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Anorectal malformations, associated congenital anomalies and their investigation in a South African setting.南非环境下的肛门直肠畸形、相关先天性异常及其调查
Pediatr Surg Int. 2017 Aug;33(8):875-882. doi: 10.1007/s00383-017-4109-0. Epub 2017 Jun 13.
2
Congenital Anorectal Malformation Severity Does Not Predict Severity of Congenital Heart Defects.先天性肛肠畸形的严重程度无法预测先天性心脏病的严重程度。
J Pediatr. 2016 Dec;179:150-153.e1. doi: 10.1016/j.jpeds.2016.08.047. Epub 2016 Sep 26.
3
Prevalence of congenital heart disease in patients undergoing surgery for major gastrointestinal malformations: an Indian study.接受重大胃肠道畸形手术患者的先天性心脏病患病率:一项印度研究。
Heart Asia. 2015 Jun 5;7(1):29-31. doi: 10.1136/heartasia-2014-010561. eCollection 2015.
4
Pulse oximetry with clinical assessment to screen for congenital heart disease in neonates in China: a prospective study.脉搏血氧饱和度联合临床评估用于中国新生儿先天性心脏病筛查的前瞻性研究。
Lancet. 2014 Aug 30;384(9945):747-54. doi: 10.1016/S0140-6736(14)60198-7. Epub 2014 Apr 22.
5
Outcome of primary posterior sagittal anorectoplasty of high anorectal malformation in well selected neonates.精心挑选的新生儿高位肛门直肠畸形一期后矢状入路肛门直肠成形术的疗效
Niger J Clin Pract. 2014 Jan-Feb;17(1):1-5. doi: 10.4103/1119-3077.122821.
6
Congenital cardiac anomalies and imperforate anus: A hospital's experience.先天性心脏异常与肛门闭锁:一家医院的经验
J Cardiovasc Dis Res. 2013 Mar;4(1):34-6. doi: 10.1016/j.jcdr.2013.02.003. Epub 2013 Feb 27.
7
Anorectal malformations.肛门直肠畸形。
Clin Perinatol. 2012 Jun;39(2):403-22. doi: 10.1016/j.clp.2012.04.001.
8
Is routine preoperative 2-dimensional echocardiography necessary for infants with esophageal atresia, omphalocele, or anorectal malformations?对于患有食管闭锁、脐膨出或肛门直肠畸形的婴儿,是否需要常规进行术前二维超声心动图检查?
J Pediatr Surg. 2010 May;45(5):876-9. doi: 10.1016/j.jpedsurg.2010.02.002.
9
Guidelines and standards for performance of a pediatric echocardiogram: a report from the Task Force of the Pediatric Council of the American Society of Echocardiography.小儿超声心动图检查的指南与标准:美国超声心动图学会小儿委员会特别工作组报告
J Am Soc Echocardiogr. 2006 Dec;19(12):1413-30. doi: 10.1016/j.echo.2006.09.001.
10
Cardiovascular anomalies with imperforate anus.心血管异常合并肛门闭锁
Arch Dis Child. 1983 Sep;58(9):747-9. doi: 10.1136/adc.58.9.747.

[肛门直肠畸形患儿先天性心脏病的发病率及相关治疗]

[Morbidity of congenital heart disease in children with anorectal malformations and related treatment].

作者信息

Liu Yun, Li Kaikai, Wu Juan, Li Hezhou, Geng Xiaoduan, Gu Yachuan

机构信息

Department of Ultrasonography, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

Department of Pediatric Surgery, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020 Oct 25;49(5):597-602. doi: 10.3785/j.issn.1008-9292.2020.10.08.

DOI:10.3785/j.issn.1008-9292.2020.10.08
PMID:33210486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8800670/
Abstract

OBJECTIVE

To investigate the morbidity of congenital heart defects(CHDs) in children with anorectal malformation, and to summarize appropriate treatment.

METHODS

The clinical data and echocardiographic findings of 155 children with congenital anorectal malformations from the Third Affiliated Hospital of Zhengzhou University during January 2016 and October 2019 were reviewed. According to the surgical findings of anorectal malformations, the patients were categorized as the high/intermediate group and the low group; the CHDs were classified as minor CHDs and major CHDs. Multiple logistic regression was used to analyze the correlation of wingspread classification, and extracardiac malformations with the severity of CHDs.

RESULTS

Out of 155 children with anorectal malformations, 47 (30.3%) had different types of cardiac structural malformations, including 18 cases of minor CHDs (11.6%) and 29 cases of major CHDs (18.7%). Sixty children (38.7%) had extracardiac malformations, of which 38 cases (24.5%) had a single extracardiac malformation, 15 cases (9.7%) had multiple extracardiac malformations, 6 had trisomy 21 syndrome, and 1 had VATER syndrome. Multivariate logistic regression analysis showed that wingspread classification of anorectal malformation and extracardiac disorders were independent risk factors for major CHDs. The probability of major CHDs in children with high/intermediate anorectal malformation was 4.709 times higher than that with low anorectal malformation (=4.709, 95% : 1.651-13.432, <0.01). The probability of major CHDs was 3.85 times higher for increasing each additional grade of extracardiac malformations(without, with single, or multiple malformations) (=3.850, 95% : 2.065-7.175, <0.01). According to the presence and severity of CHDs, children with anorectal malformations were classified into three categories: without CHDs, with minor CHDs and with major CHDs, for differential treatment and management. Anorectal malformations would be treated and managed in children without CHDs and with minor CHDs following the original plan; however, children with minor CHDs may require cardiac follow-up after surgery. In children with major CHDs, the personalization tactics were developed based on the principle of emergency first. There were increased perioperative infection rate (<0.05), longer hospital days (<0.01), reduced cure rate (<0.05) and increased mortality (<0.05) in children with major, compared with those without CHDs and minor CHDs.

CONCLUSIONS

The morbidity of major CHDs is higher in severe cases with high/intermediate anorectal malformation and acute cases without fistula or with obstructed fistula and cases with multiple congenital disorders. Echocardiography can define the type and severity of CHDs, which are useful to develop the optimal diagnosis and treatment plan for children with anorectal malformation.

摘要

目的

探讨肛门直肠畸形患儿先天性心脏病(CHD)的发病率,并总结合适的治疗方法。

方法

回顾郑州大学第三附属医院2016年1月至2019年10月期间155例先天性肛门直肠畸形患儿的临床资料和超声心动图检查结果。根据肛门直肠畸形的手术结果,将患者分为高位/中位组和低位组;CHD分为轻度CHD和重度CHD。采用多因素logistic回归分析肛门直肠畸形的翼展分类及心外畸形与CHD严重程度的相关性。

结果

155例肛门直肠畸形患儿中,47例(30.3%)有不同类型的心脏结构畸形,其中轻度CHD 18例(11.6%),重度CHD 29例(18.7%)。60例(38.7%)有心外畸形,其中38例(24.5%)有单发心外畸形,15例(9.7%)有多发性心外畸形,6例有21三体综合征,1例有VATER综合征。多因素logistic回归分析显示,肛门直肠畸形的翼展分类及心外疾病是重度CHD的独立危险因素。高位/中位肛门直肠畸形患儿发生重度CHD的概率比低位肛门直肠畸形患儿高4.709倍(比值比=4.709,95%可信区间:1.651-13.432,P<0.01)。每增加一级心外畸形(无、单发或多发畸形),重度CHD的发生概率高3.85倍(比值比=3.850,95%可信区间:2.065-7.175,P<0.01)。根据CHD的有无及严重程度,将肛门直肠畸形患儿分为三类:无CHD、轻度CHD和重度CHD,进行差异化治疗和管理。无CHD和轻度CHD的患儿按原计划进行肛门直肠畸形的治疗和管理;然而,轻度CHD患儿术后可能需要心脏随访。对于重度CHD患儿,根据急救优先原则制定个性化策略。与无CHD和轻度CHD的患儿相比,重度CHD患儿围手术期感染率增加(P<0.05)、住院天数延长(P<0.01)、治愈率降低(P<0.05)和死亡率增加(P<0.05)。

结论

高位/中位肛门直肠畸形的重症病例、无瘘或瘘管梗阻的急症病例以及合并多种先天性疾病的病例中重度CHD的发病率较高。超声心动图可明确CHD的类型和严重程度,有助于为肛门直肠畸形患儿制定最佳诊断和治疗方案。