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Association of biparietal diameter growth rate with neurodevelopment in infants with fetal growth restriction
Yoshimi Hasegawa1, Shigeru Aoki1, Kentaro Kurasawa1
1Perinatal Center for Maternity and Neonate, Yokohama City University Medical Center, Yokohama, Japan.
Insights
Poor biparietal diameter (BPD) growth in fetuses with severe growth restriction is linked to increased risks of neurodevelopmental complications. Monitoring BPD growth rate is crucial for identifying infants at risk for adverse outcomes.
Area of Science:
- Perinatology
- Fetal Medicine
- Neurodevelopmental Pediatrics
Background:
- Severe fetal growth restriction (FGR) poses significant risks to infant neurodevelopment.
- Biparietal diameter (BPD) is a key biometric parameter used in fetal assessment.
- Understanding the relationship between BPD growth patterns and neurodevelopmental outcomes is critical for early intervention.
Purpose of the Study:
- To investigate the association between biparietal diameter (BPD) growth rate and neurodevelopmental complications in infants with severe fetal growth restriction.
- To identify BPD growth delay as a potential risk factor for adverse neurodevelopmental outcomes.
Main Methods:
- Retrospective analysis of pregnant women with severe FGR (<5th percentile) before 30 weeks gestation.
- Definition of poor BPD growth: at least 50% below mean growth rate for at least 1 week.
- Assessment of neonatal morbidities, perinatal mortality, and neurodevelopmental complications at 2 years corrected age.
Main Results:
- Out of 8254 infants, 26 met criteria for severe FGR; 17 had poor BPD growth, 9 had normal BPD growth.
- No significant difference in gestational age at delivery between groups.
- Eight infants (47%) in the poor BPD growth group experienced death or neurodevelopmental complications, versus none in the normal BPD growth group (p=0.009).
Conclusions:
- BPD growth rate is significantly associated with neurodevelopmental outcomes in infants with severe FGR.
- Growth delay in BPD, compared to the mean growth rate, is a risk factor for poor neurodevelopmental outcomes.
- This highlights the importance of monitoring fetal growth parameters for predicting neurodevelopmental trajectories.
Objective:
To investigate the association between neurodevelopmental complications and biparietal diameter (BPD) growth rate.
Materials And Methods:
The patients were pregnant women with severe fetal growth restriction (< 5(th) percentile) before 30 weeks who delivered after 24 gestational weeks. We defined poor BPD growth as being at least 50% below the mean growth rate for at least 1 week. We analyzed maternal characteristics, neonatal complication morbidities, perinatal mortality rate, and neurodevelopmental complications in the child at age 2 years (corrected).
Results:
BPD growth was categorized as normal or poor. Out of 8254 infants, 26 met the above criteria. The poor BPD growth group included 17 infants and the normal BPD growth group included nine infants. The gestational age at delivery was 28.7 (24.7-31.7) weeks in the poor BPD growth group and 28.5 (26.1-32.4) weeks in the normal BPD growth group, showing no significant difference. However, death or neurodevelopmental complications occurred in eight of the 17 infants in the poor BPD growth group, whereas neither death nor neurodevelopmental complications were observed in the normal BPD growth group (p = 0.009). Moreover, in those with poor outcomes, BPD growth rates were consistently below 40% and birth weights were < 700 g.
Conclusion:
BPD growth was associated with neurodevelopmental outcomes, and growth delay as compared with the mean growth rate is a risk factor for poor neurodevelopment.
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