Morbidity and mortality in adults with a Fontan circulation beyond the fourth decade of life
Authors/Creators
- Constantine, Andrew1, 2
- Ferrero, Paolo3
- Gribaudo, Elena1
- Mitropoulou, Panagiota4
- Krishnathasan, Kaushiga1
- Costola, Giulia1
- Lwin, Myo T4
- Fitzsimmons, Samantha4
- Brida, Margarita1, 2, 5
- Montanaro, Claudia1, 2
- Kempny, Aleksander1, 2
- Heng, Ee Ling1, 2
- Chessa, Massimo3, 6
- Dimopoulos, Konstantinos1, 2
- Rafiq, Isma1, 2
- 1. Adult Congenital Heart Centre and Centre for Pulmonary Hypertension, Royal Brompton Hospital, Royal Brompton & Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, Sydney Street, SW3 6NP London, UK
- 2. National Heart and Lung Institute, Imperial College London, Guy Scadding Building, Dovehouse Street, SW3 6LY London, UK
- 3. ACHD Unit, IRCCS-Policlinico San Donato, San Donato Milanese, Milan, Italy
- 4. Congenital Cardiac Centre, Southampton General Hospital, University Hospital Southampton NHS Foundation Trust, Southampton, UK
- 5. Department of Medical Rehabilitation, Medical Faculty University of Rijeka, Rijeka, Croatia
- 6. UniSR - Vita Salute Sal Raffaele University, Milan, Italy
Description
Abstract
Aims: To evaluate the late outcomes of adults (above 35 years) with a Fontan-type circulation, for whom current data on morbidity and mortality are lacking.
Methods and results: Data were collected retrospectively on consecutive patients with Fontan circulation above the age of 35 years followed in three European specialist centres. Overall, 115 Fontan patients were included [median age 35 (range 35-48) years, 47.8% female]. The most common underlying congenital heart disease diagnosis was tricuspid atresia (n = 58, 50.4%), and the age at first Fontan completion was 9.1 (interquartile range 5.0-15.8) years. Almost two-thirds (61.7%) of patients had undergone an atriopulmonary Fontan, and 23.5% had received a total cavopulmonary connection. One-third required repeat surgery or intervention. Most patients (55.9%) were in New York Heart Association functional class II or class I (30.6%), 76 (66.1%) patients had experienced at least one arrhythmia, and eight (7.0%) protein-losing enteropathy. At a median follow-up of 5.0 (2.4-10.3) years, 15 (13.0%) patients were referred for transplantation assessment and 19 (16.5%) patients died, mainly from heart failure (84.2%). Univariable predictors of death or transplantation included lower serum albumin level [hazard ratio (HR) 1.09 per g/L decrease, 95% confidence interval (CI): 1.04-1.15, P = 0.0009], prior heart failure admission (HR 4.28, 95% CI:1.75-10.44, P = 0.001), prior atrial tachycardia or flutter (HR 3.02, 95% CI: 1.23-7.38, P = 0.02), and baseline pulmonary vasodilator therapy (HR 8.59, 95% CI:1.05-70.13, P = 0.04). Lower serum albumin and prior atrial tachycardia or flutter remained significant on bivariable analysis.
Conclusion: Our study highlights the significant morbidity and mortality in older adults with a Fontan-type circulation, emphasizing the need for lifelong specialist surveillance with frequent risk stratification, close monitoring, and early consideration for transplantation assessment.