Screening for fetal growth restriction and placental insufficiency

被引:161
作者
Audette, Melanie C. [1 ,2 ]
Kingdom, John C. [1 ,2 ,3 ]
机构
[1] Lunenfeld Tanenbaum Res Inst, 60 Murray St,6th Floor,Room 6-1020, Toronto, ON M5T 3H7, Canada
[2] Univ Toronto, Fac Med, Toronto, ON, Canada
[3] Sinai Hlth Syst, Dept Obstet & Gynaecol, Maternal Fetal Med Div, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Fetal growth restriction; Small for gestational age; Placental insufficiency; Doppler ultrasound; Biomarkers; UTERINE ARTERY DOPPLER; LOW-BIRTH-WEIGHT; EARLY-ONSET; PRETERM BIRTH; FUNDAL HEIGHT; PREGNANCY; RISK; PREDICTION; WOMEN; AGE;
D O I
10.1016/j.siny.2017.11.004
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Fetal growth restriction (FGR) continues to be a leading cause of preventable stillbirth and poor neurodevelopmental outcomes in offspring, and furthermore is strongly associated with the obstetrical complications of iatrogenic preterm birth and pre-eclampsia. The terms small for gestational age (SGA) and FGR have, for too long, been considered equivalent and therefore used interchangeably. However, the delivery of improved clinical outcomes requires that clinicians effectively distinguish fetuses that are pathologically growth-restricted from those that are constitutively small. A greater understanding of the multifactorial pathogenesis of both early- and late-onset FGR, especially the role of underlying placental pathologies, may offer insight into targeted treatment strategies that preserve placental function. The new maternal blood biomarker placenta growth factor offers much potential in this context. This review highlights new approaches to effective screening for FGR based on a comprehensive review of: etiology, diagnosis, antenatal surveillance and management. Recent advances in novel imaging methods provide the basis for stepwise multi-parametric testing that may deliver cost-effective screening within existing antenatal care systems. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:119 / 125
页数:7
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