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Risks of all-cause and site-specific fractures among hospitalized patients with COPD

Patients with chronic obstructive pulmonary disease (COPD) have a high prevalence of osteoporosis. The clinical sequel of osteoporosis is fracture. Patients with COPD who experience a fracture also have increased morbidity and mortality. Currently, the types of all-cause and site-specific fracture a...

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Autores principales: Liao, Kuang-Ming, Liang, Fu-Wen, Li, Chung-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059079/
https://www.ncbi.nlm.nih.gov/pubmed/27749576
http://dx.doi.org/10.1097/MD.0000000000005070
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author Liao, Kuang-Ming
Liang, Fu-Wen
Li, Chung-Yi
author_facet Liao, Kuang-Ming
Liang, Fu-Wen
Li, Chung-Yi
author_sort Liao, Kuang-Ming
collection PubMed
description Patients with chronic obstructive pulmonary disease (COPD) have a high prevalence of osteoporosis. The clinical sequel of osteoporosis is fracture. Patients with COPD who experience a fracture also have increased morbidity and mortality. Currently, the types of all-cause and site-specific fracture among patients with COPD are unknown. Thus, we elucidated the all-cause and site-specific fractures among patients with COPD. A retrospective, population-based, cohort study was conducted utilizing the Taiwan Longitudinal Health Insurance Database. Patients with COPD were defined as those who were hospitalized with an International Classification of Diseases, Ninth Revision, Clinical Modification code of 490 to 492 or 496 between 2001 and 2011. The index date was set as the date of discharge. The study patients were followed from the index date to the date when they sought care for any type of fracture, date of death, date of health insurance policy termination, or the last day of 2013. The types of fracture analyzed in this study included vertebral, rib, humeral, radial and ulnar/wrist, pelvic, femoral, and tibial and fibular fractures. The cohort consisted of 11,312 patients with COPD. Among these patients, 1944 experienced fractures. The most common site-specific fractures were vertebral, femoral, rib, and forearm fractures (radius, ulna, and wrist) at 32.4%, 31%, 12%, and 11.8%, respectively. The adjusted hazard ratios of fracture were 1.71 [95% confidence interval (95% CI) = 1.56–1.87] for female patient with COPD and 1.50 (95% CI = 1.39–1.52) for patients with osteoporosis after covariate adjustment. Vertebral and hip fractures are common among patients with COPD, especially among males with COPD. Many comorbidities contribute to the high risk of fracture among patients with COPD.
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spelling pubmed-50590792016-11-01 Risks of all-cause and site-specific fractures among hospitalized patients with COPD Liao, Kuang-Ming Liang, Fu-Wen Li, Chung-Yi Medicine (Baltimore) 6700 Patients with chronic obstructive pulmonary disease (COPD) have a high prevalence of osteoporosis. The clinical sequel of osteoporosis is fracture. Patients with COPD who experience a fracture also have increased morbidity and mortality. Currently, the types of all-cause and site-specific fracture among patients with COPD are unknown. Thus, we elucidated the all-cause and site-specific fractures among patients with COPD. A retrospective, population-based, cohort study was conducted utilizing the Taiwan Longitudinal Health Insurance Database. Patients with COPD were defined as those who were hospitalized with an International Classification of Diseases, Ninth Revision, Clinical Modification code of 490 to 492 or 496 between 2001 and 2011. The index date was set as the date of discharge. The study patients were followed from the index date to the date when they sought care for any type of fracture, date of death, date of health insurance policy termination, or the last day of 2013. The types of fracture analyzed in this study included vertebral, rib, humeral, radial and ulnar/wrist, pelvic, femoral, and tibial and fibular fractures. The cohort consisted of 11,312 patients with COPD. Among these patients, 1944 experienced fractures. The most common site-specific fractures were vertebral, femoral, rib, and forearm fractures (radius, ulna, and wrist) at 32.4%, 31%, 12%, and 11.8%, respectively. The adjusted hazard ratios of fracture were 1.71 [95% confidence interval (95% CI) = 1.56–1.87] for female patient with COPD and 1.50 (95% CI = 1.39–1.52) for patients with osteoporosis after covariate adjustment. Vertebral and hip fractures are common among patients with COPD, especially among males with COPD. Many comorbidities contribute to the high risk of fracture among patients with COPD. Wolters Kluwer Health 2016-10-07 /pmc/articles/PMC5059079/ /pubmed/27749576 http://dx.doi.org/10.1097/MD.0000000000005070 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 6700
Liao, Kuang-Ming
Liang, Fu-Wen
Li, Chung-Yi
Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title_full Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title_fullStr Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title_full_unstemmed Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title_short Risks of all-cause and site-specific fractures among hospitalized patients with COPD
title_sort risks of all-cause and site-specific fractures among hospitalized patients with copd
topic 6700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059079/
https://www.ncbi.nlm.nih.gov/pubmed/27749576
http://dx.doi.org/10.1097/MD.0000000000005070
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