首页良性前列腺增生治疗及预后证据详情

Outcomes and complications of naftopidil versus tamsulosin for elderly men with lower urinary tract symptoms secondary to benign prostatic hyperplasia: A systematic review and meta-analysis

原文:2021年 发布于 Andrologia 53卷 第9期 e14166 浏览量:1311次 原文链接

作者: Chai Y. Zhou Z. Cui Y. Che X. Zhang Y.

作者单位: Department of Urology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

归属分类: 良性前列腺增生治疗及预后证据

DOI: 10.1111/and.14166

关键词: Aged Humans *Lower Urinary Tract Symptoms Male Naphthalenes Piperazines Prospective Studies *Prostatic Hyperplasia Quality of Life Sulfonamides Tamsulosin Treatment Outcome benign prostatic hyperplasia lower urinary tract symptoms naftopidil tamsulosin

文献简介

We conducted a systematic review and meta-analysis to assess the outcomes and complications of naftopidil in treating elderly men with lower urinary tract symptoms secondary to benign prostatic hyperplasia and compared them with those administered with tamsulosin. A literature review was performed to identify the available randomised controlled trials concerning the comparison between naftopidil and tamsulosin for men with LUTS/BPH. We searched the following databases: the Cochrane Library Database, PubMed, Embase and Web of Science. Eleven publications involving 1,114 men (557 in the naf group and 557 in the tam group) were pooled in our analysis. We found no significant differences in the total IPSS, IPSS storage score, IPSS voiding score, quality of life index, peak urinary flow rate, average flow rate and post-void residual volumes. We assessed cardiovascular and sexual adverse events, acute urinary retention, surgical intervention, withdrawals due to any reason and withdrawals due to adverse events. The incidence of adverse events was similar among patients in naf and tam groups. In conclusion, naftopidil shared comparable efficacy and similar incidence of adverse events with tamsulosin and appears to be a promising agent for and alternative to tam. However, more prospective trials with high quality and long-term treatment duration are needed to verify this observation.

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