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Results of the FUEL Trial.
Goldberg, David J; Zak, Victor; Goldstein, Bryan H; Schumacher, Kurt R; Rhodes, Jonathan; Penny, Daniel J; Petit, Christopher J; Ginde, Salil; Menon, Shaji C; Kim, Seong-Ho; Kim, Gi Beom; Nowlen, Todd T; DiMaria, Michael V; Frischhertz, Benjamin P; Wagner, Jonathan B; McHugh, Kimberly E; McCrindle, Brian W; Shillingford, Amanda J; Sabati, Arash A; Yetman, Anji T; John, Anitha S; Richmond, Marc E; Files, Matthew D; Payne, R Mark; Mackie, Andrew S; Davis, Christopher K; Shahanavaz, Shabana; Hill, Kevin D; Garg, Ruchira; Jacobs, Jeffrey P; Hamstra, Michelle S; Woyciechowski, Stacy; Rathge, Kathleen A; McBride, Michael G; Frommelt, Peter C; Russell, Mark W; Urbina, Elaine M; Yeager, James L; Pemberton, Victoria L; Stylianou, Mario P; Pearson, Gail D; Paridon, Stephen M.
Affiliation
  • Goldberg DJ; Division of Cardiology, The Children's Hospital of Philadelphia, Perelman School of Medicine, PA (D.J.G., S.W., M.G.M., S.M.P.).
  • Zak V; New England Research Institutes, Watertown, MA (V.Z.).
  • Goldstein BH; Division of Cardiology, Cincinnati Children's Hospital Medical Center, OH (B.H.G., M.S.H., K.A.R., E.M.U.).
  • Schumacher KR; Division of Cardiology, C.S. Mott Children's Hospital, Ann Arbor, MI (K.R.S., M.W.R.).
  • Rhodes J; Department of Cardiology, Children's Hospital Boston, MA (J.R.).
  • Penny DJ; Division of Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX (D.J.P.).
  • Petit CJ; Emory University School of Medicine, Children's Healthcare of Atlanta, GA (C.J.P.).
  • Ginde S; Division of Cardiology, Medical College of Wisconsin, Children's Hospital of Wisconsin, Milwaukee (S.G., P.C.F.).
  • Menon SC; Division of Pediatric Cardiology, University of Utah, Salt Lake City (S.C.M.).
  • Kim SH; Department of Pediatrics, Sejong General Hospital, Bucheon-Si, South Korea (S.-H.K.).
  • Kim GB; Seoul National University School of Medicine, Seoul National University Children's Hospital, South Korea (G.B.K.).
  • Nowlen TT; Heart Center, Phoenix Children's Hospital, AZ (T.T.N.).
  • DiMaria MV; Department of Pediatrics, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora (M.V.D.).
  • Frischhertz BP; Division of Cardiology, Vanderbilt University School of Medicine, Nashville, TN (B.P.F.).
  • Wagner JB; Divisions of Cardiology and Clinical Pharmacology, Children's Mercy Kansas City, MO (J.B.W.).
  • McHugh KE; Division of Pediatric Cardiology, Medical University of South Carolina, Charleston (K.E.M.).
  • McCrindle BW; Division of Cardiology, The Hospital for Sick Children, University of Toronto, Ontario (B.W.M.).
  • Shillingford AJ; Nemours Cardiac Center, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, DE (A.J.S.).
  • Sabati AA; Los Angeles Children's Hospital, Division of Cardiology, CA (A.A.S.).
  • Yetman AT; Children's Hospital and Medical Center, University of Nebraska, Omaha (A.T.Y.).
  • John AS; Division of Cardiology, Children's National Health System, Washington, DC (A.S.J.).
  • Richmond ME; Division of Pediatric Cardiology, Morgan Stanley Children's Hospital, Columbia University Medical Center, New York, NY (M.E.R.).
  • Files MD; Division of Cardiology, Seattle Children's Hospital, WA (M.D.F.).
  • Payne RM; Division of Cardiology, Riley Hospital for Children, Indianapolis, IN (R.M.P.).
  • Mackie AS; Division of Cardiology, Stollery Children's Hospital, Edmonton, Alberta, Canada (A.S.M.).
  • Davis CK; Division of Cardiology, Rady Children's Hospital, San Diego, CA (C.K.D.).
  • Shahanavaz S; Division of Cardiology, St Louis Children's Hospital, MO (S.S.).
  • Hill KD; Duke Children's Pediatric and Congenital Heart Center, Durham, NC (K.D.H.).
  • Garg R; Division of Cardiology, Cedars-Sinai Medical Center, Los Angeles, CA (R.G.).
  • Jacobs JP; Johns Hopkins All Children's Hospital, Department of Surgery, St Petersburg, FL (J.P.J.).
  • Hamstra MS; Division of Cardiology, Cincinnati Children's Hospital Medical Center, OH (B.H.G., M.S.H., K.A.R., E.M.U.).
  • Woyciechowski S; Division of Cardiology, The Children's Hospital of Philadelphia, Perelman School of Medicine, PA (D.J.G., S.W., M.G.M., S.M.P.).
  • Rathge KA; Division of Cardiology, Cincinnati Children's Hospital Medical Center, OH (B.H.G., M.S.H., K.A.R., E.M.U.).
  • McBride MG; Division of Cardiology, The Children's Hospital of Philadelphia, Perelman School of Medicine, PA (D.J.G., S.W., M.G.M., S.M.P.).
  • Frommelt PC; Division of Cardiology, Medical College of Wisconsin, Children's Hospital of Wisconsin, Milwaukee (S.G., P.C.F.).
  • Russell MW; Division of Cardiology, C.S. Mott Children's Hospital, Ann Arbor, MI (K.R.S., M.W.R.).
  • Urbina EM; Division of Cardiology, Cincinnati Children's Hospital Medical Center, OH (B.H.G., M.S.H., K.A.R., E.M.U.).
  • Yeager JL; Consultant to Mezzion Pharma Co Ltd, Mezzion Pharma Co Ltd, Seoul, South Korea (J.L.Y.).
  • Pemberton VL; Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (V.L.P., M.P.S., G.D.P.).
  • Stylianou MP; Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (V.L.P., M.P.S., G.D.P.).
  • Pearson GD; Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (V.L.P., M.P.S., G.D.P.).
  • Paridon SM; Division of Cardiology, The Children's Hospital of Philadelphia, Perelman School of Medicine, PA (D.J.G., S.W., M.G.M., S.M.P.).
Circulation ; 141(8): 641-651, 2020 02 25.
Article in En | MEDLINE | ID: mdl-31736357
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 difference in change of myocardial performance index, the natural log of the 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrimidines / Sulfonamides / Phosphodiesterase 5 Inhibitors / Heart Diseases Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Circulation Year: 2020 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrimidines / Sulfonamides / Phosphodiesterase 5 Inhibitors / Heart Diseases Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Circulation Year: 2020 Document type: Article Country of publication: United States