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Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea

Aims: Obstructive sleep apnea (OSA) and insomnia commonly coexist; hypnotics are broadly prescribed for insomnia therapy. However, the safety of hypnotics use in OSA patients is unclear. We conducted a retrospective case-control study to investigate the risk of adverse respiratory events in hypnotic...

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Autores principales: Wang, Sheng-Huei, Chen, Wei-Shan, Tang, Shih-En, Lin, Hung-Che, Peng, Chung-Kan, Chu, Hsuan-Te, Kao, Chia-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330300/
https://www.ncbi.nlm.nih.gov/pubmed/30666205
http://dx.doi.org/10.3389/fphar.2018.01513
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author Wang, Sheng-Huei
Chen, Wei-Shan
Tang, Shih-En
Lin, Hung-Che
Peng, Chung-Kan
Chu, Hsuan-Te
Kao, Chia-Hung
author_facet Wang, Sheng-Huei
Chen, Wei-Shan
Tang, Shih-En
Lin, Hung-Che
Peng, Chung-Kan
Chu, Hsuan-Te
Kao, Chia-Hung
author_sort Wang, Sheng-Huei
collection PubMed
description Aims: Obstructive sleep apnea (OSA) and insomnia commonly coexist; hypnotics are broadly prescribed for insomnia therapy. However, the safety of hypnotics use in OSA patients is unclear. We conducted a retrospective case-control study to investigate the risk of adverse respiratory events in hypnotics-using OSA patients. Methods: We obtained data from the Taiwan National Health Insurance Database from 1996 to 2013. The case group included 216 OSA patients with newly diagnosed adverse respiratory events, including pneumonia and acute respiratory failure. The control group included OSA patients without adverse respiratory events, which was randomly frequency-matched to the case group at a 1:1 ratio according to age, gender, and index year. Hypnotics exposure included benzodiazepines (BZD) and non-benzodiazepines (non-BZD). A recent user was defined as a patient who had taken hypnotics for 1–30 days, while a long-term user was one who had taken hypnotics for 31–365 days. Results: Multivariable adjusted analysis showed recent BZD use is an independent risk for adverse respiratory events (OR = 2.70; 95% CI = 1.15–6.33; P < 0.001). Subgroup analysis showed both recent and long-term BZD use increased the risk of acute respiratory failure compared to never BZD use (OR = 28.6; 95% CI = 5.24–156; P < 0.001, OR = 10.1; 95% CI = 1.51–67.7; P < 0.05, respectively). Neither BZD nor non-BZD use increased the risk of pneumonia in OSA patients. Conclusion: BZD use might increase the risk of acute respiratory failure in OSA patients.
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spelling pubmed-63303002019-01-21 Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea Wang, Sheng-Huei Chen, Wei-Shan Tang, Shih-En Lin, Hung-Che Peng, Chung-Kan Chu, Hsuan-Te Kao, Chia-Hung Front Pharmacol Pharmacology Aims: Obstructive sleep apnea (OSA) and insomnia commonly coexist; hypnotics are broadly prescribed for insomnia therapy. However, the safety of hypnotics use in OSA patients is unclear. We conducted a retrospective case-control study to investigate the risk of adverse respiratory events in hypnotics-using OSA patients. Methods: We obtained data from the Taiwan National Health Insurance Database from 1996 to 2013. The case group included 216 OSA patients with newly diagnosed adverse respiratory events, including pneumonia and acute respiratory failure. The control group included OSA patients without adverse respiratory events, which was randomly frequency-matched to the case group at a 1:1 ratio according to age, gender, and index year. Hypnotics exposure included benzodiazepines (BZD) and non-benzodiazepines (non-BZD). A recent user was defined as a patient who had taken hypnotics for 1–30 days, while a long-term user was one who had taken hypnotics for 31–365 days. Results: Multivariable adjusted analysis showed recent BZD use is an independent risk for adverse respiratory events (OR = 2.70; 95% CI = 1.15–6.33; P < 0.001). Subgroup analysis showed both recent and long-term BZD use increased the risk of acute respiratory failure compared to never BZD use (OR = 28.6; 95% CI = 5.24–156; P < 0.001, OR = 10.1; 95% CI = 1.51–67.7; P < 0.05, respectively). Neither BZD nor non-BZD use increased the risk of pneumonia in OSA patients. Conclusion: BZD use might increase the risk of acute respiratory failure in OSA patients. Frontiers Media S.A. 2019-01-07 /pmc/articles/PMC6330300/ /pubmed/30666205 http://dx.doi.org/10.3389/fphar.2018.01513 Text en Copyright © 2019 Wang, Chen, Tang, Lin, Peng, Chu and Kao. 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
Wang, Sheng-Huei
Chen, Wei-Shan
Tang, Shih-En
Lin, Hung-Che
Peng, Chung-Kan
Chu, Hsuan-Te
Kao, Chia-Hung
Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title_full Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title_fullStr Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title_full_unstemmed Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title_short Benzodiazepines Associated With Acute Respiratory Failure in Patients With Obstructive Sleep Apnea
title_sort benzodiazepines associated with acute respiratory failure in patients with obstructive sleep apnea
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330300/
https://www.ncbi.nlm.nih.gov/pubmed/30666205
http://dx.doi.org/10.3389/fphar.2018.01513
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