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治疗勃起功能障碍的局部用药和口服药物。

Topical and oral agents for erectile dysfunction.

作者信息

Lue T F

机构信息

Department of Urology, University of California, San Francisco 94143-0738, USA.

出版信息

J Formos Med Assoc. 1999 Apr;98(4):233-41.

PMID:10389366
Abstract

Innovative research in the past 2 decades has shown that the hemodynamics of penile erection involve arterial dilation, sinusoidal expansion, and venous compression. Relaxation of the intracorporeal smooth muscles (trabecular and arteriolar) seems to be the final common pathway that leads to the above events. Neuropharmacologic studies have also established nitric oxide as the principal neurotransmitter for penile erection and confirmed the importance of cyclic adenosine monophosphate and cyclic guanosine monophosphate systems in penile smooth muscle relaxation. Recent years have also witnessed dramatic changes in the therapy of erectile dysfunction. The penile prosthesis, a gold standard of therapy of the 1970s, was replaced in the 1980s by the intracavernous injection and the vacuum constriction device. In the 1990s, two revolutionary concepts in erectile dysfunction therapy were added: transurethral alprostadil and oral sildenafil. However, the tremendous publicity surrounding the recent introduction of sildenafil has also created socioeconomic and ethical dilemmas, especially with regard to insurance coverage and government regulation. Medically, many problems also surfaced when large numbers of erectile dysfunction patients overwhelmed primary care physicians who were unfamiliar with the diagnosis and treatment of erectile dysfunction. This article reviews the advances in penile physiology and the clinical usefulness of topical and oral agents. In addition, a patients' goal-directed approach to the diagnosis and treatment of erectile dysfunction is presented.

摘要

过去20年的创新性研究表明,阴茎勃起的血流动力学涉及动脉扩张、海绵体窦扩张和静脉受压。体内平滑肌(小梁肌和小动脉)的松弛似乎是导致上述事件的最终共同途径。神经药理学研究也已确定一氧化氮是阴茎勃起的主要神经递质,并证实了环磷酸腺苷和环磷酸鸟苷系统在阴茎平滑肌松弛中的重要性。近年来,勃起功能障碍的治疗也发生了巨大变化。阴茎假体曾是20世纪70年代治疗的金标准,在20世纪80年代被海绵体内注射和真空紧缩装置所取代。在20世纪90年代,勃起功能障碍治疗中又增加了两个革命性概念:经尿道前列地尔和口服西地那非。然而,最近西地那非上市后的大量宣传也引发了社会经济和伦理困境,尤其是在保险覆盖范围和政府监管方面。在医学上,当大量勃起功能障碍患者让不熟悉勃起功能障碍诊断和治疗的初级保健医生应接不暇时,许多问题也浮出水面。本文综述了阴茎生理学的进展以及局部用药和口服药物的临床应用。此外,还介绍了一种以患者为导向的勃起功能障碍诊断和治疗方法。

相似文献

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Topical and oral agents for erectile dysfunction.治疗勃起功能障碍的局部用药和口服药物。
J Formos Med Assoc. 1999 Apr;98(4):233-41.
2
Switching from intracavernous prostaglandin E1 injections to oral sildenafil citrate in patients with erectile dysfunction: results of a multicenter European study. The Sildenafil Multicenter Study Group.勃起功能障碍患者从海绵体内注射前列腺素E1转换为口服枸橼酸西地那非:一项欧洲多中心研究的结果。西地那非多中心研究组
J Urol. 2000 Sep;164(3 Pt 1):708-11. doi: 10.1097/00005392-200009010-00021.
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Overview of phosphodiesterase 5 inhibition in erectile dysfunction.勃起功能障碍中磷酸二酯酶5抑制的概述。
Am J Cardiol. 2003 Nov 6;92(9A):9M-18M. doi: 10.1016/s0002-9149(03)00824-5.
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Sildenafil, a novel effective oral therapy for male erectile dysfunction.西地那非,一种治疗男性勃起功能障碍的新型有效口服疗法。
Br J Urol. 1996 Aug;78(2):257-61. doi: 10.1046/j.1464-410x.1996.10220.x.
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Mechanisms of action of PDE5 inhibition in erectile dysfunction.磷酸二酯酶5抑制剂治疗勃起功能障碍的作用机制。
Int J Impot Res. 2004 Jun;16 Suppl 1:S4-7. doi: 10.1038/sj.ijir.3901205.
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Sildenafil: medical advance or media event?西地那非:医学进步还是媒体炒作?
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Sildenafil: an orally active type 5 cyclic GMP-specific phosphodiesterase inhibitor for the treatment of penile erectile dysfunction.西地那非:一种口服活性的5型环磷酸鸟苷特异性磷酸二酯酶抑制剂,用于治疗阴茎勃起功能障碍。
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Sildenafil citrate for the management of antidepressant-associated erectile dysfunction.
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Effectiveness of sildenafil citrate (Viagra) and tadalafil (Cialis) on sexual responses in Saudi men with erectile dysfunction in routine clinical practice.枸橼酸西地那非(万艾可)和他达拉非(希爱力)在沙特勃起功能障碍男性常规临床实践中对性反应的疗效。
Pak J Pharm Sci. 2008 Jul;21(3):275-81.
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Commentary on apomorphine versus sildenafil for erectile dysfunction.阿扑吗啡与西地那非治疗勃起功能障碍的述评
J Urol. 2008 May;179(5 Suppl):S95-6. doi: 10.1016/j.juro.2008.03.002.

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