Chen Juza, Keren-Paz Gal, Bar-Yosef Yuval, Matzkin Haim
Department of Urology, Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Eur Urol. 2007 Nov;52(5):1331-9. doi: 10.1016/j.eururo.2007.08.005. Epub 2007 Aug 17.
To assess the usefulness of the phosphodiesterase type 5 inhibitors (PDE5-Is) in the treatment of premature ejaculation (PE) and to describe possible mechanisms to explain their effect.
A MedLine search was performed for peer-reviewed articles on the role of PDE5-Is in managing PE. No meta-analysis method was used.
Five manuscripts that examined the efficacy of PDE5-Is in the treatment of PE were retrieved. Three studies used sildenafil as monotherapy and two used it in combination with a serotonin selective reuptake inhibitor (SSRI). Three studies demonstrated a beneficial effect of sildenafil in the treatment of PE, as measured by intravaginal ejaculatory latency time (IELT) and by different questionnaires assessing the patients' subjective feelings of ejaculatory control, sexual satisfaction, and anxiety. One study showed the superiority of sildenafil compared to other modalities. Two studies showed that combination therapy of paroxetine and sildenafil was better than paroxetine alone. One study did not demonstrate a beneficial effect of sildenafil in prolonging IELT, but showed that sildenafil improved patients' perception of ejaculatory control. Another study showed that topical anesthetics were better than sildenafil in the treatment of PE but did not use IELT or a validated questionnaire to measure the efficacy of treatment. Several possible mechanisms could explain effectiveness of the PDE5-Is for treatment of PE: centrally, through the effect on the nitric oxide/cyclic guanosine monophosphate pathway; peripherally by causing relaxation of smooth muscle in the vas deferens, seminal vesicles, prostate, and urethra and inhibition of adrenergic transmission; or locally by inducing peripheral analgesia. Another possibility might be prolongation of the duration of erection.
Encouraging evidence supports the role of PDE5-Is for treating PE. Possible therapeutic mechanisms of action of PDE5-Is are multiple and complex and include central and peripheral effects. A large population, multicenter, randomized, double-blind, placebo-controlled study is needed to elucidate the efficacy of PDE5-Is in the treatment of PE.
评估5型磷酸二酯酶抑制剂(PDE5-Is)在治疗早泄(PE)中的有效性,并描述可能解释其作用的机制。
在MedLine上检索关于PDE5-Is在PE治疗中作用的同行评审文章。未使用荟萃分析方法。
检索到五篇研究PDE5-Is治疗PE疗效的手稿。三项研究使用西地那非作为单一疗法,两项研究将其与5-羟色胺选择性再摄取抑制剂(SSRI)联合使用。三项研究表明,以西地那非治疗PE有有益效果,通过阴道内射精潜伏期(IELT)以及评估患者射精控制主观感受、性满意度和焦虑的不同问卷来衡量。一项研究表明西地那非优于其他治疗方式。两项研究表明帕罗西汀与西地那非联合治疗优于单独使用帕罗西汀。一项研究未证明西地那非在延长IELT方面有有益效果,但表明西地那非改善了患者对射精控制的感知。另一项研究表明局部麻醉剂在PE治疗中优于西地那非,但未使用IELT或经过验证的问卷来衡量治疗效果。几种可能的机制可以解释PDE5-Is治疗PE的有效性:在中枢,通过对一氧化氮/环磷酸鸟苷途径的作用;在周围,通过引起输精管、精囊、前列腺和尿道平滑肌松弛以及抑制肾上腺素能传递;或在局部,通过诱导外周镇痛。另一种可能性可能是延长勃起持续时间。
有令人鼓舞的证据支持PDE5-Is在治疗PE中的作用。PDE5-Is可能的治疗作用机制是多样且复杂的,包括中枢和外周效应。需要进行大规模、多中心、随机、双盲、安慰剂对照研究以阐明PDE5-Is在PE治疗中的疗效。