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比较坦索罗辛治疗良性前列腺增生的疗效:系统评价和荟萃分析。

Comparison of With Tamsulosin in the Treatment of Benign Prostatic Hyperplasia: A Systematic Review and Meta-Analysis.

机构信息

Binzhou Medical University, Yantai, Shandong, China.

Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shandong, China.

出版信息

Am J Mens Health. 2020 Mar-Apr;14(2):1557988320905407. doi: 10.1177/1557988320905407.

Abstract

Studies reported that was effective in relieving lower urinary tract symptoms (LUTS). This article carried out a systematic review and meta-analysis to compare with tamsulosin in the treatment of benign prostatic hyperplasia (BPH) after at least 6-month treatment cycle. Four studies involving 1,080 patients (543 in the group and 537 in the tamsulosin group) were included in the meta-analysis. The results were as follows: compared with tamsulosin, had a same effect in treating BPH in terms of International Prostate Symptom Score (IPSS) (mean difference [MD] 0.63, 95% confidence interval [CI] [-0.33, 1.59], = 0.20), quality of life (QoL) (MD 1.51, 95% CI [-1.51, 4.52], = 0.33), maximum flow rate (Qmax) (MD 0.27, 95% CI [-0.15, 0.68], = 0.21), postvoid residual volume (PVR) (MD -4.23, 95% CI [-22.97, 14.44], = 0.65), prostate-specific antigen (PSA) (MD 0.46, 95% CI [-0.06, 0.97], = 0.08) with the exception of prostate volume (PV) (MD -0.29, 95% CI [-0.41, -0.17], < 0.00001). For side effects, was well tolerated compared with tamsulosin especially in ejaculation disorders (odds ratio [OR] = 12.56, 95% CI [3.83, 41.18], < 0.0001) and decreased libido (OR = 5.40; 95% CI [1.17, 24.87]; = 0.03). This study indicated that had the same effect in treating BPH compared with tamsulosin in terms of IPSS, QoL, and PVR after at least 6-month treatment cycle, however, the latter had a greater improvement in PV compared with the former. And did not increase the risk of adverse events especially with respect to ejaculation disorders and libido decrease.

摘要

研究表明[药物名称]在缓解下尿路症状(LUTS)方面有效。本文进行了系统评价和荟萃分析,比较了[药物名称]与坦索罗辛在至少 6 个月治疗周期后治疗良性前列腺增生(BPH)的疗效。四项研究共纳入 1080 名患者([药物名称]组 543 名,坦索罗辛组 537 名)纳入荟萃分析。结果如下:与坦索罗辛相比,[药物名称]在国际前列腺症状评分(IPSS)(均数差[MD]0.63,95%置信区间[CI]-0.33,1.59],=0.20)、生活质量(QoL)(MD1.51,95%CI-1.51,4.52],=0.33)、最大尿流率(Qmax)(MD0.27,95%CI-0.15,0.68],=0.21)、残余尿量(PVR)(MD-4.23,95%CI-22.97,14.44],=0.65)和前列腺特异性抗原(PSA)(MD0.46,95%CI-0.06,0.97],=0.08)方面,治疗 BPH 的效果与坦索罗辛相当,除前列腺体积(PV)(MD-0.29,95%CI-0.41,-0.17],<0.00001)外。在副作用方面,[药物名称]与坦索罗辛相比耐受性更好,尤其是在射精障碍(比值比[OR]12.56,95%CI3.83,41.18],<0.0001)和性欲降低(OR5.40,95%CI1.17,24.87],=0.03)方面。本研究表明,在至少 6 个月的治疗周期后,[药物名称]在 IPSS、QoL 和 PVR 方面与坦索罗辛治疗 BPH 的效果相当,但后者在 PV 方面的改善程度大于前者。并且[药物名称]不会增加不良反应的风险,尤其是在射精障碍和性欲降低方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51d9/7153190/5d3e4d209dfe/10.1177_1557988320905407-fig1.jpg

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