Augmentation cystoplasty and continent catheterizable channels in the bladder exstrophy-epispadias complex: A 20-year experience.

IF 2 3区 医学 Q2 PEDIATRICS
Victoria Maxon, Carolyn Im, Ahmad Haffar, Alexander Hirsch, David Heap, Chad Crigger, Heather Di Carlo, John Gearhart
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引用次数: 0

Abstract

Introduction: The variable presentation of the exstrophy-epispadias complex (EEC) has led to a variety of surgical and medical care practices for management of the condition. Augmentation cystoplasty (AC) is a procedure that can be used to increase the volume and compliance of the bladder to facilitate a functional storage vessel for urine that does not put the upper urinary tract under high pressure.

Objective: To determine risk factors for complications after augmentation cystoplasty (AC) with continent catheterizable channel (CCC) in the EEC.

Study design: An IRB approved institutional database of EEC patients was reviewed retrospectively. Patients that had primary augmentation performed at our institution between 2003 and 2023 were included. Gender, race, primary closure outcome, bowel segment choice for augmentation and stoma, preoperative bladder capacity, bladder neck status, age at augmentation, 30- and 90-day complications, number of stomal revisions, and length of longer term follow-ups were reviewed. Comparisons were made among different risk factors and complications across AC type and CCC type.

Results: 186 patients underwent primary AC with CCC at our institution and 157 met final inclusion criteria (Table 1). The patients included 148 (94.3 %) classic bladder exstrophy, 6 (3.8 %) male epispadias and 3 (1.9 %) female epispadias. The mean age at time of AC was 11.3 years with a median follow up of 6.46 years. There was no significant difference in the length of bowel harvested by the ileum and colon groups (p = 0.0836) or closure outcome (p = 0.3013). There was increased usage of Monti stoma in patients with an ileum AC (p = 0.0034). Stomal revisions were also significantly more common in the ileum group (p = 0.0392). Closure outcome did not influence the rate of 30- and 90-day complications (p = 0.6560, p = 0.6761) or stoma choice (p = 0.7384). There was no significant difference between the ileum and colon augment groups in terms of 30- and 90-day complications (p = 0.8329, p = 0.2923, respectively). Multivariate Cox regression showed no significant association between stoma or augmentation type and time to postoperative complication (p = 0.94 and p = 0.77, respectively). Patients with a history of primary successful closure had a shorter hospital stay (p = 0.0042) but there was no difference in hospital stay between the ileum and colon groups (p = 0.6632).

Discussion: Bowel segment choice for AC does not influence the risk for complications in the EEC population. History of a failed primary closure leads to a longer hospital stay after AC, but there is no increased risk for complications.

Conclusion: Risks factors in the EEC population for complications after AC with CCC remain unknown.

膀胱膨大成形术和膀胱外翻-尿道外膈复合的大陆导尿通道:20年的经验。
简介:外翻-上膈肌复合体(EEC)的不同表现导致了各种手术和医疗保健实践的管理条件。膀胱增强成形术(AC)是一种可用于增加膀胱体积和顺应性的手术,以促进尿液的功能储存血管,而不会使上尿路处于高压状态。前言:目的:探讨膀胱扩张成形术(AC)后膀胱持续导尿通道(CCC)并发症的危险因素。研究设计:回顾性回顾了经IRB批准的脑电图患者机构数据库。纳入了2003年至2023年间在我们机构接受过初级隆胸手术的患者。我们回顾了性别、种族、主要闭合结果、增加术和造口的肠段选择、术前膀胱容量、膀胱颈部状态、增加术时年龄、30天和90天并发症、造口修复次数和长期随访时间。比较AC型和CCC型患者不同危险因素及并发症。结果:186例患者在我院接受了原发性AC伴CCC, 157例符合最终纳入标准(表1)。典型膀胱外翻148例(94.3%),男性6例(3.8%),女性3例(1.9%)。AC时的平均年龄为11.3岁,中位随访时间为6.46年。回肠组和结肠组的肠长度(p = 0.0836)和闭合结果(p = 0.3013)无显著差异。回肠AC患者Monti造口术的使用增加(p = 0.0034)。回肠组的造口修复也明显更常见(p = 0.0392)。闭合结果不影响30天和90天并发症发生率(p = 0.6560, p = 0.6761)或造口选择(p = 0.7384)。在30天和90天并发症方面,回肠组和结肠组之间无显著差异(p = 0.8329, p = 0.2923)。多因素Cox回归显示造口或隆胸类型与术后并发症发生时间无显著相关性(p = 0.94, p = 0.77)。有首次成功闭合病史的患者住院时间较短(p = 0.0042),但回肠组和结肠组的住院时间无差异(p = 0.6632)。讨论:AC的肠段选择不影响EEC人群并发症的风险。初次关闭失败的历史导致AC术后住院时间更长,但并发症的风险没有增加。结论:EEC人群AC合并CCC术后并发症的危险因素尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pediatric Urology
Journal of Pediatric Urology PEDIATRICS-UROLOGY & NEPHROLOGY
CiteScore
3.70
自引率
15.00%
发文量
330
审稿时长
4-8 weeks
期刊介绍: The Journal of Pediatric Urology publishes submitted research and clinical articles relating to Pediatric Urology which have been accepted after adequate peer review. It publishes regular articles that have been submitted after invitation, that cover the curriculum of Pediatric Urology, and enable trainee surgeons to attain theoretical competence of the sub-specialty. It publishes regular reviews of pediatric urological articles appearing in other journals. It publishes invited review articles by recognised experts on modern or controversial aspects of the sub-specialty. It enables any affiliated society to advertise society events or information in the journal without charge and will publish abstracts of papers to be read at society meetings.
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