Literature DB >> 10798428

Congenital Heart Surgery Nomenclature and Database Project: pediatric cardiomyopathies and end-stage congenital heart disease.

R E Delius1.   

Abstract

The extant nomenclature for cardiomyopathy is reviewed for the purpose of establishing a unified reporting system. The subject was debated and reviewed by members of the STS-Congenital Heart Surgery Database Committee and representatives from the European Association for Cardiothoracic Surgery. All efforts were made to include all relevant nomenclature categories using synonyms where appropriate. A functional classification based on pathophysiology is proposed. Cardiomyopathy is subdivided into: dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy, right ventricular cardiomyopathy, and end-stage congenital heart disease. A comprehensive database set is presented that is based on a hierarchical scheme. Data are entered at various levels of complexity and detail that can be determined by the clinician. These data can lay the foundation for comprehensive risk stratification analyses. A minimum database set is also presented that will allow for data sharing and would lend itself to basic interpretation of trends. Outcome tables relating diagnoses, procedures, and various risk factors are presented.

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Year:  2000        PMID: 10798428     DOI: 10.1016/s0003-4975(99)01243-6

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  1 in total

1.  [Neonatal hypertrophic cardiomyopathy of difficult etiologic diagnosis].

Authors:  Rania Hammami; Sana Ouali; Ilyes Naffeti; Sami Hammas; Slim Kacem; Rim Gribaa; Fahmi Remedi; Essia Boughzela
Journal:  Pan Afr Med J       Date:  2011-12-19
  1 in total

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