Congenital Heart Defects and Outcome in a Large Cohort of Down Syndrome: A Single-Center Experience from Turkey.

IF 1.3 Q3 PEDIATRICS
Dilek Uludağ Alkaya, Birol Öztürk, Aylin Yüksel Ülker, Serdar Bozlak, Esra Öztürk, Reyhan Dedeoğlu, Ayşe Güler Eroğlu, Funda Öztunç, Beyhan Tüysüz
{"title":"Congenital Heart Defects and Outcome in a Large Cohort of Down Syndrome: A Single-Center Experience from Turkey.","authors":"Dilek Uludağ Alkaya,&nbsp;Birol Öztürk,&nbsp;Aylin Yüksel Ülker,&nbsp;Serdar Bozlak,&nbsp;Esra Öztürk,&nbsp;Reyhan Dedeoğlu,&nbsp;Ayşe Güler Eroğlu,&nbsp;Funda Öztunç,&nbsp;Beyhan Tüysüz","doi":"10.5152/TurkArchPediatr.2023.23041","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Congenital heart defects occur in approximately 50% of children with Down syndrome and they contribute considerably to morbidity and mortality. The aim of this study is to investigate the prevalence, classification, and survival of congenital heart defects in Down syndrome.</p><p><strong>Materials and methods: </strong>About 1731 Down syndrome patients who underwent echocardiography between 1986 and 2022 were evaluated. The median follow-up duration was 8.7 years (range 1-35.8 years). Congenital heart defect was grouped as cyanotic and acyanotic.</p><p><strong>Results: </strong>Among the 1731 patients, 52.1% had congenital heart defects. Congenital heart defect was significantly more common in females than males. The most common cardiac defect was ventricular septal defect (35%), followed by atrial septal defect (31.8%), atrioventricular septal defect (23.4%), tetralogy of Fallot (5%), and patent ductus arteriosus (3.6%). In the follow-up, 43.2% of atrial septal defect, 17.8% of ventricular septal defect, and a total of 20% of congenital heart defects were closed spontaneously. About 34.4% of congenital heart defect was corrected by cardiac surgery/intervention. Five-year survival rate was 97.4% in patients without congenital heart defects, whereas it was 95.6% in mild congenital heart defects and 86.1% in moderate to severe congenital heart defects. There was no relationship between consanguinity, parental age, maternal disease, folic acid supplementation before/during pregnancy, gestational age, birth weight, and congenital heart defects. Neuromotor development was similar in patients with and without congenital heart defects.</p><p><strong>Conclusion: </strong>We demonstrated that almost half of the patients had congenital heart defects; ventricular septal defect was the most common congenital heart defect type. This study is valuable in terms of the largest single-center study describing the classification, prognostic factors, and survival of Down syndrome patients with congenital heart defect from Turkey.</p>","PeriodicalId":75267,"journal":{"name":"Turkish archives of pediatrics","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7c/2e/tap-58-5-473.PMC10544380.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish archives of pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5152/TurkArchPediatr.2023.23041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Congenital heart defects occur in approximately 50% of children with Down syndrome and they contribute considerably to morbidity and mortality. The aim of this study is to investigate the prevalence, classification, and survival of congenital heart defects in Down syndrome.

Materials and methods: About 1731 Down syndrome patients who underwent echocardiography between 1986 and 2022 were evaluated. The median follow-up duration was 8.7 years (range 1-35.8 years). Congenital heart defect was grouped as cyanotic and acyanotic.

Results: Among the 1731 patients, 52.1% had congenital heart defects. Congenital heart defect was significantly more common in females than males. The most common cardiac defect was ventricular septal defect (35%), followed by atrial septal defect (31.8%), atrioventricular septal defect (23.4%), tetralogy of Fallot (5%), and patent ductus arteriosus (3.6%). In the follow-up, 43.2% of atrial septal defect, 17.8% of ventricular septal defect, and a total of 20% of congenital heart defects were closed spontaneously. About 34.4% of congenital heart defect was corrected by cardiac surgery/intervention. Five-year survival rate was 97.4% in patients without congenital heart defects, whereas it was 95.6% in mild congenital heart defects and 86.1% in moderate to severe congenital heart defects. There was no relationship between consanguinity, parental age, maternal disease, folic acid supplementation before/during pregnancy, gestational age, birth weight, and congenital heart defects. Neuromotor development was similar in patients with and without congenital heart defects.

Conclusion: We demonstrated that almost half of the patients had congenital heart defects; ventricular septal defect was the most common congenital heart defect type. This study is valuable in terms of the largest single-center study describing the classification, prognostic factors, and survival of Down syndrome patients with congenital heart defect from Turkey.

Abstract Image

Abstract Image

先天性心脏缺陷与唐氏综合征患者的预后:土耳其的一项单中心经验。
目的:先天性心脏缺陷发生在约50%的唐氏综合症儿童中,它们对发病率和死亡率有很大影响。本研究的目的是调查唐氏综合征先天性心脏缺陷的患病率、分类和生存率。材料和方法:对1986年至2022年间接受超声心动图检查的约1731名唐氏综合征患者进行评估。中位随访时间为8.7年(1-35.8年)。先天性心脏缺陷分为青紫性和非青紫性。结果:1731例患者中,52.1%为先天性心脏病。先天性心脏缺陷在女性中明显比男性更常见。最常见的心脏缺陷是室间隔缺损(35%),其次是房间间隔缺损(31.8%)、房室间隔缺损(23.4%)、法洛四联症(5%)和动脉导管未闭(3.6%)。在随访中,43.2%的房间间隔缺损、17.8%的室间隔缺损和共20%的先天性心脏缺陷是自发闭合的。约34.4%的先天性心脏缺陷通过心脏手术/干预得到纠正。无先天性心脏缺陷患者的五年生存率为97.4%,而轻度先天性心脏缺损患者的五周生存率为95.6%,中度至重度先天性心脏病患者的五岁生存率为86.1%。血亲、父母年龄、母亲疾病、孕前/孕期叶酸补充、胎龄、出生体重和先天性心脏缺陷之间没有关系。先天性心脏缺陷和非先天性心脏病患者的神经运动发育相似。结论:我们证明,几乎一半的患者有先天性心脏缺陷;室间隔缺损是最常见的先天性心脏缺损类型。这项研究在描述土耳其先天性心脏缺陷唐氏综合征患者的分类、预后因素和生存率的最大单中心研究中具有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.00
自引率
0.00%
发文量
0
文献相关原料
公司名称 产品信息 采购帮参考价格
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信