Passavanti Giandomenico, Bragaglia Alessandro, Paolini Riccardo
Department of Urology Misericordia Hospital, Grosseto, Italy.
Arch Ital Urol Androl. 2009 Dec;81(4):242-4.
The better knowledge concerning the anatomo-physiology of erection has brought important changes to the management of priapism. We experimented with a staged therapeutic protocol forthis condition.
17 patients, aged from 27 to 71 (mean age 43) were treated for ischemic priapism; the pathogenesis was idiopathic in 9 cases, in 4 cases secondary to intracavernous injection (IcI) of PGE1, in 2 cases to papaverine Icd, in 1 case to haemolympho-pathy and in another patient to treatement with heparin. Cavernous PO2, PCO2 and pH were checked. All patients underwent removal of 100 cc of blood, irrigation with NaHCO3 solution of the cavernous corpora and Methylen blue (MB) IcI 10 mg every 5 minutes 10 times, repeated twice.
From 3 to 6 hours from the beginning of therapy, detumescence was achieved in 10 cases. In 5 cases the priapism persisted and we administered adrenaline 20 pg every 5-10 minutes: 2 cases had detumescence respectively in 5 and 7 hours whereas in the patient with leukaemia the erection persisted and we desisted from further therapy; in 2 other cases the erection persisted and we did a distal cavernosum-glans shunt and the detumescence a was achieved in 30 and 58 hours respectively. In the last 2 cases, before adrenaline we administered an IcI of ethylephrine 5 mg every 5 minutes for 4-5 times but finally we had to perform a shunt. In all cases, during the treatment, and during the following 6-8 hours, we administered 200 mg of MB intravenous.
The introduction of oral drugs has changed the epidemiology of priapism. A better knowledge of the molecular mechanisms that govern the cavernous contraction and myorelaxation has allowed us to use adrenergic drugs and also the MB. This staged therapeutic protocol goes from a less invasive therapy (irrigation with NaHCO3, MB, ethylephrine, adrenaline) to a surgical procedure which must not be delayed and this progression could allow a reduction in the collateral effects.
对勃起的解剖生理学有了更深入的了解,这给阴茎异常勃起的治疗带来了重要变化。我们针对这种情况试验了一种分阶段治疗方案。
17例年龄在27至71岁(平均年龄43岁)的患者接受了缺血性阴茎异常勃起的治疗;9例病因不明,4例继发于海绵体内注射前列腺素E1(IcI),2例继发于海绵体内注射罂粟碱,1例继发于血液系统疾病,另1例继发于肝素治疗。检查了海绵体内的氧分压(PO2)、二氧化碳分压(PCO2)和pH值。所有患者均抽取100毫升血液,用碳酸氢钠溶液冲洗海绵体,并每5分钟进行一次10毫克亚甲蓝(MB)的海绵体内注射,共注射10次,重复两次。
治疗开始后3至6小时,10例患者阴茎消肿。5例患者阴茎异常勃起持续存在,我们每5至10分钟给予20微克肾上腺素:2例分别在5小时和7小时消肿,而白血病患者的勃起持续存在,我们停止了进一步治疗;另外2例患者的勃起持续存在,我们进行了远端海绵体-龟头分流术,分别在30小时和58小时消肿。在最后2例患者中,在使用肾上腺素之前,我们每5分钟进行一次5毫克乙基肾上腺素的海绵体内注射,共注射4至5次,但最终我们不得不进行分流术。在所有病例中,治疗期间及之后的6至8小时内,我们静脉注射了200毫克亚甲蓝。
口服药物的出现改变了阴茎异常勃起的流行病学。对控制海绵体收缩和舒张的分子机制有了更好的了解,使我们能够使用肾上腺素能药物以及亚甲蓝。这种分阶段治疗方案从侵入性较小的治疗(用碳酸氢钠、亚甲蓝、乙基肾上腺素、肾上腺素冲洗)过渡到不得延迟的外科手术,这种进展可能会减少副作用。