胎儿斑点追踪超声心动图测量先天性心脏病的整体纵向应变和应变率:系统回顾与元分析》。

IF 2.7 2区 医学 Q2 GENETICS & HEREDITY
Prenatal Diagnosis Pub Date : 2024-10-04 DOI:10.1002/pd.6672
Sarah van den Wildenberg, Ingrid M van Beynum, Malou E C Havermans, Eric Boersma, Greggory R DeVore, John M Simpson, Eric A P Steegers, Attie T J I Go, Jérôme M J Cornette
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引用次数: 0

摘要

胎儿二维斑点追踪超声心动图(2D-STE)是一种新型技术,它通过测量全纵向应变(GLS)和全纵向应变率(GLSR)来提供胎儿心脏功能的信息。这些特征可评估胎儿心壁的纵向变形。2D-STE 对患有先天性心脏病(CHD)的儿童和成人具有预后价值。因此,也应考虑其在胎儿期的重要性。本系统综述和荟萃分析概述了有关先天性心脏病胎儿二维-STE(GLS/GLSR)的文献,重点关注左心室和右心室(LV/RV)。研究结果表明,与对照组相比,主动脉共动脉症(CoA)和法洛氏四联症(ToF)胎儿的左心室-GLS明显较低。相反,单左心室胎儿的左心室-GLS较高。与对照组相比,左心发育不全综合征(HLHS)和法洛氏四联症胎儿的左心室-GLS明显较低。CoA 胎儿的左心室-GLSR 明显较低。总体而言,观察到相当大的异质性,这可能是由于研究设计的差异造成的。考虑到异质性参数,对患有先天性心脏病的胎儿进行更多的二维-STE前瞻性纵向研究,可为这一前景广阔的技术提供更好的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetal Speckle Tracking Echocardiography Measured Global Longitudinal Strain and Strain Rate in Congenital Heart Disease: A Systematic Review and Meta-Analysis.

Fetal two-dimensional speckle tracking echocardiography (2D-STE) is a novel technique that provides information on fetal heart function by measuring global longitudinal strain (GLS) and global longitudinal strain rate (GLSR). These features assess the longitudinal deformity of the fetal cardiac wall. 2D-STE is shown to be of prognostic value in children and adults with congenital heart disease (CHD). Therefore, its importance in fetal life should also be considered. This systematic review and meta-analysis provides an overview of the literature on 2D-STE (GLS/GLSR) in fetuses with CHD, focusing on the left and right ventricles (LV/RV). Findings indicated that LV-GLS was significantly lower in fetuses with coarctation of the aorta (CoA) and Tetralogy of Fallot (ToF) compared to controls. Conversely, fetuses with a single left ventricle exhibited higher LV-GLS. RV-GLS was significantly lower in fetuses with hypoplastic left heart syndrome (HLHS) and ToF compared to controls. LV-GLSR was significantly lower in fetuses with CoA. Overall, considerable heterogeneity was observed, possibly due to differences in study design. More prospective longitudinal studies on 2D-STE in fetuses with CHD, considering heterogeneity parameters, could offer better insights into this promising technique.

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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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