Vanden Bossche M, Abi Aad A, Vandendris M, Van Cangh P, Schulman C
Service d'Urologié, Hôpital Universitaire Erasme, Bruxelles.
Acta Urol Belg. 1991;59(1):93-104.
Seventy one patients were treated with mepartricin or placebo in three urological centres for a mean duration of 102 days (extremes: 60 and 142 days). An analysis of the results was carried out for 34 patients in the placebo group and 36 patients in the mepartricin group. The results indicate a significant improvement in both the placebo group and the mepartricin group. The irritative and obstructive symptoms are improved in the active treatment group with a response rate of the order of 70%, compared to approx. 45% in the placebo group. An improvement of the values on the flow meter, though not statistically significant, is observed following treatment with mepartricin, compared to the placebo group. There were no significant differences in the evolution of the prostate gland volume, determined by ultrasound in the placebo group and the active treatment group. Side-effects were minor and only one patient reported epigastric pain.
71名患者在三个泌尿中心接受了美帕曲星或安慰剂治疗,平均治疗时长为102天(范围:60至142天)。对安慰剂组的34名患者和美帕曲星组的36名患者进行了结果分析。结果显示,安慰剂组和美帕曲星组均有显著改善。与安慰剂组约45%的有效率相比,积极治疗组的刺激性和梗阻性症状得到改善,有效率约为70%。与安慰剂组相比,美帕曲星治疗后虽未达到统计学显著差异,但流量计数值有所改善。安慰剂组和积极治疗组通过超声测定的前列腺体积变化无显著差异。副作用较小,仅有一名患者报告有上腹部疼痛。