Circulation: Heart Failure. 2008;1:72-76
doi: 10.1161/CIRCHEARTFAILURE.108.770826
Controversies in Heart Failure |
Is the 2006 American Heart Association classification of cardiomyopathies the gold standard?
The 2006 American Heart Association Classification of Cardiomyopathies Is the Gold Standard
Barry J. Maron, MD
From the Hypertrophic Cardiomyopathy Center, Minneapolis Heart Institute Foundation, Minneapolis, Minn.
Correspondence to Barry J. Maron, MD, Hypertrophic Cardiomyopathy Center, 920 E 28th St, Suite 620, Minneapolis, MN 55407. E-mail hcm.maron@mhif.org
An extract of the first 250 words of the full text is provided, because this article has no abstract.
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Introduction
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The cardiomyopathies are an important and complex group of heart
muscle diseases with multiple etiologies and heterogeneous phenotypic
expression.
1 Awareness and knowledge of these diseases in both
the public and medical communities have historically been impaired
by periodic confusion surrounding definitions and nomenclature.
Therefore, formal and systematic classifications have traditionally
been viewed as useful exercises promoting greater understanding
of the heart muscle diseases.
1–10 Indeed, a multitude
of such cardiomyopathy classifications have been advanced over
the years by individual investigators and consensus panels sanctioned
by medically related organizations such as the World Health
Organization (WHO).
2,4 These classification schemes have evolved
in concert with the level of scientific understanding.
Response by Elliott p 76
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Historical Context to the Debate
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Remarkably, it was not until 50 years ago (1957) that the term
cardiomyopathy was used for the first time.
1 Over the next 25
years, a number of definitions for cardiomyopathies were advanced.
Indeed, in the original 1980 WHO classification,
4 cardiomyopathies
were defined only as "heart muscle diseases of unknown cause,"
reflecting a general lack of available information about basic
disease mechanisms. In 1968, the WHO defined cardiomyopathies
as "diseases of different and often unknown etiology in which
the dominant feature is cardiomegaly and heart failure."
1,3 The final WHO classification published in 1995
2 proposed "diseases
of myocardium associated with cardiac dysfunction" and included
for the first time arrhythmogenic right ventricular cardiomyopathy/dysplasia,
as well as primary restrictive cardiomyopathy.
Therefore, why was it necessary to offer yet another classification scheme for cardiomyopathies in 2006 under the auspices of the American Heart . . . [Full Text of this Article]