Ventilator-associated Pneumonia caused by commensal oropharyngeal a retrospective Analysis of a prospectively collected Database

نویسندگان

  • Johannes B. J. Scholte
  • Johan I. M. van der Velde
  • Catharina F. M. Linssen
  • Helke A. van Dessel
  • Dennis C. J. J. Bergmans
  • Paul H. M. Savelkoul
  • Paul M. H. J. Roekaerts
  • Walther N. K. A. van Mook
چکیده

Background: The significance of commensal oropharyngeal flora (COF) as a potential cause of ventilator-associated pneumonia (VAP) is scarcely investigated and consequently unknown. Therefore, the aim of this study was to explore whether COF may cause VAP. Methods: Retrospective clinical, microbiological and radiographic analysis of all prospectively collected suspected VAP cases in which bronchoalveolar lavage fluid exclusively yielded ≥ 10 cfu/ml COF during a 9.5-year period. Characteristics of 899 recent intensive care unit (ICU) admissions were used as a reference population. Results: Out of the prospectively collected database containing 159 VAP cases, 23 patients were included. In these patients, VAP developed after a median of 8 days of mechanical ventilation. The patients faced a prolonged total ICU length of stay (35 days [P < .001]), hospital length of stay (45 days [P = .001]), and a trend to higher mortality (39 % vs. 26 %, [P = .158]; standardized mortality ratio 1.26 vs. 0.77, [P = .137]) compared to the reference population. After clinical, microbiological and radiographic analysis, COF was the most likely cause of respiratory deterioration in 15 patients (9.4 % of all VAP cases) and a possible cause in 2 patients. Conclusion: Commensal oropharyngeal flora appears to be a potential cause of VAP in limited numbers of ICU patients as is probably associated with an increased length of stay in both ICU and hospital. As COF-VAP develops late in the course of ICU admission, it is possibly associated with the immunocompromised status of ICU patients.

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Erratum to: ‘Ventilator-associated Pneumonia caused by commensal oropharyngeal a retrospective Analysis of a prospectively collected Database’

Author details Department of Intensive Care Medicine, Luzerner Kantonspital, Luzern 16 6000, Switzerland. Department of Intensive Care Medicine, Maastricht University Medical Centre+, P.O. box 5800, Maastricht 6202 AZ, The Netherlands. Department of Medical Microbiology, Atrium Medical Centre, P.O. box 4446, Heerlen 6401 CX, The Netherlands. Department of Medical Microbiology, Maastricht Univer...

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عنوان ژورنال:

دوره 15  شماره 

صفحات  -

تاریخ انتشار 2015