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Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease
BACKGROUND: Studies on the association between polymyositis/dermatomyositis (PM/DM) and acute respiratory failure (ARF) are considerably limited. We investigated whether ARF is associated with PM/DM using a nationwide cohort study. METHODS: We identified 1,374 patients with newly diagnosed PM/DM and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154474/ https://www.ncbi.nlm.nih.gov/pubmed/32309349 http://dx.doi.org/10.21037/atm.2020.01.56 |
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author | Syue, Shih-Huei Chang, Yi-Hua Shih, Pei-Ju Lin, Cheng-Li Yeh, Jun-Jun Kao, Chia-Hung |
author_facet | Syue, Shih-Huei Chang, Yi-Hua Shih, Pei-Ju Lin, Cheng-Li Yeh, Jun-Jun Kao, Chia-Hung |
author_sort | Syue, Shih-Huei |
collection | PubMed |
description | BACKGROUND: Studies on the association between polymyositis/dermatomyositis (PM/DM) and acute respiratory failure (ARF) are considerably limited. We investigated whether ARF is associated with PM/DM using a nationwide cohort study. METHODS: We identified 1,374 patients with newly diagnosed PM/DM and 13,740 comparison individuals without PM/DM (non-PM/DM) randomly selected from the general population; frequency matched by age, sex, and index year using the National Health Insurance Research Database; and followed up until the end of 2011 to measure the incidence of ARF. Cox proportional hazards regression analysis was used to measure the hazard ratio (HR) of ARF for the PM/DM cohort in comparison with the non-PM/DM cohort. RESULTS: The adjusted HR of ARF was 5.05 for the PM/DM cohort compared with the non-PM/DM cohort after adjusting for sex, age, comorbidities, Charlson comorbidity index (CCI) score and medicine. The risk of ARF significantly increased irrespective of age, sex, comorbidities and medicine. Meanwhile, the PM/DM cohort with comorbidities, such as cardiac disease (hypertension), pulmonary disease (chronic obstructive pulmonary disease and pneumonia), and pulmonary vascular diseases had additive effects on the incident ARF. CONCLUSIONS: This study determined the cross-reaction of pulmonary heart disease in the PM/DM cohort with incident ARF even without comorbidities. |
format | Online Article Text |
id | pubmed-7154474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-71544742020-04-17 Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease Syue, Shih-Huei Chang, Yi-Hua Shih, Pei-Ju Lin, Cheng-Li Yeh, Jun-Jun Kao, Chia-Hung Ann Transl Med Original Article BACKGROUND: Studies on the association between polymyositis/dermatomyositis (PM/DM) and acute respiratory failure (ARF) are considerably limited. We investigated whether ARF is associated with PM/DM using a nationwide cohort study. METHODS: We identified 1,374 patients with newly diagnosed PM/DM and 13,740 comparison individuals without PM/DM (non-PM/DM) randomly selected from the general population; frequency matched by age, sex, and index year using the National Health Insurance Research Database; and followed up until the end of 2011 to measure the incidence of ARF. Cox proportional hazards regression analysis was used to measure the hazard ratio (HR) of ARF for the PM/DM cohort in comparison with the non-PM/DM cohort. RESULTS: The adjusted HR of ARF was 5.05 for the PM/DM cohort compared with the non-PM/DM cohort after adjusting for sex, age, comorbidities, Charlson comorbidity index (CCI) score and medicine. The risk of ARF significantly increased irrespective of age, sex, comorbidities and medicine. Meanwhile, the PM/DM cohort with comorbidities, such as cardiac disease (hypertension), pulmonary disease (chronic obstructive pulmonary disease and pneumonia), and pulmonary vascular diseases had additive effects on the incident ARF. CONCLUSIONS: This study determined the cross-reaction of pulmonary heart disease in the PM/DM cohort with incident ARF even without comorbidities. AME Publishing Company 2020-03 /pmc/articles/PMC7154474/ /pubmed/32309349 http://dx.doi.org/10.21037/atm.2020.01.56 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Syue, Shih-Huei Chang, Yi-Hua Shih, Pei-Ju Lin, Cheng-Li Yeh, Jun-Jun Kao, Chia-Hung Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title | Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title_full | Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title_fullStr | Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title_full_unstemmed | Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title_short | Polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
title_sort | polymyositis/dermatomyositis is a potential risk factor for acute respiratory failure: a pulmonary heart disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154474/ https://www.ncbi.nlm.nih.gov/pubmed/32309349 http://dx.doi.org/10.21037/atm.2020.01.56 |
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