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孤立性 II 型房间隔缺损病例的出生结局——一项基于人群的病例对照研究。

Birth outcomes of cases with isolated atrial septal defect type II--a population-based case-control study.

机构信息

Versys Clinics, Human Reproduction Institute, Budapest, Hungary.

出版信息

Acta Obstet Gynecol Scand. 2013 Jul;92(7):824-9. doi: 10.1111/aogs.12062. Epub 2013 Jan 21.

Abstract

OBJECTIVES

In general, epidemiological studies have evaluated cases with congenital cardiovascular abnormalities together. The aim of this study is to describe the birth outcomes of cases with isolated/single atrial septal defect type II (ASD-II, i.e. only a fossa ovalis defect) after surgical correction or lethal outcome in the light of maternal sociodemographic data.

DESIGN

Comparison of birth outcomes and maternal characteristics of cases with ASD-II and controls without defect.

SETTING

The population-based Hungarian Case-Control Surveillance of Congenital Abnormalities.

POPULATION

Hungarian newborn infants with or without ASD-II.

METHODS

Medically recorded birth outcomes, maternal age and birth order were evaluated. Marital and employment status was based on maternal information. The lifestyle factors were analyzed in a subsample of mothers visited at home based on a personal interview with mothers and their close relatives, and the family consensus was accepted.

MAIN OUTCOME MEASURES

Mean gestational age at delivery and birthweight, rate of preterm birth and low birthweight, maternal age, birth order, marital and employment status.

RESULTS

The evaluation of 471 cases with ASD-II and 38,151 controls without any defects showed a female excess in cases with ASD-II, having shorter gestational age and lower mean birthweight, and thus a higher rate of preterm births and low birthweight.

CONCLUSIONS

Intrauterine growth restriction and shorter gestational age were found in cases with ASD-II, particularly in female children. These factors may have a general developmental process in which there was not closure of the foramen ovale, thus echocardiographic screening of these babies might be of value.

摘要

目的

一般来说,流行病学研究将先天性心血管异常病例合并评估。本研究旨在根据母体社会人口统计学数据,描述单纯/单发 II 型房间隔缺损(ASD-II,即仅卵圆孔未闭)病例经手术矫正或致死结局后的出生结局。

设计

ASD-II 病例与无缺陷对照组的出生结局和母体特征比较。

设置

基于人群的匈牙利先天性异常病例对照监测。

人群

匈牙利有或无 ASD-II 的新生儿。

方法

评估了医学记录的出生结局、母亲年龄和出生顺序。婚姻和就业状况基于母亲的信息。生活方式因素在基于母亲及其近亲的家访基础上对母亲的子样本进行了分析,并接受了家庭共识。

主要观察指标

平均分娩孕周和出生体重、早产和低出生体重发生率、母亲年龄、出生顺序、婚姻和就业状况。

结果

对 471 例 ASD-II 病例和 38151 例无任何缺陷的对照进行评估,结果显示 ASD-II 病例中女性偏多,其妊娠周数较短,平均出生体重较低,因此早产和低出生体重的发生率较高。

结论

ASD-II 病例中存在宫内生长受限和妊娠周数较短的情况,尤其是女性患儿。这些因素可能具有普遍的发育过程,卵圆孔未闭合,因此对这些婴儿进行超声心动图筛查可能具有一定价值。

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