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早孕期静脉导管筛查心脏缺陷:一项荟萃分析。

First-trimester ductus venosus screening for cardiac defects: a meta-analysis.

机构信息

Department of Obstetrics and Gynaecology, University of Ioannina School of Medicine, Greece.

出版信息

BJOG. 2011 Nov;118(12):1438-45. doi: 10.1111/j.1471-0528.2011.03029.x. Epub 2011 Jun 14.

DOI:10.1111/j.1471-0528.2011.03029.x
PMID:21668765
Abstract

BACKGROUND

Heart defects are the most common congenital abnormalities.

OBJECTIVE

We aimed to evaluate in a meta-analysis the screening performance of abnormal ductus venosus (DV) Doppler waveform for detection of congenital heart disease (CHD) in chromosomally normal fetuses.

SEARCH STRATEGY

Studies were retrieved from a search of MEDLINE, ISI, SCOPUS and EMBASE (from 1999 to March 2011) using the keywords 'ductus venosus', 'DV', 'chromosomal abnormalities', 'congenital heart disease' and 'nuchal translucency'.

SELECTION CRITERIA

We considered all studies that examined the diagnostic performance of DV in the first trimester for CHD in chromosomally normal fetuses. We included studies that were limited to fetuses with increased nuchal translucency (NT), normal NT, and studies that examined fetuses regardless of NT status.

DATA COLLECTION AND ANALYSIS

Seven studies (n = 50,354) regardless of the NT status, nine studies (n = 2908) with increased NT and seven studies (n = 47,610) with normal NT were included in the meta-analysis. We drew hierarchical summary receiver operating characteristic (HSROC) curves using the parameters of the fitted models.

MAIN RESULTS

In populations including participants regardless of NT status, the summary sensitivity and specificity of DV for detecting CHD were 50 and 93%, respectively. In participants with increased NT, the summary sensitivity and specificity were 83 and 80%, and in those with normal NT, they were 19 and 96%, respectively.

AUTHORS' CONCLUSIONS: The estimated performance of DV assessment for detection of CHD in chromosomally normal fetuses can be considered in evaluating the potential use and limitations of this screening test.

摘要

背景

心脏缺陷是最常见的先天性异常。

目的

我们旨在通过荟萃分析评估异常静脉导管(DV)多普勒波形在检测染色体正常胎儿先天性心脏病(CHD)中的筛查性能。

搜索策略

使用“静脉导管”、“DV”、“染色体异常”、“先天性心脏病”和“颈项透明层”等关键词,从 MEDLINE、ISI、SCOPUS 和 EMBASE 中检索研究(从 1999 年至 2011 年 3 月)。

选择标准

我们考虑了所有在染色体正常胎儿中检查第一孕期 DV 对 CHD 的诊断性能的研究。我们纳入了仅针对颈项透明层增加(NT)、正常 NT 和检查胎儿无论 NT 状态的研究。

数据收集和分析

无论 NT 状态如何,有 7 项研究(n = 50354),NT 增加有 9 项研究(n = 2908),NT 正常有 7 项研究(n = 47610)被纳入荟萃分析。我们使用拟合模型的参数绘制了分层综合受试者工作特征(HSROC)曲线。

主要结果

在包括无论 NT 状态如何的参与者的人群中,DV 检测 CHD 的汇总敏感性和特异性分别为 50%和 93%。在 NT 增加的参与者中,汇总敏感性和特异性分别为 83%和 80%,而在 NT 正常的参与者中,分别为 19%和 96%。

作者结论

可以考虑静脉导管评估在染色体正常胎儿中检测 CHD 的估计性能,以评估这种筛查试验的潜在用途和局限性。

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