Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy

The purpose of the present study was to validate the quantitative culture and cellularity of bronchoalveolar lavage (BAL) for the diagnosis of ventilator-associated pneumonia (VAP). A prospective validation test trial was carried out between 1992 and 1997 in a general adult intensive care unit of a...

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Main Authors: A.B. Balthazar, A. Von Nowakonski, E.M. De Capitani, P.V. Bottini, R.G.G. Terzi, S. Araújo
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2001-08-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001000800004
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author A.B. Balthazar
A. Von Nowakonski
E.M. De Capitani
P.V. Bottini
R.G.G. Terzi
S. Araújo
author_facet A.B. Balthazar
A. Von Nowakonski
E.M. De Capitani
P.V. Bottini
R.G.G. Terzi
S. Araújo
author_sort A.B. Balthazar
collection DOAJ
description The purpose of the present study was to validate the quantitative culture and cellularity of bronchoalveolar lavage (BAL) for the diagnosis of ventilator-associated pneumonia (VAP). A prospective validation test trial was carried out between 1992 and 1997 in a general adult intensive care unit of a teaching hospital. Thirty-seven patients on mechanical ventilation with suspected VAP who died at most three days after a BAL diagnostic procedure were submitted to a postmortem lung biopsy. BAL effluent was submitted to Gram staining, quantitative culture and cellularity count. Postmortem lung tissue quantitative culture and histopathological findings were considered to be the gold standard exams for VAP diagnosis. According to these criteria, 20 patients (54%) were diagnosed as having VAP and 17 (46%) as not having the condition. Quantitative culture of BAL effluent showed 90% sensitivity (18/20), 94.1% specificity (16/17), 94.7% positive predictive value and 88.8% negative predictive value. Fever and leukocytosis were useless for VAP diagnosis. Gram staining of BAL effluent was negative in 94.1% of the patients without VAP (16/17). Regarding the total cellularity of BAL, a cut-off point of 400,000 cells/ml showed a specificity of 94.1% (16/17), and a cut-off point of 50% of BAL neutrophils showed a sensitivity of 90% (19/20). In conclusion, BAL quantitative culture, Gram staining and cellularity might be useful in the diagnostic investigation of VAP.
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spelling doaj.art-ac14ecdd984b4b4c9ccabe32ea0969bb2022-12-22T00:48:29ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2001-08-01348993100110.1590/S0100-879X2001000800004Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsyA.B. BalthazarA. Von NowakonskiE.M. De CapitaniP.V. BottiniR.G.G. TerziS. AraújoThe purpose of the present study was to validate the quantitative culture and cellularity of bronchoalveolar lavage (BAL) for the diagnosis of ventilator-associated pneumonia (VAP). A prospective validation test trial was carried out between 1992 and 1997 in a general adult intensive care unit of a teaching hospital. Thirty-seven patients on mechanical ventilation with suspected VAP who died at most three days after a BAL diagnostic procedure were submitted to a postmortem lung biopsy. BAL effluent was submitted to Gram staining, quantitative culture and cellularity count. Postmortem lung tissue quantitative culture and histopathological findings were considered to be the gold standard exams for VAP diagnosis. According to these criteria, 20 patients (54%) were diagnosed as having VAP and 17 (46%) as not having the condition. Quantitative culture of BAL effluent showed 90% sensitivity (18/20), 94.1% specificity (16/17), 94.7% positive predictive value and 88.8% negative predictive value. Fever and leukocytosis were useless for VAP diagnosis. Gram staining of BAL effluent was negative in 94.1% of the patients without VAP (16/17). Regarding the total cellularity of BAL, a cut-off point of 400,000 cells/ml showed a specificity of 94.1% (16/17), and a cut-off point of 50% of BAL neutrophils showed a sensitivity of 90% (19/20). In conclusion, BAL quantitative culture, Gram staining and cellularity might be useful in the diagnostic investigation of VAP.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001000800004nosocomial pneumoniamechanical ventilationdiagnostic techniquesbronchoalveolar lavagelung biopsyventilator-associated pneumonia
spellingShingle A.B. Balthazar
A. Von Nowakonski
E.M. De Capitani
P.V. Bottini
R.G.G. Terzi
S. Araújo
Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
Brazilian Journal of Medical and Biological Research
nosocomial pneumonia
mechanical ventilation
diagnostic techniques
bronchoalveolar lavage
lung biopsy
ventilator-associated pneumonia
title Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
title_full Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
title_fullStr Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
title_full_unstemmed Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
title_short Diagnostic investigation of ventilator-associated pneumonia using bronchoalveolar lavage: comparative study with a postmortem lung biopsy
title_sort diagnostic investigation of ventilator associated pneumonia using bronchoalveolar lavage comparative study with a postmortem lung biopsy
topic nosocomial pneumonia
mechanical ventilation
diagnostic techniques
bronchoalveolar lavage
lung biopsy
ventilator-associated pneumonia
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001000800004
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