[Congenital heart disease in Down's syndrome].

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Rebeca Arias-Lobo, Edgar Lupinta-Paredes, Juan Calderón-Colmenero, Jorge L Cervantes-Salazar, José A García-Montes, Emilia J Patiño-Bahena, Antonio Benita-Bordes
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引用次数: 0

Abstract

Background: Down syndrome is the most common chromosomal abnormality, it is associated with a wide variety of congenital heart defects, being considered as clinical elements of high infant morbidity and mortality. Objective.

Objective: To describe the clinical outcomes of patients with Down syndrome undergoing surgery and interventionism as treatment for congenital heart disease at this Institution.

Material and methods: 368 patients with Down syndrome and associated congenital heart disease were diagnosed. The variables studied were weight, stature, sex, age, type of heart disease, corrective procedure, length of stay in the hospital and intensive care unit, morbidity and mortality.

Results: 368 pediatric patients underwent surgical or interventional correction. Of which 197 (54%) were female, the median age was 24 months (interquartile range [IQR]: 14-48) in the surgical group and 36 months (IQR: 17-85) in the interventional group. The most frequent congenital heart diseases were: PCA (31%), IVC (28%), CAV (20%), ASD (16%) and tetralogy of Fallot with 4% respectively. Hospital stay was 9 days (IQR: 7-15) in the surgical group and 3 days (IQR: 2-5) in the hemodynamic group. Morbidities were postoperative infection in 30 patients (14%) and complete atrioventricular block in 19 patients (9%). Overall mortality including both surgical and interventional was 2%.

Conclusions: The therapeutic, surgical and interventional results in children with Down syndrome and congenital heart disease have improved very satisfactorily. The lower prevalence of the atrioventricular canal in the Mexican population is noteworthy. It is essential to carry out a cardiological evaluation of children with Down syndrome and those with congenital heart disease to correct them in a timely manner to promote survival and quality of life.

[唐氏综合症中的先天性心脏病]。
背景:唐氏综合征是最常见的染色体异常,它与多种先天性心脏缺陷有关,被认为是婴儿高发病率和死亡率的临床因素。目标。目的:描述本院唐氏综合征患者接受手术和介入治疗先天性心脏病的临床结果。材料与方法:对368例唐氏综合征及相关先天性心脏病患者进行诊断。研究的变量包括体重、身高、性别、年龄、心脏病类型、矫正手术、在医院和重症监护病房的住院时间、发病率和死亡率。结果:368例患儿接受了手术或介入矫正。其中女性197例(54%),手术组中位年龄为24个月(四分位间距[IQR]: 14-48),介入组中位年龄为36个月(IQR: 17-85)。最常见的先天性心脏病是:PCA(31%)、IVC(28%)、CAV(20%)、ASD(16%)和法洛四联症(4%)。手术组住院9天(IQR: 7 ~ 15),血流动力学组住院3天(IQR: 2 ~ 5)。发病率为术后感染30例(14%),完全性房室传导阻滞19例(9%)。包括手术和介入术在内的总死亡率为2%。结论:儿童唐氏综合征合并先天性心脏病的治疗、手术及介入治疗效果均有令人满意的改善。值得注意的是,在墨西哥人群中房室管的患病率较低。对唐氏综合征患儿及先天性心脏病患儿进行心脏学评估,及时进行纠正,提高患儿的生存率和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archivos de cardiologia de Mexico
Archivos de cardiologia de Mexico Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.80
自引率
20.00%
发文量
176
审稿时长
18 weeks
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