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出生时患有肛门直肠畸形且无瘘管的新生儿肠穿孔。

Bowel perforation in newborn with anorectal malformation and no fistula at presentation.

作者信息

Chan Kin Wai Edwin, Lee Kim Hung, Tsui Siu Yan Bess, Wong Yuen Shan, Pang Kit Yi Kristine, Mou Jennifer Wai Cheung, Tam Yuk Him

机构信息

Department of Surgery, Division of Paediatric Surgery and Paediatric Urology, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.

Department of Surgery, Division of Paediatric Surgery and Paediatric Urology, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.

出版信息

J Pediatr Surg. 2014 Mar;49(3):390-4. doi: 10.1016/j.jpedsurg.2013.07.009.

DOI:10.1016/j.jpedsurg.2013.07.009
PMID:24650463
Abstract

PURPOSE

Anorectal malformation (ARM) in newborns with no fistula at presentation resembles intestinal obstruction. The aim of this study is to study the factors associated with bowel perforation in this group of patients.

METHODS

From 2000 to 2012, 106 newborns with ARM were managed in our hospital. Thirty neonates without fistula at presentation were included in this study. Demographic data and the incidence of bowel perforation were studied.

RESULTS

Twenty-nine male and 1 female were included in the study. Five patients were born premature and six patients had low birth weight. Six patients had Down's syndrome and 12 patients had associated anomalies. Cross-table lateral x-ray in prone position was performed from 20 to 24 hours after birth. All operations were performed within 48 hours after birth. One neonate underwent primary anoplasty. Twenty-nine neonates underwent colostomy. Two males developed bowel perforation before surgery (at 33 and 36 hours after birth). Perforation was associated with low birth weight (p=0.034) and was not associated with prematurity (p=0.31), Down's syndrome (p=0.634) or the presence of other associated anomalies (p=0.687).

CONCLUSIONS

In newborns with ARM, bowel perforation can occur within 36 hours after birth. Forty-eight hours of waiting is too long as it risks perforation. In this study, a neonate with low birth weight was trended toward bowel perforation.

摘要

目的

出生时无瘘管的新生儿肛门直肠畸形(ARM)类似于肠梗阻。本研究的目的是探讨该组患者中与肠穿孔相关的因素。

方法

2000年至2012年,我院收治了106例患有ARM的新生儿。本研究纳入了30例出生时无瘘管的新生儿。研究了人口统计学数据和肠穿孔的发生率。

结果

研究纳入了29名男性和1名女性。5例为早产儿,6例出生体重低。6例患有唐氏综合征,12例伴有其他畸形。出生后20至24小时进行俯卧位交叉侧位x光检查。所有手术均在出生后48小时内进行。1例新生儿接受了一期肛门成形术。29例新生儿接受了结肠造口术。2名男性在手术前(出生后33和36小时)发生了肠穿孔。穿孔与低出生体重相关(p = 0.034),与早产(p = 0.31)、唐氏综合征(p = 0.634)或其他相关畸形的存在(p = 0.687)无关。

结论

在患有ARM的新生儿中,肠穿孔可在出生后36小时内发生。等待48小时太长,因为有穿孔的风险。在本研究中,低出生体重的新生儿有肠穿孔的倾向。

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引用本文的文献

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Front Pediatr. 2022 Feb 7;10:807607. doi: 10.3389/fped.2022.807607. eCollection 2022.
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Spontaneous ileal perforation complicating low anorectal malformation.自发性回肠穿孔并发低位肛门直肠畸形
Afr J Paediatr Surg. 2015 Apr-Jun;12(2):152-4. doi: 10.4103/0189-6725.160411.