Maternal Predictors of Disparate Outcomes in Children With Single Ventricle Congenital Heart Disease

Author:

Asrani Priyanka1ORCID,Pinto Nelangi M.1,Puchalski Michael D.1,Ou Zhining2,Silver Robert M.3,Zinkhan Erin K.4,Heuser Cara C.3,Nance Amy5,Miller Thomas A.1

Affiliation:

1. Division of Pediatric Cardiology Department of Pediatrics University of Utah Salt Lake City UT

2. Center for Clinical and Translational Science Study Design and Biostatistics Center University of Utah Salt Lake City UT

3. Division of Maternal‐Fetal Medicine Department of Obstetrics and Gynecology University of Utah Salt Lake City UT

4. Division of Neonatology Department of Pediatrics University of Utah Salt Lake City UT

5. Utah Birth Defects Network Utah Department of Health Salt Lake City UT

Abstract

Background Significant variability in morbidity and mortality persists for children with functionally single ventricle congenital heart disease (SV‐CHD) despite standardization in medical and surgical care. We hypothesized that maternal health factors may be associated with an increased risk of poor outcomes in children with SV‐CHD. Methods and Results This retrospective, observational, cohort study included term maternal‐infant pairs with a diagnosis of SV‐CHD who underwent surgical palliation from 2006 to 2015 at Primary Children's Hospital. Pairs lacking maternal variables of interest or infant follow‐up data were excluded. The association of maternal risk factors of abnormal pre‐pregnancy body mass index, abnormal gestational weight gain (<7 or >20 kg), hypertensive disorders, and gestational diabetes mellitus with death/transplant and hemodynamics were analyzed using regression models. Of 190 infants, 135 (71%) maternal‐infant dyads had complete data for inclusion. Death or transplant occurred in 48 infants (36%) during an average follow‐up of 2.2 years (0.1–11.7 years). Abnormal gestational weight gain was associated with an increased risk of death and/or transplant in logistic regression (odds ratio, 3.22; 95% CI, 1.32–7.86; P =0.01), but not Cox regression (hazard ratio, 1.9; 95% CI, 1.0–3.7; P =0.055). Mean pulmonary artery pressures were higher in the setting of abnormal gestational weight gain (16.5±2.9 versus 14.7±3.0 mm Hg; P <0.001), and abnormal pre‐pregnancy body mass index (15.7±3.5 versus 14.2±2.1 mm Hg; P <0.001) in the systemic right ventricle group. Conclusions Abnormal gestational weight gain (excessive or inadequate) is a novel risk factor for worse outcomes in SV‐CHD. The fetoplacental environment may alter the trajectory of vascular development to impact outcomes in infants with SV‐CHD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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