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低强度脉冲超声(LIPUS)联合他达拉非治疗重度勃起功能障碍的疗效和安全性:一项回顾性队列研究

Efficacy and safety of low-intensity pulsed ultrasound (LIPUS) combined with tadalafil in the treatment of severe erectile dysfunction: a retrospective cohort study.

作者信息

Gao Qing-Qiang, Wang Jing, Li Da-Sheng, Dai Yu-Tian, Li Zhi-Ran, Zhao Xiao-Zhi

机构信息

Department of Andrology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, China.

出版信息

Transl Androl Urol. 2024 Sep 30;13(9):2045-2054. doi: 10.21037/tau-24-154. Epub 2024 Sep 25.

Abstract

BACKGROUND

Low-intensity pulsed ultrasound (LIPUS) is an effective and safe treatment for mild to moderate erectile dysfunction (ED). This study aimed to investigate the efficacy and safety of combining LIPUS with tadalafil in treating severe ED.

METHODS

The data from 27 patients treated with LIPUS alone (group A) and 21 patients treated with a combination of LIPUS and daily 10 mg tadalafil (group B) were retrospectively analyzed. The LIPUS regimen consisted of twice-weekly treatments for 4 consecutive weeks. The treatment was considered effective if the change in International Index of Erectile Function-Erectile Function Domain (IIEF-EF) score after treatment was greater than or equal to the minimal clinically important difference (MCID) (the MCID for severe ED is 7 points). The effectiveness, IIEF-EF score, erectile hardness score (EHS), peak systolic velocity (PSV), end diastolic velocity (EDV), and adverse events were evaluated before treatment, 4 weeks after treatment, and 12 weeks after treatment.

RESULTS

Compared to pre-treatment, both groups showed significant improvement in IIEF-EF score and EHS at 4 and 12 weeks after treatment (P<0.001), with no statistically significant difference between the two time points (P>0.05). The effective rate did not significantly differ between group A (9/27, 33.3%) and group B (10/21, 47.62%) at 4 weeks or between group A (9/27, 33.3%) and group B (12/21, 57.14%) at 12 weeks after treatment (P=0.32, P=0.10). However, in patients without comorbidities, the effective rate of group B (12/18, 66.67%) was higher than that of group A (9/25, 36.00%) at 12 weeks after treatment (P=0.047). After LIPUS treatment, the PSV level significantly increased and the EDV level significantly decreased compared with before treatment (P<0.05). No adverse events were reported.

CONCLUSIONS

The study suggests that LIPUS has a therapeutic effect on severe ED patients, especially those without comorbidities. It may have a synergistic or overlapping effect with phosphodiesterase type 5 inhibitors (PDE5Is) on severe ED patients without comorbidities.

摘要

背景

低强度脉冲超声(LIPUS)是治疗轻至中度勃起功能障碍(ED)的一种有效且安全的方法。本研究旨在探讨LIPUS联合他达拉非治疗重度ED的疗效和安全性。

方法

回顾性分析27例仅接受LIPUS治疗的患者(A组)和21例接受LIPUS联合每日10 mg他达拉非治疗的患者(B组)的数据。LIPUS治疗方案为每周两次,连续治疗4周。如果治疗后国际勃起功能指数-勃起功能领域(IIEF-EF)评分的变化大于或等于最小临床重要差异(MCID)(重度ED的MCID为7分),则认为治疗有效。在治疗前、治疗后4周和治疗后12周评估疗效、IIEF-EF评分、勃起硬度评分(EHS)、收缩期峰值流速(PSV)、舒张末期流速(EDV)和不良事件。

结果

与治疗前相比,两组在治疗后4周和12周时IIEF-EF评分和EHS均有显著改善(P<0.001),两个时间点之间无统计学显著差异(P>0.05)。治疗后4周,A组(9/27,33.3%)和B组(10/21,47.62%)的有效率无显著差异;治疗后12周,A组(9/27,33.3%)和B组(12/21,57.14%)的有效率也无显著差异(P=0.32,P=0.10)。然而,在无合并症的患者中,治疗后12周B组的有效率(12/18,66.67%)高于A组(9/25,36.00%)(P=0.047)。LIPUS治疗后,与治疗前相比,PSV水平显著升高,EDV水平显著降低(P<0.05)。未报告不良事件。

结论

该研究表明,LIPUS对重度ED患者有治疗作用,尤其是对无合并症的患者。对于无合并症的重度ED患者,它可能与5型磷酸二酯酶抑制剂(PDE5Is)有协同或重叠作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0918/11491205/b9506a93e441/tau-13-09-2045-f1.jpg

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