Pattanaik Smita, Sandhu Harbhupinder Singh, Mavuduru Ravimohan Suryanarayan, Singh Shrawan Kumar, Mandal Arup Kumar
Department of Pharmacology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Surgery, Government Medical College, Patiala, Punjab, India.
Indian J Urol. 2019 Jan-Mar;35(1):25-33. doi: 10.4103/iju.IJU_147_18.
Tadalafil and Tamsulosin have both been approved for use in the management of lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH). This study compared the differential effects of these two on BPH-LUTS using a cross over study design.
Men ≥45 years of age, with an International Prostate Symptom Score (IPSS) ≥8 due to BPH-LUTS were included. The patients were randomized into sequence AB (tadalafil 10 mg OD followed by tamsulosin 0.4 mg OD) or BA in a double blind manner. All patients received a placebo lead-in period for 2 weeks, followed by an active drug for 6 weeks; placebo wash out for 4 weeks and then crossed over to second active drug for another 6 weeks. IPSS scores, Uroflowmetry parameters and International Index of Erectile Function-5 scores were recorded.
Out of the 40 patients, 36 completed the study. Demographic and baseline characteristics were comparable between the two groups (AB and BA). No significant placebo effects were observed. Tadalafil and tamsulosin significantly improved the total IPSS score and quality of life ( < 0.05) as compared to the baseline. However, there were no significant differences between the two drugs with respect to extent of observed effect and which drug was prescribed 1 in the sequence respectively ( > 0.05). Significant period effect was observed ( < 0.05) i.e., the symptoms did not return to the baseline before the second treatment. Half of the nonresponders to either of the drugs responded when the drug was changed to the other. Tadalafil showed better improvement in EF score as compared to Tamsulosin.
Both Tadalafil and Tamsulosin improved LUTS and erectile function and those patients who did not respond to Tadalafil showed improvement with Tamsulosin and vice-a-versa.
他达拉非和坦索罗辛均已获批用于治疗良性前列腺增生(BPH)继发的下尿路症状(LUTS)。本研究采用交叉研究设计比较了二者对BPH-LUTS的不同作用。
纳入年龄≥45岁、因BPH-LUTS导致国际前列腺症状评分(IPSS)≥8的男性患者。患者以双盲方式随机分为AB组(先服用他达拉非10 mg每日一次,随后服用坦索罗辛0.4 mg每日一次)或BA组。所有患者均接受为期2周的安慰剂导入期,随后服用活性药物6周;停用安慰剂4周,然后交叉服用另一种活性药物6周。记录IPSS评分、尿流率参数和国际勃起功能指数-5评分。
40例患者中,36例完成了研究。两组(AB组和BA组)的人口统计学和基线特征具有可比性。未观察到显著的安慰剂效应。与基线相比,他达拉非和坦索罗辛均显著改善了总IPSS评分和生活质量(P<0.05)。然而,两种药物在观察到的疗效程度以及给药顺序方面均无显著差异(P>0.05)。观察到显著的周期效应(P<0.05),即第二次治疗前症状未恢复到基线水平。两种药物的无反应者中,有一半在更换药物后出现反应。与坦索罗辛相比,他达拉非在勃起功能评分方面改善更明显。
他达拉非和坦索罗辛均改善了LUTS和勃起功能,对他达拉非无反应的患者使用坦索罗辛有改善,反之亦然。