Characteristics and consequences of airway colonization by filamentous fungi in 201 adult patients with cystic fibrosis in France

A total of 657 sputum samples from 201 cystic fibrosis adult patients were collected during a 24-month period (2005-2006). We retrospectively analyzed the fungal colonization of the respiratory tract of these individuals by linking medical records and microbiological data. Filamentous fungi were iso...

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Published inMedical mycology (Oxford) Vol. 48 Suppl 1; p. S32
Main Authors Paugam, André, Baixench, Marie-Thérèse, Demazes-Dufeu, Nadine, Burgel, Pierre-Régis, Sauter, Elise, Kanaan, Reem, Dusser, Daniel, Dupouy-Camet, Jean, Hubert, Dominique
Format Journal Article
LanguageEnglish
Published England 01.11.2010
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Abstract A total of 657 sputum samples from 201 cystic fibrosis adult patients were collected during a 24-month period (2005-2006). We retrospectively analyzed the fungal colonization of the respiratory tract of these individuals by linking medical records and microbiological data. Filamentous fungi were isolated from specimens of 65.6% of the patients, with Aspergillus fumigatus being the predominant species recovered as it was found in specimens of 56.7% of the patients. We observed no difference for gender, pancreatic status and cirrhosis in patients with or without A. fumigatus colonization. We found a higher percentage of recovery of Pseudomonas aeruginosa, Stenotrophomonas maltophilia and nontuberculous mycobacteria in patients with A. fumigatus colonization. During the follow-up period of the study, 8.9% of the patients were diagnosed with allergic bronchopulmonary aspergillosis (ABPA). By a multivariate analysis we demonstrated that Scedosporium apiospermum was significantly associated with ABPA (Odds ratio = 13 [2-80]) as opposed to A. fumigatus (Odds ratio = 1.58 [0.49-5.05]).
AbstractList A total of 657 sputum samples from 201 cystic fibrosis adult patients were collected during a 24-month period (2005-2006). We retrospectively analyzed the fungal colonization of the respiratory tract of these individuals by linking medical records and microbiological data. Filamentous fungi were isolated from specimens of 65.6% of the patients, with Aspergillus fumigatus being the predominant species recovered as it was found in specimens of 56.7% of the patients. We observed no difference for gender, pancreatic status and cirrhosis in patients with or without A. fumigatus colonization. We found a higher percentage of recovery of Pseudomonas aeruginosa, Stenotrophomonas maltophilia and nontuberculous mycobacteria in patients with A. fumigatus colonization. During the follow-up period of the study, 8.9% of the patients were diagnosed with allergic bronchopulmonary aspergillosis (ABPA). By a multivariate analysis we demonstrated that Scedosporium apiospermum was significantly associated with ABPA (Odds ratio = 13 [2-80]) as opposed to A. fumigatus (Odds ratio = 1.58 [0.49-5.05]).
Author Baixench, Marie-Thérèse
Hubert, Dominique
Dupouy-Camet, Jean
Burgel, Pierre-Régis
Dusser, Daniel
Kanaan, Reem
Paugam, André
Demazes-Dufeu, Nadine
Sauter, Elise
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  givenname: Marie-Thérèse
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Snippet A total of 657 sputum samples from 201 cystic fibrosis adult patients were collected during a 24-month period (2005-2006). We retrospectively analyzed the...
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StartPage S32
SubjectTerms Adolescent
Adult
Aged
Aspergillosis, Allergic Bronchopulmonary - epidemiology
Aspergillosis, Allergic Bronchopulmonary - microbiology
Aspergillus fumigatus - classification
Aspergillus fumigatus - isolation & purification
Cystic Fibrosis - complications
Cystic Fibrosis - epidemiology
Cystic Fibrosis - microbiology
Female
France - epidemiology
Fungi - isolation & purification
Humans
Lung Diseases, Fungal - epidemiology
Lung Diseases, Fungal - microbiology
Lung Diseases, Fungal - physiopathology
Male
Middle Aged
Multivariate Analysis
Scedosporium - classification
Scedosporium - isolation & purification
Sputum - microbiology
Young Adult
Title Characteristics and consequences of airway colonization by filamentous fungi in 201 adult patients with cystic fibrosis in France
URI https://www.ncbi.nlm.nih.gov/pubmed/21067327
Volume 48 Suppl 1
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