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采用自动注射器给予血管活性肠肽和甲磺酸酚妥拉明治疗对其他海绵体内药物耐药的勃起功能障碍患者。

Vasoactive intestinal polypeptide and phentolamine mesylate administered by autoinjector in the treatment of patients with erectile dysfunction resistant to other intracavernosal agents.

作者信息

Dinsmore W W, Alderdice D K

机构信息

Department of Genito-Urinary Medicine, Royal Victoria Hospital, Belfast, Northern Ireland, UK.

出版信息

Br J Urol. 1998 Mar;81(3):437-40. doi: 10.1046/j.1464-410x.1998.00564.x.

DOI:10.1046/j.1464-410x.1998.00564.x
PMID:9523666
Abstract

OBJECTIVE

To study the effect of vasoactive intestinal polypeptide (VIP) and phentolamine mesylate (PM) on patients in whom previous intracavernosal therapy had failed.

PATIENTS AND METHOD

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).

RESULT

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.

CONCLUSION

The combination of VIP and PM at the dose used was a safe and effective treatment in patients in whom other therapies had failed.

摘要

目的

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。

患者与方法

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)。

结果

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。

结论

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。

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