Cargando…

Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study

BACKGROUND: Blocking muscarinic receptors could have an effect on cardiac function, especially among elderly patients with overactive bladder (OAB). STUDY OBJECTIVE: To investigate the risk of cardiovascular (CV) events in users of antimuscarinic drugs to treat OAB. DESIGN, SETTING, AND PARTICIPANTS...

Descripción completa

Detalles Bibliográficos
Autores principales: Arana, Alejandro, Margulis, Andrea V., McQuay, Lisa J., Ziemiecki, Ryan, Bartsch, Jennifer L., Rothman, Kenneth J., Franks, Billy, D'Silva, Milbhor, Appenteng, Kwame, Varas‐Lorenzo, Cristina, Perez‐Gutthann, Susana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033092/
https://www.ncbi.nlm.nih.gov/pubmed/29723926
http://dx.doi.org/10.1002/phar.2121
_version_ 1783337633022214144
author Arana, Alejandro
Margulis, Andrea V.
McQuay, Lisa J.
Ziemiecki, Ryan
Bartsch, Jennifer L.
Rothman, Kenneth J.
Franks, Billy
D'Silva, Milbhor
Appenteng, Kwame
Varas‐Lorenzo, Cristina
Perez‐Gutthann, Susana
author_facet Arana, Alejandro
Margulis, Andrea V.
McQuay, Lisa J.
Ziemiecki, Ryan
Bartsch, Jennifer L.
Rothman, Kenneth J.
Franks, Billy
D'Silva, Milbhor
Appenteng, Kwame
Varas‐Lorenzo, Cristina
Perez‐Gutthann, Susana
author_sort Arana, Alejandro
collection PubMed
description BACKGROUND: Blocking muscarinic receptors could have an effect on cardiac function, especially among elderly patients with overactive bladder (OAB). STUDY OBJECTIVE: To investigate the risk of cardiovascular (CV) events in users of antimuscarinic drugs to treat OAB. DESIGN, SETTING, AND PARTICIPANTS: Cohort study of new users of darifenacin, fesoterodine, oxybutynin, solifenacin, tolterodine, or trospium, 18 years or older, in the United Kingdom's Clinical Practice Research Datalink (CPRD), 2004–2012. OUTCOME MEASUREMENTS AND MAIN RESULTS: Using tolterodine as the reference, we estimated propensity‐score–stratified incidence rate ratios (IRRs) for acute myocardial infarction, stroke, CV mortality, major adverse cardiac events (MACE, a combined end point of the previous three), and all‐cause death for individual antimuscarinic drugs. The study cohort included 119,912 new users of OAB drugs. The mean age at cohort entry was 62 years, 70% were female, and the mean follow‐up was 3.3 years. The adjusted IRR for MACE and current use of oxybutynin compared with current use of tolterodine was 1.14 (95% confidence interval [CI] 1.01–1.30). In contrast, the IRR was 0.65 (CI 0.56–0.76) for current use of solifenacin compared with tolterodine. In this study, performed with health care data, the distribution of risk factors was relatively similar across users of different OAB drugs and, although our analyses controlled for a range of measured potential confounders, residual confounding cannot be ruled out. CONCLUSIONS: In an observational comparative study of users of medications to treat OAB conducted in routine clinical practice, the risk for CV side effects was increased in users of oxybutynin and decreased in users of solifenacin compared with users of tolterodine.
format Online
Article
Text
id pubmed-6033092
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-60330922018-07-12 Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study Arana, Alejandro Margulis, Andrea V. McQuay, Lisa J. Ziemiecki, Ryan Bartsch, Jennifer L. Rothman, Kenneth J. Franks, Billy D'Silva, Milbhor Appenteng, Kwame Varas‐Lorenzo, Cristina Perez‐Gutthann, Susana Pharmacotherapy Regular Manuscripts BACKGROUND: Blocking muscarinic receptors could have an effect on cardiac function, especially among elderly patients with overactive bladder (OAB). STUDY OBJECTIVE: To investigate the risk of cardiovascular (CV) events in users of antimuscarinic drugs to treat OAB. DESIGN, SETTING, AND PARTICIPANTS: Cohort study of new users of darifenacin, fesoterodine, oxybutynin, solifenacin, tolterodine, or trospium, 18 years or older, in the United Kingdom's Clinical Practice Research Datalink (CPRD), 2004–2012. OUTCOME MEASUREMENTS AND MAIN RESULTS: Using tolterodine as the reference, we estimated propensity‐score–stratified incidence rate ratios (IRRs) for acute myocardial infarction, stroke, CV mortality, major adverse cardiac events (MACE, a combined end point of the previous three), and all‐cause death for individual antimuscarinic drugs. The study cohort included 119,912 new users of OAB drugs. The mean age at cohort entry was 62 years, 70% were female, and the mean follow‐up was 3.3 years. The adjusted IRR for MACE and current use of oxybutynin compared with current use of tolterodine was 1.14 (95% confidence interval [CI] 1.01–1.30). In contrast, the IRR was 0.65 (CI 0.56–0.76) for current use of solifenacin compared with tolterodine. In this study, performed with health care data, the distribution of risk factors was relatively similar across users of different OAB drugs and, although our analyses controlled for a range of measured potential confounders, residual confounding cannot be ruled out. CONCLUSIONS: In an observational comparative study of users of medications to treat OAB conducted in routine clinical practice, the risk for CV side effects was increased in users of oxybutynin and decreased in users of solifenacin compared with users of tolterodine. John Wiley and Sons Inc. 2018-06-21 2018-06 /pmc/articles/PMC6033092/ /pubmed/29723926 http://dx.doi.org/10.1002/phar.2121 Text en © 2018 RTI Health Solutions. Pharmacotherapy published by Wiley Periodicals, Inc. on behalf of Pharmacotherapy Publications, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Regular Manuscripts
Arana, Alejandro
Margulis, Andrea V.
McQuay, Lisa J.
Ziemiecki, Ryan
Bartsch, Jennifer L.
Rothman, Kenneth J.
Franks, Billy
D'Silva, Milbhor
Appenteng, Kwame
Varas‐Lorenzo, Cristina
Perez‐Gutthann, Susana
Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title_full Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title_fullStr Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title_full_unstemmed Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title_short Variation in Cardiovascular Risk Related to Individual Antimuscarinic Drugs Used to Treat Overactive Bladder: A UK Cohort Study
title_sort variation in cardiovascular risk related to individual antimuscarinic drugs used to treat overactive bladder: a uk cohort study
topic Regular Manuscripts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033092/
https://www.ncbi.nlm.nih.gov/pubmed/29723926
http://dx.doi.org/10.1002/phar.2121
work_keys_str_mv AT aranaalejandro variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT margulisandreav variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT mcquaylisaj variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT ziemieckiryan variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT bartschjenniferl variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT rothmankennethj variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT franksbilly variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT dsilvamilbhor variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT appentengkwame variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT varaslorenzocristina variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy
AT perezgutthannsusana variationincardiovascularriskrelatedtoindividualantimuscarinicdrugsusedtotreatoveractivebladderaukcohortstudy