McMahon Chris G
Australian Centre for Sexual Health, Sydney, NSW, Australia.
Sex Med Rev. 2015 Jul;3(3):183-202. doi: 10.1002/smrj.49. Epub 2015 Oct 8.
Over the past 20-30 years, the premature ejaculation (PE) treatment paradigm, previously limited to behavioral psychotherapy, has expanded to include drug treatment. Pharmacotherapy for PE predominantly targets the multiple neurotransmitters and receptors involved in the control of ejaculation, which include serotonin, dopamine, oxytocin, norepinephrine, gamma amino-butyric acid (GABA) and nitric oxide (NO).
The objective of this article is to review current and emerging PE interventions.
Contemporary data on the treatment of PE were reviewed and critiqued using the principles of evidence-based medicine.
Integrated pharmacotherapy and cognitive behavioral therapy (CBT) may achieve superior treatment outcomes in some patients. Phosphodiesterase type 5 inhibitors alone or in combination with selective serotonin reuptake inhibitors (SSRIs) should be limited to men with acquired PE secondary to comorbid erectile dysfunction (ED). New on-demand rapid-acting SSRIs, oxytocin receptor antagonists, or single agents that target multiple receptors may form the foundation of more effective future on-demand medication.
Multiple well-controlled evidence-based studies have demonstrated the efficacy and safety of SSRIs in delaying ejaculation, confirming their role as first-line agents for the medical treatment of lifelong and acquired PE. Daily dosing of SSRIs is likely to be associated with superior fold increases in intravaginal ejaculation latency time compared with on-demand SSRIs. On-demand SSRIs are less effective but may fulfill the treatment goals of many patients.
Current evidence suggests that psychosexual CBT has a limited role in the contemporary management of PE and confirms the efficacy and safety of dapoxetine, off-label SSRI drugs, and topical anesthetics drugs. Treatment with tramadol, α1-adrenoceptor antagonists cannot be recommended until the results of large, well-designed randomized controlled trials are published in major international peer-reviewed medical journals. As our understanding of the neurochemical control of ejaculation improves, new therapeutic targets and candidate molecules will be identified, which may increase our pharmacotherepeutic armamentarium. McMahon CG. Current and emerging treatments for premature ejaculation. Sex Med Rev 2015;3:183-202.
在过去20至30年中,早泄(PE)的治疗模式已从先前仅限于行为心理治疗扩展到包括药物治疗。PE的药物治疗主要针对参与射精控制的多种神经递质和受体,其中包括5-羟色胺、多巴胺、催产素、去甲肾上腺素、γ-氨基丁酸(GABA)和一氧化氮(NO)。
本文的目的是综述当前和新兴的PE干预措施。
使用循证医学原则对有关PE治疗的当代数据进行综述和评判。
综合药物治疗和认知行为疗法(CBT)在某些患者中可能取得更好的治疗效果。5型磷酸二酯酶抑制剂单独使用或与选择性5-羟色胺再摄取抑制剂(SSRI)联合使用应限于继发于合并勃起功能障碍(ED)的获得性PE患者。新型按需速效SSRI、催产素受体拮抗剂或靶向多种受体的单一药物可能成为未来更有效按需用药的基础。
多项严格对照的循证研究已证明SSRI在延迟射精方面的有效性和安全性,证实了它们作为治疗终身性和获得性PE的一线药物的作用。与按需服用SSRI相比,每日服用SSRI可能会使阴道内射精潜伏期时间有更高倍数的增加。按需服用SSRI效果较差,但可能实现许多患者的治疗目标。
当前证据表明,性心理CBT在当代PE管理中的作用有限,并证实了达泊西汀、非标签SSRI药物和局部麻醉药物的有效性和安全性。在大型、设计良好的随机对照试验结果在主要国际同行评审医学期刊上发表之前,不建议使用曲马多、α1-肾上腺素能受体拮抗剂进行治疗。随着我们对射精神经化学控制的理解不断提高,将确定新的治疗靶点和候选分子,这可能会增加我们的药物治疗手段。麦克马洪CG。早泄的当前和新兴治疗方法。性医学评论2015;3:183-202。