Sexual and Reproductive Medicine Program, Urology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
Sexual and Reproductive Medicine Program, Urology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
J Sex Med. 2019 Oct;16(10):1541-1546. doi: 10.1016/j.jsxm.2019.07.013. Epub 2019 Aug 20.
There exists little literature on the outcomes of the medical management of men with erectile dysfunction (ED) with no overt organic etiology.
This study was conducted to assess the outcomes of men with nonorganic ED treated medically.
All patients had normal hormone profiles and vascular assessment. All were given a trial of a phosphodiesterase type 5 inhibitor (PDE5i). If no improvement was experienced, intracavernosal injection (ICI) therapy was administered. All patients were encouraged to seek a consultation with a mental health professional.
Patient demographics, medical comorbidities, hormone and hemodynamics assessments, and change in International Index of Erectile Function scores of patients were recorded.
116 men with a mean age or 38 ± 19 (range 16-57) years were studied. 21% had mild ED, 47% had moderate ED, and 32% had severe ED. 21% had seen a psychiatrist. 81% of patients responded to PDE5i with a penetration hardness erection on follow-up (mean duration of 7 ± 3 months postcommencement of PDE5i). However, only 68% of these were capable of a consistently good response. The mean Erectile Function domain score on PDE5i for the entire group improved from 18 ± 11 to 22 ± 6 (P = .01), and for PDE5i responders it was 27 ± 4 (P < .001). 28% of men (22 PDE5i failures and 10 with a mixed response to PDE5i) attempted ICI, all obtaining consistently functional erections. At a mean time point of 11 ± 5 months, 83% of those responding to PDE5i had ceased using PDE5i due to a lack of need. 11% of those using ICI continued to use them 6 months after starting ICI; the remainder had been transitioned back to PDE5i. Of the 29 patients in the latter subgroup, 66% were no longer using PDE5i consistently due to a lack of need.
Not all men with nonorganic ED respond to PDE5i initially and many of those who respond do so only intermittently; such patients are potentially curable, using erectogenic pharmacotherapy for erectile confidence restoration, most men are capable of being weaned from drug therapy.
STRENGTHS & LIMITATIONS: The strengths of the study are the large number of patients and the use of serial validated instruments to assess erectile function outcomes. As a weakness, despite normal hormone and vascular assessments, the diagnosis of nonorganic ED is still a presumptive one.
Medical management of nonorganic ED utilizing the process of care model results in cure in a large proportion of such patients. The transient use of ICI in some patients permits successful PDE5i rechallenge. Jenkins LC, Hall M, Deveci S, et al. An Evaluation of a Clinical Care Pathway for the Management of Men With Nonorganic Erectile Dysfunction. J Sex Med 2019;16:1541-1546.
关于没有明显器质性病因的勃起功能障碍(ED)男性的医学管理结果,文献记载甚少。
本研究旨在评估非器质性 ED 男性的医学治疗结果。
所有患者的激素水平和血管评估均正常。所有患者均接受了磷酸二酯酶 5 抑制剂(PDE5i)治疗试验。如果没有改善,则给予阴茎海绵体内注射(ICI)治疗。所有患者均被鼓励咨询心理健康专家。
记录患者的人口统计学特征、合并症、激素和血液动力学评估以及国际勃起功能指数评分的变化。
共研究了 116 名平均年龄为 38±19 岁(16-57 岁)的男性。21%的患者有轻度 ED,47%的患者有中度 ED,32%的患者有重度 ED。21%的患者看过心理医生。81%的患者在接受 PDE5i 治疗后(平均开始 PDE5i 治疗后 7±3 个月)勃起硬度有所改善。然而,只有 68%的患者能够持续获得良好的反应。整个组的 PDE5i 勃起功能域评分从 18±11 提高到 22±6(P=0.01),PDE5i 应答者的评分提高到 27±4(P<0.001)。28%的男性(22 名 PDE5i 失败者和 10 名 PDE5i 反应混合者)尝试了 ICI,均获得了持续的功能勃起。在平均 11±5 个月的时间点,83%对 PDE5i 有反应的患者由于不再需要而停止使用 PDE5i。开始 ICI 后 6 个月,继续使用 ICI 的有 11%;其余患者已转回 PDE5i。在后者亚组的 29 名患者中,由于不再需要,66%的患者不再持续使用 PDE5i。
并非所有非器质性 ED 患者最初都对 PDE5i 有反应,而且许多有反应的患者只是间歇性反应;这种情况下,使用勃起功能药物治疗来恢复勃起信心,可以治愈,大多数男性能够停药。
该研究的优势在于患者数量多,以及使用一系列经过验证的工具来评估勃起功能结果。不足之处在于,尽管进行了激素和血管评估,但非器质性 ED 的诊断仍然是一种推测。
利用医疗管理流程对非器质性 ED 进行医学管理,可使大多数患者获得治愈。一些患者暂用 ICI,可成功重新挑战 PDE5i。