Late outcome of extracardiac Fontan patients: 32 years of follow-up

Author:

Giannico Salvatore1,Trezzi Matteo2,Cantarutti Nicoletta1,Cafiero Giulia3,Ravà Lucilla4,Adorisio Rachele1,Brancaccio Gianluca2,Albanese Sonia2ORCID,Drago Fabrizio1ORCID,Carotti Adriano2ORCID,Amodeo Antonio2,Galletti Lorenzo2ORCID

Affiliation:

1. Pediatric Cardiology and Cardiac Arrhythmia Unit, Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, IRCCS , Rome, Italy

2. Cardiac Surgery Unit, Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, IRCCS , Rome, Italy

3. Department of Pediatric Cardiology and Cardiac Surgery, Sports Medicine Unit, Bambino Gesù Children's Hospital, IRCCS , Rome, Italy

4. Department of Pediatric Cardiology and Cardiac Surgery, Clinical Epidemiology Unit, Bambino Gesù Children's Hospital, IRCCS , Rome, Italy

Abstract

Abstract OBJECTIVES We sought to evaluate the long-term survival and risk factors for morbidity and mortality in our cohort of patients after extracardiac (EC) Fontan. METHODS We collected and analysed follow-up data until September 2020 for all patients who underwent EC Fontan operation at our institution from November 1988 to November 2015. RESULTS Out of 406 patients treated with EC Fontan at a mean age of 5.4 ± 4.5 years, 372 (91.6%) were discharged home; 15% were lost to follow-up. The median follow-up was 14.6 years (interquartile range 8.7–20.3). Two hundred patients (54%) had a good long-term outcome, with an event-free long-term survival, but late adverse events of any kind needing interventional or surgical reoperations were reported in 128 patients (34%). Forty-four patients (12%) developed late Fontan failure. Thirty-seven survivors (10%) had late arrhythmias, with the need for pacemaker implantation. Obstruction of the cavopulmonary pathway occurred in 49 patients (13%), but just 8 patients needed conduit surgical replacement. At 32 years, the survival probability was 84%. The risk of orthotopic heart transplant, considering death as a competing event (showed as cumulative incidence), was 12.5%. A preoperative diagnosis of hypoplastic left heart syndrome was an independent risk factor for the need for heart transplant. CONCLUSIONS The EC Fontan shows satisfactory long-term survival and low incidence of adverse events and late failure. Conduit replacement is rare, and its longevity may not represent a substantial issue in these patients. However, as with other technical variants, the need for reoperations during long-term follow-up is a significant challenge.

Publisher

Oxford University Press (OUP)

Subject

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

Reference35 articles.

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2. Staging toward the Fontan operation;Giannico;Semin Thorac Cardiovasc Surg,1994

3. An operation for the correction of tricuspid atresia;Kreutzer;J Thorac Cardiovasc Surg,1973

4. Four decades of Fontan palliation;de Leval;Nat Rev Cardiol,2010

5. Total cavopulmonary connection: a logical alternative to atriopulmonary connection for complex Fontan operations;de Leval;J Thorac Cardiovasc Surg,1988

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