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肠闭锁和短肠婴儿的渐减式肠成形术

Tapering enteroplasty in infants with bowel atresia and short gut.

作者信息

Weber T R, Vane D W, Grosfeld J L

出版信息

Arch Surg. 1982 May;117(5):684-8. doi: 10.1001/archsurg.1982.01380290130023.

Abstract

Antimesenteric tapering enteroplasty was evaluated as an alternative to resection in 16 babies. Tapering enteroplasty was done for jejunal atresia (11), ileal atresia (three), total colonic aganglionosis (one), and colonic atresia (one). Most had short gut with proximal bowel dilation. There were no anastomotic leaks but slight functional delay (eight to 14 days). One patient with 14 jejunoileal atresias received continuous-drip feeding while the remainder took regular diet. Mean weight gain was in the 25th percentile at 1 year of age, and the 35th percentile at 2 years of age. There were two deaths from liver failure and brain damage. Antimesenteric tapering enteroplasty is particularly useful in selected instances of intestinal atresia associated with short gut, where preservation of bowel length may be essential for survival. Gastrointestinal function, bowel movement patterns and growth and development have been gratifying.

摘要

对16例婴儿进行了评估,以抗肠系膜逐渐变细肠成形术作为切除术的替代方法。逐渐变细肠成形术用于空肠闭锁(11例)、回肠闭锁(3例)、全结肠无神经节症(1例)和结肠闭锁(1例)。大多数患儿肠道短且近端肠管扩张。无吻合口漏,但有轻微功能延迟(8至14天)。1例有14处空回肠闭锁的患儿接受持续滴注喂养,其余患儿采用常规饮食。1岁时平均体重增长处于第25百分位,2岁时处于第35百分位。有2例死于肝功能衰竭和脑损伤。抗肠系膜逐渐变细肠成形术在某些与短肠相关的肠闭锁病例中特别有用,在这些病例中,保留肠长度对生存可能至关重要。胃肠功能、排便模式以及生长发育情况都令人满意。

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