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Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients

Although atypical bacteria are important causes of lower airway infections, data on their role in immunocompromised patients are scarce. The aim of the study was to evaluate the prevalence of atypical pulmonary infections in patients with various types of immunosuppression, and to analyze clinical c...

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Autores principales: Grabczak, E. M., Krenke, R., Przybylski, M., Kolkowska-Lesniak, A., Chazan, R., Dzieciatkowski, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120206/
https://www.ncbi.nlm.nih.gov/pubmed/27334731
http://dx.doi.org/10.1007/5584_2016_28
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author Grabczak, E. M.
Krenke, R.
Przybylski, M.
Kolkowska-Lesniak, A.
Chazan, R.
Dzieciatkowski, T.
author_facet Grabczak, E. M.
Krenke, R.
Przybylski, M.
Kolkowska-Lesniak, A.
Chazan, R.
Dzieciatkowski, T.
author_sort Grabczak, E. M.
collection PubMed
description Although atypical bacteria are important causes of lower airway infections, data on their role in immunocompromised patients are scarce. The aim of the study was to evaluate the prevalence of atypical pulmonary infections in patients with various types of immunosuppression, and to analyze clinical characteristics of these infections. Eighty non-HIV immunocompromised patients with different underlying diseases and clinical and radiological signs of pulmonary infection were enrolled. Due to incomplete data on eight patients, 72 patients were eligible for final analysis (median age 58 years). All patients underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Bronchoalveolar lavage fluid (BALF) fluid samples were sent for direct microscopy, cultures, and fungal antigen detection, when appropriate. Commercial qualitative amplification assay (PNEUMOTRIS oligomix Alert Kit(®)), based on nested PCR method, was used to detect specific DNA sequences of L. pneumophila, C. pneumoniae, and M. pneumoniae in BALF. There were 61 (84.7 %) patients with hematologic diseases, 3 (4.2 %) after solid organ transplantation, and 8 (11.1 %) with miscellaneous diseases affecting immune status. Specific sequences of M. pneumoniae, C. pneumoniae, and L. pneumophila DNA were found in 7 (9.7 %), 2 (2.8 %), and 0 patients, respectively. In 8 of these patients co-infections with different microorganisms were demonstrated. Co-infection with A. baumanii and P. aeruginosa was diagnosed in three patients who died. We conclude that atypical lower airway infections are uncommon in immunocompromised patients. The majority of these infections are co-infections rather than single pathogen infections.
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spelling pubmed-71202062020-04-06 Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients Grabczak, E. M. Krenke, R. Przybylski, M. Kolkowska-Lesniak, A. Chazan, R. Dzieciatkowski, T. Pulmonary Infection and Inflammation Article Although atypical bacteria are important causes of lower airway infections, data on their role in immunocompromised patients are scarce. The aim of the study was to evaluate the prevalence of atypical pulmonary infections in patients with various types of immunosuppression, and to analyze clinical characteristics of these infections. Eighty non-HIV immunocompromised patients with different underlying diseases and clinical and radiological signs of pulmonary infection were enrolled. Due to incomplete data on eight patients, 72 patients were eligible for final analysis (median age 58 years). All patients underwent fiberoptic bronchoscopy and bronchoalveolar lavage. Bronchoalveolar lavage fluid (BALF) fluid samples were sent for direct microscopy, cultures, and fungal antigen detection, when appropriate. Commercial qualitative amplification assay (PNEUMOTRIS oligomix Alert Kit(®)), based on nested PCR method, was used to detect specific DNA sequences of L. pneumophila, C. pneumoniae, and M. pneumoniae in BALF. There were 61 (84.7 %) patients with hematologic diseases, 3 (4.2 %) after solid organ transplantation, and 8 (11.1 %) with miscellaneous diseases affecting immune status. Specific sequences of M. pneumoniae, C. pneumoniae, and L. pneumophila DNA were found in 7 (9.7 %), 2 (2.8 %), and 0 patients, respectively. In 8 of these patients co-infections with different microorganisms were demonstrated. Co-infection with A. baumanii and P. aeruginosa was diagnosed in three patients who died. We conclude that atypical lower airway infections are uncommon in immunocompromised patients. The majority of these infections are co-infections rather than single pathogen infections. 2016-06-23 /pmc/articles/PMC7120206/ /pubmed/27334731 http://dx.doi.org/10.1007/5584_2016_28 Text en © Springer International Publishing Switzerland 2016 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Grabczak, E. M.
Krenke, R.
Przybylski, M.
Kolkowska-Lesniak, A.
Chazan, R.
Dzieciatkowski, T.
Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title_full Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title_fullStr Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title_full_unstemmed Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title_short Prevalence of Pulmonary Infections Caused by Atypical Pathogens in non-HIV Immunocompromised Patients
title_sort prevalence of pulmonary infections caused by atypical pathogens in non-hiv immunocompromised patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7120206/
https://www.ncbi.nlm.nih.gov/pubmed/27334731
http://dx.doi.org/10.1007/5584_2016_28
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