Risk Factors and Mode of Death in Isolated Hypertrophic Cardiomyopathy in Children

Jamie A. Decker, Joseph W. Rossano, E. O.Brian Smith, Bryan Cannon, Sarah K. Clunie, Corey Gates, John Jefferies, Jeffrey J. Kim, Jack F. Price, William J. Dreyer, Jeffrey Towbin, Susan W. Denfield

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

Objectives: This study was designed to review outcomes of pediatric isolated hypertrophic cardiomyopathy (HCM) managed uniformly at a single institution and assess whether reported adult risk factors for sudden death are predictive in pediatric HCM. Background: Cardiac death in HCM occurs suddenly (SCD) or may be nonsudden (non-SCD). Little data exists on non-SCD in children. Risk factors for SCD in adult HCM are characterized and consensus management strategies detailed. Their application to children is uncertain and treatment strategies vary. Methods: A retrospective cohort study of children with HCM was performed. Primary end points were cardiac death and transplantation. Frequency and outcomes of known adult risk factors were assessed. Outcomes analysis was performed using Kaplan-Meier curves and Cox regression analysis. Results: Ninety-six patients were included. The average age at diagnosis was 10.6 ± 5.4 years, and mean follow-up was 6.4 ± 5.2 years. Primary end points occurred in 11 patients over the 20-year follow-up (11%), 4 underwent cardiac transplant and 7 died (3 suddenly). Extreme left ventricular hypertrophy (z-score: >6) and an abnormal blood pressure response to exercise were predictive of non-SCD (p < 0.02 and p < 0.03, respectively). Kaplan-Meier survival analysis predicts an 82% survival over a 20-year period. Conclusions: In children with isolated HCM managed primarily with exercise restriction and medication, cardiac death occurred infrequently. Non-SCD or transplant was at least as common as SCD. Extreme left ventricular hypertrophy and blunted blood pressure response to exercise were associated with an increased risk of non-SCD.

Original languageEnglish (US)
Pages (from-to)250-254
Number of pages5
JournalJournal of the American College of Cardiology
Volume54
Issue number3
DOIs
StatePublished - Jul 14 2009

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Hypertrophic Cardiomyopathy
Left Ventricular Hypertrophy
Exercise
Pediatrics
Blood Pressure
Transplants
Kaplan-Meier Estimate
Heart Transplantation
Survival Analysis
Sudden Death
Cohort Studies
Retrospective Studies
Regression Analysis
Survival

All Science Journal Classification (ASJC) codes

  • Cardiology and Cardiovascular Medicine

Cite this

Decker, J. A., Rossano, J. W., Smith, E. O. B., Cannon, B., Clunie, S. K., Gates, C., ... Denfield, S. W. (2009). Risk Factors and Mode of Death in Isolated Hypertrophic Cardiomyopathy in Children. Journal of the American College of Cardiology, 54(3), 250-254. https://doi.org/10.1016/j.jacc.2009.03.051

Risk Factors and Mode of Death in Isolated Hypertrophic Cardiomyopathy in Children. / Decker, Jamie A.; Rossano, Joseph W.; Smith, E. O.Brian; Cannon, Bryan; Clunie, Sarah K.; Gates, Corey; Jefferies, John; Kim, Jeffrey J.; Price, Jack F.; Dreyer, William J.; Towbin, Jeffrey; Denfield, Susan W.

In: Journal of the American College of Cardiology, Vol. 54, No. 3, 14.07.2009, p. 250-254.

Research output: Contribution to journalArticle

Decker, JA, Rossano, JW, Smith, EOB, Cannon, B, Clunie, SK, Gates, C, Jefferies, J, Kim, JJ, Price, JF, Dreyer, WJ, Towbin, J & Denfield, SW 2009, 'Risk Factors and Mode of Death in Isolated Hypertrophic Cardiomyopathy in Children', Journal of the American College of Cardiology, vol. 54, no. 3, pp. 250-254. https://doi.org/10.1016/j.jacc.2009.03.051
Decker, Jamie A. ; Rossano, Joseph W. ; Smith, E. O.Brian ; Cannon, Bryan ; Clunie, Sarah K. ; Gates, Corey ; Jefferies, John ; Kim, Jeffrey J. ; Price, Jack F. ; Dreyer, William J. ; Towbin, Jeffrey ; Denfield, Susan W. / Risk Factors and Mode of Death in Isolated Hypertrophic Cardiomyopathy in Children. In: Journal of the American College of Cardiology. 2009 ; Vol. 54, No. 3. pp. 250-254.
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abstract = "Objectives: This study was designed to review outcomes of pediatric isolated hypertrophic cardiomyopathy (HCM) managed uniformly at a single institution and assess whether reported adult risk factors for sudden death are predictive in pediatric HCM. Background: Cardiac death in HCM occurs suddenly (SCD) or may be nonsudden (non-SCD). Little data exists on non-SCD in children. Risk factors for SCD in adult HCM are characterized and consensus management strategies detailed. Their application to children is uncertain and treatment strategies vary. Methods: A retrospective cohort study of children with HCM was performed. Primary end points were cardiac death and transplantation. Frequency and outcomes of known adult risk factors were assessed. Outcomes analysis was performed using Kaplan-Meier curves and Cox regression analysis. Results: Ninety-six patients were included. The average age at diagnosis was 10.6 ± 5.4 years, and mean follow-up was 6.4 ± 5.2 years. Primary end points occurred in 11 patients over the 20-year follow-up (11{\%}), 4 underwent cardiac transplant and 7 died (3 suddenly). Extreme left ventricular hypertrophy (z-score: >6) and an abnormal blood pressure response to exercise were predictive of non-SCD (p < 0.02 and p < 0.03, respectively). Kaplan-Meier survival analysis predicts an 82{\%} survival over a 20-year period. Conclusions: In children with isolated HCM managed primarily with exercise restriction and medication, cardiac death occurred infrequently. Non-SCD or transplant was at least as common as SCD. Extreme left ventricular hypertrophy and blunted blood pressure response to exercise were associated with an increased risk of non-SCD.",
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AU - Decker, Jamie A.

AU - Rossano, Joseph W.

AU - Smith, E. O.Brian

AU - Cannon, Bryan

AU - Clunie, Sarah K.

AU - Gates, Corey

AU - Jefferies, John

AU - Kim, Jeffrey J.

AU - Price, Jack F.

AU - Dreyer, William J.

AU - Towbin, Jeffrey

AU - Denfield, Susan W.

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N2 - Objectives: This study was designed to review outcomes of pediatric isolated hypertrophic cardiomyopathy (HCM) managed uniformly at a single institution and assess whether reported adult risk factors for sudden death are predictive in pediatric HCM. Background: Cardiac death in HCM occurs suddenly (SCD) or may be nonsudden (non-SCD). Little data exists on non-SCD in children. Risk factors for SCD in adult HCM are characterized and consensus management strategies detailed. Their application to children is uncertain and treatment strategies vary. Methods: A retrospective cohort study of children with HCM was performed. Primary end points were cardiac death and transplantation. Frequency and outcomes of known adult risk factors were assessed. Outcomes analysis was performed using Kaplan-Meier curves and Cox regression analysis. Results: Ninety-six patients were included. The average age at diagnosis was 10.6 ± 5.4 years, and mean follow-up was 6.4 ± 5.2 years. Primary end points occurred in 11 patients over the 20-year follow-up (11%), 4 underwent cardiac transplant and 7 died (3 suddenly). Extreme left ventricular hypertrophy (z-score: >6) and an abnormal blood pressure response to exercise were predictive of non-SCD (p < 0.02 and p < 0.03, respectively). Kaplan-Meier survival analysis predicts an 82% survival over a 20-year period. Conclusions: In children with isolated HCM managed primarily with exercise restriction and medication, cardiac death occurred infrequently. Non-SCD or transplant was at least as common as SCD. Extreme left ventricular hypertrophy and blunted blood pressure response to exercise were associated with an increased risk of non-SCD.

AB - Objectives: This study was designed to review outcomes of pediatric isolated hypertrophic cardiomyopathy (HCM) managed uniformly at a single institution and assess whether reported adult risk factors for sudden death are predictive in pediatric HCM. Background: Cardiac death in HCM occurs suddenly (SCD) or may be nonsudden (non-SCD). Little data exists on non-SCD in children. Risk factors for SCD in adult HCM are characterized and consensus management strategies detailed. Their application to children is uncertain and treatment strategies vary. Methods: A retrospective cohort study of children with HCM was performed. Primary end points were cardiac death and transplantation. Frequency and outcomes of known adult risk factors were assessed. Outcomes analysis was performed using Kaplan-Meier curves and Cox regression analysis. Results: Ninety-six patients were included. The average age at diagnosis was 10.6 ± 5.4 years, and mean follow-up was 6.4 ± 5.2 years. Primary end points occurred in 11 patients over the 20-year follow-up (11%), 4 underwent cardiac transplant and 7 died (3 suddenly). Extreme left ventricular hypertrophy (z-score: >6) and an abnormal blood pressure response to exercise were predictive of non-SCD (p < 0.02 and p < 0.03, respectively). Kaplan-Meier survival analysis predicts an 82% survival over a 20-year period. Conclusions: In children with isolated HCM managed primarily with exercise restriction and medication, cardiac death occurred infrequently. Non-SCD or transplant was at least as common as SCD. Extreme left ventricular hypertrophy and blunted blood pressure response to exercise were associated with an increased risk of non-SCD.

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JO - Journal of the American College of Cardiology

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