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The risk and severity of developing symptomatic palpitations when prescribed mirabegron for overactive bladder
Aswini A Balachandran1, Jonathan R A Duckett1
1Department of Obstetrics and Gynaecology, Medway Maritime Hospital, Windmill Road, Gillingham Kent ME7 5NY, UK.
Palpitations occurred in 2.9% of patients taking mirabegron for overactive bladder. While generally mild and resolving upon discontinuation, some cases saw worsening symptoms, suggesting potential cardiovascular effects.
Area of Science:
- Pharmacology
- Cardiology
- Urology
Background:
- Mirabegron, a selective β3-adrenoreceptor agonist, is used for overactive bladder (OAB).
- Clinical trials indicate mirabegron has a favorable side-effect profile.
- Limited data exists on mirabegron's risks in unselected patient populations, particularly concerning cardiovascular events due to β-adrenoreceptor presence in cardiac and vascular tissues.
Purpose of the Study:
- To assess the risk and severity of palpitations in patients with OAB treated with mirabegron.
- To identify potential risk factors for developing palpitations while on mirabegron.
- To evaluate cardiovascular safety in an unselected OAB population using mirabegron.
Main Methods:
- A consecutive cohort study of 279 OAB patients prescribed 50mg daily mirabegron.
- Outcomes assessed at 6 weeks, excluding patients with known cardiac arrhythmias.
- Palpitations, symptoms, medical history, and 12-lead ECGs (heart rate, QT interval) were documented.
Main Results:
- Eight patients (2.9%) reported palpitations.
- Two patients with prior palpitations experienced worsening symptoms.
- Two patients showed QT interval prolongation; three reported chest pain/tightness. Palpitations resolved upon stopping mirabegron without serious adverse events.
Conclusions:
- The incidence of palpitations with mirabegron in an unselected population mirrors previous trial data.
- Palpitations may indicate a potential for worsening cardiovascular dysfunction in some patients.
- Mirabegron appears generally safe, with palpitations being the primary noted adverse event, typically manageable.
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