首页> 外文期刊>The Journal of Urology >Effects of acute treatment with tamsulosin versus alfuzosin on ejaculatory function in normal volunteers.
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Effects of acute treatment with tamsulosin versus alfuzosin on ejaculatory function in normal volunteers.

机译:坦索罗辛与阿夫唑嗪急性治疗对正常志愿者射精功能的影响。

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PURPOSE: The frequency of ejaculatory dysfunction in men varies among the alpha-blockers used in the treatment of lower urinary tract symptoms associated with benign prostatic hyperplasia. We assessed the effect of acute administration of tamsulosin, alfuzosin and placebo on ejaculate volume and sperm concentration in post-ejaculate urine, and addressed the mechanism of action of tamsulosin and alfuzosin on ejaculation. MATERIALS AND METHODS: Using a randomized, 3-way crossover design, the effects of 5 days of treatment with 0.8 mg tamsulosin daily, 10 mg alfuzosin daily and placebo on ejaculation in healthy adult men were compared. The primary end points of the study were ejaculate volume and sperm concentration in post-ejaculate urine on each treatment. To aid in clinical interpretation of primary efficacy end points, each primary end point was transformed into a binary outcome, that is subjects with a greater than 20% decrease in ejaculate volume and subjects with a greater than 20% increase in sperm concentration in post-ejaculate urine. RESULTS: In healthy volunteers who completed the study (48), tamsulosin resulted in significantly decreased ejaculate volume (-2.4 +/- 0.17 ml) compared to alfuzosin (+0.3 +/- 0.18 ml, p < 0.0001 vs tamsulosin) or placebo (+0.4 +/- 0.18 ml, p < 0.0001 vs tamsulosin, p = nonsignificant vs alfuzosin). Among completers the incidence of more than 20% decreased ejaculate volume was significantly greater with tamsulosin (89.6%) compared to alfuzosin (20.8%, p < 0.0001 vs tamsulosin) or placebo (12.5%, p < 0.0001 vs tamsulosin, p = nonsignificant vs alfuzosin). While on tamsulosin 35.4% of 48 completers had complete lack of ejaculation (anejaculation) and no subjects experienced anejaculation while on alfuzosin or placebo. CONCLUSIONS: On 0.8 mg tamsulosin daily ejaculatory function in subjects was marked by decreased ejaculate volume in almost 90% of subjects and anejaculation in approximately 35% of participants. These ejaculatory disorders with tamsulosin were not attributed to retrograde ejaculation. In contrast, anejaculation was not observed in any subjects in the alfuzosin or placebo groups.
机译:目的:男性射精功能障碍的频率因用于治疗与良性前列腺增生相关的下尿路症状的α-受体阻滞剂而异。我们评估了坦索罗辛,阿夫唑嗪和安慰剂的急性给药对射精后尿液中射精量和精子浓度的影响,并探讨了坦索罗辛和阿夫唑嗪对射精的作用机理。材料与方法:采用随机,三向交叉设计,比较了健康成年男子每天0.8 mg坦索罗辛,每天10 mg阿夫唑嗪和安慰剂治疗5天对射精的影响。该研究的主要终点是每次治疗时射精后尿液中的射精量和精子浓度。为了帮助对主要功效终点进行临床解释,将每个主要终点转换为二元结局,即在治疗后射精量减少大于20%的受试者,精子浓度增加大于20%的受试者。射出尿液。结果:在完成研究的健康志愿者中(48),坦洛新导致射精量(-2.4 +/- 0.17 ml)显着低于阿夫唑嗪(+0.3 +/- 0.18 ml,与坦洛新相比p <0.0001)或安慰剂( +0.4 +/- 0.18 ml,相对于坦洛新,p <0.0001,相对于阿夫唑嗪,p =无显着性。在完成者中,坦索罗辛(89.6%)的射精量减少超过20%的发生率显着高于阿夫唑嗪(20.8%,与坦索罗辛相比,p <0.0001)或安慰剂(对坦索罗辛而言为12.5%,p <0.0001,p =不显着与阿夫唑嗪)。在坦索罗辛治疗的48名完成者中,有35.4%的人完全没有射精(射精),并且在使用阿夫唑嗪或安慰剂时没有受试者发生射精。结论:在0.8 mg坦索罗辛中,受试者的每日射精功能以近90%的受试者射精量减少和约35%的受试者射精为特征。坦索罗辛的这些射精障碍并非归因于射精逆行。相反,在阿夫唑嗪或安慰剂组的任何受试者中均未观察到射精。

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