Journal article

Head Biometry in Fetuses with Isolated Congenital Heart Disease


Authors listGraupner, Oliver; Koch, Jessica; Enzensberger, Christian; Goette, Malena; Wolter, Aline; Mueller, Vera; Kawecki, Andreea; Herrmann, Johannes; Axt-Fliedner, Roland

Publication year2020

Pages69-76

JournalUltraschall in der Medizin = European journal of ultrasound

Volume number41

Issue number1

ISSN0172-4614

eISSN1438-8782

DOI Linkhttps://doi.org/10.1055/a-0796-6502

PublisherThieme


Abstract

Purpose Altered cerebral hemodynamics are involved in changes in head biometry in fetuses with congenital heart disease (CHD). We compared head growth in different CHD groups with published normative values and investigated whether CHD groups differ from each other in terms of head circumference (HC) development over gestational age (GA).

Materials and Methods Retrospective cohort study consisting of 248 CHD fetuses. Subgroups were generated according to the expected ascending aorta oxygen saturation: Low placental blood content (BC) and therefore low oxygen delivery to the brain (group 1: n = 108), intermediate placental and systemic BC due to intracardiac mixing of blood (group 2: n = 103), high placental BC (group 3: n = 13) and low placental BC and low oxygen delivery to the brain without mixing of blood (group 4: n = 24). Furthermore, group 1 was divided into antegrade (n = 34) and retrograde (n = 74) flow through the aortic arch. Comparisons were made at a GA of 22, 30 and 38 weeks.

Results Estimated values of zHC (z-score transformed) were not significantly different between the four CHD groups at the three time points in gestation (all p > 0.05). Within group 1 fetuses with retrograde aortic arch flow showed a significant negative association between HC and GA compared to reference values (b = -0.054, p < 0.001) and had significantly lower zHC values at 38 weeks (-0.836) compared to fetuses with antegrade flow (0.366, p = 0.009).

Conclusion Our data do not confirmthat CHD fetuses in general have a significantly smaller HC. HC becomes smaller throughout gestation depending on the direction of aortic arch flow.




Citation Styles

Harvard Citation styleGraupner, O., Koch, J., Enzensberger, C., Goette, M., Wolter, A., Mueller, V., et al. (2020) Head Biometry in Fetuses with Isolated Congenital Heart Disease, European Journal of Ultrasound, 41(1), pp. 69-76. https://doi.org/10.1055/a-0796-6502

APA Citation styleGraupner, O., Koch, J., Enzensberger, C., Goette, M., Wolter, A., Mueller, V., Kawecki, A., Herrmann, J., & Axt-Fliedner, R. (2020). Head Biometry in Fetuses with Isolated Congenital Heart Disease. European Journal of Ultrasound. 41(1), 69-76. https://doi.org/10.1055/a-0796-6502



Keywords


APOLIPOPROTEIN-E GENOTYPECARDIOVASCULAR MALFORMATIONScongenital heart diseaseFetal Echocardiographyfetal head biometryNEURODEVELOPMENTAL OUTCOMESplacental blood contentPREDICTORSTRANSPOSITION

Last updated on 2025-21-05 at 18:24