Cardiovascular safety of mirabegron in individuals treated for spinal cord injury- or multiple sclerosis-induced neurogenic detrusor overactivity

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F21%3AA22028KG" target="_blank" >RIV/61988987:17110/21:A22028KG - isvavai.cz</a>

Alternative codes found

RIV/00064190:_____/21:N0000105 RIV/00216208:11120/21:43920929 RIV/00843989:_____/21:E0109023 RIV/00216208:11110/21:10420155

Result on the web

<a href="https://link.springer.com/article/10.1007/s11255-020-02774-7" target="_blank" >https://link.springer.com/article/10.1007/s11255-020-02774-7</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/s11255-020-02774-7" target="_blank" >10.1007/s11255-020-02774-7</a>

Result language

angličtina

Original language name

Cardiovascular safety of mirabegron in individuals treated for spinal cord injury- or multiple sclerosis-induced neurogenic detrusor overactivity

Original language description

Purpose To analyze cardiovascular safety of mirabegron in patients with spinal cord injury (SCI)- and multiple sclerosis (MS)-induced neurogenic detrusor overactivity (NDO) in a prospective, randomized, double-blind, placebo-controlled study. Methods Seventy-eight patients were enrolled into the study, and 66 of them were included into the final analysis. In 49 (74.2%), NDO developed due to suprasacral SCI, 17 (25.8%) suffered from NDO due to MS. Eleven patients were previously treated for hypertension and one for arrhythmia. All study participants received placebo for 2 weeks run-in period. Subsequently, eligible subjects were randomized for 4 weeks of active treatment with mirabegron 50 mg once daily (Group A; n = 32) or placebo (Group B; n = 34). Data from resting electrocardiography (ECG), 24-h ECG and blood pressure monitoring, and echocardiographic examination, were used for cardiovascular safety assessment. All reported variables were evaluated at time of randomization and at the end of the study. Longitudinal changes of variables within the groups and differences between the groups were assessed using nonparametric Kruskal-Wallis test, and p <= 0.05 was considered statistically significant. Results No statistically significant longitudinal changes were found in safety variables, except for prolongation of QT interval in placebo group (p = 0.0328) recorded by resting ECG. No significant difference between the Groups A and B, in any of the variables, was observed. A single cardiovascular study drug-related adverse event was recorded in a patient with cervical SCI (3.13%). Conclusions Our results suggest that mirabegron can be safely used in the treatment of patients with SCI- and MS-induced NDO.

Czech name

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Czech description

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Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

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OECD FORD branch

30217 - Urology and nephrology

Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2021

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

International Urology and Nephrology

ISSN

0301-1623

e-ISSN

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Volume of the periodical

53

Issue of the periodical within the volume

6

Country of publishing house

NL - THE KINGDOM OF THE NETHERLANDS

Number of pages

6

Pages from-to

1089-1095

UT code for WoS article

000606282300001

EID of the result in the Scopus database

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