Long-term outcomes after heart transplantation in adult patients with univentricular versus biventricular congenital heart disease

Author:

Dib Nabil1,Iserin Laurence2,Varnous Shaida3,Guillemain Romain4,Hascoet Sebastien56,Belli Emre1,Cohen Sarah57

Affiliation:

1. Marie Lannelongue Hospital, Pediatric and Congenital Cardiac Surgery, M3C, Reference Center for Complex Congenital Heart Diseases , Le Plessis Robinson, France

2. Adult Congenital Heart Disease Unit, Cardiology Department, M3C, Reference Center for Complex Congenital Heart Diseases, European George Pompidou Hospital, AP-HP , Paris, France

3. Cardio-Thoracic Surgery Unit and Pathology Department, La Pitié-Salpétrière Hospital, APHP , Paris, France

4. European George Pompidou Hospital, AP-HP Department of Cardiovascular Surgery, , Paris, France

5. Marie Lannelongue Hospital, Pediatric and Congenital Cardiac Cardiology, M3C, Reference Center for Complex Congenital Heart Diseases , Le Plessis Robinson, France

6. Inserm UMR-S 999, Le Plessis-Robinson, France Paris-Saclay University

7. Université Paris-Saclay, UVSQ, Inserm, CESP U1018, Le Kremlin-Bicêtre, France; Marie Lannelongue

Abstract

Abstract OBJECTIVE Heart transplantation (HT) is the only life-extending therapy in adults with congenital heart disease (CHD) and end-stage heart failure. HT is considered at high risk in complex CHD given the anatomical complexity and past medical history. Little is known about long-term outcomes after HT in these patients. We aimed to evaluate early and long-term outcomes after HT in adult patients with univentricular versus biventricular CHD. METHODS This multicentre retrospective cohort study included all adult CHD patients who underwent HT between 1988 and 2021 in 3 tertiary centers. Factors associated with early (<30 days) and conditional long-term survival were assessed in the entire cohort. RESULTS Over a mean follow-up of 10.1 ± 7.8 years, 149 patients were included, of whom 55 (36.9%) had univentricular CHD. Sixty-four patients died during follow-up including 47 deaths before discharge from hospital. In multivariable analysis, univentricular physiology and female recipient gender were independently associated with a higher risk of early mortality (OR 2.99; 95% CI [1.33– 6.74] and OR 2.76; 95% CI [1.23– 6.20], respectively). For patients who survive the early period, conditional long-term survival was excellent for both groups and was not different between two groups (p = 0.764). CONCLUSION Adult CHD patients have a high incidence of overall mortality due to a high rate of early mortality. Univentricular physiology was associated with a significant increased risk of early death compared to biventricular physiology. However late mortality was excellent and no longer different between the two physiologies.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,General Medicine,Surgery

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