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Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study.
Lampert, Rachel; Day, Sharlene; Ainsworth, Barbara; Burg, Matthew; Marino, Bradley S; Salberg, Lisa; Tome Esteban, Maria Teresa; Abrams, Dominic J; Aziz, Peter F; Barth, Cheryl; Behr, Elijah R; Bell, Cheyanne; Berul, Charles I; Bos, Johan M; Bradley, David; Cannom, David S; Cannon, Bryan C; Concannon, Maryann Anandi; Cerrone, Marina; Czosek, Richard J; Dubin, Anne M; Dziura, James; Erickson, Christopher C; Estes, N A Mark; Etheridge, Susan P; Goldenberg, Ilan; Gray, Belinda; Haglund-Turnquist, Carla; Harmon, Kimberly; James, Cynthia A; Johnsrude, Christopher; Kannankeril, Prince; Lara, Alice; Law, Ian H; Li, Fangyong; Link, Mark S; Molossi, Silvana M; Olshansky, Brian; Noseworthy, Peter A; Saarel, Elizabeth V; Sanatani, Shubhayan; Shah, Maully; Simone, Laura; Skinner, Jonathan; Tomaselli, Gordon F; Ware, James Simon; Webster, Gregory; Zareba, Wojciech; Zipes, Douglas P; Ackerman, Michael J.
Afiliación
  • Lampert R; Yale School of Medicine, New Haven, CT (R.L., M.B., C. Barth, J.D., F.L, L.S.).
  • Day S; University of Pennsylvania, Philadelphia (S.D.).
  • Ainsworth B; University of Michigan Hospital, Ann Arbor (S.D., M.A.C.).
  • Burg M; School of Exercise and Health, Shanghai University of Sport, China (B.A.).
  • Marino BS; College of Health Solutions/Arizona State University, Phoenix (B.A.).
  • Salberg L; Yale School of Medicine, New Haven, CT (R.L., M.B., C. Barth, J.D., F.L, L.S.).
  • Tome Esteban MT; VA Hospital, West Haven, CT (M.B.).
  • Abrams DJ; Cleveland Clinic, OH (B.S.M., P.F.A.).
  • Aziz PF; Lurie Children's Hospital, Chicago, IL (B.S.M., G.W.).
  • Barth C; Hypertrophic Cardiomyopathy Association, Denville, NJ (L.S.).
  • Behr ER; Cardiology Section, Cardiovascular and Genomics Research Institute, St. George's, University of London, UK (M.T.T.E., E.R.B.).
  • Bell C; Cardiology Department, St. George's University Hospitals NHS Foundation Trust, London, UK (M.T.T.E., E.R.B.).
  • Berul CI; Boston Children's Hospital, MA (D.J.A.).
  • Bos JM; Cleveland Clinic, OH (B.S.M., P.F.A.).
  • Bradley D; Yale School of Medicine, New Haven, CT (R.L., M.B., C. Barth, J.D., F.L, L.S.).
  • Cannom DS; Cardiology Section, Cardiovascular and Genomics Research Institute, St. George's, University of London, UK (M.T.T.E., E.R.B.).
  • Cannon BC; Cardiology Department, St. George's University Hospitals NHS Foundation Trust, London, UK (M.T.T.E., E.R.B.).
  • Concannon MA; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology and Experimental Therapeutics; Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN (C. Bell, J.M.B., B.C.C., C.H.
  • Cerrone M; Children's National Hospital, Washington, DC (C.I.B.).
  • Czosek RJ; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology and Experimental Therapeutics; Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN (C. Bell, J.M.B., B.C.C., C.H.
  • Dubin AM; C.S. Mott Children's Hospital, Ann Arbor, MI (D.B.).
  • Dziura J; Keck Medicine of USC, Los Angeles, CA (D.S.C.).
  • Erickson CC; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology and Experimental Therapeutics; Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN (C. Bell, J.M.B., B.C.C., C.H.
  • Estes NAM; University of Michigan Hospital, Ann Arbor (S.D., M.A.C.).
  • Etheridge SP; Leon H. Charney Division of Cardiology, NYU Grossman Sch of Medicine, New York (M.C.).
  • Goldenberg I; The Heart Institute, Cincinnati Children's Hospital Med Center, OH (R.J.C.).
  • Gray B; Stanford University School of Medicine, Palo Alto, CA (A.M.D.).
  • Haglund-Turnquist C; Yale School of Medicine, New Haven, CT (R.L., M.B., C. Barth, J.D., F.L, L.S.).
  • Harmon K; University of Nebraska Medical Center, Children's Nebraska, Omaha (C.C.E.).
  • James CA; Tufts Medical Center, Boston, MA (N.A.M.E., M.S.L.).
  • Johnsrude C; UPMC, Pittsburgh, PA (N.A.M.E.).
  • Kannankeril P; University of Utah, Salt Lake City (S.P.E.).
  • Lara A; Division of Cardiology, University of Rochester Medical Center, NY (I.G., W.Z.).
  • Law IH; Faculty of Medicine and Health, University of Sydney/Royal Prince Alfred Hospital, Australia (B.G.).
  • Li F; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology and Experimental Therapeutics; Divisions of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN (C. Bell, J.M.B., B.C.C., C.H.
  • Link MS; Department of Family Medicine, University of Washington, Seattle (K.H.).
  • Molossi SM; Johns Hopkins University, Baltimore, MD (C.A.J.,G.F.T.).
  • Olshansky B; University of Louisville School of Medicine, KY (C.J.).
  • Noseworthy PA; Department of Pediatrics, Monroe Carell Jr Children's Hospital at Vanderbilt and Vanderbilt University, Nashville, TN (P.K.).
  • Saarel EV; Sudden Arrhythmia Death Syndrome Foundation, Salt Lake City, UT (A.L.).
  • Sanatani S; University of Iowa Carver College of Medicine, Iowa City (I.H.L., B.O.).
  • Shah M; Yale School of Medicine, New Haven, CT (R.L., M.B., C. Barth, J.D., F.L, L.S.).
  • Simone L; Tufts Medical Center, Boston, MA (N.A.M.E., M.S.L.).
  • Skinner J; UT Southwestern Medical Center, Dallas, TX (M.S.L.).
  • Tomaselli GF; Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston (S.M.M.).
  • Ware JS; University of Iowa Carver College of Medicine, Iowa City (I.H.L., B.O.).
  • Webster G; Department of Medicine/Cardiology, Mayo Clinic, Rochester, MN (P.A.N.).
  • Zareba W; St. Lukes Medical Center/Primary Children's Hospital, Boise, ID (E.V.S.).
  • Zipes DP; Institution British Columbia Children's Hospital, University of British Columbia, Vancouver, Canada (S.S.).
  • Ackerman MJ; University of Pennsylvania School of Medicine, Children's Hospital of Philadelphia (M.S.).
Circulation ; 150(7): 516-530, 2024 Aug 13.
Article en En | MEDLINE | ID: mdl-39051104
ABSTRACT

BACKGROUND:

Whether vigorous exercise increases risk of ventricular arrhythmias for individuals diagnosed and treated for congenital long QT syndrome (LQTS) remains unknown.

METHODS:

The National Institutes of Health-funded LIVE-LQTS study (Lifestyle and Exercise in the Long QT Syndrome) prospectively enrolled individuals 8 to 60 years of age with phenotypic and/or genotypic LQTS from 37 sites in 5 countries from May 2015 to February 2019. Participants (or parents) answered physical activity and clinical events surveys every 6 months for 3 years with follow-up completed in February 2022. Vigorous exercise was defined as ≥6 metabolic equivalents for >60 hours per year. A blinded Clinical Events Committee adjudicated the composite end point of sudden death, sudden cardiac arrest, ventricular arrhythmia treated by an implantable cardioverter defibrillator, and likely arrhythmic syncope. A National Death Index search ascertained vital status for those with incomplete follow-up. A noninferiority hypothesis (boundary of 1.5) between vigorous exercisers and others was tested with multivariable Cox regression analysis.

RESULTS:

Among the 1413 participants (13% <18 years of age, 35% 18-25 years of age, 67% female, 25% with implantable cardioverter defibrillators, 90% genotype positive, 49% with LQT1, 91% were treated with beta-blockers, left cardiac sympathetic denervation, and/or implantable cardioverter defibrillator), 52% participated in vigorous exercise (55% of these competitively). Thirty-seven individuals experienced the composite end point (including one sudden cardiac arrest and one sudden death in the nonvigorous group, one sudden cardiac arrest in the vigorous group) with overall event rates at 3 years of 2.6% in the vigorous and 2.7% in the nonvigorous exercise groups. The unadjusted hazard ratio for experience of events for the vigorous group compared with the nonvigorous group was 0.97 (90% CI, 0.57-1.67), with an adjusted hazard ratio of 1.17 (90% CI, 0.67-2.04). The upper 95% one-sided confidence level extended beyond the 1.5 boundary. Neither vigorous or nonvigorous exercise was found to be superior in any group or subgroup.

CONCLUSIONS:

Among individuals diagnosed with phenotypic and/or genotypic LQTS who were risk assessed and treated in experienced centers, LQTS-associated cardiac event rates were low and similar between those exercising vigorously and those not exercising vigorously. Consistent with the low event rate, CIs are wide, and noninferiority was not demonstrated. These data further inform shared decision-making discussions between patient and physician about exercise and competitive sports participation. REGISTRATION URL https//www.clinicaltrials.gov; Unique identifier NCT02549664.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Ejercicio Físico Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Ejercicio Físico Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Año: 2024 Tipo del documento: Article