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Indications and early results of sildenafil (Viagra) in erectile dysfunction.

机译:西地那非(伟哥)勃起功能障碍的适应症和早期结果。

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OBJECTIVES: To assess the acceptability, feasibility, and early results of sildenafil (Viagra) in a nonselected cohort of 316 patients (median age 58 years) who sought treatment for male sexual dysfunction during a 10-week period. METHODS: Erectile status and activity were evaluated by questionnaire; erectile function was assessed by pharmacologic testing and visual sexual stimulation. Cardiovascular contraindications were assessed. Patients selected for the trial received treatment for 2 months. Results based on the possibility of penetration and individual satisfaction (scale from 0 to 10) were classified as good, fair, or bad. Multifactorial analysis was performed to define factors influencing the response to sildenafil. RESULTS: Twenty-five percent of the patients from the initial cohort refused or did not meet the criteria for oral treatment; 25% of the remaining had a cardiovascular contraindication. At the end of the trial, 157 patients (88.7%) had completed the study; the efficacy of and satisfaction with sildenafil were considered good for 50 (31.84%), fair for 46 (29.29%), and bad for 61 (38.85%). Spontaneous nocturnal erections, organic etiologies, especially cavernovenous impotence, and previous treatment with self-intracavernous injections were significant factors influencing responses to oral treatment. Finally, 32% of the patients after completing the trial (17.2% of the initial cohort) were using sildenafil as their sole treatment, 34% chose self-intracavernous injections, and 25% decided to alternate between oral and local therapy. CONCLUSIONS: In the present study, sildenafil had a 60% efficacy rate and was chosen as the sole treatment by only 30% of the patients tested. We propose pretreatment tests to help to predict the response to this medication.
机译:目的:评估西地那非(Viagra)在非选择队列中的316名患者(中位年龄58岁)在10周内寻求男性性功能障碍的治疗的可接受性,可行性和早期结果。方法:通过问卷评估勃起状态和活动。通过药理测试和视觉性刺激评估勃起功能。评估了心血管禁忌症。选择参加试验的患者接受了2个月的治疗。根据渗透率和个人满意度(范围从0到10)的结果分为好,中或坏。进行多因素分析以定义影响对西地那非反应的因素。结果:最初队列中25%的患者拒绝或不符合口服治疗标准;其余的25%有心血管禁忌症。在试验结束时,有157名患者(88.7%)完成了研究;西地那非的疗效和满意度被认为是良好(50(31.84%),中等(46)(29.29%),不良(61)(38.85%)。夜间自发性勃起,器质性病因,尤其是海绵状阳imp,以及先前自体海绵体注射的治疗是影响口服治疗反应的重要因素。最后,完成试验的患者中有32%(最初队列的17.2%)使用西地那非作为唯一治疗药物,有34%的患者选择了自腹腔注射,另有25%的患者选择了口服和局部治疗。结论:在本研究中,西地那非的疗效率为60%,仅30%的受试患者被选为唯一的治疗方法。我们建议进行预处理测试,以帮助预测对该药物的反应。

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