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 inThe Journal of heart and lung transplantation Vol. 37; no. 7; pp. 879 - 885
Main Authors Mahle, William T., Hu, Chenwei, Trachtenberg, Felicia, Menteer, JonDavid, Kindel, Steven J., Dipchand, Anne I., Richmond, Marc E., Daly, Kevin P., Henderson, Heather T., Lin, Kimberly Y., McCulloch, Michael, Lal, Ashwin K., Schumacher, Kurt R., Jacobs, Jeffrey P., Atz, Andrew M., Villa, Chet R., Burns, Kristin M., Newburger, Jane W.
Format Journal Article
LanguageEnglish
Published 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.
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.
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  organization: Duke University Hospital and Department of Pediatrics, Division of Cardiology Duke University, Durham, NC (H.T.H.)
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  givenname: Kimberly Y.
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  surname: McCulloch
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  organization: Alfred I. DuPont Hospital for Children and Department of Pediatrics, Division of Cardiology Thomas Jefferson University, Wilmington, DE (M.M.)
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  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.)
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  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.)
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  givenname: Jeffrey P.
  surname: Jacobs
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  organization: Johns Hopkins All Children’s Heart Institute and Department of Surgery, Division of Cardiothoracic Surgery, St. Petersburg, FL (J.P.J.)
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  givenname: Andrew M.
  surname: Atz
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  givenname: Chet R.
  surname: Villa
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  organization: National Heart, Lung, and Blood Institute, Bethesda, MD (K.M.B.)
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  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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congenital heart disease
cardiac surgery
single ventricle
congenital heart defect
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Snippet Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood procedure. We...
Heart failure results in significant morbidity and mortality in young children with hypoplastic left heart syndrome (HLHS) after the Norwood...
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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
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1053249818313597
https://dx.doi.org/10.1016/j.healun.2018.02.009
https://www.ncbi.nlm.nih.gov/pubmed/29571602
https://www.proquest.com/docview/2018031502
Volume 37
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