Shi Tian-Hao, Fu Yu-Li, Zhang Qi, Huang Wen-Jie, Lü Bo-Dong
The First Affiliated Hospital Zhejiang University School of Medicine Liangzhu Branch, Hangzhou, Zhejiang 311105, China.
The Second School of Clinical Medicine, Zhejiang University of Chinese Medicine,Hangzhou, Zhejiang 310053, China.
Zhonghua Nan Ke Xue. 2023 Oct;29(10):888-893.
This study aimed to evaluate the efficacy and safety of applying 5% lidocaine cream to the sensitive area of the glans penis after its precise localization under the penile biological vibration threshold test for the treatment of primary premature ejaculation.
Eighty patients diagnosed with primary premature ejaculation in an outpatient setting were included in this study. They were randomly scored into two groups. Group 1 (n = 40) was given 1 ml of 5% lidocaine cream on demand. They were instructed to apply the lidocaine cream evenly in a circular pattern to the glans penis without precise application to the sensitive area of the glans penis. The treatment lasted for a total of 4 weeks. Group 2 (n = 40) had a penile biological vibration threshold test performed to detect loci with a lower threshold. They were instructed to apply 1 ml of 5% lidocaine cream to the sensitive loci on the glans penis for 4 weeks. Lidocaine cream was applied topically or uniformly to the glans penis 20 minutes before planned intercourse in both groups .The efficacy and side effects before and after treatment were evaluated by the intravaginal ejaculation latency (IELTs) before and after treatment, combined with the Arabic Index of Premature Ejaculation and IIEF-5 score.
After treatment, IELTs in both groups were significantly improved compared with those before treatment(P<0.05);The Arab premature ejaculation index and IIEF-5 score of the precise smear group are higher than those of the uniform smear group(P<0.05).
This study infers that applying lidocaine according to the threshold of penile and glans vibration has a positive effect and fewer adverse event reports compared with the traditional method of using surface anesthetics, which is worthy of clinical promotion.
本研究旨在评估在阴茎生物振动阈值测试精确定位后,将5%利多卡因乳膏应用于阴茎头敏感区域治疗原发性早泄的疗效和安全性。
本研究纳入80例门诊诊断为原发性早泄的患者。他们被随机分为两组。第1组(n = 40)按需给予1毫升5%利多卡因乳膏。指导他们将利多卡因乳膏以环形均匀涂抹于阴茎头,但未精确涂抹于阴茎头敏感区域。治疗共持续4周。第2组(n = 40)进行阴茎生物振动阈值测试以检测阈值较低的位点。指导他们将1毫升5%利多卡因乳膏涂抹于阴茎头的敏感位点,持续4周。两组均在计划性交前20分钟将利多卡因乳膏局部或均匀涂抹于阴茎头。通过治疗前后的阴道内射精潜伏期(IELT),结合阿拉伯早泄指数和IIEF-5评分评估治疗前后的疗效和副作用。
治疗后,两组的IELT均较治疗前显著改善(P<0.05);精确涂抹组的阿拉伯早泄指数和IIEF-5评分高于均匀涂抹组(P<0.05)。
本研究推断,与传统使用表面麻醉剂的方法相比,根据阴茎和龟头振动阈值应用利多卡因具有积极效果且不良事件报告较少,值得临床推广。