Medicine (RMH) - Research Publications

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    Body Mass Index Trajectory and Outcome Post Fontan Procedure
    Payne, E ; Garden, F ; D'Udekem, Y ; McCallum, Z ; Wightman, H ; Zannino, D ; Zentner, D ; Cordina, R ; Weintraub, R ; Wilson, TG ; Ayer, J (WILEY, 2022-09-20)
    Background Patients with a single ventricle who experience early life growth failure suffer high morbidity and mortality in the perisurgical period. However, long-term implications of poor infant growth, as well as associations between body mass index (BMI) and outcome in adulthood, remain unclear. We aimed to model BMI trajectories of patients with a single ventricle undergoing a Fontan procedure to determine trajectory-based differences in baseline characteristics and long-term clinical outcomes. Methods and Results We performed a retrospective analysis of medical records from patients in the Australia and New Zealand Fontan Registry receiving treatment at the Royal Children's Hospital, The Children's Hospital at Westmead, Royal Melbourne Hospital, and Royal Prince Alfred Hospital from 1981 to 2018. BMI trajectories were modeled in 496 patients using latent class growth analysis from 0 to 6 months, 6 to 60 months, and 5 to 16 years. Trajectories were compared regarding long-term incidence of severe Fontan failure (defined as mortality, heart transplantation, Fontan takedown, or New York Heart Association class III/IV heart failure). Three trajectories were found for male and female subjects at each age group-lower, middle, higher. Subjects in the lower trajectory at 0 to 6 months were more likely to have an atriopulmonary Fontan and experienced increased mortality long term. No association was found between higher BMI trajectory, current BMI, and long-term outcome. Conclusions Poor growth in early life correlates with increased long-term severe Fontan failure. Delineation of distinct BMI trajectories can be used in larger and older cohorts to find optimal BMI targets for patient outcome.
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    Exercise Intolerance, Benefits, and Prescription for People Living With a Fontan Circulation: The Fontan Fitness Intervention Trial (F-FIT)-Rationale and Design
    Tran, DL ; Gibson, H ; Maiorana, AJ ; Verrall, CE ; Baker, DW ; Clode, M ; Lubans, DR ; Zannino, D ; Bullock, A ; Ferrie, S ; Briody, J ; Simm, P ; Wijesekera, V ; D'Almeida, M ; Gosbell, SE ; Davis, GM ; Weintraub, R ; Keech, AC ; Puranik, R ; Ugander, M ; Justo, R ; Zentner, D ; Majumdar, A ; Grigg, L ; Coombes, JS ; d'Udekem, Y ; Morris, NR ; Ayer, J ; Celermajer, DS ; Cordina, R (FRONTIERS MEDIA SA, 2022-01-06)
    Background: Despite developments in surgical techniques and medical care, people with a Fontan circulation still experience long-term complications; non-invasive therapies to optimize the circulation have not been established. Exercise intolerance affects the majority of the population and is associated with worse prognosis. Historically, people living with a Fontan circulation were advised to avoid physical activity, but a small number of heterogenous, predominantly uncontrolled studies have shown that exercise training is safe-and for unique reasons, may even be of heightened importance in the setting of Fontan physiology. The mechanisms underlying improvements in aerobic exercise capacity and the effects of exercise training on circulatory and end-organ function remain incompletely understood. Furthermore, the optimal methods of exercise prescription are poorly characterized. This highlights the need for large, well-designed, multi-center, randomized, controlled trials. Aims and Methods: The Fontan Fitness Intervention Trial (F-FIT)-a phase III clinical trial-aims to optimize exercise prescription and delivery in people with a Fontan circulation. In this multi-center, randomized, controlled study, eligible Fontan participants will be randomized to either a 4-month supervised aerobic and resistance exercise training program of moderate-to-vigorous intensity followed by an 8-month maintenance phase; or usual care (control group). Adolescent and adult (≥16 years) Fontan participants will be randomized to either traditional face-to-face exercise training, telehealth exercise training, or usual care in a three-arm trial with an allocation of 2:2:1 (traditional:telehealth:control). Children (<16 years) will be randomized to either a physical activity and exercise program of moderate-to-vigorous intensity or usual care in a two-arm trial with a 1:1 allocation. The primary outcome is a change in aerobic exercise capacity (peak oxygen uptake) at 4-months. Secondary outcomes include safety, and changes in cardiopulmonary exercise testing measures, peripheral venous pressure, respiratory muscle and lung function, body composition, liver stiffness, neuropsychological and neurocognitive function, physical activity levels, dietary and nutritional status, vascular function, neurohormonal activation, metabolites, cardiac function, quality of life, musculoskeletal fitness, and health care utilization. Outcome measures will be assessed at baseline, 4-months, and 12-months. This manuscript will describe the pathophysiology of exercise intolerance in the Fontan circulation and the rationale and protocol for the F-FIT.
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    Management of People With a Fontan Circulation: a Cardiac Society of Australia and New Zealand Position Statement
    Zentner, D ; Celermajer, DS ; Gentles, T ; d'Udekem, Y ; Ayer, J ; Blue, GM ; Bridgman, C ; Burchill, L ; Cheung, M ; Cordina, R ; Culnane, E ; Davis, A ; du Plessis, K ; Eagleson, K ; Finucane, K ; Frank, B ; Greenway, S ; Grigg, L ; Hardikar, W ; Hornung, T ; Hynson, J ; Iyengar, AJ ; James, P ; Justo, R ; Kalman, J ; Kasparian, N ; Le, B ; Marshall, K ; Mathew, J ; McGiffin, D ; McGuire, M ; Monagle, P ; Moore, B ; Neilsen, J ; O'Connor, B ; O'Donnell, C ; Pflaumer, A ; Rice, K ; Sholler, G ; Skinner, JR ; Sood, S ; Ward, J ; Weintraub, R ; Wilson, T ; Wilson, W ; Winlaw, D ; Wood, A (ELSEVIER SCIENCE INC, 2020-01)
    The Fontan circulation describes the circulatory state resulting from an operation in congenital heart disease where systemic venous return is directed to the lungs without an intervening active pumping chamber. As survival increases, so too does recognition of the potential health challenges. This document aims to allow clinicians, people with a Fontan circulation, and their families to benefit from consensus agreement about management of the person with a Fontan circulation. The document was crafted with input from a multidisciplinary group of health care providers as well as individuals with a Fontan circulation and families. It is hoped that the shared common vision of long-term wellbeing will continue to drive improvements in care and quality of life in this patient population and eventually translate into improved survival. KEYPOINTS.