Department of Urology, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Department of Pediatric Urology, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, 6 Weizmann St., Tel-Aviv 6423906, Israel.
J Pediatr Surg. 2022 Nov;57(11):676-680. doi: 10.1016/j.jpedsurg.2022.06.021. Epub 2022 Jul 11.
To present the results of hypospadias repair in the absence of preputial skin following neonatal circumcision, and the analyses of surgical techniques and predictors of procedural success.
Records of all children who underwent hypospadias repair between 10/1999 and 12/2018 were retrospectively reviewed. All of those who underwent neonatal circumcision prior to surgery were included. Patients with any prior penile reconstruction surgery and those with the megameatus intact prepuce variant were excluded. The primary endpoint was the need for reoperation.
A total of 69 patients with a history of neonatal circumcision underwent surgical reconstruction of hypospadias during the study period. Their mean age at surgery was 14 months (interquartile range [IQR] 9,22). Forty-five cases (65%) involved distal hypospadias, and ventral curvature was present in 24 (35%). Dartos flaps were harvested from the dorsal aspect in 37/58 (64%) patients and from the ventral aspect in 21/58 (36%). Twenty-two patients (22/69, 32%) required reoperation after a median follow-up of 9 years (IQR 6,13). Indications for revision surgery included urethral fistula (n = 16, 22%), meatal stenosis (n = 5, 7%), and skin redundancy (n = 1). Ventral curvature (odds ratio [OR] 3.5, p = 0.02) and higher grades of hypospadias. (OR 3.3, p = 0.03) had a higher probability of reoperation (univariate logistic regression).
Hypospadias repair following neonatal circumcision in the absence of preputial skin is a challenging reconstruction. The reoperation rate in our cohort was 30%, similar to reoperative hypospadias surgery. Parents of newborns diagnosed with hypospadias should be encouraged to refrain from pre surgical neonatal circumcision.
Treatment study, level IV.
介绍新生儿包皮环切术后缺乏包皮皮肤的尿道下裂修复结果,并分析手术技术和手术成功的预测因素。
回顾性分析 1999 年 10 月至 2018 年 12 月期间所有接受尿道下裂修复的患儿记录。所有手术前均接受新生儿包皮环切术的患儿均纳入本研究。排除既往有阴茎重建手术和保留完整舟状窝包皮变异的患儿。主要终点是需要再次手术。
研究期间共有 69 例有新生儿包皮环切术史的患儿接受了尿道下裂手术重建。他们的手术时年龄平均为 14 个月(四分位距[IQR]9,22)。45 例(65%)为远端尿道下裂,24 例(35%)存在腹侧弯曲。37/58 例(64%)患儿从背侧取 Dartos 皮瓣,21/58 例(36%)从腹侧取 Dartos 皮瓣。中位随访 9 年(IQR 6,13)后,22 例(22/69,32%)患儿需要再次手术。再次手术的指征包括尿道瘘(n=16,22%)、尿道口狭窄(n=5,7%)和皮肤冗余(n=1)。腹侧弯曲(优势比[OR]3.5,p=0.02)和较高等级的尿道下裂(OR 3.3,p=0.03)再次手术的可能性更高(单因素 logistic 回归)。
新生儿包皮环切术后缺乏包皮皮肤的尿道下裂修复是一种具有挑战性的重建。我们的队列中再次手术率为 30%,与再次手术的尿道下裂手术相似。诊断为尿道下裂的新生儿的父母应鼓励其避免术前新生儿包皮环切术。
治疗研究,IV 级。