Outcomes for Children With Congenital Heart Disease Undergoing Ventricular Assist Device Implantation: An ACTION Registry Analysis
- PMID: 39772369
- DOI: 10.1016/j.jacc.2024.10.083
Outcomes for Children With Congenital Heart Disease Undergoing Ventricular Assist Device Implantation: An ACTION Registry Analysis
Abstract
Background: There are no contemporary reports that highlight the national outcomes for children with congenital heart disease (CHD) undergoing ventricular assist device (VAD) implantation.
Objectives: This study sought to evaluate differences in VAD outcomes for children with CHD to those with non-CHD as well as those with univentricular CHD to those with biventricular CHD.
Methods: Data for CHD and non-CHD patients from the multicenter ACTION (Advanced Cardiac Therapies Improving Outcomes Network) undergoing VAD implantation from April 2018 to February 2023 were included. Preimplantation characteristics were compared between CHD and non-CHD as well as univentricular and biventricular CHD patients. Postimplantation survival and adverse events were compared between these cohorts.
Results: Of 966 patients undergoing VAD implantation, 352 (36%) had CHD, the majority of whom had univentricular CHD (230; 65%). Compared to non-CHD, CHD patients were younger (median age: 1.2 vs 9.4 years), were listed as INTERMACS (Interagency Registry for Mechanically Assisted Circulatory Support) 1 (36.1% vs 28.7%), were on mechanical ventilation (67.0% vs 44.1%), received total parenteral nutrition (63.6% vs 45.1%), and were on extracorporeal membrane oxygenation (ECMO) preimplantation (33.2% vs 20.5%) (P < 0.05 for all). Except for lower estimated glomerular filtration rate in children with univentricular CHD (median: 47.3 vs 59.9 mL/min/1.73 m2), there were no significant differences in clinical characteristics in univentricular vs biventricular CHD patients. Children with CHD compared to non-CHD were more likely to experience major adverse events (stroke, bleeding, infection, respiratory failure, renal and hepatic dysfunction) and have worse adjusted survival (HR: 2.05; 95% CI: 1.39-3.02; P < 0.001). There were no differences in adjusted survival in univentricular vs biventricular CHD (P > 0.05).
Conclusions: CHD patients are more likely in extremis at VAD implantation and experience higher rates of adverse events and worse survival compared to those with non-CHD. Timely referral for patients with CHD experiencing worsening heart failure and a proactive approach to VAD implantation has the potential to improve outcomes for this vulnerable cohort.
Keywords: children; congenital heart defect; heart failure; morbidity; mortality; outcomes; pediatric; univentricular congenital heart defect; ventricular assist device.
Copyright © 2025 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures ACTION receives funding from Abbott, Abiomed, and Berlin Heart. Dr Amdani is the site principal investigator for a multicenter study led by the University of Michigan and site principal investigator for FUEL-2 (Fontan Udenafil Exercise Longitudinal Assessment Trial, Mezzion) and has received no salary support. Dr Lorts has received research funding from Abbott, Abiomed, Berlin Heart Inc, and Bayer; is the principal investigator for the Berlin ACTIVE driver study; and has served as a consultant and speaker for Abbott. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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