Dinsmore W W, Alderdice D K
Department of Genito-Urinary Medicine, Royal Victoria Hospital, Belfast, Northern Ireland, UK.
Br J Urol. 1998 Mar;81(3):437-40. doi: 10.1046/j.1464-410x.1998.00564.x.
To study the effect of vasoactive intestinal polypeptide (VIP) and phentolamine mesylate (PM) on patients in whom previous intracavernosal therapy had failed.
The study comprised 70 consecutive patients attending a clinic for erectile dysfunction, in whom previous therapy with intracavernosal prostaglandin-E1 (20 microg and papaverine (30 mg) combined with 1 mg PM had failed. They were given intracavernosal injections, initially with 25 microg VIP/1 mg PM (VIP1) and if unsuccessful, 25 microg VIP/2 mg PM (VIP2). Both VIP1 and VIP2 were administered using a pre-filled ready-to-use autoinjector fitted with a 29 G needle. The patients were diagnosed as having spinal cord lesion (eight), diabetes (21), ischaemic heart disease (12), hypertension (six), other diagnoses (nine), or idiopathic causes (14).
Forty-seven (67%) of patients achieved erections sufficient for sexual intercourse (33 on VIP1 and 14 on VIP2), initially under clinical supervision and subsequently during home use. Minor side-effects were transient facial flushing in 37 (53%), truncal flushing in six (9%), bruising in 14 (20%) and pain from the injection needle in eight (11%). No patients reported priapism or other serious adverse events.
The combination of VIP and PM at the dose used was a safe and effective treatment in patients in whom other therapies had failed.
研究血管活性肠肽(VIP)和甲磺酸酚妥拉明(PM)对既往海绵体内注射治疗无效患者的疗效。
本研究纳入了70例连续就诊于勃起功能障碍门诊的患者,他们既往接受海绵体内注射前列腺素E1(20微克)和罂粟碱(30毫克)联合1毫克PM治疗均失败。给予他们海绵体内注射,初始剂量为25微克VIP/1毫克PM(VIP1),若无效则给予25微克VIP/2毫克PM(VIP2)。VIP1和VIP2均使用预装即用型自动注射器并配备29G针头进行给药。患者的诊断包括脊髓损伤(8例)、糖尿病(21例)、缺血性心脏病(12例)、高血压(6例)、其他诊断(9例)或特发性病因(14例)。
47例(67%)患者实现了足以进行性交的勃起(33例在VIP1治疗后,14例在VIP2治疗后),最初在临床监督下,随后在家中使用期间。轻微副作用包括37例(53%)出现短暂面部潮红、6例(9%)出现躯干潮红、14例(20%)出现瘀斑以及8例(11%)出现注射针疼痛。没有患者报告阴茎异常勃起或其他严重不良事件。
所使用剂量的VIP和PM联合治疗对其他治疗失败的患者是一种安全有效的治疗方法。