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A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD
OBJECTIVE: To investigate a possible increased risk observed in tiotropium clinical trials of stroke and other adverse events. DESIGN: New users of long-acting anticholinergic therapy (tiotropium HandiHaler®) were compared with new users of long-acting β-agonist (LABA) monotherapy, and propensity sc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364448/ https://www.ncbi.nlm.nih.gov/pubmed/22619266 http://dx.doi.org/10.1136/bmjopen-2012-000841 |
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author | Jara, Michele Wentworth, Charles Lanes, Stephan |
author_facet | Jara, Michele Wentworth, Charles Lanes, Stephan |
author_sort | Jara, Michele |
collection | PubMed |
description | OBJECTIVE: To investigate a possible increased risk observed in tiotropium clinical trials of stroke and other adverse events. DESIGN: New users of long-acting anticholinergic therapy (tiotropium HandiHaler®) were compared with new users of long-acting β-agonist (LABA) monotherapy, and propensity scores were used to control confounding. SETTING: UK healthcare system general practitioner electronic medical record database. PARTICIPANTS: 10 840 patients newly prescribed tiotropium (n=4767) or LABA (n=6073), at least 40 years old, and not having asthma as their only respiratory illness. PRIMARY AND SECONDARY OUTCOME MEASURES: Incidence rates of total stroke, myocardial infarction, angina and other adverse events. RESULTS: Tiotropium was associated with increased rates of stroke (HR=1.49, 95% CI 0.91 to 2.45), angina (HR=1.38, 95% CI 0.88 to 2.16) and myocardial infarction (HR=1.26, 95% CI 0.72 to 2.21). Groups had similar rates of chronic obstructive pulmonary disease exacerbation (HR=0.95, 95% CI 0.80 to 1.12) and pneumonia (HR=0.96, 95% CI 0.58 to 1.58). Tiotropium was associated with a lower rate of total mortality (HR=0.70, 95% CI 0.56 to 0.89) and asthma exacerbations (HR=0.46, 95% CI 0.36 to 0.57) than users of LABA. CONCLUSION: Small increased risks of serious ischaemic cardiovascular events have been reported with inhaled anticholinergic medication from randomised and nonrandomized studies of ipratropium, tiotropium HandiHaler® and tiotropium Respimat®. Additional research is needed to understand the full extent of cardiovascular effects of inhaled anticholinergic medications and the patients who may be most susceptible. |
format | Online Article Text |
id | pubmed-3364448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33644482012-06-04 A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD Jara, Michele Wentworth, Charles Lanes, Stephan BMJ Open Pharmacology and Therapeutics OBJECTIVE: To investigate a possible increased risk observed in tiotropium clinical trials of stroke and other adverse events. DESIGN: New users of long-acting anticholinergic therapy (tiotropium HandiHaler®) were compared with new users of long-acting β-agonist (LABA) monotherapy, and propensity scores were used to control confounding. SETTING: UK healthcare system general practitioner electronic medical record database. PARTICIPANTS: 10 840 patients newly prescribed tiotropium (n=4767) or LABA (n=6073), at least 40 years old, and not having asthma as their only respiratory illness. PRIMARY AND SECONDARY OUTCOME MEASURES: Incidence rates of total stroke, myocardial infarction, angina and other adverse events. RESULTS: Tiotropium was associated with increased rates of stroke (HR=1.49, 95% CI 0.91 to 2.45), angina (HR=1.38, 95% CI 0.88 to 2.16) and myocardial infarction (HR=1.26, 95% CI 0.72 to 2.21). Groups had similar rates of chronic obstructive pulmonary disease exacerbation (HR=0.95, 95% CI 0.80 to 1.12) and pneumonia (HR=0.96, 95% CI 0.58 to 1.58). Tiotropium was associated with a lower rate of total mortality (HR=0.70, 95% CI 0.56 to 0.89) and asthma exacerbations (HR=0.46, 95% CI 0.36 to 0.57) than users of LABA. CONCLUSION: Small increased risks of serious ischaemic cardiovascular events have been reported with inhaled anticholinergic medication from randomised and nonrandomized studies of ipratropium, tiotropium HandiHaler® and tiotropium Respimat®. Additional research is needed to understand the full extent of cardiovascular effects of inhaled anticholinergic medications and the patients who may be most susceptible. BMJ Group 2012-05-22 /pmc/articles/PMC3364448/ /pubmed/22619266 http://dx.doi.org/10.1136/bmjopen-2012-000841 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Pharmacology and Therapeutics Jara, Michele Wentworth, Charles Lanes, Stephan A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title | A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title_full | A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title_fullStr | A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title_full_unstemmed | A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title_short | A new user cohort study comparing the safety of long-acting inhaled bronchodilators in COPD |
title_sort | new user cohort study comparing the safety of long-acting inhaled bronchodilators in copd |
topic | Pharmacology and Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364448/ https://www.ncbi.nlm.nih.gov/pubmed/22619266 http://dx.doi.org/10.1136/bmjopen-2012-000841 |
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