Cardiovascular Risk in Users of Mirabegron Compared with Users of Antimuscarinic Treatments for Overactive Bladder: Findings from a Non-Interventional, Multinational, Cohort Study.
Journal
Drug safety
ISSN: 1179-1942
Titre abrégé: Drug Saf
Pays: New Zealand
ID NLM: 9002928
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
accepted:
30
06
2021
pubmed:
9
7
2021
medline:
21
4
2022
entrez:
8
7
2021
Statut:
ppublish
Résumé
During clinical trials, mirabegron, a β3-adrenoreceptor agonist, was associated with increased vital signs vs placebo in patients with overactive bladder. The purpose of this study was to compare incidence rates of adverse cardiovascular (CV) outcomes following mirabegron or antimuscarinic use. We conducted an observational post-marketing safety study utilising real-world data. The study population was identified within five sources: Danish and Swedish National Registers, Clinical Practice Research Datalink (UK), Optum (USA) and Humana (USA). Episodes of time when patients were new users of mirabegron or antimuscarinics (October 2012-December 2018) were sourced from prescriptions and matched on propensity scores. Occurrences of major adverse cardiovascular events (MACE), acute myocardial infarction (AMI), stroke, CV mortality and all-cause mortality were identified. Outcome incidence rates and hazard ratios from Cox models were estimated. Overall, 152,026 mirabegron and 152,026 antimuscarinic episodes were matched. The population consisted of 63.1% women and 72.6% were ≥ 65 years old. There were no appreciable differences in the incidence rates of MACE, AMI or stroke between users of mirabegron and antimuscarinics. Incidence rates of CV mortality (hazard ratio 0.83, 95% confidence interval 0.73-0.95) and all-cause mortality (hazard ratio 0.80, 95% confidence interval 0.76-0.84) were no higher with mirabegron vs antimuscarinics. Results restricted to episodes at high risk for CV events or stratified by age (< 65 years, ≥ 65 years) or prior overactive bladder medication use were consistent with overall findings. This large, multinational study found no higher risk of MACE, AMI, stroke, CV mortality or all-cause mortality among users of mirabegron relative to users of antimuscarinics. During clinical trials, mirabegron, which is a treatment for overactive bladder, was associated with small increases in heart rate and blood pressure. This study was conducted to compare the frequency of cardiac events following the use of mirabegron or antimuscarinics, a group of treatments also used to treat overactive bladder. We obtained the data for this study from four countries: Denmark, Sweden, the UK and the USA. We identified people who were new users of mirabegron or antimuscarinics from 2012 to 2018 using prescription or dispensing records. Occurrences of major cardiac events, heart attack, stroke, death due to cardiac events and death from any cause were evaluated. Overall, we identified 152,026 times when mirabegron or antimuscarinics were each used as new treatments. Most of the people in the study were women (63.1%) and at least 65 years old (72.6%). There were no notable differences between the treatment groups with regard to how often major cardiac events, heart attack or stroke occurred. Further, death due to cardiac events and death from any cause were no higher with mirabegron compared with antimuscarinics. We obtained similar results when the data were assessed for patients who were at high risk for cardiac events or split by age (less than 65 years or at least 65 years) or a history of overactive bladder medication use. In conclusion, this large study involving data from several countries found no higher risk of major cardiac events, heart attack, stroke or death among people prescribed mirabegron compared with antimuscarinics.
Autres résumés
Type: plain-language-summary
(eng)
During clinical trials, mirabegron, which is a treatment for overactive bladder, was associated with small increases in heart rate and blood pressure. This study was conducted to compare the frequency of cardiac events following the use of mirabegron or antimuscarinics, a group of treatments also used to treat overactive bladder. We obtained the data for this study from four countries: Denmark, Sweden, the UK and the USA. We identified people who were new users of mirabegron or antimuscarinics from 2012 to 2018 using prescription or dispensing records. Occurrences of major cardiac events, heart attack, stroke, death due to cardiac events and death from any cause were evaluated. Overall, we identified 152,026 times when mirabegron or antimuscarinics were each used as new treatments. Most of the people in the study were women (63.1%) and at least 65 years old (72.6%). There were no notable differences between the treatment groups with regard to how often major cardiac events, heart attack or stroke occurred. Further, death due to cardiac events and death from any cause were no higher with mirabegron compared with antimuscarinics. We obtained similar results when the data were assessed for patients who were at high risk for cardiac events or split by age (less than 65 years or at least 65 years) or a history of overactive bladder medication use. In conclusion, this large study involving data from several countries found no higher risk of major cardiac events, heart attack, stroke or death among people prescribed mirabegron compared with antimuscarinics.
Identifiants
pubmed: 34236595
doi: 10.1007/s40264-021-01095-7
pii: 10.1007/s40264-021-01095-7
pmc: PMC8280006
doi:
Substances chimiques
Acetanilides
0
Muscarinic Antagonists
0
Thiazoles
0
mirabegron
MVR3JL3B2V
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
899-915Investigateurs
Cheryl Enger
(C)
John Seeger
(J)
Veena Hoffman
(V)
Kelesitse Phiri
(K)
Jesper Hallas
(J)
Morten Olesen
(M)
Nina Sahlertz Kristiansen
(NS)
Shahram Bahmanyar
(S)
Marie Linder
(M)
Helle Kieler
(H)
Ingvild Odsbu
(I)
Alejandro Arana
(A)
Lisa McQuay
(L)
Andrea Margulis
(A)
Susana Perez-Gutthann
(S)
Ryan Ziemiecki
(R)
Su Bunniran
(S)
Brandon Suehs
(B)
Claudia Uribe
(C)
Yihua Xu
(Y)
Libby Horter
(L)
Kwame Appenteng
(K)
Stefan de Vogel
(S)
Noah Jamie Robinson
(NJ)
Songlin Xue
(S)
Josie Wolfram
(J)
Achim Steup
(A)
Jena Giese-Pagac
(J)
Raymond van Aarle
(R)
Neha Sheth
(N)
David Burns
(D)
Natalie Boone
(N)
Mary Beth Blauwet
(MB)
Milbhor D'Silva
(M)
Billy Franks
(B)
Willem Jan Atsma
(WJ)
Tim Auton
(T)
Edeltraut Garbe
(E)
Anders Ekbom
(A)
Todd Lee
(T)
Noel Weiss
(N)
John Rumsfeld
(J)
Sara Yuewen Gao
(SY)
Laura Karslake
(L)
Nan Liu
(N)
Katherine Reed
(K)
Bruce Turnbull
(B)
Jing Yang
(J)
Nicole Brooks
(N)
Kathleen Mortimer
(K)
Informations de copyright
© 2021. The Author(s).
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