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按需服用舍曲林、达泊西汀与每日服用舍曲林治疗终身性早泄患者的安全性和有效性比较:一项前瞻性随机研究。

Comparison of the safety and efficacy of the on-demand use of sertraline, dapoxetine, and daily use of sertraline in the treatment of patients with lifelong premature ejaculation: A prospective randomised study.

作者信息

Sahan Ahmet, Cubuk Alkan, Ozkaptan Orkunt, Toprak Tuncay, Ozcan Tolga, Ertas Kasım, Canguven Onder, Tarhan Fatih

机构信息

Department of Urology, Health Science University, Kartal Dr. Lutfi Kirdar Training and Research Hospital, Istanbul, Turkey.

Department of Urology, Health Science University, Fatih Sultan Mehmet Training and Research Hospital, Istanbul, Turkey.

出版信息

Andrologia. 2020 Dec;52(11):e13854. doi: 10.1111/and.13854. Epub 2020 Oct 28.

DOI:10.1111/and.13854
PMID:33113277
Abstract

This study compared the safety and efficacy of the on-demand (OD) use of sertraline (50 mg), sertraline (100 mg) and dapoxetine (30 mg), and the daily use of sertraline (50 mg) in the treatment of patients with premature ejaculation (PE). This prospective randomised study involved 120 lifelong PE patients (intravaginal ejaculatory latency time [IELT]: <1 min; Arabic Index of Premature Ejaculation [AIPE] score: < 30) without secondary causes of PE, identified between March 2018 and May 2020. Patients were divided into 4 groups (30 patients per group) and treated for 8 weeks. Assessments were conducted using the AIPE form as a diagnostic tool. Sertraline (50 mg, daily; 196.7 ± 115.5 s) and sertraline (100 mg, OD; 173.3 ± 97.0 s) had similar IELT and AIPE scores. The latter groups had better results in comparison with sertraline (50 mg, OD; 100.5 ± 54.4 s) and dapoxetine (93.7 ± 53.5 s; p < 0.01). Sertraline (100 mg, OD) had a similar efficacy to that of sertraline (50 mg, daily) and was more effective than sertraline (50 mg, OD) and dapoxetine (30 mg, OD). Sertraline (100 mg, OD) can be considered in the treatment of lifelong PE treatment, having tolerable side effects.

摘要

本研究比较了按需服用舍曲林(50毫克)、舍曲林(100毫克)和达泊西汀(30毫克)以及每日服用舍曲林(50毫克)治疗早泄(PE)患者的安全性和有效性。这项前瞻性随机研究纳入了2018年3月至2020年5月期间确诊的120例原发性早泄患者(阴道内射精潜伏期[IELT]:<1分钟;阿拉伯早泄指数[AIPE]评分:<30),且不存在导致早泄的继发性病因。患者被分为4组(每组30例),并接受8周的治疗。使用AIPE表格作为诊断工具进行评估。舍曲林(每日50毫克;196.7±115.5秒)和舍曲林(按需服用100毫克;173.3±97.0秒)的IELT和AIPE评分相似。与舍曲林(按需服用50毫克;100.5±54.4秒)和达泊西汀(93.7±53.5秒;p<0.01)相比,后两组的效果更好。舍曲林(按需服用100毫克)与舍曲林(每日50毫克)疗效相似,且比舍曲林(按需服用50毫克)和达泊西汀(按需服用30毫克)更有效。舍曲林(按需服用100毫克)可用于原发性早泄的治疗,且副作用可耐受。

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