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先天性心脏病的产前检测 - 2013-2017 年瑞典筛查计划的结果。

Prenatal detection of congenital heart disease - results of a Swedish screening program 2013-2017.

机构信息

Department of Obstetrics and Gynecology, Region Västra Götaland, Sahlgrenska University Hospital, Diagnosvägen 15, Paviljong 7b, 416 85, Gothenburg, Sweden.

Pediatric Heart Center, Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

BMC Pregnancy Childbirth. 2021 Aug 22;21(1):579. doi: 10.1186/s12884-021-04028-5.

Abstract

BACKGROUND

This report evaluates results of a screening program on prenatal detection of congenital heart defects in a geographical cohort of western Sweden between January 1st, 2013 and June 31st, 2017. During the study period 88,230 children were born in VGR.

METHODS

Retrospective data on pregnant women from the Västra Götaland region that were referred to fetal cardiologists in Gothenburg were retrieved. To determine prenatal detection rate, all neonates who underwent surgery or catheter intervention for a critical congenital heart defect born between January 1st, 2014 and December 31st, 2016 were included. The four-chamber view was implemented into the routine scan in 2009 and implementation of the ISUOG guidelines, including the outflow tracts, started in the region in 2015.

RESULTS

113 fetuses received a prenatal diagnosis of a major congenital heart defect. 89% of these were referred because of a suspected cardiac malformation and 88% were diagnosed before 22 completed weeks. 59% of the patients diagnosed before 22 completed weeks opted for termination of pregnancy. During 2014-2016, 61 fetuses had a prenatal diagnosis of a critical congenital heart defect and a further 47 were diagnosed after birth, hence 56% were diagnosed prenatally, 82% for those which had a combination with an extracardiac abnormality and/or chromosomal aberration compared to 50% if an isolated critical congenital heart defect was diagnosed. For single ventricle cardiac defects such as hypoplastic left heart syndrome, double inlet left ventricle and tricuspid atresia, the detection rate was 100%. The detection rate for transposition of the great arteries and coarctation of the aorta was 9 and 18% respectively.

CONCLUSIONS

56% of all fetuses with a critical congenital heart defect were diagnosed prenatally during 2014-2016 and approximately 53% of all major congenital heart defects 2013-2017 as compared to 13.8% in 2009 in the same region. An increased focus towards the fetal heart in the routine scan improved the prenatal detection rate of major congenital heart defects. The detection of congenital heart defects affecting the four-chamber view seems sufficient, but more training is needed to improve the quality of the examination of the outflow tracts.

摘要

背景

本报告评估了 2013 年 1 月 1 日至 2017 年 6 月 31 日期间,在瑞典西部一个地理队列中进行的产前先天性心脏病筛查项目的结果。在研究期间,VGR 有 88230 名儿童出生。

方法

检索了哥德堡胎儿心脏病专家转诊的来自西瑞典地区的孕妇的回顾性数据。为了确定产前检出率,将 2014 年 1 月 1 日至 2016 年 12 月 31 日期间因严重先天性心脏缺陷而接受手术或导管介入治疗的所有新生儿均纳入研究。四腔心切面于 2009 年纳入常规扫描,ISUOG 指南(包括流出道)于 2015 年在该地区开始实施。

结果

113 例胎儿产前诊断为严重先天性心脏病。其中 89%因疑似心脏畸形而转诊,88%在 22 周前完成诊断。59%在 22 周前完成诊断的患者选择终止妊娠。2014-2016 年期间,61 例胎儿产前诊断为严重先天性心脏缺陷,另有 47 例出生后诊断,因此 56%产前诊断,82%对于伴有心脏外异常和/或染色体异常的患者,与仅诊断为严重先天性心脏缺陷的患者(50%)相比。对于左心发育不良综合征、左心室双入口和三尖瓣闭锁等单心室心脏缺陷,检出率为 100%。大动脉转位和主动脉缩窄的检出率分别为 9%和 18%。

结论

2014-2016 年期间,所有严重先天性心脏缺陷胎儿中有 56%产前诊断,而在同一地区 2013-2017 年所有重大先天性心脏缺陷中有 53%产前诊断,而在 2009 年为 13.8%。在常规扫描中更加关注胎儿心脏,提高了重大先天性心脏缺陷的产前检出率。四腔心切面先天性心脏缺陷的检出似乎足够,但需要更多的培训来提高流出道检查的质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f6/8380393/6d4319651e73/12884_2021_4028_Fig1_HTML.jpg

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