Durable left ventricular assist device explantation following recovery in paediatric patients: Determinants and outcome after explantation

Author:

Rohde Sofie1,Miera Oliver2,Sliwka Joanna3ORCID,Sandica Eugen4ORCID,Amodeo Antonio5ORCID,Veen Kevin1,de By Theo M M H6,Bogers Ad J J C1ORCID,Schweiger Martin7ORCID

Affiliation:

1. Department of Cardio-thoracic surgery, Erasmus University Medical Center , Rotterdam, Netherlands

2. Department of Congenital Heart Disease and Pediatric Cardiology, Deutsches Herzzentrum der Charité , Berlin, Germany

3. Department of Cardiac Surgery, Transplantology and Vascular Surgery, Silesian Center for Heart Diseases , Zabrze, Poland

4. Clinic for Pediatric Cardiac Surgery and Congenital Heart Defects, Heart and Diabetes Centre North Rhine-Westphalia, Ruhr-University of Bochum , Bad Oeynhausen, Germany

5. Heart Failure, Transplant and MCS Unit, Bambino Gesù Children Hospital & Research Institute, Rome, Italy, Catholic University of Sacred Heart, Department of Cardiac Surgery , Rome, Italy

6. EUROMACS, EACTS House , Windsor, United Kingdom

7. Children′s Hospital Zurich, Pediatric Heart Centre, Department for congenital heart surgery , Zurich, Switzerland

Abstract

Abstract OBJECTIVES Myocardial recovery in children supported by a durable left ventricular assist device is a rare, but highly desirable outcome because it could potentially eliminate the need for a cardiac transplant and the lifelong need for immunosuppressant therapy and the risk of complications. However, experience with this specific outcome is extremely limited. METHODS All patients < 19 years old supported by a durable left ventricular assist device from the European Registry for Patients with Mechanical Circulatory Support database were included. Participating centres were approached for additional follow-up data after explantation. Associated factors for explantation due to myocardial recovery were explored using Cox proportional hazard models. RESULTS The incidence of recovery in children supported by a durable left ventricular assist device was 11.7% (52/445; median duration of support, 122.0 days). Multivariable analyses showed body surface area (hazard ratio 0.229; confidence interval 0.093–0.565; P = 0.001) and a primary diagnosis of myocarditis (hazard ratio 4.597; confidence interval 2.545–8.303; P < 0.001) to be associated with recovery. Left ventricular end-diastolic diameter in children with myocarditis was not associated with recovery. Follow-up after recovery was obtained for 46 patients (88.5%). Sustained myocardial recovery was reported in 33/46 (71.7%) at the end of the follow-up period (28/33; >2 year). Transplants were performed in 6/46 (11.4%) (in 5 after a ventricular assist device was reimplanted). Death occurred in 7/46 (15.2%). CONCLUSIONS Myocardial recovery occurs in a substantial portion of paediatric patients supported with durable left ventricular assist devices, and sustainable recovery is seen in around three-quarters of them. Even children with severely dilated ventricles due to myocarditis can show recovery. Clinicians should be attentive to (developing) myocardial recovery. These results can be used to develop internationally approved paediatric weaning guidelines.

Funder

European Association for Cardio-Thoracic Surgery

Publisher

Oxford University Press (OUP)

Reference29 articles.

1. Pediatric ventricular assist devices;Stiller;Pediatr Crit Care Med,2013

2. The European Registry for Patients with Mechanical Circulatory Support (EUROMACS): third Paediatric (Paedi-EUROMACS) report;de By;Eur J Cardiothorac Surg,2022

3. Fifth Annual Pediatric Interagency Registry for Mechanical Circulatory Support (Pedimacs) Report;Rossano;Ann Thorac Surg,2021

4. Myocardial recovery in children supported with a durable ventricular assist device-a systematic review;Rohde;Eur J Cardiothorac Surg,2023

5. The European Registry for Patients with Mechanical Circulatory Support (EUROMACS): first annual report;de By;Eur J Cardiothorac Surg,2015

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