Original Investigation
Clinical Outcomes in Adolescents and Adults After the Fontan Procedure

https://doi.org/10.1016/j.jacc.2017.12.054Get rights and content
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Abstract

Background

Long-term outcomes of Fontan patients who survive to age ≥16 years have not been well characterized. The Australian and New Zealand Fontan Registry (ANZFR) provides a unique opportunity to understand survival and complication rates in Fontan patients who transition to adult congenital heart disease centers.

Objectives

This study sought to describe the survival and complications of adult patients who have had a Fontan procedure.

Methods

The study analyzed outcomes in patients ≥16 years of age who were prospectively enrolled in the ANZFR.

Results

Data from all 683 adult survivors from the ANZFR were analyzed. Mortality status was confirmed from the National Death Index. There were 201 atriopulmonary (AP) connections and 482 total cavopulmonary connections (249 lateral tunnels and 233 extracardiac conduits). For these subjects, the survival rate at age 30 years was 90% (95% CI: 87% to 93%), and it was 80% (95% CI: 75% to 87%) at 40 years of age. Survival at age 30 years was significantly worse for the patients with AP connections (p = 0.03). At latest follow-up, only 53% of patients were in New York Heart Association functional class I. After the age of 16 years, 136 (20%) had experienced at least 1 new arrhythmia, 42 (6%) required a permanent pacemaker, 45 (7%) had a thromboembolic event, and 135 (21%) required a surgical reintervention. Only 41% (95% CI: 33% to 51%) of Fontan patients were free of serious adverse events at 40 years of age.

Conclusions

This comprehensively followed cohort showed that a variety of morbid complications is common in Fontan adults, and that there is a substantial incidence of premature death, particularly in patients with AP connections.

Key Words

adult congenital heart disease
arrhythmia
Fontan
single ventricle

Abbreviations and Acronyms

ACHD
adult congenital heart disease
ANZFR
Australian and New Zealand Fontan Registry
AP
atriopulmonary
AV
atrioventricular
ECC
extracardiac conduit
LT
lateral tunnel
PLE
protein-losing enteropathy
SVT
supraventricular tachycardia
TCPC
total cavopulmonary connection

Cited by (0)

This work was supported by a National Health and Medical Research Council (NHMRC) Partnership Grant (1076849). Dr. d’Udekem is a Clinician Practitioner Fellow of the National Health and Medical Research Council (NHMRC) (1082186); and has received consulting fees from Merck Sharp & Dohme and Actelion. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

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