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穆拉戈医院乌干达心脏研究所收治儿童的先天性心脏病模式:一项为期7年的回顾

Pattern of congenital heart disease among children presenting to the Uganda Heart Institute, Mulago Hospital: a 7-year review.

作者信息

Namuyonga Judith, Lubega Sulaiman, Aliku Twalib, Omagino John, Sable Craig, Lwabi Peter

机构信息

Uganda Heart Institute.

Makerere University College of Health Sciences.

出版信息

Afr Health Sci. 2020 Jun;20(2):745-752. doi: 10.4314/ahs.v20i2.26.

Abstract

BACKGROUND

Congenital heart disease (CHD) is the most common congenital anomaly in children. Over half of the deaths due to CHD occur in the neonatal period. Most children with unrepaired complex heart lesions do not live to celebrate their first birthday. We describe the spectrum of congenital heart disease in Uganda.

METHODS

We retrospectively reviewed the data of children with CHD who presented to the Uganda Heart Institute (UHI), Mulago Hospital Complex from 2007 to 2014.

RESULTS

A total of 4621 children were seen at the UHI during the study period. Of these, 3526 (76.3%) had CHD; 1941(55%) were females. Isolated ventricular septal defect (VSD) was the most common CHD seen in 923 (27.2%) children followed by Patent ductus arteriosus (PDA) 760 (22%) and atrial septal defects (ASD) 332 (9.4%). Tetralogy of Fallot (TOF) and Truncus arteriosus were the most common cyanotic heart defects (7% and 5% respectively). Dysmorphic features were diagnosed in 185 children, of which 61 underwent genetic testing (Down syndrome=24, 22q11.2 deletion syndrome n=10). Children with confirmed 22q11.2 deletion had conotruncal abnormalities.

CONCLUSION

Isolated VSD and Tetralogy of Fallot are the most common acyanotic and cyanotic congenital heart defects. We report an unusually high occurrence of Truncus arteriosus.

摘要

背景

先天性心脏病(CHD)是儿童中最常见的先天性畸形。超过一半的先天性心脏病相关死亡发生在新生儿期。大多数患有未经修复的复杂心脏病变的儿童活不到一岁生日。我们描述了乌干达先天性心脏病的情况。

方法

我们回顾性分析了2007年至2014年期间在穆拉戈医院综合院区乌干达心脏研究所(UHI)就诊的先天性心脏病患儿的数据。

结果

在研究期间,UHI共接诊了4621名儿童。其中,3526名(76.3%)患有先天性心脏病;1941名(55%)为女性。单纯室间隔缺损(VSD)是最常见的先天性心脏病,923名(27.2%)儿童患有该病,其次是动脉导管未闭(PDA)760名(22%)和房间隔缺损(ASD)332名(9.4%)。法洛四联症(TOF)和动脉干畸形是最常见的紫绀型心脏缺陷(分别为7%和5%)。185名儿童被诊断出有畸形特征,其中61名接受了基因检测(唐氏综合征=24例,22q11.2缺失综合征n = 10例)。确诊为22q11.2缺失的儿童有圆锥动脉干异常。

结论

单纯室间隔缺损和法洛四联症是最常见的非紫绀型和紫绀型先天性心脏缺陷。我们报告了动脉干畸形异常高的发生率。

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