首页> 外文OA文献 >Silodosin in the treatment of benign prostatic hyperplasia.
【2h】

Silodosin in the treatment of benign prostatic hyperplasia.

机译:西洛多辛治疗良性前列腺增生。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Benign prostatic hyperplasia (BPH)-associated lower urinary tract symptoms (LUTS) are highly prevalent in older men. Medical therapy is the first-line treatment for LUTS due to BPH. Alpha-adrenergic receptor blockers remain one of the mainstays in the treatment of male LUTS and clinical BPH. They exhibit early onset of efficacy with regard to both symptoms and flow rate improvement, and this is clearly demonstrated in placebo-controlled trials with extensions out to five years. These agents have been shown to prevent symptomatic progression of the disease. The aim of this article is to offer a critical review of the current literature on silodosin, formerly known as KMD-3213, a novel alpha-blocker with unprecedented selectivity for α(1A)-adrenergic receptors, as compared with both α(1B)- and α(1D) -adrenoceptors, exceeding the selectivity of all currently used α(1)-blockers, and with clinically promising effects.
机译:良性前列腺增生(BPH)相关的下尿路症状(LUTS)在老年男性中非常普遍。由于BPH,药物治疗是LUTS的一线治疗。 α-肾上腺素能受体阻滞剂仍然是治疗男性LUTS和临床BPH的主要手段之一。它们在症状和流速改善方面均显示出较早的功效,并且在延长至五年的安慰剂对照试验中清楚地证明了这一点。这些药物已显示可预防疾病的症状发展。本文的目的是对当前有关西洛多辛的文献(以前称为KMD-3213)进行批判性回顾,西洛多辛是一种新型的α-受体阻滞剂,与α(1B)和α(1B)相比,对α(1A)-肾上腺素受体具有前所未有的选择性-和α(1D)-肾上腺素能受体,超过了目前所有使用的α(1)-受体阻滞剂的选择性,并在临床上有希望的效果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号