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脊髓发育不良患儿的回肠膀胱扩大术

Augmentation ileocystoplasty in children with myelodysplasia.

作者信息

Webber E M, Crofts P G, Pomeroy C, Coleman G U, Arnold W J, Johnson H W

机构信息

Department of Surgery, B.C. Children's Hospital, University of British Columbia, Vancouver.

出版信息

Can J Surg. 1990 Apr;33(2):135-8.

PMID:2268813
Abstract

Over the past 8 years 20 children suffering from myelodysplasia were selected to undergo augmentation ileocystoplasty for urinary incontinence refractory to treatment by clean, intermittent catheterization and anticholinergic agents, or as part of urinary undiversion. The children ranged in age from 5 to 17 years, and the follow-up ranged from 6 months to 7 years. Three children underwent undiversion, two had vesicostomy closure and six had bladder outlet repair at the time of augmentation. In one patient, surgery was technically impossible. Postoperatively 16 children were fully continent on clean, intermittent catheterization and anticholinergic medication. Three boys failed to achieve satisfactory continence. Delayed perforation, a potentially serious complication, occurred in two patients several months postoperatively.

摘要

在过去8年中,选择了20名患有骨髓发育不良的儿童,对其进行回肠膀胱扩大术,用于治疗经清洁间歇性导尿和抗胆碱能药物治疗后仍难治的尿失禁,或作为尿路改道逆转的一部分。这些儿童年龄在5至17岁之间,随访时间为6个月至7年。3名儿童进行了尿路改道逆转,2名进行了膀胱造瘘口闭合术,6名在扩大术时进行了膀胱出口修复。1例患者因技术原因无法进行手术。术后,16名儿童通过清洁间歇性导尿和抗胆碱能药物实现了完全控尿。3名男孩未能实现令人满意的控尿。2例患者在术后数月发生了延迟穿孔,这是一种潜在的严重并发症。

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