Christiansen E, Guirguis W R, Cox D, Osterloh I H
Andrology Center, Oslo, Norway.
Int J Impot Res. 2000 Jun;12(3):177-82. doi: 10.1038/sj.ijir.3900527.
The long-term efficacy and safety of oral Viagra (sildenafil citrate), a selective phosphodiesterase 5 inhibitor, and the effect of withdrawing treatment were evaluated in men with erectile dysfunction (ED). In 233 men with ED of psychogenic or mixed organic/psychogenic aetiology, 16 weeks of open-label, flexible-dose sildenafil treatment (10-100 mg) was followed by eight weeks of double-blind, fixed-dose, randomised withdrawal to placebo or continued treatment with sildenafil. Sildenafil was taken as needed (not more than once daily) approximately 1 h prior to sexual activity. The main outcome measures were a global efficacy question, a sexual function questionnaire, an event log of erections, and adverse event recording. In the open-label phase, 200 of 216 patients (93%) reported improved erections with sildenafil; 28 patients (12%) discontinued treatment. In the double-blind phase, the significant improvements in the frequency and duration of erections were maintained in the sildenafil group but returned to pre-treatment values in patients on placebo (P values < 0.0001 versus placebo). The most frequent adverse events in the sildenafil group during the double-blind phase were flushing (7%), headache (6%), and dyspepsia (5%). Of the 192 patients enrolled in the 1-y extension, 90% completed the study; only two patients (1%) were withdrawn due to lack of efficacy. In men with ED of psychogenic or mixed aetiology, oral sildenafil is effective and well-tolerated both at the initiation of therapy and during long-term treatment. For most patients, sildenafil treatment must be continued for improvements in erectile function to be maintained.
对患有勃起功能障碍(ED)的男性,评估了口服万艾可(枸橼酸西地那非)这一选择性磷酸二酯酶5抑制剂的长期疗效和安全性,以及停药的影响。在233名患有心因性或混合性器质性/心因性病因的勃起功能障碍男性中,先进行了16周的开放标签、灵活剂量西地那非治疗(10 - 100毫克),随后是8周的双盲、固定剂量、随机停药至安慰剂组或继续用西地那非治疗。西地那非在性活动前约1小时按需服用(每日不超过1次)。主要结局指标包括一个总体疗效问题、一份性功能问卷、勃起事件记录以及不良事件记录。在开放标签阶段,216名患者中有200名(93%)报告使用西地那非后勃起功能改善;28名患者(12%)停止治疗。在双盲阶段,西地那非组勃起频率和持续时间仍有显著改善,但安慰剂组患者的这些指标恢复到治疗前水平(与安慰剂组相比,P值<0.0001)。双盲阶段西地那非组最常见的不良事件是潮红(7%)、头痛(6%)和消化不良(5%)。在参加1年延长期研究的192名患者中,90%完成了研究;只有2名患者(1%)因疗效不佳而退出。对于患有心因性或混合性病因勃起功能障碍的男性,口服西地那非在治疗开始时和长期治疗期间均有效且耐受性良好。对于大多数患者,必须持续使用西地那非治疗才能维持勃起功能的改善。