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1.
Figure 2

Figure 2. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Freedom from death or transplantation for 1423 children with pure dilated cardiomyopathy, by cause. Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Towbin JA, Lowe AM, Colan SD, et al. Incidence, causes, and outcomes of dilated cardiomyopathy in children. JAMA 2006;296:1873, with permission.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.
2.
Figure 1

Figure 1. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Freedom from death or transplant for 491 children in the retrospective cohort and 935 children in the prospective cohort with pure dilated cardiomyopathy (P= 0.71). Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Towbin JA, Lowe AM, Colan SD, et al. Incidence, causes, and outcomes of dilated cardiomyopathy in children. JAMA 2006;296:1869, with permission.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.
3.
Figure 3

Figure 3. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Freedom from death or transplantation for 855 children with idiopathic hypertrophic cardiomyopathy, by age at diagnosis. Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Colan SD, Lipshultz SE, Lowe AM, et al. Epidemiology and cause specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry. Circulation 2007;115:777, with permission.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.
4.
Figure 5

Figure 5. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Physical and psychosocial function, as measured by the Child Health Questionnaire, of 294 children with cardiomyopathy, by functional type. Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Sleeper LA, Towbin JA, Colan SD, et al. Functional Status is Impaired and Correlated with Clinical Status in Pediatric Cardiomyopathy [abstract]. In: Proc 5th World Cong Pediatr Cardiol and Cardiac Surg 2009;5:134.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.
5.
Figure 4

Figure 4. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Risk of death or transplant in 882 children with hypertrophic cardiomyopathy, by number of cause-specific risk factors. Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Lipshultz SE, Orav EJ, Wilkinson JD, Towbin JA, Messere J, Lowe AM, Sleeper LA, Clunie SK, Cox GF, Lurie PR, Hsu DT, Canter CE, Colan SD. A risk stratification analysis of predictors of death or transplant in children with hypertrophic cardiomyopathy. Circulation Supplement. 2008;118:4956.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.
6.
Figure 6

Figure 6. From: The Pediatric Cardiomyopathy Registry and Heart Failure: Key Results from the First 15 Years.

Child Health Questionnaire domain mean z scores for 303 children with cardiomyopathy in the Pediatric Cardiomyopathy Registry. Scores for the physical domains, general health, self-esteem, and parental impact-emotional domains were significantly below the average for healthy children. Scores for mental health and behavior did not differ significantly from those of healthy children. (PF = physical functioning; RE = role/social limits-emotional; RP = role/social limits-physical; PAIN= bodily pain; BEH = behavior; MH = mental health; SE = self-esteem; GH = general health perception; PE = parental impact-emotional; PT= parental impact-time). Data are from the Pediatric Cardiomyopathy Registry for the period between 1990 and 2002. [From Sleeper LA, Towbin JA, Colan SD, et al. Functional Status is Impaired and Correlated with Clinical Status in Pediatric Cardiomyopathy [abstract]. In: Proc 5th World Cong Pediatr Cardiol and Cardiac Surg 2009;5:134.]

James D. Wilkinson, et al. Heart Fail Clin. ;6(4):401-413.

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