Abstract:Objectives
To determine the incidence of and predictors for recovery of normal echocardiographic function among children with idiopathic dilated cardiomyopathy (DCM).
Background
Most children with idiopathic DCM have poor outcomes; however, some improve.
Methods
We studied children less than 18 years old in the Pediatric Cardiomyopathy Registry who had both depressed left ventricular (LV) function (fractional shortening [FS] or ejection fraction [EF] z-score <−2) and LV dilation (end-diastolic dimension [L… Show more
“…In other groups of patients such as the dilated cardiomyopathy cohort, myocardial recovery is a well-documented phenomenon (Everitt et al 2014;Alexander et al 2013) patients were able to proceed to stage II. This is demonstrating that myocardial recovery is possible in this population as well.…”
Section: Ventricular Dysfunction Is Not Always a Permanent Diagnosismentioning
confidence: 99%
“…A more dilated ventricle that works harder for the same result would result in a decreased circulatory reserve. The physiology associated with ventricular dilation might explain why this is an independent risk factor for death or transplant in multiple other cardiac conditions (Alexander et al 2012, Abe et al 2013, Everitt et al 2014, Therrien et al 2005). Figure 37.…”
Section: Right Ventricular Dilatation 521 the Laplace Lawmentioning
confidence: 99%
“…Therefore, ventricular dilatation is usually observed when there is significant ventricular dysfunction. (Matsumura et al 2013;Alexander et al 2013) In other diseases, such as dilated cardiomyopathy, ventricular dilatation is one of the main predictors of outcome where ejection fraction is often not an important predictor (Everitt et al 2014;Alexander et al 2013). In other congenital diseases, such as Tetralogy of Fallot, right ventricular dilatation has also been shown to be one of the main outcome drivers (Therrien et al 2005;Henkens et al 2007).…”
Section: The Relation Between Ventricular Dysfunction and Ventricularmentioning
We investigated patient and procedural factors associated with failure of staged palliation after the Norwood procedure in patients with right ventricular dysfunction (RVDfx).Patients from the Pediatric Heart Network Single Ventricle Reconstruction (SVR) Trial dataset were selected if RVDfx was present, defined as an ejection fraction of less than 44% and a fractional area of change of less than 35% on the post-Norwood echocardiogram. Transplantfree survival after the Norwood procedure was analyzed using multiphase parametric hazard analysis and factors associated with death or transplant were identified.In the SVR cohort, 123 (34%) infants had RVDfx. The six-month transplant-free survival was 87% (70%CI 82-91%). The independent factors associated with increased risk of death or transplant were BT shunt, increased RV size, infectious disease complications and low surgeon volume.Patient factors can help identify which patient with RVDfx is at higher risk of death and help decision making around early transplant listing.iii
“…In other groups of patients such as the dilated cardiomyopathy cohort, myocardial recovery is a well-documented phenomenon (Everitt et al 2014;Alexander et al 2013) patients were able to proceed to stage II. This is demonstrating that myocardial recovery is possible in this population as well.…”
Section: Ventricular Dysfunction Is Not Always a Permanent Diagnosismentioning
confidence: 99%
“…A more dilated ventricle that works harder for the same result would result in a decreased circulatory reserve. The physiology associated with ventricular dilation might explain why this is an independent risk factor for death or transplant in multiple other cardiac conditions (Alexander et al 2012, Abe et al 2013, Everitt et al 2014, Therrien et al 2005). Figure 37.…”
Section: Right Ventricular Dilatation 521 the Laplace Lawmentioning
confidence: 99%
“…Therefore, ventricular dilatation is usually observed when there is significant ventricular dysfunction. (Matsumura et al 2013;Alexander et al 2013) In other diseases, such as dilated cardiomyopathy, ventricular dilatation is one of the main predictors of outcome where ejection fraction is often not an important predictor (Everitt et al 2014;Alexander et al 2013). In other congenital diseases, such as Tetralogy of Fallot, right ventricular dilatation has also been shown to be one of the main outcome drivers (Therrien et al 2005;Henkens et al 2007).…”
Section: The Relation Between Ventricular Dysfunction and Ventricularmentioning
We investigated patient and procedural factors associated with failure of staged palliation after the Norwood procedure in patients with right ventricular dysfunction (RVDfx).Patients from the Pediatric Heart Network Single Ventricle Reconstruction (SVR) Trial dataset were selected if RVDfx was present, defined as an ejection fraction of less than 44% and a fractional area of change of less than 35% on the post-Norwood echocardiogram. Transplantfree survival after the Norwood procedure was analyzed using multiphase parametric hazard analysis and factors associated with death or transplant were identified.In the SVR cohort, 123 (34%) infants had RVDfx. The six-month transplant-free survival was 87% (70%CI 82-91%). The independent factors associated with increased risk of death or transplant were BT shunt, increased RV size, infectious disease complications and low surgeon volume.Patient factors can help identify which patient with RVDfx is at higher risk of death and help decision making around early transplant listing.iii
“…Sixteen (16) prospective or retrospective studies meeting the inclusion criteria were included in this meta-analysis [12,24,26,30,31,[54][55][56][57][58][59][60][61][62][63][64]. Altogether, the studies investigated a total sample of 6,665 patients aged younger than 18 years with pediatric cardiomyopathies having mean high mortality rate of 12% within five years of diagnosis.…”
Section: Characteristics Of Included Studiesmentioning
confidence: 99%
“…Altogether, the studies investigated a total sample of 6,665 patients aged younger than 18 years with pediatric cardiomyopathies having mean high mortality rate of 12% within five years of diagnosis. The study period ranged from 1958 [12] to 2012 [61]. Echocardiographic defined left ventricular dysfunction (also used in the recruitment of pediatric patients constituting the PCMR data), was the dominant method of diagnosis adopted by 14 studies (87.5%) [12,24,26,30,31,[54][55][56][59][60][61][62][63][64].…”
Section: Characteristics Of Included Studiesmentioning
Cardiomyopathies define a heterogeneous group of heart muscle disorders. They are an important cause of heart failure and a leading indication for heart transplantation in pediatric patients. Research on cardiomyopathy has however focused on the adult populations with fewer dedicated clinical trials investigating pediatric cardiomyopathy. Diagnosis and clinical management of pediatric cardiomyopathy are also challenging because of the lack of specific methods for diagnosis and treatment. Assessment of ventricular structure using absolute values in adults are not useful in children because of their constantly changing body surface area. Therapies developed for adults applied to pediatric patients also have had varied clinical outcomes. This paper therefore reviews existing research evidence on pediatric cardiomyopathy, with the objective of broadening its clinical understanding and management.
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