Diab Tamer, Noah Kareem, Farag Mahmoud, Shaher Hussein
Urology Department, Faculty of Medicine, Benha University, Benha, 13511, Qalyubiyya Governorate, Egypt.
Int Urol Nephrol. 2025 Jan;57(1):99-106. doi: 10.1007/s11255-024-04147-w. Epub 2024 Aug 6.
To determine the optimum combination therapy of Silodosin-Tadalafil versus Silodosin-Vardenafil in terms of both tolerability and efficacy for the management of distal ureteric stones.
This prospective, double blinded, randomized clinical trial included 140 patients with distal ureteric stones, randomized into two groups: Group I (n = 67) received Silodosin 8 mg once daily combined with Tadalafil 5 mg once daily, and Group II (n = 68) received Silodosin 8 mg once daily combined with Vardenafil 10 mg once daily. The primary outcome was the tolerability of the combination therapies, assessed through the incidence of adverse events. Secondary outcomes included stone expulsion rate, expulsion time, and the need for analgesics.
Both combination therapies demonstrated similar efficacy, with no significant differences in stone expulsion rate (70.1% vs. 67.6%, P = 0.754), expulsion time (19 ± 3 days for both groups, P = 0.793), and analgesic requirements (P > 0.05). However, the Silodosin-Tadalafil combination showed a significantly lower occurrence of adverse events, with notable differences in headache (23.9% vs. 57.4%, P < 0.001), dizziness (32.8% vs. 60.3%, P = 0.001), and gastrointestinal upset (9% vs. 66.2%, P < 0.001), and other adverse effects. The overall occurrence of any adverse event was significantly lower in the Silodosin-Tadalafil group (88.1% vs. 98.5%, P = 0.017).
Both Silodosin-Tadalafil and Silodosin-Vardenafil therapies are effective in managing distal ureteric stones. However, the Silodosin-Tadalafil combination is associated with a significantly lower incidence of adverse events, making it a more tolerable option for patients.
在治疗远端输尿管结石的耐受性和疗效方面,确定西洛多辛 - 他达拉非与西洛多辛 - 伐地那非的最佳联合治疗方案。
这项前瞻性、双盲、随机临床试验纳入了140例远端输尿管结石患者,随机分为两组:第一组(n = 67)每日一次服用8毫克西洛多辛联合每日一次服用5毫克他达拉非,第二组(n = 68)每日一次服用8毫克西洛多辛联合每日一次服用10毫克伐地那非。主要结局是联合治疗的耐受性,通过不良事件发生率进行评估。次要结局包括结石排出率、排出时间和镇痛需求。
两种联合治疗方案疗效相似,结石排出率(70.1%对67.6%,P = 0.754)、排出时间(两组均为19±3天,P = 0.793)和镇痛需求(P>0.05)均无显著差异。然而,西洛多辛 - 他达拉非联合治疗的不良事件发生率显著较低,在头痛(23.9%对57.4%,P<0.001)、头晕(32.8%对60.3%,P = 0.001)和胃肠道不适(9%对66.2%,P<0.001)及其他不良反应方面存在显著差异。西洛多辛 - 他达拉非组任何不良事件的总体发生率显著较低(88.1%对98.5%,P = 0.017)。
西洛多辛 - 他达拉非和西洛多辛 - 伐地那非治疗方案在治疗远端输尿管结石方面均有效。然而,西洛多辛 - 他达拉非联合治疗的不良事件发生率显著较低,使其成为患者更易耐受的选择。