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The efficacy of mirabegron additional therapy for lower urinary tract symptoms after treatment with α1-adrenergic receptor blocker monotherapy: prospective analysis of elderly men

机译:米拉贝隆联合治疗α1-肾上腺素受体阻滞剂单一疗法治疗下尿路症状的疗效:老年男性的前瞻性分析

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Background Mirabegron is a β3-adrenoreceptor agonist developed for treatment of overactive bladder (OAB). α1-Adrenergic receptor blockers are effective for lower urinary tract symptoms (LUTS) in male patients. However, the efficacy of mirabegron additional treatment in elderly male patients with persistent male LUTS, especially in OAB after monotherapy with α1-adrenergic blockers, is not fully understood. Methods This study was conducted in male LUTS patients who were?≥?65?years of age and had persistent OAB symptoms, regardless of whether they took an α1-adrenergic receptor blocker orally. Before and 12?weeks after mirabegron additional therapy (50?mg once daily), we evaluated the efficacy of this treatment using the Overactive Bladder Symptom Score (OABSS) and International Prostate Symptom Score (IPSS), and changes in the maximum flow rate (Qmax) and post-void residual urine volume (PVR). We evaluated patients overall and divided into two groups by age: young-old (from 65 to 74?years old) and old-old (from 75 to 84?years old). Results Fifty men were enrolled in this study. Mirabegron additional therapy improved the total OABSS, total IPSS, and IPSS-quality of life (QOL) score. The voided volume (VV) and Qmax improved after treatment in patients overall. However, there was no significant change in PVR. The total OABSS, total IPSS, and IPSS-QOL score significantly improved in both of the young-old and old-old groups. However, a significant increasing of VV was detected in the young-old group. There were no significant differences in the Qmax or PVR in either group. Conclusions Mirabegron additional therapy was effective for male patients whose persistent LUTS and particularly OAB was not controlled with α1-adrenergic receptor blocker monotherapy, and mirabegron did not have negative effects on voiding function. Additionally, mirabegron additional therapy was considered effective regardless of patient age. Trial registration Trial registration number (TRN) trial registration number (TRN) and date of registration: ISRCTN16759097 in July 8, 2016.
机译:背景Mirabegron是为治疗膀胱过度活动症(OAB)而开发的β3-肾上腺素受体激动剂。 α1-肾上腺素能受体阻滞剂可有效治疗男性患者的下尿路症状(LUTS)。然而,米拉贝隆在顽固性男性LUTS的老年男性患者中,特别是在α1-肾上腺素能阻断剂单药治疗后的OAB中,对其他男性患者的疗效尚不完全清楚。方法本研究针对年龄≥65岁且持续存在OAB症状的男性LUTS患者,无论是否口服α1-肾上腺素受体阻滞剂。在米拉贝隆追加治疗之前和之后12周(每天50 mg),我们使用膀胱过度活动症症状评分(OABSS)和国际前列腺症状评分(IPSS)评估了该疗法的疗效,并评估了最大流量的变化( Qmax)和排尿后残余尿量(PVR)。我们对患者进行了总体评估,并按年龄将其分为两组:年轻人(65至74岁)和老年人(75至84岁)。结果本研究共招募了50名男性。 Mirabegron的其他治疗改善了总OABSS,总IPSS和IPSS生活质量(QOL)评分。治疗后总体患者的排尿量(VV)和Qmax有所改善。但是,PVR没有明显变化。在年轻组和老年组中,总的OABSS,总IPSS和IPSS-QOL得分均显着提高。但是,在年轻组中检测到VV显着增加。两组的Qmax或PVR均无显着差异。结论Mirabegron补充治疗对持续性LUTS特别是OAB不能通过α1-肾上腺素能受体阻滞剂单一疗法控制的男性患者有效,并且mirabegron对排尿功能没有负面影响。此外,无论患者年龄如何,米拉贝隆辅助治疗均被认为有效。试用注册试用注册号(TRN)试用注册号(TRN)和注册日期:2016年7月8日为ISRCTN16759097。

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