Related Experiment Video
Updated: Aug 10, 2025

Fetal Echocardiography and Pulsed-wave Doppler Ultrasound in a Rabbit Model of Intrauterine Growth Restriction
Published on: June 29, 2013
Common Issues in Prenatal Care: Fetal Growth Restriction
Nicholas LeFevre1, Brandon Williamson2, Allison Kolker2
1Department of Family and Community Medicine - University of Missouri School of Medicine-Columbia, 1 Hospital Dr, Columbia, MO 65201.
Insights
Fetal growth restriction (FGR), affecting 10% of pregnancies, increases risks for babies. Early diagnosis and tailored delivery timing are key for managing FGR and improving outcomes.
Area of Science:
- Obstetrics and Gynecology
- Perinatology
- Neonatology
Background:
- Fetal growth restriction (FGR) affects up to 10% of pregnancies.
- FGR is associated with increased risks of intrauterine mortality and significant postnatal complications.
- These complications include intraventricular hemorrhage, necrotizing enterocolitis, respiratory distress, hypoglycemia, and developmental issues.
Purpose of the Study:
- To define FGR and outline diagnostic and management strategies.
- To highlight the importance of early diagnosis and appropriate interventions for FGR.
- To discuss the role of genetic testing and delivery timing in managing FGR.
Main Methods:
- Definition of FGR based on ultrasound (US) parameters (estimated fetal weight or abdominal circumference <10th percentile).
- Recommendation for detailed US in early-onset FGR (<32 weeks' gestation).
- Consideration of genetic testing (including chromosomal microarray) when FGR is associated with polyhydramnios or fetal anomalies.
Main Results:
- FGR significantly elevates risks for adverse fetal and neonatal outcomes.
- Early-onset FGR necessitates detailed US evaluation.
- Genetic testing is indicated in specific FGR cases with additional anomalies.
- Delivery timing is guided by growth restriction severity and fetal well-being tests.
Conclusions:
- FGR management requires a multi-faceted approach including accurate diagnosis and risk assessment.
- Tailored delivery timing based on fetal well-being is crucial.
- Low-dose aspirin may reduce FGR risk in high-risk preeclampsia patients, but no routine prevention is recommended for FGR itself.
Abstract:
Fetal growth restriction (FGR) is defined as an ultrasound (US)-determined estimated fetal weight or abdominal circumference less than the 10th percentile according to a population level reference curve. FGR affects up to 10% of pregnancies. Fetuses with FGR are at increased risk of intrauterine mortality and, postnatally, neonatal intraventricular hemorrhage, necrotizing enterocolitis, respiratory distress, hypoglycemia, and suboptimal neurologic, behavioral, and cognitive development. In early-onset FGR (ie, less than 32 weeks' gestation), a detailed US examination is recommended. When FGR is accompanied by polyhydramnios and/or fetal anomalies, genetic testing should be obtained, including chromosomal microarray analysis. The timing of delivery strategy should be based on the severity of growth restriction and findings on fetal tests of well-being (eg, nonstress testing, umbilical artery Doppler velocimetry). No routine prevention strategies are recommended. However, it has been shown that daily low-dose aspirin (ie, 81 mg/day) reduces the risk of FGR when taken by patients with a high risk of preeclampsia.
Related Concept Videos
Teratogenicity
Nature and Nurture
Fetal Circulation
Two umbilical arteries transport blood from the fetus to the placenta. At the placenta, the blood absorbs oxygen and nutrients while simultaneously eliminating waste products. This oxygen-enriched and nutrient-rich blood then returns to the fetus through one...
Pathophysiology of Diabetes
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Diabetes Mellitus: Type 2 and Gestational
Mitral Valve Prolapse III: Nursing Management

