Mirabegron in patients with Parkinson disease and overactive bladder symptoms: A retrospective cohort

被引:34
|
作者
Peyronnet, Benoit [1 ,2 ]
Vurture, Gregory [1 ]
Palma, Jose-Alberto [3 ]
Malacarne, Dominique R. [1 ]
Feigin, Andrew [4 ]
Sussman, Rachael D. [1 ]
Biagioni, Milton C. [4 ]
Palmerola, Ricardo [1 ]
Gilbert, Rebecca [4 ]
Rosenblum, Nirit [1 ]
Frucht, Steven [4 ]
Kaufmann, Horacio [3 ]
Nitti, Victor W. [1 ]
Brucker, Benjamin M. [1 ]
机构
[1] NYU, Sch Med, Dept Urol, New York, NY 10003 USA
[2] Univ Rennes, Dept Urol, Rennes, France
[3] NYU, Dept Neurol, Sch Med, Dysautonomia Ctr, New York, NY 10016 USA
[4] NYU, Sch Med, Marlene & Paolo Fresco Inst Parkinsons & Movement, New York, NY USA
关键词
Urinary bladder; Detrusor overactivity; Parkinson; Beta3-agonist; Outcomes; PERSISTENCE; DYSFUNCTION; PREVALENCE; DEMENTIA; AGONIST; TRIALS; OAB;
D O I
10.1016/j.parkreldis.2018.07.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: This study aimed to assess the outcomes of mirabegron for the treatment of overactive bladder (CAB) symptoms in patients with Parkinson disease (PD). Methods: A retrospective study was conducted including patients with PD who received mirabegron 50 mg once daily for OAB symptoms between 2012 and 2017. The primary endpoint was clinical success defined as any improvement in overactive bladder symptoms self-assessed by the patients 6 weeks after mirabegron initiation. Secondary endpoints included number of pads per day, number of nocturia episodes and adverse events. Results: Fifty patients (mean 74 years old) were included. Before being treated with mirabegron, 56% had failed prior anticholinergic therapy. After 6 weeks of mirabegron 50 mg, five patients (11.4%) had a complete resolution of their OAB symptoms; 25 patients (50%) reported improvement, 23 (46%) reported no change and 2(4%) reported worsening of their OAB symptoms. The number of pads per day decreased from 1.5 to 0.9 (p = 0.01) and so did the number of nocturia episodes (from 3 to 2.6/night; p = 0.02). Only 2 adverse events were reported during mirabegron treatment (4%): one dizziness and one diaphoresis, that disappeared after mirabegron discontinuation. After a median follow-up of 19 months, 23 patients (46%) persisted on mirabegron. Persistence rates were 51.5%, 44.6% and 36.4% at 1, 2 and 3 years respectively. Conclusion; Mirabegron has an excellent safety profile and appears to be an effective treatment for overactive bladder symptoms in patients with PD. Further prospective randomized trials are needed to properly assess mirabegron in PD patients.
引用
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页码:22 / 26
页数:5
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