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1
Simultaneous Single-staged Repair of Anorectal Malformation with Tracheoesophageal Fistula: Lessons Learned.肛门直肠畸形合并气管食管瘘的同期单阶段修复:经验教训
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2
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J Neonatal Surg. 2016 Oct 10;5(4):43. doi: 10.21699/jns.v5i4.449. eCollection 2016 Oct-Dec.

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Challenges in scaling up of special care newborn units--lessons from India.提升新生儿特别护理单元规模面临的挑战——来自印度的经验教训。
Indian Pediatr. 2011 Dec;48(12):931-5. doi: 10.1007/s13312-011-0149-z.
2
Prognosis of congenital tracheoesophageal fistula with esophageal atresia on the basis of gap length.基于间隙长度的先天性食管闭锁合并气管食管瘘的预后
Pediatr Surg Int. 2007 Aug;23(8):767-71. doi: 10.1007/s00383-007-1964-0. Epub 2007 Jun 20.
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Anorectal malformations and their impact on survival.肛门直肠畸形及其对生存的影响。
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Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.食管闭锁、气管食管瘘与VACTERL综合征:遗传学与流行病学综述
J Med Genet. 2006 Jul;43(7):545-54. doi: 10.1136/jmg.2005.038158. Epub 2005 Nov 18.
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Oesophageal atresia: what has changed in the last 3 decades?食管闭锁:过去30年有哪些变化?
Pediatr Surg Int. 2004 Oct;20(10):768-72. doi: 10.1007/s00383-004-1139-1.
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Cost of neonatal intensive care.新生儿重症监护的费用。
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The effects of Down syndrome and other chromosomal abnormalities on survival and management in oesophageal atresia.唐氏综合征及其他染色体异常对食管闭锁患儿生存及治疗的影响。
Pediatr Surg Int. 1997;12(8):550-1. doi: 10.1007/BF01371897.
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The epidemiology of tracheo-oesophageal fistula and oesophageal atresia in Europe. EUROCAT Working Group.欧洲气管食管瘘与食管闭锁的流行病学。欧洲先天性异常监测系统工作组
Arch Dis Child. 1993 Jun;68(6):743-8. doi: 10.1136/adc.68.6.743.
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Status of neonatal intensive care units in India.印度新生儿重症监护病房的现状。
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食管闭锁合并肛门直肠畸形:在资源有限的情况下,分两期手术的术后效果会更好吗?

Esophageal atresia associated with anorectal malformation: Is the outcome better after surgery in two stages in a limited resources scenario?

作者信息

Singh Sunita, Wakhlu Ashish, Pandey Anand, Singh Anita, Kureel Shiv N, Rawat Jiledar, Srivastava Payal Mishra

机构信息

Department of Pediatric Surgery, CSM Medical University (Erstwhile King George Medical University), Lucknow, Uttar Pradesh, India.

出版信息

J Indian Assoc Pediatr Surg. 2012 Jul;17(3):107-10. doi: 10.4103/0971-9261.98123.

DOI:10.4103/0971-9261.98123
PMID:22869975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3409897/
Abstract

AIMS

To analyze whether outcome of neonates having esophageal atresia with or without tracheoesophageal fistula (EA±TEF) associated with anorectal malformation (ARM) can be improved by doing surgery in 2 stages.

MATERIALS AND METHODS

A prospective study of neonates having both EA±TEF and ARM from 2004 to 2011. The patients with favorable parameters were operated in a single stage, whereas others underwent first-stage decompression surgery for ARM. Thereafter, once septicemia was under control and ventilator care available, second-stage surgery for EA±TEF was performed.

RESULTS

Total 70 neonates (single stage = 20, 2 stages = 30, expired after colostomy = 9, only EA±TEF repair needed = 11) were enrolled. The admission rate for this association was 1 per 290. Forty-one percent (24/70) neonates had VACTERL association and 8.6% (6/70) neonates had multiple gastrointestinal atresias. Sepsis screen was positive in 71.4% (50/70). The survival was 45% (9/20) in neonates operated in a single stage and 53.3% (16/30) when operated in 2 stages (P = 0.04). Data analysis of 50 patients revealed that the survived neonates had significantly better birth weight, better gestational age, negative sepsis screen, no cardiac diseases, no pneumonia, and 2-stage surgery (P value 0.002, 0.003, 0.02, 0.02, 0.04, and 0.04, respectively). The day of presentation and abdominal distension had no significant effect (P value 0.06 and 0.06, respectively). This was further supported by stepwise logistic regression analysis.

CONCLUSIONS

In a limited resources scenario, the survival rate of babies with this association can be improved by treating ARM first and then for EA±TEF in second stage, once mechanical ventilator care became available and sepsis was under control.

摘要

目的

分析对于患有食管闭锁伴或不伴气管食管瘘(EA±TEF)且合并肛门直肠畸形(ARM)的新生儿,分两阶段进行手术是否能改善其预后。

材料与方法

对2004年至2011年期间患有EA±TEF和ARM的新生儿进行前瞻性研究。参数良好的患者进行一期手术,而其他患者则先接受ARM的一期减压手术。此后,一旦败血症得到控制且有呼吸机护理条件,便进行EA±TEF的二期手术。

结果

共纳入70例新生儿(一期手术 = 20例,两期手术 = 30例,结肠造口术后死亡 = 9例,仅需进行EA±TEF修复 = 11例)。这种关联的发病率为每290例中有1例。41%(24/70)的新生儿患有VACTERL综合征,8.6%(6/70)的新生儿患有多处胃肠道闭锁。71.4%(50/70)的败血症筛查呈阳性。一期手术的新生儿存活率为45%(9/20),两期手术时为53.3%(16/30)(P = 0.04)。对50例患者的数据分析显示,存活的新生儿出生体重明显更高、孕周更好、败血症筛查阴性、无心脏病、无肺炎且接受两期手术(P值分别为0.002、0.003、0.02、0.02、0.04和0.04)。就诊时间和腹胀无显著影响(P值分别为0.06和0.06)。逐步逻辑回归分析进一步支持了这一点。

结论

在资源有限的情况下,对于患有这种关联疾病的婴儿,先治疗ARM然后在有机械通气护理且败血症得到控制后进行二期EA±TEF手术,可提高存活率。