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α1肾上腺素能受体拮抗剂对男性性功能的影响。

Effects of alpha(1)-adrenoceptor antagonists on male sexual function.

作者信息

van Dijk Marleen M, de la Rosette Jean J M C H, Michel Martin C

机构信息

Department of Urology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Drugs. 2006;66(3):287-301. doi: 10.2165/00003495-200666030-00002.

Abstract

alpha(1)-Adrenoceptor antagonists such as alfuzosin, doxazosin, tamsulosin and terazosin are first-line agents for the treatment of lower urinary tract symptoms suggestive of benign prostatic hyperplasia (BPH), but are only second-line agents (doxazosin and terazosin only) for the treatment of arterial hypertension. Sexual function is complex and includes multiple domains such as sexual desire (libido), erectile function and ejaculatory function. Erectile and ejaculatory functions are frequently reduced in patients with BPH and can impact on their quality of life. Therefore, the treatment of BPH should aim to maintain or even restore sexual function.alpha(1)-Adrenoceptor antagonists lack major effects on sexual desire in placebo-controlled studies. Reports on erectile function are inconsistent, with both beneficial and adverse effects being reported, but impotence can occur in some patients without clear differences between drugs. Ejaculatory dysfunction during treatment may represent (relative) an ejaculation. It occurs more frequently with tamsulosin than with other drugs of this class, but the differences are not big enough to be consistently detectable in directly comparative studies. We propose that such differences between drugs should be weighed against differences in cardiovascular tolerability when choosing the optimal treatment for each patient.

摘要

α1-肾上腺素能受体拮抗剂,如阿夫唑嗪、多沙唑嗪、坦索罗辛和特拉唑嗪,是治疗提示良性前列腺增生(BPH)的下尿路症状的一线药物,但仅是治疗动脉高血压的二线药物(仅多沙唑嗪和特拉唑嗪)。性功能很复杂,包括多个方面,如性欲、勃起功能和射精功能。BPH患者的勃起和射精功能常常减退,这会影响他们的生活质量。因此,BPH的治疗应旨在维持甚至恢复性功能。在安慰剂对照研究中,α1-肾上腺素能受体拮抗剂对性欲缺乏主要影响。关于勃起功能的报道并不一致,既有有益作用也有不良反应的报道,但有些患者可能会出现阳痿,且不同药物之间无明显差异。治疗期间的射精功能障碍可能表现为(相对的)射精。坦索罗辛比该类其他药物更常出现这种情况,但差异不够大,在直接比较研究中无法始终检测到。我们建议,在为每位患者选择最佳治疗方案时,应将药物之间的这种差异与心血管耐受性差异进行权衡。

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