Cited by 250Nosocomial Infections in ICURespiratory Support and MechanismsAntifungal resistance and susceptibility

Nosocomial pneumonia in patients with acute respiratory distress syndrome

CHASTRE, JEAN, TROUILLET, JEAN LOUIS, VUAGNAT, ALBERT, JOLY-GUILLOU, MARIE LAURE, CLAVIER, HERVÉ, DOMBRET, MARIE CHRISTINE, GIBERT, CLAUDE·1998·American Journal of Respiratory and Critical Care Medicine

Abstract

To describe the epidemiologic and microbial aspects of ventilator-associated pneumonia (VAP) in patients with acute respiratory distress syndrome (ARDS), we prospectively evaluated 243 consecutive patients who required mechanical ventilation (MV) for > or = 48 h, 56 of whom developed ARDS as defined by a Murray lung injury score > 2.5. We did this with bronchoscopic techniques when VAP was clinically suspected, before any modification of existing antimicrobial therapy. For all patients, the diagnosis of pneumonia was established on the basis of culture results of protected-specimen brush (PSB) (> or = 10(3) cfu/ml) and bronchoalvelolar lavage fluid (BALF) (> or = 10(4) cfu/ml) specimens, and direct examination of cells recovered by bronchoalveolar lavage (BAL) (< or = 5% of infected cells). Thirty-one (55%) of the 56 patients with ARDS developed VAP for a total of 41 episodes, as compared with only 53 (28%) of the 187 patients without ARDS for a total of 65 episodes (p = 0.0005). Only 10% of first episodes of VAP in patients with ARDS occurred before Day 7 of MV, as compared with 40% of the episodes in patients without ARDS (p = 0.005). All but two patients with ARDS who developed VAP had received antimicrobial treatment (mostly with broad-spectrum antibiotics) before the onset of infection, as compared with only 35 patients without ARDS (p = 0.004). The organisms most frequently isolated from patients with ARDS and VAP were methicillin-resistant Staphylococcus aureus (23%), nonfermenting gram-negative bacilli (21%), and Enterobacteriaceae (21%). These findings confirm that microbiologically provable VAP occurs far more often in patients with ARDS than in other ventilated patients. Because these patients are often treated with antibiotics early in the course of the syndrome, the onset of VAP is frequently delayed after the first week of MV, and is then caused mainly by methicillin-resistant S. aureus and other multiresistant microorganisms.

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Crossref · 10.1164/ajrccm.157.4.9708057

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  • Roughly half of patients with established ARDS develop pneumonia during intensive care.

    “roughly half of patients with established ARDS develop pneumonia during intensive care.”

    From The microbiome and critical illness (2016) · cites this paper as [115]

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References 34 · Cited by 250

Authors
CHASTRE, J., TROUILLET, J. L., VUAGNAT, A., JOLY-GUILLOU, M. L., CLAVIER, H., DOMBRET, M. C., & GIBERT, C.
Affiliations
  • Hôpital Bichat-Claude-Bernard (FR)
  • Services de Réanimation Médicale, Microbiologie, and Pneumologie, Hôpital Bichat, Paris, France
Venue
American Journal of Respiratory and Critical Care Medicine
Published
1998-04-01
Volume
157
Issue
4
Pages
1165-1172
ISSN
  • 1073-449X (ISSN-L)
  • 1535-4970
OpenAlex
W2080930943
Cited by
250
References
34
Citations by year
2026: 1 · 2025: 4 · 2024: 1 · 2023: 6 · 2022: 6 · 2021: 3 · 2020: 12 · 2019: 5 · 2018: 6 · 2017: 6 · 2016: 13 · 2015: 6 · 2014: 12 · 2013: 6 · 2012: 9
FWCI
11.11
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Respiratory and Critical Care Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Nosocomial Infections in ICU
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
Keywords
ventilator-associated pneumonia, acute respiratory distress syndrome, nosocomial pneumonia, mechanical ventilation, methicillin-resistant Staphylococcus aureus, non-fermenting Gram-negative bacilli, Enterobacteriaceae, antibiotic prophylaxis, broad-spectrum antibiotics, multidrug resistance, bronchoalveolar lavage, protected specimen brush
MeSH terms
Aged, Bronchoalveolar Lavage Fluid, Bronchoscopy, Cross Infection, Female, Humans, Male, Middle Aged, Prospective Studies, Respiration, Artificial, Respiratory Distress Syndrome, Survival Rate, Pneumonia, Bacterial

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