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Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease

Purpose: Many comorbidities, including depression, anxiety, and insomnia, occur in patients with chronic obstructive pulmonary disease (COPD). These patients may be prescribed benzodiazepines (BZDs). However, there are some concerns that benzodiazepines increase the risk of drug overdose, hypercapni...

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Autores principales: Liao, Yi-Hsiang, Chen, Liang-Yu, Liao, Kuang-Ming, Chen, Chung-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793820/
https://www.ncbi.nlm.nih.gov/pubmed/33424603
http://dx.doi.org/10.3389/fphar.2020.592910
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author Liao, Yi-Hsiang
Chen, Liang-Yu
Liao, Kuang-Ming
Chen, Chung-Yu
author_facet Liao, Yi-Hsiang
Chen, Liang-Yu
Liao, Kuang-Ming
Chen, Chung-Yu
author_sort Liao, Yi-Hsiang
collection PubMed
description Purpose: Many comorbidities, including depression, anxiety, and insomnia, occur in patients with chronic obstructive pulmonary disease (COPD). These patients may be prescribed benzodiazepines (BZDs). However, there are some concerns that benzodiazepines increase the risk of drug overdose, hypercapnic respiratory failure, acute exacerbation and increased mortality. The aim of our study was to evaluate the drug safety of BZDs in patients with COPD. Methods: We used the National Health Insurance Research database in Taiwan from 2002 to 2016 to perform a retrospective cohort study. We enrolled patients who were exposed to the first prescription of BZDs, non-BZDs or a combination (mix user) after COPD diagnosis. We performed 1:1:1 propensity score matching in three groups. The outcomes were COPD with acute exacerbation and all-cause mortality. Poisson regression analysis was performed to evaluate the incidence rate ratios for the outcomes in the groups. Results: After propensity score matching, there were 2,856 patients in each group. After adjusting for confounding factors, we found that compared to BZD users, non-BZD and mix users had nonsignificant differences in outpatient management of acute exacerbations, hospitalization management of acute exacerbations, emergency department management of acute exacerbations and all-cause mortality. BZD and mix groups showed significantly increased admission for acute exacerbation of COPD compared with that of the nonuser group, with IRRs of 2.52 (95% CI, 1.52–4.18; p = 0.0004) and 2.63 (95% CI, 1.57–4.40; p = 0.0002), respectively. Conclusion: BZD, non-BZD, and mix users showed increased COPD-related respiratory events compared to nonusers in Asian subjects.
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spelling pubmed-77938202021-01-09 Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease Liao, Yi-Hsiang Chen, Liang-Yu Liao, Kuang-Ming Chen, Chung-Yu Front Pharmacol Pharmacology Purpose: Many comorbidities, including depression, anxiety, and insomnia, occur in patients with chronic obstructive pulmonary disease (COPD). These patients may be prescribed benzodiazepines (BZDs). However, there are some concerns that benzodiazepines increase the risk of drug overdose, hypercapnic respiratory failure, acute exacerbation and increased mortality. The aim of our study was to evaluate the drug safety of BZDs in patients with COPD. Methods: We used the National Health Insurance Research database in Taiwan from 2002 to 2016 to perform a retrospective cohort study. We enrolled patients who were exposed to the first prescription of BZDs, non-BZDs or a combination (mix user) after COPD diagnosis. We performed 1:1:1 propensity score matching in three groups. The outcomes were COPD with acute exacerbation and all-cause mortality. Poisson regression analysis was performed to evaluate the incidence rate ratios for the outcomes in the groups. Results: After propensity score matching, there were 2,856 patients in each group. After adjusting for confounding factors, we found that compared to BZD users, non-BZD and mix users had nonsignificant differences in outpatient management of acute exacerbations, hospitalization management of acute exacerbations, emergency department management of acute exacerbations and all-cause mortality. BZD and mix groups showed significantly increased admission for acute exacerbation of COPD compared with that of the nonuser group, with IRRs of 2.52 (95% CI, 1.52–4.18; p = 0.0004) and 2.63 (95% CI, 1.57–4.40; p = 0.0002), respectively. Conclusion: BZD, non-BZD, and mix users showed increased COPD-related respiratory events compared to nonusers in Asian subjects. Frontiers Media S.A. 2020-12-09 /pmc/articles/PMC7793820/ /pubmed/33424603 http://dx.doi.org/10.3389/fphar.2020.592910 Text en Copyright © 2020 Liao, Chen, Liao and Chen http://Creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Liao, Yi-Hsiang
Chen, Liang-Yu
Liao, Kuang-Ming
Chen, Chung-Yu
Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title_full Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title_fullStr Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title_full_unstemmed Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title_short Drug Safety of Benzodiazepines in Asian Patients With Chronic Obstructive Pulmonary Disease
title_sort drug safety of benzodiazepines in asian patients with chronic obstructive pulmonary disease
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793820/
https://www.ncbi.nlm.nih.gov/pubmed/33424603
http://dx.doi.org/10.3389/fphar.2020.592910
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