1. Fetal cerebrovascular impedance is reduced in left congenital diaphragmatic hernia
- Author
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Kosiv, KA, Moon‐Grady, A, Hogan, W, Keller, R, Rapoport, R, Rogers, E, Feldstein, VA, Lee, H, and Peyvandi, S
- Subjects
Neurosciences ,Digestive Diseases ,Pediatric ,Infant Mortality ,Perinatal Period - Conditions Originating in Perinatal Period ,Brain Disorders ,Cardiovascular ,Biomedical Imaging ,Clinical Research ,Reproductive health and childbirth ,Adaptation ,Physiological ,Cardiography ,Impedance ,Case-Control Studies ,Cerebrovascular Circulation ,Echocardiography ,Electric Impedance ,Female ,Fetal Development ,Fetus ,Functional Laterality ,Gestational Age ,Hernias ,Diaphragmatic ,Congenital ,Humans ,Middle Cerebral Artery ,Neurodevelopmental Disorders ,Pregnancy ,Pulsatile Flow ,Ultrasonography ,Prenatal ,Umbilical Arteries ,cerebral sparing ,cerebrovascular resistance ,congenital diaphragmatic hernia ,middle cerebral artery pulsatility index ,neurodevelopment ,Paediatrics and Reproductive Medicine ,Obstetrics & Reproductive Medicine - Abstract
ObjectivesCongenital diaphragmatic hernia (CDH) can cause a significant mass effect in the fetal thorax, displacing the heart into the opposite hemithorax. In left-sided CDH (L-CDH), this is associated with smaller left-sided cardiac structures and reduced left-ventricular cardiac output (LVCO). The effect of these physiologic changes on cerebral blood flow is not well understood. We sought to describe the middle cerebral artery (MCA) pulsatility index (PI), a measure of cerebrovascular impedance, in fetuses with L-CDH and those with right-sided CDH (R-CDH) compared with unaffected fetuses, and the relationship between MCA-PI and LVCO. We hypothesized that MCA-PI would be lower in fetuses with L-CDH and similar in those with R-CDH compared to controls, and that MCA-PI would be correlated with LVCO.MethodsWe identified all fetuses with CDH evaluated at The University of California San Francisco, San Francisco, CA, USA from 2011 to 2018. Fetal echocardiograms and ultrasound scans were reviewed. Umbilical artery and MCA Doppler examinations were assessed to calculate pulsatility indices. Ventricular outputs were calculated using Doppler-derived stroke volume and fetal heart rate. Lung-to-head ratio (LHR), estimated fetal weight, biparietal diameter (BPD) and head circumference (HC) were obtained from fetal sonograms. Measurements in fetuses with CDH, according to the side of the defect, were compared with those in unaffected, gestational age-matched controls. A subset of CDH survivors had available data on neurodevelopmental outcome, as assessed using the Bayley Scales of Infant Development, 3rd edition.ResultsA total of 64 fetuses with CDH (L-CDH, n = 53; R-CDH, n = 11) comprised the study groups, with 27 unaffected fetuses serving as controls. Mean gestational age at evaluation was similar between the three groups. Compared to controls, fetuses with L-CDH had significantly lower LVCO expressed as a percentage of combined cardiac output (CCO) (32%; 95% CI, 29-35% vs 38%; 95% CI, 33-42%; P = 0.04) and lower MCA-PI Z-score (-1.3; 95% CI, -1.7 to -1.0 vs 0.08; 95% CI, -0.5 to 0.6; P
- Published
- 2021