Service d'urologie, Hôpital Carémeau, Nîmes, France.
J Sex Med. 2013 Jul;10(7):1850-60. doi: 10.1111/jsm.12186. Epub 2013 May 16.
Phosphodiesterase type 5 inhibitors (PDE5is) as oral treatment for erectile dysfunction (ED) facilitate the management of ED in primary care. Still, compliance is low and general practitioners (GPs) do not always feel confident with this pathology. AIM.: The aim of this paper is to evaluate the impact of a first treatment with PDE5i on the patient and his partner and the management of ED by GPs.
The Evaluation après traitement de la dyfonction erectile, du bien-êtré émotionnel d'un patient en fonction de la rigidité de son érection survey was a longitudinal, observational French study with prospective collection of data from the GP, the patient, and his partner at baseline and after 3 months of treatment. GPs benefited from a short educational session before starting the survey.
The main outcome measures are the Erection Hardness Score (EHS), Self-Esteem and Relationship (SEAR) questionnaire, Index of Sexual Life (ISL), and Erectile Dysfunction Inventory of Treatment Satisfaction.
A total of 478 men aged 19-80 years (mean 57 years) were included in the survey by 229 GPs. Before treatment, EHS was mostly grade 1 (28%) or 2 (44%). At the end of the survey, an improvement was reported for 88% of the patients and 58% achieved maximum score EHS 4 (penis completely hard and fully rigid). Mean SEAR scores significantly increased after 3 months for self-esteem, overall and sexual relationship, and more notably with greater improvement in EHS (P < 0.001). Improvement in partners' ISL scores was significantly higher with greater improvement in EHS (P < 0.001) and in SEAR score for self-esteem. The safety profile of PDE5i was good with few adverse events, mostly headaches. More than 80% of the participating GPs considered that the survey had changed their management of ED.
After 3 months of treatment with PDE5i, a significant improvement in self-esteem was observed in patients with ED, associated with improvement in erection.
磷酸二酯酶 5 抑制剂(PDE5i)作为治疗勃起功能障碍(ED)的口服药物,便于初级保健医生对 ED 进行管理。尽管如此,患者的依从性仍然较低,全科医生(GP)对此类疾病也并不总是有信心。目的:本文旨在评估首次使用 PDE5i 对患者及其伴侣的影响,以及 GP 对 ED 的管理。
该研究是一项纵向、观察性的法国研究,通过 GP、患者及其伴侣在基线和治疗 3 个月时前瞻性地收集数据,评估勃起功能治疗后患者及其伴侣的幸福感。在开始调查前,GP 接受了简短的教育课程。主要观察指标:主要观察指标是勃起硬度评分(EHS)、自尊和关系(SEAR)问卷、性生活指数(ISL)和治疗满意度勃起功能障碍问卷。
共纳入 229 名 GP 治疗的 478 名 19-80 岁(平均 57 岁)男性患者。治疗前,EHS 主要为 1 级(28%)或 2 级(44%)。在调查结束时,88%的患者报告症状改善,58%的患者达到最大 EHS 评分 4 级(阴茎完全坚硬且完全刚性)。3 个月后,自尊、整体和性关系的 SEAR 评分显著提高,EHS 改善程度越大,评分提高越显著(P<0.001)。EHS 改善程度越大,伴侣的 ISL 评分改善越显著(P<0.001),SEAR 评分中自尊得分提高越显著。PDE5i 的安全性良好,不良事件少,主要为头痛。超过 80%的参与 GP 认为该调查改变了他们对 ED 的管理。
在使用 PDE5i 治疗 3 个月后,ED 患者的自尊显著提高,与勃起改善相关。