Fukuoka H, Ishibashi Y, Shiba T, Tuchiya F, Sakanishi S
Department of Urology, Yokohama Minami Kyosai Hospital.
Hinyokika Kiyo. 1993 Jul;39(7):679-83.
The efficacy and safety of allylestrenol were studied in 22 patients with benign prostatic hypertrophy. A 25 mg allylestrenol tablet (Perselin tablet) was administered twice a day. A significant decrease in frequency of nocturnal urination was observed and improvement rates of subjective symptoms, such as sensation of residual urine, delay in start of urination, straining during urination and strength of urinary stream, were 59.1-68.2%. The rate of decrease of maximum area of transverse plane of prostate estimated by transrectal sonography was 13.2% and presumed circle area ratio (PCAR) improved significantly. The incidence of total side effects was 22.7%, whereas a decrease in sexual potency was observed in only 4.5% of the cases. The final global improvement rating of allylestrenol was 72.2% and the rate of usefulness was estimated in 63.6% of the patients. The present findings confirmed that allylestrenol is a useful and safe drug for the treatment of benign prostatic hypertrophy.
对22例良性前列腺增生患者研究了烯丙雌醇的疗效和安全性。给予25毫克烯丙雌醇片(普赛林片),每日两次。观察到夜间排尿次数显著减少,主观症状如残余尿感、排尿起始延迟、排尿时用力及尿流强度的改善率为59.1%-68.2%。经直肠超声检查估计前列腺横截面积最大减小率为13.2%,推测圆形面积比(PCAR)显著改善。总副作用发生率为22.7%,而仅4.5%的病例观察到性功能减退。烯丙雌醇的最终总体改善率为72.2%,估计63.6%的患者使用有效。目前的研究结果证实,烯丙雌醇是治疗良性前列腺增生的一种有效且安全的药物。