used confidently for the diagnosis of bacterial ventilator-associated pneumonia (VAP) without taking dilution into account.
Design
Prospective observational cohort study.
Setting
A 12-bed medical ICU in a teaching hospital.
Patients
A total of 241 BAL (three 50-mL aliquots) were performed in 127 patients presenting a suspicion of VAP.
Interventions
All consecutive adults who were ventilated more than 48 h were included if VAP was clinically suspected. A dilution factor, k, was developed according to the formula: dilution factor k = concentration of urea in plasma/concentration of urea in lavage fluid recovered. Using this dilution factor, the quantitative bacterial counts were interpreted accordingly with a corrected positive threshold at 105 colony forming unit (CFU) mL−1.
Measurements and results
Eighty-nine BAL with at least one micro-organism ≥104 CFU mL−1 were identified (37%). In 176 BAL (73%), k ranged from 10 to 100. Median k was 24.4 (9.7–40.2) in VAP group and 24.6 (13.1–57.8) in patients without pneumonia (NS). Among the 25 BAL with micro-organism counts of 104 CFU mL−1, 3 had a dilution factor lower than 10, resulting in corrected counts below the threshold of 105 CFU mL−1. Two out of 15 patients with micro-organism counts of 103 CFU mL−1 had corrected micro-organism counts of 105 CFU mL−1. Finally, only five BAL (2.1%) were misclassified when the dilution correction factor was applied.
Conclusions
Using urea as dilution factor, we showed that BAL dilution variations did not alter the interpretation of BAL quantitative bacterial culture when administrating three aliquots of 50 mL of saline.