Literature DB >> 8087940

Infantile dilated cardiomyopathy. Relation of outcome to left ventricular mechanics, hemodynamics, and histology at the time of presentation.

A Matitiau1, A Perez-Atayde, S P Sanders, T Sluysmans, I A Parness, P J Spevak, S D Colan.   

Abstract

BACKGROUND: For patients with acute dilated cardiomyopathy, definition of prognosis and of clinical features predictive of outcome is particularly important due to the availability of cardiac transplantation and other innovative treatment strategies. METHODS AND
RESULTS: We reviewed our experience with 24 children under 2 years of age with dilated congestive cardiomyopathy to determine outcome and potential predictive variables. Clinical, serological, ECG, echocardiographic, hemodynamic, and histological findings were analyzed. Idiopathic cardiomyopathy or myocarditis constituted 29% of the patients presenting with congestive heart failure without structural heart disease. Among these patients, 45% recovered completely, 25% survived with persistent left ventricular dysfunction, and 30% died. All except one of the deaths occurred during the first 2 months after presentation. Poorer outcome and higher mortality were associated with a more severely depressed left ventricular ejection fraction and/or a more spherical left ventricular shape at presentation. Histological evidence of myocardial inflammation was a favorable prognostic indicator, whereas histological evidence of endocardial fibroelastosis was associated with a poor outcome. During the recovery phase, diastolic volume fell rapidly. Ventricular mass was elevated from the earliest observations and fell more slowly, with persistent elevation of the mass-to-volume ratio up to 2 years. Function and contractility improved over the first several months in most patients who recovered, although in occasional patients continued improvement was seen for as long as 2 years after presentation.
CONCLUSIONS: Histological and echocardiographic features can be used to identify patients at particularly high risk for death. To have any impact on outcome, decisions about cardiac transplantation must be reached rapidly, since almost all deaths occurred within the first 2 months after presentation. Recovery of function is often rapid, but continued improvement may be seen for as long as 2 years.

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Year:  1994        PMID: 8087940     DOI: 10.1161/01.cir.90.3.1310

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  21 in total

1.  Impaired cardiac adrenergic innervation assessed by MIBG imaging as a predictor of treatment response in childhood dilated cardiomyopathy.

Authors:  P Acar; P Merlet; L Iserin; D Bonnet; D Sidi; A Syrota; J Kachaner
Journal:  Heart       Date:  2001-06       Impact factor: 5.994

2.  Presentation, management and outcomes of thrombosis for children with cardiomyopathy.

Authors:  Brian W McCrindle; Tara Karamlou; Harvey Wong; Nirupama Gangam; Kalyani R Trivedi; Kyong-Jin Lee; Lee N Benson
Journal:  Can J Cardiol       Date:  2006-06       Impact factor: 5.223

3.  Cardiac function assessment in patients with family history of nonhypertrophic cardiomyopathy: a prenatal and postnatal study.

Authors:  S R F F Pedra; L K Hornberger; S M Leal; G P Taylor; J F Smallhorn
Journal:  Pediatr Cardiol       Date:  2005 Sep-Oct       Impact factor: 1.655

4.  NT-proBNP as a marker for persistent cardiac disease in children with history of dilated cardiomyopathy and myocarditis.

Authors:  N Nasser; Z Perles; A J J T Rein; A Nir
Journal:  Pediatr Cardiol       Date:  2006 Jan-Feb       Impact factor: 1.655

Review 5.  Genetic abnormalities responsible for dilated cardiomyopathy.

Authors:  J A Towbin; N E Bowles
Journal:  Curr Cardiol Rep       Date:  2000-09       Impact factor: 2.931

6.  Clinical outcomes of acute myocarditis in childhood.

Authors:  K J Lee; B W McCrindle; D J Bohn; G J Wilson; G P Taylor; R M Freedom; J F Smallhorn; L N Benson
Journal:  Heart       Date:  1999-08       Impact factor: 5.994

Review 7.  Echocardiographic methods, quality review, and measurement accuracy in a randomized multicenter clinical trial of Marfan syndrome.

Authors:  Elif Seda Selamet Tierney; Jami C Levine; Shan Chen; Timothy J Bradley; Gail D Pearson; Steven D Colan; Lynn A Sleeper; M Jay Campbell; Meryl S Cohen; Julie De Backer; Lin T Guey; Haleh Heydarian; Wyman W Lai; Mark B Lewin; Edward Marcus; Christopher R Mart; Ricardo H Pignatelli; Beth F Printz; Angela M Sharkey; Girish S Shirali; Shubhika Srivastava; Ronald V Lacro
Journal:  J Am Soc Echocardiogr       Date:  2013-04-10       Impact factor: 5.251

8.  Nontransplant cardiac surgery as a bridge to heart transplantation in pediatric dilated cardiomyopathy.

Authors:  Ron-Bin Hsu; Chen-Yen Chien; Shoei-Shen Wang; Shu-Hsun Chu
Journal:  Tex Heart Inst J       Date:  2002

9.  Use of 123I-MIBG scintigraphy to assess the impact of carvedilol on cardiac adrenergic neuronal function in childhood dilated cardiomyopathy.

Authors:  Christophe Maunoury; Philippe Acar; Daniel Sidi
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-09-23       Impact factor: 9.236

10.  Outcome Predictors for Pediatric Dilated Cardiomyopathy: A Systematic Review.

Authors:  Jorge A Alvarez; James D Wilkinson; Steven E Lipshultz
Journal:  Prog Pediatr Cardiol       Date:  2007-09-01
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