Borisov V V
FGAOU VO I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
Urologiia. 2020 Jun(3):50-55.
To evaluate the efficacy and safety of combination therapy with 1-blocker and phosphodiesterase type 5 inhibitor (PDE5) in patients with benign prostatic hyperplasia (BPH) and erectile dysfunction (ED).
The observational multicenter program involving 18 medical institutions in Moscow included 315 men aged 40-65 years with BPH and ED. The inclusion criteria were a total IPSS score more than 8 points, QoL score of more than 3 points and clinical manifestations of ED ( less or equal 20 points on the IIEF-5 score). All patients received combined pharmacotherapy with Alfuprost MP 10 mg/day and Viatail 50 mg/day (if necessary, the dose was increased to 100 mg/day) for 3 months.
The combination therapy showed a high clinical efficiency and a favorable safety profile. Lower urinary tract symptoms improved by more than 60%, QoL increased by 64% and erectile function improved in more than 80% of patients. At the end of treatment, the average patient satisfaction score on the Likert scale was 4.2 (high and very high satisfaction), while doctors satisfaction with the clinical response of patients to the treatment was 4.35 points, which also corresponds to high and very high efficacy of therapy.
Combination of Alfuprost MP 10 mg/day and Viatail 50 mg/day (100 mg, if necessary) can be considered as one of the best options for non-surgical treatment of patients with BPH and ED.
评估α-受体阻滞剂与5型磷酸二酯酶抑制剂(PDE5)联合治疗良性前列腺增生(BPH)合并勃起功能障碍(ED)患者的疗效和安全性。
这项观察性多中心项目涉及莫斯科的18家医疗机构,纳入了315名年龄在40-65岁之间的BPH合并ED男性患者。纳入标准为国际前列腺症状评分(IPSS)总分超过8分、生活质量评分超过3分以及存在ED的临床表现(国际勃起功能指数-5评分小于或等于20分)。所有患者接受Alfuprost MP 10毫克/天和Viatail 50毫克/天的联合药物治疗(必要时剂量增加至100毫克/天),为期3个月。
联合治疗显示出较高的临床疗效和良好的安全性。下尿路症状改善超过60%,生活质量提高64%,超过80%的患者勃起功能得到改善。治疗结束时,患者在李克特量表上的平均满意度评分为4.2(高满意度和非常高满意度),而医生对患者治疗临床反应的满意度为4.35分,这也对应着治疗的高疗效和非常高疗效。
Alfuprost MP 10毫克/天与Viatail 50毫克/天(必要时100毫克)联合用药可被视为BPH合并ED患者非手术治疗的最佳选择之一。