Jardin A
Service d'Urologie, Hôpital Universitaire de Bicêtre, Le Kremlin Bicêtre.
Ann Urol (Paris). 1988;22(5):333-40.
The use of alfuzosin (a competitive post-junctional alpha-blocker) is based on the finding of alpha-adrenoceptors in trigone, urethra and adenoma tissue. Thirty-one European centers participated in this randomized study with parallel groups (alfuzosin versus placebo). The treatment period lasted 6 months with assessments on D14 and every 6 weeks thereafter. The dose was either 7.5 mg or 10 mg/day. Four hundred and seventeen patients were included (alfuzosin = 205, placebo = 212). The demographic data and the characteristics of the benign prostatic hypertrophy were comparable in both groups. There were 30 drop-outs due to inefficacy in the placebo group and 15 in the alfuzosin group. The difference is significant (p = 0.01). Five patients had to leave the study for emergency treatment of acute urinary retention (4 in the placebo group and 1 in the alfuzosin group). Early improvement was observed in the total score (urgency (p = 0.001) and quality of the stream), assessed on the basis of the functional symptoms (diurnal frequency and nocturia, hesitancy, post-void dribbling, urgency, sensation of incomplete emptying of the bladder and quality of the stream). Alfuzosin was demonstrated to be effective with respect to out-flow obstructive symptoms (quality of the stream, hesitancy, sensation of incomplete emptying of the bladder) and other functional symptoms (diurnal frequency and nocturia). The good total score results favor alfuzosin primarily because of its action on urgency and dysuria. The drug was well tolerated clinically. In conclusion, alfuzosin is useful in moderate dysuria in young subjects, during acute episodes in elderly patients and in patients when surgery has to be delayed.
阿夫唑嗪(一种竞争性节后α受体阻滞剂)的应用基于在三角区、尿道和腺瘤组织中发现α肾上腺素能受体。31个欧洲中心参与了这项平行组随机研究(阿夫唑嗪与安慰剂对照)。治疗期持续6个月,在第14天进行评估,此后每6周评估一次。剂量为7.5毫克或10毫克/天。共纳入417例患者(阿夫唑嗪组205例,安慰剂组212例)。两组的人口统计学数据和良性前列腺增生的特征具有可比性。安慰剂组有30例因无效退出研究,阿夫唑嗪组有15例。差异具有统计学意义(p = 0.01)。5例患者因急性尿潴留的紧急治疗而不得不退出研究(安慰剂组4例,阿夫唑嗪组1例)。根据功能症状(日间排尿频率、夜尿、排尿犹豫、排尿后滴沥、尿急、膀胱未完全排空感和尿流质量)评估,总分(尿急(p = 0.001)和尿流质量)出现早期改善。阿夫唑嗪在改善流出道梗阻症状(尿流质量、排尿犹豫、膀胱未完全排空感)和其他功能症状(日间排尿频率和夜尿)方面被证明是有效的。良好的总分结果主要因阿夫唑嗪对尿急和排尿困难的作用而有利于它。该药物在临床上耐受性良好。总之,阿夫唑嗪适用于年轻患者的中度排尿困难、老年患者的急性发作期以及手术不得不推迟的患者。