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Comorbidities and survival in patients with chronic hypersensitivity pneumonitis
INTRODUCTION: Chronic Hypersensitivity Pneumonitis (cHP) is a fibrotic interstitial lung disease (ILD) resulting from repeated exposure to an offending antigen. Prognostication in cHP remains challenging, and the relationship between comorbidities and survival has yet to be characterized. The aim of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953142/ https://www.ncbi.nlm.nih.gov/pubmed/31918716 http://dx.doi.org/10.1186/s12931-020-1283-8 |
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author | Wälscher, Julia Gross, Benjamin Morisset, Julie Johannson, Kerri A. Vasakova, Martina Bruhwyler, Jacques Kreuter, Michael |
author_facet | Wälscher, Julia Gross, Benjamin Morisset, Julie Johannson, Kerri A. Vasakova, Martina Bruhwyler, Jacques Kreuter, Michael |
author_sort | Wälscher, Julia |
collection | PubMed |
description | INTRODUCTION: Chronic Hypersensitivity Pneumonitis (cHP) is a fibrotic interstitial lung disease (ILD) resulting from repeated exposure to an offending antigen. Prognostication in cHP remains challenging, and the relationship between comorbidities and survival has yet to be characterized. The aim of this study was to describe the relationship between comorbid conditions and survival in patients with cHP. METHODS: The prospective database from a tertiary referral centre for ILD was reviewed for patient-reported comorbidities, their frequency, and relationship with survival in cHP patients. Comorbidities were assessed by direct questioning of the patient at the baseline visit and by a standardized questionnaire for the diagnosis of interstitial lung diseases. During the follow-up examinations, patients were asked about newly diagnosed comorbidities. RESULTS: Two hundred eleven patients with cHP were identified (mean age 63 years, 53% male, mean FVC 73%), with mean follow-up of 32 months. The mean number of comorbidities was 3 (10% had 0, 59% 1–3 and 31% ≥4 comorbidities). Most frequent comorbidities groups were cardiovascular (65%) and respiratory (26%), most common comorbidities were hypertension (56%), gastro-esophageal reflux disease (GERD) (24%), diabetes (20%) and coronary heart disease (18%). In general, deceased patients had more comorbidities than survivors (p = 0.005), yet there was no association between the absolute number of comorbidities and survival. Pulmonary hypertension (30.8% versus 5.7%, p = 0.001;), diastolic dysfunction (26.9% versus 6.4%, p = 0.004) and cerebrovascular disease were more frequent in non-survivors (23.1% versus 7.6%, p = 0.026). Lung cancer was not observed, and neither GERD nor antacid drugs were associated with outcome (p = 0.357 and p = 0.961, respectively). CONCLUSIONS: Comorbidities are common in cHP are associated with survival. Further work should determine whether interventions for these specific comorbidities can positively affect survival. |
format | Online Article Text |
id | pubmed-6953142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69531422020-01-14 Comorbidities and survival in patients with chronic hypersensitivity pneumonitis Wälscher, Julia Gross, Benjamin Morisset, Julie Johannson, Kerri A. Vasakova, Martina Bruhwyler, Jacques Kreuter, Michael Respir Res Research INTRODUCTION: Chronic Hypersensitivity Pneumonitis (cHP) is a fibrotic interstitial lung disease (ILD) resulting from repeated exposure to an offending antigen. Prognostication in cHP remains challenging, and the relationship between comorbidities and survival has yet to be characterized. The aim of this study was to describe the relationship between comorbid conditions and survival in patients with cHP. METHODS: The prospective database from a tertiary referral centre for ILD was reviewed for patient-reported comorbidities, their frequency, and relationship with survival in cHP patients. Comorbidities were assessed by direct questioning of the patient at the baseline visit and by a standardized questionnaire for the diagnosis of interstitial lung diseases. During the follow-up examinations, patients were asked about newly diagnosed comorbidities. RESULTS: Two hundred eleven patients with cHP were identified (mean age 63 years, 53% male, mean FVC 73%), with mean follow-up of 32 months. The mean number of comorbidities was 3 (10% had 0, 59% 1–3 and 31% ≥4 comorbidities). Most frequent comorbidities groups were cardiovascular (65%) and respiratory (26%), most common comorbidities were hypertension (56%), gastro-esophageal reflux disease (GERD) (24%), diabetes (20%) and coronary heart disease (18%). In general, deceased patients had more comorbidities than survivors (p = 0.005), yet there was no association between the absolute number of comorbidities and survival. Pulmonary hypertension (30.8% versus 5.7%, p = 0.001;), diastolic dysfunction (26.9% versus 6.4%, p = 0.004) and cerebrovascular disease were more frequent in non-survivors (23.1% versus 7.6%, p = 0.026). Lung cancer was not observed, and neither GERD nor antacid drugs were associated with outcome (p = 0.357 and p = 0.961, respectively). CONCLUSIONS: Comorbidities are common in cHP are associated with survival. Further work should determine whether interventions for these specific comorbidities can positively affect survival. BioMed Central 2020-01-09 2020 /pmc/articles/PMC6953142/ /pubmed/31918716 http://dx.doi.org/10.1186/s12931-020-1283-8 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wälscher, Julia Gross, Benjamin Morisset, Julie Johannson, Kerri A. Vasakova, Martina Bruhwyler, Jacques Kreuter, Michael Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title | Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title_full | Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title_fullStr | Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title_full_unstemmed | Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title_short | Comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
title_sort | comorbidities and survival in patients with chronic hypersensitivity pneumonitis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953142/ https://www.ncbi.nlm.nih.gov/pubmed/31918716 http://dx.doi.org/10.1186/s12931-020-1283-8 |
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