Results of the FUEL Trial

David Goldberg(Children's Hospital of Philadelphia), Victor Zak(New England Research Institutes), Bryan H. Goldstein(Cincinnati Children's Hospital Medical Center), Kurt R. Schumacher(C. S. Mott Children's Hospital), Jonathan Rhodes(Boston Children's Hospital), Daniel J. Penny(Texas Children's Hospital), Christopher J. Petit(Children's Healthcare of Atlanta), Salil Ginde(Children's Hospital of Wisconsin), Shaji C. Menon(University of Utah), Seong Ho Kim(Sejong General Hospital), Gi Beom Kim(Seoul National University Children's Hospital), Todd Nowlen(Arizona Heart Hospital), Michael V. DiMaria(Children's Hospital Colorado), Benjamin P. Frischhertz(Vanderbilt University), Jonathan B. Wagner(Children's Mercy Hospital), Kimberly E. McHugh(Medical University of South Carolina), Brian W. McCrindle(Hospital for Sick Children), Amanda J. Shillingford(Alfred I. duPont Hospital for Children), Arash Sabati(Children's Hospital of Los Angeles), Anji T. Yetman(Children's Hospital & Medical Center), Anitha S. John(Children's National), Marc E. Richmond(Morgan Stanley Children's Hospital), Matthew D. Files(Seattle Children's Hospital), R. Mark Payne(Riley Hospital for Children), Andrew S. Mackie(Stollery Children's Hospital), Christopher K. Davis(Rady Children's Hospital-San Diego), Shabana Shahanavaz(St. Louis Children's Hospital), Kevin D. Hill(Duke Children's Hospital & Health Center), Ruchira Garg(Cedars-Sinai Medical Center), Jeffrey P. Jacobs(Johns Hopkins University), Michelle Hamstra(Cincinnati Children's Hospital Medical Center), Stacy Woyciechowski(Children's Hospital of Philadelphia), Kathleen A. Rathge(Cincinnati Children's Hospital Medical Center), Michael G. McBride(Children's Hospital of Philadelphia), Peter C. Frommelt(Children's Hospital of Wisconsin), Mark W. Russell(C. S. Mott Children's Hospital), Elaine M. Urbina(Cincinnati Children's Hospital Medical Center), James L. Yeager(Korea Pharma (South Korea)), Victoria L. Pemberton(National Heart Lung and Blood Institute), Mario Stylianou(National Heart Lung and Blood Institute), Gail D. Pearson(National Heart Lung and Blood Institute), Stephen M. Paridon(Children's Hospital of Philadelphia), For the Pediatric Heart Network Investigators
Circulation
November 17, 2019
Cited by 156Open Access
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Abstract

Background: The Fontan operation creates a total cavopulmonary connection, a circulation in which the importance of pulmonary vascular resistance is magnified. Over time, this circulation leads to deterioration of cardiovascular efficiency associated with a decline in exercise performance. Rigorous clinical trials aimed at improving physiology and guiding pharmacotherapy are lacking. Methods: The FUEL trial (Fontan Udenafil Exercise Longitudinal) was a phase III clinical trial conducted at 30 centers. Participants were randomly assigned udenafil, 87.5 mg twice daily, or placebo in a 1:1 ratio. The primary outcome was the between-group difference in change in oxygen consumption at peak exercise. Secondary outcomes included between-group differences in changes in submaximal exercise at the ventilatory anaerobic threshold, the myocardial performance index, the natural log of the reactive hyperemia index, and serum brain-type natriuretic peptide. Results: Between 2017 and 2019, 30 clinical sites in North America and the Republic of Korea randomly assigned 400 participants with Fontan physiology. The mean age at randomization was 15.5±2 years; 60% of participants were male, and 81% were white. All 400 participants were included in the primary analysis with imputation of the 26-week end point for 21 participants with missing data (11 randomly assigned to udenafil and 10 to placebo). Among randomly assigned participants, peak oxygen consumption increased by 44±245 mL/min (2.8%) in the udenafil group and declined by 3.7±228 mL/min (–0.2%) in the placebo group ( P =0.071). Analysis at ventilatory anaerobic threshold demonstrated improvements in the udenafil group versus the placebo group in oxygen consumption (+33±185 [3.2%] versus –9±193 [–0.9%] mL/min, P =0.012), ventilatory equivalents of carbon dioxide (–0.8 versus –0.06, P =0.014), and work rate (+3.8 versus +0.34 W, P =0.021). There was no an improvement in myocardial performance index (–0.02 vs 0.01, P =0.030), but no change in reactive hyperemia index, or serum brain-type natriuretic peptide level. Conclusions: In the FUEL trial, treatment with udenafil (87.5 mg twice daily) was not associated with an improvement in oxygen consumption at peak exercise but was associated with improvements in multiple measures of exercise performance at the ventilatory anaerobic threshold. Clinical Trial Registration: URL: https://www.clinicaltrials.gov . Unique identifier: NCT02741115.


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