Prevalence and pattern of congenital heart disease among children with Down syndrome seen in a Federal Medical Centre in the Niger Delta Region, Nigeria

Susan Ujuanbi Amenawon, Chiemerie Onyeka Adaeze
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引用次数: 1

Abstract

Background: Down syndrome (DS), or Trisomy 21, is the most common genetic disorder in the world and congenital heart disease (CHD) contributes significantly to morbidity and mortality in this population. Early diagnosis and prompt cardiac intervention improve their quality of life. This study was done to determine the prevalence and pattern of congenital heart disease among children with Down syndrome seen at the Paediatric Cardiology Unit of Federal Medical Centre (FMC), Bayelsa State. Method: A prospective study of children with Down syndrome referred for cardiac evaluation and echocardiography at the Paediatric Cardiology Unit of FMC, Bayelsa State over four years from 1st January 2016 to 30th December 2019. Data on socio-demographic information, echocardiographic diagnosis, and outcome were retrieved from the study proforma and analyzed. Results: A total of 24 children with Down syndrome were seen over the study period. Their age ranged from 0 to 16years. The majority, 20 (83.3%) of the children with Down syndrome were aged 5 years and below. There were 13 males and 11 females with a male to female ratio of 1.2:1. A total of 23 (95.8%) of the children with Down syndrome had CHD. The most common CHD was AVSD (including complete, partial, isolated, or in association with other defects) in 66.6% followed by TOF in 8.3%. Multiple CHDs were seen in 43.5% of the children. Only one child (4.2%) had a structurally normal heart on echocardiography. All the children with Down syndrome had pericardial effusion of varying severity while 33% had pulmonary artery hypertension (PAH). The fatality rate among the children seen with Down syndrome over the study period was 34.8% and only one child (4.2%) had open-heart surgery with the total repair of cardiac defect during the study period. Conclusion: Morbidity and mortality are high among children with Down syndrome due to the high prevalence of CHD. Early referral, diagnosis, and prompt intervention are encouraged.
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尼日利亚尼日尔三角洲地区联邦医疗中心唐氏综合症儿童先天性心脏病的患病率和发病模式
背景:唐氏综合症(DS)或21三体是世界上最常见的遗传性疾病,先天性心脏病(CHD)是这一人群发病率和死亡率的重要因素。早期诊断和及时的心脏干预可以提高他们的生活质量。这项研究是为了确定在巴耶尔萨州联邦医疗中心(FMC)儿科心脏病科就诊的唐氏综合症儿童中先天性心脏病的患病率和模式。方法:对2016年1月1日至2019年12月30日期间在巴耶尔萨州FMC儿科心脏病科进行心脏评估和超声心动图检查的唐氏综合征儿童进行前瞻性研究。从研究形式中检索社会人口统计信息、超声心动图诊断和结果数据并进行分析。结果:在研究期间共观察到24名唐氏综合症儿童。他们的年龄从0岁到16岁不等。多数唐氏综合征患儿年龄在5岁及以下,20例(83.3%)。男性13人,女性11人,男女比例为1.2:1。共有23例(95.8%)唐氏综合征患儿患有冠心病。最常见的冠心病是AVSD(包括完全、部分、孤立或与其他缺陷相关),占66.6%,其次是TOF(8.3%)。43.5%的儿童出现多重冠心病。超声心动图显示,仅有1名儿童(4.2%)心脏结构正常。所有唐氏综合征患儿均有不同程度的心包积液,33%有肺动脉高压(PAH)。在研究期间,唐氏综合症患儿的死亡率为34.8%,只有一名患儿(4.2%)在研究期间进行了心脏直视手术,完全修复了心脏缺陷。结论:由于冠心病的高发,唐氏综合征患儿的发病率和死亡率较高。鼓励早期转诊、诊断和及时干预。
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