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Fetal Echocardiography and Pulsed-wave Doppler Ultrasound in a Rabbit Model of Intrauterine Growth Restriction
Published on: June 29, 2013
Screening for fetal growth restriction and placental insufficiency
Melanie C Audette1, John C Kingdom2
1Lunenfeld-Tanenbaum Research Institute, Toronto, Canada; Faculty of Medicine, University of Toronto, Toronto, Canada.
Insights
Distinguishing fetal growth restriction (FGR) from constitutionally small fetuses is crucial for improving outcomes. New screening methods, including placental growth factor biomarkers and advanced imaging, offer potential for better antenatal care.
Area of Science:
- Obstetrics and Gynecology
- Fetal Medicine
- Biomarker Discovery
Background:
- Fetal growth restriction (FGR) is a major cause of stillbirth and poor neurodevelopmental outcomes.
- FGR is often conflated with small for gestational age (SGA), hindering effective clinical management.
- Distinguishing pathological FGR from constitutionally small fetuses is essential for improved outcomes.
Purpose of the Study:
- To review current understanding of FGR etiology, diagnosis, and management.
- To highlight novel approaches for effective FGR screening.
- To emphasize the potential of new biomarkers and imaging techniques in antenatal care.
Main Methods:
- Comprehensive review of literature on FGR etiology, diagnosis, antenatal surveillance, and management.
- Analysis of recent advances in novel imaging methods for fetal assessment.
- Evaluation of maternal blood biomarkers, such as placenta growth factor, for FGR detection.
Main Results:
- Understanding the multifactorial pathogenesis of FGR, including placental pathologies, is key to developing targeted treatments.
- Maternal blood biomarker placenta growth factor shows significant potential for FGR screening.
- Stepwise multi-parametric testing using novel imaging offers a basis for cost-effective FGR screening.
Conclusions:
- Effective distinction between pathological FGR and constitutionally small fetuses is critical for clinical practice.
- Integrating novel biomarkers and advanced imaging into antenatal care systems can improve FGR screening.
- Targeted treatment strategies preserving placental function are needed for better fetal outcomes.
Abstract:
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.
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