Am. J. Respir. Crit. Care Med., Vol 154, No. 1, Jul 1996, 116-123.
Mortality of nosocomial pneumonia in ventilated patients: influence of diagnostic tools
JF Timsit, S Chevret, J Valcke, B Misset, B Renaud, FW Goldstein, P Vaury and J Carlet
Intensive Care Unit, Hopital Saint Joseph, Paris, France.
The overmortality induced by nosocomial infections, especially pneumonia in
ventilated patients (VNP), is still a matter of controversy because it is
difficult to know precisely the respective effects of VNP per se and both
the underlying illness and the severity of the disease that indicates ICU
stay. During a 3-yr period, for each patient mechanically ventilated for
more than 48 h we recorded underlying illness, reason for mechanical
ventilation, clinical and therapeutic data collected during the first 48 h
of ventilation, and death in the ICU. Patients with suspicion of VNP
(S-VNP) according to clinical, radiologic, and biologic criteria underwent
bronchoscopy with protected specimen brush (PSB) and bronchoalveolar lavage
culture (BAL- C). VNP was confirmed (C-VNP) if PSB > or = 10(3) cfu/ml
and/or BAL-C > or = 10(4) cfu/ml. Prognostic multivariate analysis was
performed introducing S-VNP and C-VNP as time-dependent covariates. Of the
387 studied patients, 112 S-VNP and 56 C-VNP were observed with overall
mortality of 43% (168 patients). MacCabe, APACHE II score, shock, use of
sedatives and absence of enteral nutrition were additively associated with
an increased mortality as well as C-VNP (relative risk [RR]: 1.8, p =
0.007). Nevertheless, when S-VNP and C-VNP were simultaneously introduced
in the Cox model, only S-VNP remained associated with increased mortality.
In patients suspected of VNP, confirmation of VNP using PSB and/or BAL-C
adds no prognostic information. Whether this could be explained by the lack
of sensitivity of protected distal samples or the severity of underlying
conditions of S-VNP patients is still an open issue. A multivariate
analysis based on follow-up data during the ICU course of ventilated
patients will be initiated in the near future.
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Copyright © 1996 American Thoracic Society
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