Allen R P, Engel R M, Smolev J K, Brendler C B
Department of Urology, Johns Hopkins Hospital, Baltimore, Maryland.
J Urol. 1992 Oct;148(4):1181-3. doi: 10.1016/s0022-5347(17)36853-2.
We performed a double-blind, crossover study using objective measurements to compare maximum rigidity and duration of erections with papaverine hydrochloride in combination with phentolamine mesylate and/or prostaglandin E1. The rationale for the protocol was to combine a smooth muscle relaxant (papaverine) with either or both vasodilating agents (phentolamine and prostaglandin E1) commonly used for injection therapy. The 7 volunteer patients with organic impotence documented by abnormal nocturnal penile tumescence testing were injected with 0.5 to 1.0 ml. papaverine (30 mg./ml.) in combination with phentolamine (0.5 mg./ml.) and/or prostaglandin E1 (5 micrograms./ml.). Each patient received 2 injections on each of 2 testing dates; injection 2 was given after tumescence resulting from injection 1 had subsided completely. The medications were given in a randomized, counterbalanced order following double-blind procedures. Patients evaluated the erections subjectively. In addition, the RigiScan device was used to measure maximum rigidity and duration of erections. All patients observed increased duration of erections with both combinations containing prostaglandin E1. Analysis of RigiScan measurements showed no statistically significant differences for maximum rigidity (p greater than 0.1) but significantly greater duration of erections with papaverine plus prostaglandin E1, and papaverine plus phentolamine plus prostaglandin E1 compared to papaverine plus phentolamine (p less than 0.001). There was no statistical difference in rigidity or duration of erections between papaverine plus prostaglandin E1 and papaverine plus phentolamine plus prostaglandin E1. No patient reported significant penile pain with any of the injections. We conclude that the combination of papaverine and prostaglandin E1 produces erections of longer duration than papaverine plus phentolamine and that no additional benefit is gained by adding phentolamine to a combination of papaverine and prostaglandin E1. Further studies are in progress to define optimal dose response curves for papaverine and prostaglandin E1 as individual agents and in combination.
我们进行了一项双盲交叉研究,采用客观测量方法,比较盐酸罂粟碱联合甲磺酸酚妥拉明和/或前列腺素E1后勃起的最大硬度和持续时间。该方案的基本原理是将平滑肌松弛剂(罂粟碱)与通常用于注射治疗的一种或两种血管扩张剂(酚妥拉明和前列腺素E1)联合使用。7例经夜间阴茎勃起功能测试异常确诊为器质性阳痿的志愿者患者,注射了0.5至1.0毫升罂粟碱(30毫克/毫升)联合酚妥拉明(0.5毫克/毫升)和/或前列腺素E1(5微克/毫升)。每位患者在2个测试日中的每一天都接受2次注射;在第1次注射引起的勃起完全消退后进行第2次注射。按照双盲程序,药物以随机、平衡的顺序给药。患者对勃起进行主观评估。此外,使用RigiScan设备测量勃起的最大硬度和持续时间。所有患者观察到,含前列腺素E1的两种联合用药方案均使勃起持续时间增加。RigiScan测量分析显示,最大硬度无统计学显著差异(p大于0.1),但与罂粟碱加酚妥拉明相比,罂粟碱加前列腺素E1以及罂粟碱加酚妥拉明加前列腺素E1的勃起持续时间显著更长(p小于0.001)。罂粟碱加前列腺素E1与罂粟碱加酚妥拉明加前列腺素E1之间,勃起的硬度和持续时间无统计学差异。没有患者报告任何一次注射后出现明显的阴茎疼痛。我们得出结论,罂粟碱与前列腺素E1联合用药产生的勃起持续时间比罂粟碱加酚妥拉明更长,并且在罂粟碱与前列腺素E1联合用药中添加酚妥拉明不会带来额外益处。目前正在进行进一步研究,以确定罂粟碱和前列腺素E1单独使用及联合使用时的最佳剂量反应曲线。