Ananda I Gede Yogi Prema, Surya Radika Naufal Hadi, Surya Prima Ardiansah, Putratama Alfin, Andhika Dimas Panca
Department of Urology, Klungkung General Hospital, Klungkung, Bali, Indonesia.
Intan Medika Hospital, Lamongan, East Java, Indonesia.
Urol Ann. 2025 Jan-Mar;17(1):2-8. doi: 10.4103/ua.ua_30_24. Epub 2025 Jan 18.
Overactive bladder (OAB) is a chronic disease with the symptoms of urgency with or without incontinence. Solifenacin is an antimuscarinic drug that Excels in OAB treatment due to its specific bladder receptor targeting. While previous research had positive outcomes, reports of adverse events (AEs) highlight the need for regular updates on the safety and efficacy of solifenacin for OAB management. This study followed PRISMA 2020 guidelines and was registered to PROSPERO CRD42023445318. A comprehensive search of PubMed, ScienceDirect, and Scopus databases was conducted until July 2023. Data were analyzed using Review Manager version 5.4 (The Cochrane Collaboration, The Nordic Cochrane Centre, Copenhagen, Denmark). Solifenacin had a significantly better effect in decreasing urgency episode (mean difference (MD) = -1.09, 95% confidence interval [CI]: -1.29--0.89, < 0.00001), incontinence episode (MD = -0.56, 95% CI: -0.80--0.32, < 0.00001), micturition frequency (MD = -1.01, 95% CI: -1.16--0.85, < 0.00001), nocturia episode (MD = -0.13, 95% CI: -0.25--0.01, = 0.04), and had a higher urine volume (MD = 26.88, 95% CI: 24.17-29.59, < 0.00001) per 24 h compared to placebo. Solifenacin had a significant number of AEs compared to placebo (MD = 1.75, 95% CI: 1.25-2.45, = 0.001). Solifenacin significantly decreased urgency episode, incontinence episodes, micturition frequency, and nocturia episode, and had a higher urine volume per 24 h. There was a significant number of AEs in patients receiving solifenacin.
膀胱过度活动症(OAB)是一种伴有尿急症状(有无尿失禁均可)的慢性疾病。索利那新是一种抗毒蕈碱药物,因其对膀胱特定受体具有靶向作用,在OAB治疗方面表现出色。尽管先前的研究取得了积极成果,但不良事件(AE)报告凸显了定期更新索利那新治疗OAB的安全性和有效性的必要性。本研究遵循PRISMA 2020指南,并已在PROSPERO注册,注册号为CRD42023445318。对PubMed、ScienceDirect和Scopus数据库进行了全面检索,直至2023年7月。使用Review Manager 5.4版(丹麦哥本哈根北欧科克伦中心科克伦协作网)对数据进行分析。与安慰剂相比,索利那新在减少尿急发作次数(平均差(MD)=-1.09,95%置信区间[CI]:-1.29--0.89,P<0.00001)、尿失禁发作次数(MD=-0.56,95%CI:-0.80--0.32,P<0.00001)、排尿频率(MD=-1.01,95%CI:-1.16--0.85,P<0.00001)、夜尿发作次数(MD=-0.13,95%CI:-0.25--0.01,P=0.04)方面效果显著更好,且每24小时尿量更高(MD=26.88,95%CI:24.17-29.59,P<0.00001)。与安慰剂相比,索利那新的不良事件数量显著更多(MD=1.75,95%CI:1.25-2.45,P=0.001)。索利那新显著减少了尿急发作次数、尿失禁发作次数、排尿频率和夜尿发作次数,且每24小时尿量更高。接受索利那新治疗的患者不良事件数量显著增多。