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Invasive Aspergillus infections in hospitalized patients with chronic lung disease
BACKGROUND: Although invasive pulmonary aspergillosis (IPA) is more prevalent in immunocompromised patients, critical care clinicians need to be aware of the occurrence of IPA in the nontraditional host, such as a patient with chronic lung disease. The purpose of this study was to describe the IPA p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674018/ https://www.ncbi.nlm.nih.gov/pubmed/23761976 http://dx.doi.org/10.2147/IDR.S43069 |
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author | Wessolossky, Mireya Welch, Verna L Sen, Ajanta Babu, Tara M Luke, David R |
author_facet | Wessolossky, Mireya Welch, Verna L Sen, Ajanta Babu, Tara M Luke, David R |
author_sort | Wessolossky, Mireya |
collection | PubMed |
description | BACKGROUND: Although invasive pulmonary aspergillosis (IPA) is more prevalent in immunocompromised patients, critical care clinicians need to be aware of the occurrence of IPA in the nontraditional host, such as a patient with chronic lung disease. The purpose of this study was to describe the IPA patient with chronic lung disease and compare the data with that of immunocompromised patients. METHODS: The records of 351 patients with Aspergillus were evaluated in this single-center, retrospective study for evidence and outcomes of IPA. The outcomes of 57 patients with chronic lung disease and 56 immunocompromised patients were compared. Patients with chronic lung disease were defined by one of the following descriptive terms: emphysema, asthma, idiopathic lung disease, bronchitis, bronchiectasis, sarcoid, or pulmonary leukostasis. RESULTS: Baseline demographics were similar between the two groups. Patients with chronic lung disease were primarily defined by emphysema (61%) and asthma (18%), and immunocompromised patients primarily had malignancies (27%) and bone marrow transplants (14%). A higher proportion of patients with chronic lung disease had a diagnosis of IPA by bronchoalveolar lavage versus the immunocompromised group (P < 0.03). The major risk factors for IPA were found to be steroid use in the chronic lung disease group and neutropenia and prior surgical procedures in the immunocompromised group. Overall, 53% and 69% of chronic lung disease and immunocompromised patients were cured (P = 0.14); 55% of chronic lung patients and 47% of immunocompromised patients survived one month (P = 0.75). CONCLUSION: Nontraditional patients with IPA, such as those with chronic lung disease, have outcomes and mortality similar to that in the more traditional immunocompromised population. |
format | Online Article Text |
id | pubmed-3674018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36740182013-06-12 Invasive Aspergillus infections in hospitalized patients with chronic lung disease Wessolossky, Mireya Welch, Verna L Sen, Ajanta Babu, Tara M Luke, David R Infect Drug Resist Original Research BACKGROUND: Although invasive pulmonary aspergillosis (IPA) is more prevalent in immunocompromised patients, critical care clinicians need to be aware of the occurrence of IPA in the nontraditional host, such as a patient with chronic lung disease. The purpose of this study was to describe the IPA patient with chronic lung disease and compare the data with that of immunocompromised patients. METHODS: The records of 351 patients with Aspergillus were evaluated in this single-center, retrospective study for evidence and outcomes of IPA. The outcomes of 57 patients with chronic lung disease and 56 immunocompromised patients were compared. Patients with chronic lung disease were defined by one of the following descriptive terms: emphysema, asthma, idiopathic lung disease, bronchitis, bronchiectasis, sarcoid, or pulmonary leukostasis. RESULTS: Baseline demographics were similar between the two groups. Patients with chronic lung disease were primarily defined by emphysema (61%) and asthma (18%), and immunocompromised patients primarily had malignancies (27%) and bone marrow transplants (14%). A higher proportion of patients with chronic lung disease had a diagnosis of IPA by bronchoalveolar lavage versus the immunocompromised group (P < 0.03). The major risk factors for IPA were found to be steroid use in the chronic lung disease group and neutropenia and prior surgical procedures in the immunocompromised group. Overall, 53% and 69% of chronic lung disease and immunocompromised patients were cured (P = 0.14); 55% of chronic lung patients and 47% of immunocompromised patients survived one month (P = 0.75). CONCLUSION: Nontraditional patients with IPA, such as those with chronic lung disease, have outcomes and mortality similar to that in the more traditional immunocompromised population. Dove Medical Press 2013-05-27 /pmc/articles/PMC3674018/ /pubmed/23761976 http://dx.doi.org/10.2147/IDR.S43069 Text en © 2013 Wessolossky et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Wessolossky, Mireya Welch, Verna L Sen, Ajanta Babu, Tara M Luke, David R Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title | Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title_full | Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title_fullStr | Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title_full_unstemmed | Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title_short | Invasive Aspergillus infections in hospitalized patients with chronic lung disease |
title_sort | invasive aspergillus infections in hospitalized patients with chronic lung disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674018/ https://www.ncbi.nlm.nih.gov/pubmed/23761976 http://dx.doi.org/10.2147/IDR.S43069 |
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