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Monotherapy with tadalafil or tamsulosin similarly improved lower urinary tract symptoms suggestive of benign prostatic hyperplasia in an international, randomised, parallel, placebo-controlled clinical trial.在一项国际性、随机、平行、安慰剂对照的临床试验中,单用他达拉非或坦索罗辛同样改善了良性前列腺增生症的下尿路症状。
Eur Urol. 2012 May;61(5):917-25. doi: 10.1016/j.eururo.2012.01.013. Epub 2012 Jan 20.
2
Tadalafil 2.5 or 5 mg administered once daily for 12 weeks in men with both erectile dysfunction and signs and symptoms of benign prostatic hyperplasia: results of a randomized, placebo-controlled, double-blind study.他达拉非 2.5 或 5 毫克每日一次治疗 12 周治疗勃起功能障碍合并良性前列腺增生症状和体征的男性患者:一项随机、安慰剂对照、双盲研究的结果。
J Sex Med. 2012 Jan;9(1):271-81. doi: 10.1111/j.1743-6109.2011.02504.x. Epub 2011 Oct 7.
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Efficacy and safety of tadalafil once daily in the treatment of men with lower urinary tract symptoms suggestive of benign prostatic hyperplasia: results of an international randomized, double-blind, placebo-controlled trial.每日一次他达拉非治疗下尿路症状提示良性前列腺增生症男性患者的疗效和安全性:一项国际随机、双盲、安慰剂对照试验的结果。
Eur Urol. 2011 Nov;60(5):1105-13. doi: 10.1016/j.eururo.2011.08.005. Epub 2011 Aug 12.
4
Efficacy and safety of tadalafil 20 mg on demand vs. tadalafil 5 mg once-a-day in the treatment of post-radiotherapy erectile dysfunction in prostate cancer men: a randomized phase II trial.按需服用他达拉非 20 毫克与每日一次服用他达拉非 5 毫克治疗前列腺癌放疗后勃起功能障碍的疗效和安全性:一项随机 II 期试验。
J Sex Med. 2010 Aug;7(8):2851-9. doi: 10.1111/j.1743-6109.2010.01890.x.
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Endothelial apoptosis decrease following tadalafil administration in patients with arterial ED does not last after its discontinuation.他达拉非治疗动脉性 ED 患者后内皮细胞凋亡减少,停药后不会持续。
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Efficacy and safety of once-daily dosing of udenafil in the treatment of erectile dysfunction: results of a multicenter, randomized, double-blind, placebo-controlled trial.乌地那非每日 1 次治疗勃起功能障碍的疗效和安全性:多中心、随机、双盲、安慰剂对照试验的结果。
Eur Urol. 2011 Aug;60(2):380-7. doi: 10.1016/j.eururo.2011.03.025. Epub 2011 Apr 1.
7
Chronic administration of udenafil, a selective phosphodiesterase type 5 inhibitor, promotes erectile function recovery in an animal model of bilateral cavernous nerve crush injury.慢性给予乌地那非(一种选择性磷酸二酯酶 5 抑制剂)可促进海绵体神经挤压损伤动物模型的勃起功能恢复。
J Sex Med. 2011 May;8(5):1330-40. doi: 10.1111/j.1743-6109.2011.02228.x. Epub 2011 Mar 2.
8
Chronic vardenafil treatment improves erectile function via structural maintenance of penile corpora cavernosa in rats with acute arteriogenic erectile dysfunction.慢性伐地那非治疗通过维持急性动脉性勃起功能障碍大鼠海绵体结构改善勃起功能。
J Sex Med. 2011 Mar;8(3):705-11. doi: 10.1111/j.1743-6109.2010.02153.x. Epub 2010 Dec 8.
9
Onset of efficacy of tadalafil once daily in men with erectile dysfunction: a randomized, double-blind, placebo controlled trial.每日一次他达拉非治疗男性勃起功能障碍的疗效发作:一项随机、双盲、安慰剂对照试验。
J Urol. 2011 Jan;185(1):243-8. doi: 10.1016/j.juro.2010.09.035. Epub 2010 Nov 13.
10
Efficacy and Safety of Tadalafil 5 mg Administered Once Daily in Korean Men with Erectile Dysfunction: A Prospective, Multicenter Study.他达拉非5毫克每日一次给药对韩国勃起功能障碍男性的疗效和安全性:一项前瞻性多中心研究。
Korean J Urol. 2010 Sep;51(9):647-52. doi: 10.4111/kju.2010.51.9.647. Epub 2010 Sep 17.

慢性低剂量使用5型磷酸二酯酶抑制剂治疗勃起功能障碍。

Chronic low dosing of phosphodiesterase type 5 inhibitor for erectile dysfunction.

作者信息

Sung Hyun Hwan, Lee Sung Won

机构信息

Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Korean J Urol. 2012 Jun;53(6):377-85. doi: 10.4111/kju.2012.53.6.377. Epub 2012 Jun 19.

DOI:10.4111/kju.2012.53.6.377
PMID:22741044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3382685/
Abstract

Oral phosphodiesterase type 5 (PDE5) inhibitors have provided non-invasive, effective, and well-tolerated treatments for patients with erectile dysfunction (ED). However, many patients with ED are unresponsive to 'on-demand' PDE5 inhibitors. In addition, the lack of spontaneity and naturalness of the on-demand regimen could be a reason for decreased compliance with PDE5 inhibitors. Recently, tadalafil and udenafil were approved for low-dose daily administration for the treatment of ED. Since the introduction of the concept of daily administration of PDE5 inhibitors, several reports have supported the potential benefits of this therapy for disease modification, improvement of the treatment response in difficult-to-treat populations, spontaneity, and safety, although further research is needed to better address these hypotheses. In this article, we reviewed the daily administration of PDE5 inhibitors in terms of pharmacokinetics, safety, efficacy, and distinct features.

摘要

口服5型磷酸二酯酶(PDE5)抑制剂为勃起功能障碍(ED)患者提供了非侵入性、有效且耐受性良好的治疗方法。然而,许多ED患者对“按需服用”的PDE5抑制剂无反应。此外,按需治疗方案缺乏自发性和自然性可能是导致PDE5抑制剂依从性降低的一个原因。最近,他达拉非和伐地那非被批准用于低剂量每日给药治疗ED。自从引入PDE5抑制剂每日给药的概念以来,尽管需要进一步研究以更好地验证这些假设,但已有几份报告支持了这种治疗方法在疾病改善、改善难治性人群的治疗反应、自发性和安全性方面的潜在益处。在本文中,我们从药代动力学、安全性、疗效和独特特征方面对PDE5抑制剂的每日给药进行了综述。