Division of Pediatric Surgery, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.
Department of Pediatrics and Adolescent Medicine, Medical Faculty and University Hospital Cologne, University of Cologne, Cologne, Germany.
World J Urol. 2024 Oct 23;42(1):589. doi: 10.1007/s00345-024-05307-4.
Intrauterine vesicoamniotic shunting (VAS) was shown to affect survival of male fetuses with megacystis in suspected lower urinary tract obstruction (LUTO). Data on postnatal management are largely lacking. We aim to describe the pathologies diagnosed in children born after vesicoamniotic shunt placement in early pregnancy for megacystis.
All newborns with previous intrauterine VAS treated in our institution were analyzed retrospectively. We evaluated the clinical spectrum of urethral pathologies. We also compared patients who received a shunt before the 17th gestational week with those who received it later.
Between 2014 and 2023, 26 patients (all male) with a history of VAS for suspected LUTO were treated in our institution postnatally. Five fetuses with dislocated shunts underwent re-implantation in utero. Overall, premature birth before the 38th week of gestation was observed in 14 patients. Seven patients received a Harrison shunt whereas 19 received a Somatex shunt. Twelve patients required surgical shunt removal under general anesthesia due to shunt migration/embedding. Posterior urethral valves were found in 10/26 patients, 10/26 patients showed a urethral hypoplasia [Fig. 1] and two patients had urethral duplications. In two patients, we identified a prune belly syndrome. One patient had posterior and anterior urethral valves. One patient had a high grade bilateral vesicoureteral reflux without LUTO. The 11 patients shunted early (before 17GW) showed a trend towards a higher proportion of urethral hypoplasia in the early shunt group (54% vs. 26%) without statistical significance.
In our observation, patients treated with VAS had a noticeable high proportion of complex urethral pathologies such as urethral hypoplasia. These data should be taken into consideration for prenatal counselling of parents and planning of postnatal management.
子宫内膀胱羊膜分流术(VAS)已被证明可影响疑似下尿路梗阻(LUTO)所致巨膀胱男性胎儿的存活率。关于产后管理的数据在很大程度上仍然缺乏。我们旨在描述在早孕时因巨膀胱而行 VAS 治疗的儿童出生后的病理诊断。
回顾性分析我院接受宫内 VAS 治疗的所有新生儿。我们评估了尿道病变的临床谱。我们还比较了 17 孕周前接受分流术的患者与 17 孕周后接受分流术的患者。
2014 年至 2023 年,我院共治疗 26 例(均为男性)因疑似 LUTO 而行 VAS 治疗的新生儿。5 例分流器移位的胎儿在宫内重新植入。总体而言,14 例患者在妊娠 38 周前早产。7 例患者接受了 Harrison 分流术,19 例患者接受了 Somatex 分流术。12 例患者因分流器移位/嵌入需要全身麻醉下手术移除分流器。26 例患者中 10 例发现后尿道瓣膜,26 例患者中有 10 例存在尿道发育不良[图 1],2 例患者存在尿道重复。2 例患者存在脐疝。1 例患者同时存在后尿道瓣膜和前尿道瓣膜。1 例患者存在双侧高级别膀胱输尿管反流但无 LUTO。11 例早期(17GW 前)分流的患者中,早期分流组尿道发育不良的比例较高(54%比 26%),但无统计学意义。
在我们的观察中,接受 VAS 治疗的患者存在显著较高比例的复杂尿道病变,如尿道发育不良。这些数据应在为父母提供产前咨询和规划产后管理时予以考虑。