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[哥斯达黎加先天性心脏病的流行病学与登记情况]

[Epidemiology and registry of congenital heart disease in Costa Rica].

作者信息

Benavides-Lara Adriana, Faerron Ángel Jorge Enrique, Umaña Solís Lila, Romero Zúñiga Juan José

机构信息

Unidad de Enfermedades Congénitas, Instituto Costarricense de Investigación y Enseñanza en Nutrición y Salud, Cartago, Costa Rica.

出版信息

Rev Panam Salud Publica. 2011 Jul;30(1):31-8.

Abstract

OBJECTIVE

Characterize the population of children born with congenital heart disease (CHD) in Costa Rica and evaluate the country's registry processes.

METHODS

Exploratory observational study that included all children with CHD diagnosed at the National Children's Hospital between 1 May 2006 and 1 May 2007. Considering children under 1 year of age and their respective birth cohort, prevalence was estimated by sex, type of heart disease, age at diagnosis, maternal age, habitual residence, and associated extracardiac malformations, with 95% confidence intervals (95% CI). The data was compared with those of the Congenital Disease Registry Center (CREC).

RESULTS

During the period studied, 534 cases with CHD were diagnosed. There were 473 cases in children under 1 year of age in a birth cohort of 77 140 children. Prevalence was 0.6% (95% CI: 0.5-0.7). Based on CREC data, it was demonstrated that 71% of the cases were not detected at birth. The average age of diagnosis in infants under 1 year of age was 46.6 days. There were no differences by sex. Prevalence of CHD in children of mothers aged 35 years or over was significantly higher. However, when chromosomal abnormalities were excluded, the risk was no longer statistically significant. The provinces in the country with maritime ports were the areas with the highest risk in children of adolescent mothers. The most common CHDs were ventricular and atrial septal defects, patent ductus arteriosus, pulmonary valve stenosis, atrioventricular septal defects, coarctation of the aorta, and tetralogy of Fallot. Thirty-four percent of the cases of CHD were multiple, 11.2% were associated with chromosomal abnormalities, and 19% had associated congenital malformations.

CONCLUSIONS

CHD prevalence in Costa Rica is within the range reported globally. Significant underreporting of CHD was found in the CREC, primarily due to the age criteria applied. The results suggest that maternal age (under 20 and over 34) is a factor associated with CHD.

摘要

目的

描述哥斯达黎加先天性心脏病(CHD)患儿的群体特征,并评估该国的登记流程。

方法

探索性观察性研究,纳入2006年5月1日至2007年5月1日期间在国家儿童医院被诊断为CHD的所有患儿。考虑1岁以下儿童及其各自的出生队列,按性别、心脏病类型、诊断时年龄、母亲年龄、常住地和相关心脏外畸形估计患病率,并计算95%置信区间(95%CI)。将数据与先天性疾病登记中心(CREC)的数据进行比较。

结果

在研究期间,共诊断出534例CHD病例。在77140名儿童的出生队列中,1岁以下儿童有473例。患病率为0.6%(95%CI:0.5 - 0.7)。根据CREC数据,表明71%的病例在出生时未被发现。1岁以下婴儿的平均诊断年龄为46.6天。性别之间无差异。35岁及以上母亲的子女中CHD患病率显著更高。然而,排除染色体异常后,该风险不再具有统计学意义。该国拥有海港的省份是青少年母亲子女中风险最高的地区。最常见的CHD类型为室间隔和房间隔缺损、动脉导管未闭、肺动脉瓣狭窄、房室间隔缺损、主动脉缩窄和法洛四联症。34%的CHD病例为多发,11.2%与染色体异常相关,19%伴有先天性畸形。

结论

哥斯达黎加的CHD患病率在全球报告的范围内。CREC中CHD漏报情况严重,主要是由于所采用的年龄标准。结果表明母亲年龄(20岁以下和34岁以上)是与CHD相关的一个因素。

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