Heart failure after the Norwood procedure: An analysis of the Single Ventricle Reconstruction Trial
Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure. We studied subjects enrolled in the prospective Single Ventricle Reconstruction (SVR) Trial who survived to hospital discharge after a Norwood opera...
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Published in | The Journal of heart and lung transplantation Vol. 37; no. 7; pp. 879 - 885 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.07.2018
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Abstract | Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure.
We studied subjects enrolled in the prospective Single Ventricle Reconstruction (SVR) Trial who survived to hospital discharge after a Norwood operation and were followed up to age 6 years. The primary outcome was heart failure, defined as heart transplant listing after Norwood hospitalization, death attributable to heart failure, or symptomatic heart failure (New York Heart Association [NYHA] Class IV). Multivariate modeling was undertaken using Cox regression methodology to determine variables associated with heart failure.
Of the 461 subjects discharged home following a Norwood procedure, 66 (14.3%) met the criteria for heart failure. Among these, 15 died from heart failure, 39 were listed for transplant (22 had a transplant, 12 died after listing, and 5 were alive and not yet transplanted), and 12 had NYHA Class IV heart failure but were never listed. The median age at heart failure identification was 1.28 (interquartile range 0.30 to 4.69) years. Factors associated with early heart failure included post-Norwood lower fractional area change, need for extracorporeal membrane oxygenation, non-Hispanic ethnicity, Norwood perfusion type, and total support time (p < 0.05).
By 6 years of age, heart failure developed in nearly 15% of children after the Norwood procedure. Although transplant listing was common, many patients died from heart failure before receiving a transplant or without being listed. Shunt type did not impact the risk of developing heart failure. |
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AbstractList | Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure.
We studied subjects enrolled in the prospective Single Ventricle Reconstruction (SVR) Trial who survived to hospital discharge after a Norwood operation and were followed up to age 6 years. The primary outcome was heart failure, defined as heart transplant listing after Norwood hospitalization, death attributable to heart failure, or symptomatic heart failure (New York Heart Association [NYHA] Class IV). Multivariate modeling was undertaken using Cox regression methodology to determine variables associated with heart failure.
Of the 461 subjects discharged home following a Norwood procedure, 66 (14.3%) met the criteria for heart failure. Among these, 15 died from heart failure, 39 were listed for transplant (22 had a transplant, 12 died after listing, and 5 were alive and not yet transplanted), and 12 had NYHA Class IV heart failure but were never listed. The median age at heart failure identification was 1.28 (interquartile range 0.30 to 4.69) years. Factors associated with early heart failure included post-Norwood lower fractional area change, need for extracorporeal membrane oxygenation, non-Hispanic ethnicity, Norwood perfusion type, and total support time (p < 0.05).
By 6 years of age, heart failure developed in nearly 15% of children after the Norwood procedure. Although transplant listing was common, many patients died from heart failure before receiving a transplant or without being listed. Shunt type did not impact the risk of developing heart failure. Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure.BACKGROUNDHeart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure.We studied subjects enrolled in the prospective Single Ventricle Reconstruction (SVR) Trial who survived to hospital discharge after a Norwood operation and were followed up to age 6 years. The primary outcome was heart failure, defined as heart transplant listing after Norwood hospitalization, death attributable to heart failure, or symptomatic heart failure (New York Heart Association [NYHA] Class IV). Multivariate modeling was undertaken using Cox regression methodology to determine variables associated with heart failure.METHODSWe studied subjects enrolled in the prospective Single Ventricle Reconstruction (SVR) Trial who survived to hospital discharge after a Norwood operation and were followed up to age 6 years. The primary outcome was heart failure, defined as heart transplant listing after Norwood hospitalization, death attributable to heart failure, or symptomatic heart failure (New York Heart Association [NYHA] Class IV). Multivariate modeling was undertaken using Cox regression methodology to determine variables associated with heart failure.Of the 461 subjects discharged home following a Norwood procedure, 66 (14.3%) met the criteria for heart failure. Among these, 15 died from heart failure, 39 were listed for transplant (22 had a transplant, 12 died after listing, and 5 were alive and not yet transplanted), and 12 had NYHA Class IV heart failure but were never listed. The median age at heart failure identification was 1.28 (interquartile range 0.30 to 4.69) years. Factors associated with early heart failure included post-Norwood lower fractional area change, need for extracorporeal membrane oxygenation, non-Hispanic ethnicity, Norwood perfusion type, and total support time (p < 0.05).RESULTSOf the 461 subjects discharged home following a Norwood procedure, 66 (14.3%) met the criteria for heart failure. Among these, 15 died from heart failure, 39 were listed for transplant (22 had a transplant, 12 died after listing, and 5 were alive and not yet transplanted), and 12 had NYHA Class IV heart failure but were never listed. The median age at heart failure identification was 1.28 (interquartile range 0.30 to 4.69) years. Factors associated with early heart failure included post-Norwood lower fractional area change, need for extracorporeal membrane oxygenation, non-Hispanic ethnicity, Norwood perfusion type, and total support time (p < 0.05).By 6 years of age, heart failure developed in nearly 15% of children after the Norwood procedure. Although transplant listing was common, many patients died from heart failure before receiving a transplant or without being listed. Shunt type did not impact the risk of developing heart failure.CONCLUSIONSBy 6 years of age, heart failure developed in nearly 15% of children after the Norwood procedure. Although transplant listing was common, many patients died from heart failure before receiving a transplant or without being listed. Shunt type did not impact the risk of developing heart failure. |
Author | Villa, Chet R. Henderson, Heather T. McCulloch, Michael Dipchand, Anne I. Hu, Chenwei Richmond, Marc E. Mahle, William T. Jacobs, Jeffrey P. Atz, Andrew M. Trachtenberg, Felicia Menteer, JonDavid Daly, Kevin P. Lin, Kimberly Y. Lal, Ashwin K. Burns, Kristin M. Kindel, Steven J. Schumacher, Kurt R. Newburger, Jane W. |
Author_xml | – sequence: 1 givenname: William T. surname: Mahle fullname: Mahle, William T. email: wmahle@emory.edu organization: Children’s Healthcare of Atlanta and Department of Pediatrics, Division of Cardiology Emory University Atlanta, GA (W.T.M) – sequence: 2 givenname: Chenwei surname: Hu fullname: Hu, Chenwei organization: New England Research Institutes, Watertown, MA (F.T., C.H.) – sequence: 3 givenname: Felicia surname: Trachtenberg fullname: Trachtenberg, Felicia organization: New England Research Institutes, Watertown, MA (F.T., C.H.) – sequence: 4 givenname: JonDavid surname: Menteer fullname: Menteer, JonDavid organization: Children’s Hospital Los Angeles and Department of Pediatrics, Division of Cardiology University of Southern California, Los Angeles, CA (J.M.) – sequence: 5 givenname: Steven J. surname: Kindel fullname: Kindel, Steven J. organization: Children’s Hospital of Wisconsin, Milwaukee and Department of Pediatrics, Division of Cardiology University of Wisconsin Milwaukee, WI (S.J.K.) – sequence: 6 givenname: Anne I. surname: Dipchand fullname: Dipchand, Anne I. organization: The Hospital for Sick Children and Department of Pediatrics, Division of Cardiology University of Toronto, Toronto, Ontario (A.I.D.) – sequence: 7 givenname: Marc E. surname: Richmond fullname: Richmond, Marc E. organization: Morgan Stanley Children’s Hospital of New York Presbyterian Columbia University Medical Center and Department of Pediatrics, Division of Cardiology Columbia University, New York, NY (M.E.R.) – sequence: 8 givenname: Kevin P. surname: Daly fullname: Daly, Kevin P. organization: Boston Children’s Hospital and Department of Pediatrics Cardiology Harvard School of Medicine, Boston, MA (K.PD., J.W.N.) – sequence: 9 givenname: Heather T. surname: Henderson fullname: Henderson, Heather T. organization: Duke University Hospital and Department of Pediatrics, Division of Cardiology Duke University, Durham, NC (H.T.H.) – sequence: 10 givenname: Kimberly Y. surname: Lin fullname: Lin, Kimberly Y. organization: Children’s Hospital of Philadelphia and Department of Pediatrics, Division of Cardiology University of Pennsylvania, Philadelphia, PA (K.L.) – sequence: 11 givenname: Michael surname: McCulloch fullname: McCulloch, Michael organization: Alfred I. DuPont Hospital for Children and Department of Pediatrics, Division of Cardiology Thomas Jefferson University, Wilmington, DE (M.M.) – sequence: 12 givenname: Ashwin K. surname: Lal fullname: Lal, Ashwin K. organization: Primary Children’s Medical Center and Department of Pediatrics, Division of Cardiology University of Utah, Salt Lake City, UT (A.K.L.) – sequence: 13 givenname: Kurt R. surname: Schumacher fullname: Schumacher, Kurt R. organization: University of Michigan Health System and Department of Pediatrics, Division of Cardiology University of Michigan, Ann Arbor, MI (K.S.) – sequence: 14 givenname: Jeffrey P. surname: Jacobs fullname: Jacobs, Jeffrey P. organization: Johns Hopkins All Children’s Heart Institute and Department of Surgery, Division of Cardiothoracic Surgery, St. Petersburg, FL (J.P.J.) – sequence: 15 givenname: Andrew M. surname: Atz fullname: Atz, Andrew M. organization: Department of Pediatrics, Division of Cardiology Medical University of South Carolina, Charleston, SC (A.M.A.) – sequence: 16 givenname: Chet R. surname: Villa fullname: Villa, Chet R. organization: Cincinnati Children's Hospital Medical Center and Department of Pediatrics, Division of Cardiology University of Cincinnati, Cincinnati, OH (C.R.V.) – sequence: 17 givenname: Kristin M. surname: Burns fullname: Burns, Kristin M. organization: National Heart, Lung, and Blood Institute, Bethesda, MD (K.M.B.) – sequence: 18 givenname: Jane W. surname: Newburger fullname: Newburger, Jane W. organization: Boston Children’s Hospital and Department of Pediatrics Cardiology Harvard School of Medicine, Boston, MA (K.PD., J.W.N.) |
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Keywords | Norwood procedure congenital heart disease cardiac surgery single ventricle congenital heart defect |
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SubjectTerms | cardiac surgery Child Child, Preschool congenital heart defect congenital heart disease Follow-Up Studies Heart Failure - epidemiology Heart Failure - etiology Humans Hypoplastic Left Heart Syndrome - surgery Infant Norwood procedure Norwood Procedures - adverse effects Postoperative Complications - epidemiology Postoperative Complications - etiology Prospective Studies single ventricle Time Factors |
Title | Heart failure after the Norwood procedure: An analysis of the Single Ventricle Reconstruction Trial |
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