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患有VACTERL综合征的婴儿气管食管瘘和食管闭锁的手术矫正:一项回顾性病例对照研究。

Surgical correction of tracheo-oesophageal fistula and oesophageal atresia in infants with VACTERL association: a retrospective case-control study.

作者信息

Morgan Robert D, O'Callaghan John M, Wagener Silke, Grant Hugh W, Lakhoo Kokila

机构信息

Department of Paediatric Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Headley Way, Headington, Oxford, OX3 9DU, UK.

出版信息

Pediatr Surg Int. 2012 Oct;28(10):967-70. doi: 10.1007/s00383-012-3165-8. Epub 2012 Aug 22.

Abstract

INTRODUCTION

VACTERL is a rare, non-random association comprising at least three major component features defined by the acronym, and including Vertebral anomalies, Anorectal malformations, Cardiac defects, Tracheo-oEsophageal fistula with or without oesophageal atresia (TOF/OA), Renal abnormalities and Limb anomalies. The aim of this study was to compare the post-operative outcomes following surgical correction of TOF/OA in infants with VACTERL and isolated TOF/OA.

METHODS

A retrospective case-control study comparing infants with VACTERL (case group) versus infants with isolated TOF/OA (control group) that underwent surgical correction of TOF/OA at our centre between January 2006 and December 2011. Patient demographics, types of anomalies, operative techniques and post-operative outcomes were collected using inpatient and outpatient records.

RESULTS

We identified 30 consecutive infants with TOF/OA. Five infants had VACTERL (17 %) and 15 infants had isolated TOF/OA (50 %). There was no significant difference in the gestational age (P = 0.79), birth weight (P = 0.69) or operative repair (P = 0.14) between groups. Overall, surgical correction of TOF/OA led to satisfactory morbidity. Infants with VACTERL were not at higher risk of post-operative complications, such as oesophageal stricture (P = 0.17) or gastro-oesophageal reflux (P = 1.0), compared to infants with isolated TOF/OA.

CONCLUSIONS

VACTERL association does not increase the risk of post-operative complications following TOF/OA repair.

摘要

引言

VACTERL是一种罕见的、非随机的综合征,由至少三个主要组成特征构成,其首字母缩写词包含以下特征:椎体异常、肛门直肠畸形、心脏缺陷、伴有或不伴有食管闭锁的气管食管瘘(TOF/OA)、肾脏异常和肢体异常。本研究的目的是比较VACTERL患儿与单纯TOF/OA患儿在接受TOF/OA手术矫正后的术后结果。

方法

一项回顾性病例对照研究,比较2006年1月至2011年12月期间在本中心接受TOF/OA手术矫正的VACTERL患儿(病例组)与单纯TOF/OA患儿(对照组)。通过住院和门诊记录收集患者人口统计学资料、异常类型、手术技术和术后结果。

结果

我们连续纳入了30例TOF/OA患儿。5例患儿患有VACTERL(17%),15例患儿患有单纯TOF/OA(50%)。两组之间的胎龄(P = 0.79)、出生体重(P = 0.69)或手术修复情况(P = 0.14)无显著差异。总体而言,TOF/OA的手术矫正导致的发病率令人满意。与单纯TOF/OA患儿相比,VACTERL患儿术后发生并发症的风险并不更高,如食管狭窄(P = 0.17)或胃食管反流(P = 1.0)。

结论

VACTERL综合征不会增加TOF/OA修复术后的并发症风险。

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