Dilated cardiomyopathy classification: Difference between revisions
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{{CMG}}; {{AE}} {{AIA}} | {{CMG}}; {{AE}} {{AIA}} | ||
==Overview== | ==Overview== | ||
Dilated cardiomyopathy can be classified in terms of etiology | [[Dilated cardiomyopathy]] can be classified in terms of [[etiology]], according to the presence of [[ischemia]] (ischemic and non-ischemic) or the mode of [[Heredity|inheritance]] ([[Familial]] and non-familial). | ||
==Classification== | ==Classification== | ||
[[Dilated cardiomyopathy]] can be classified in terms of etiology: | [[Dilated cardiomyopathy]] can be classified in terms of etiology: | ||
* Based on the presence of [[ischemia]] | * Based on the presence of [[ischemia]] | ||
** [[Ischemia|Ischemic]] [[Dilated cardiomyopathy|DCM]]: In which the underlying cause is related to ischemia like [[Coronary heart disease|coronary artery disease]]. | ** [[Ischemia|Ischemic]] [[Dilated cardiomyopathy|DCM]]: In which the underlying cause is related to ischemia like [[Coronary heart disease|coronary artery disease]]. | ||
** Non-ischemic [[Dilated cardiomyopathy|DCM]]: In which ischemia was not he main driver of DCM [[pathogenesis]]. | ** Non-ischemic [[Dilated cardiomyopathy|DCM]]: In which ischemia was not he main driver of DCM [[pathogenesis]]. | ||
* Based on the mode of [[Inheritance (genetic algorithm)|inheritance]]: | |||
** [[Familial]]: In which an inherited genetic [[mutation]] started the [[myopathy]] process | |||
** Non-familial: related to other causes as [[Infection|infections]], [[Toxin|toxins]], [[:Category:Drugs|drugs]], and [[peripartum cardiomyopathy]] | |||
* | * | ||
Revision as of 12:24, 30 December 2019
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Dilated cardiomyopathy Microchapters |
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Dilated cardiomyopathy classification On the Web |
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American Roentgen Ray Society Images of Dilated cardiomyopathy classification |
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Risk calculators and risk factors for Dilated cardiomyopathy classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdelrahman Ibrahim Abushouk, MD[2]
Overview
Dilated cardiomyopathy can be classified in terms of etiology, according to the presence of ischemia (ischemic and non-ischemic) or the mode of inheritance (Familial and non-familial).
Classification
Dilated cardiomyopathy can be classified in terms of etiology:
- Based on the presence of ischemia
- Ischemic DCM: In which the underlying cause is related to ischemia like coronary artery disease.
- Non-ischemic DCM: In which ischemia was not he main driver of DCM pathogenesis.
- Based on the mode of inheritance:
- Familial: In which an inherited genetic mutation started the myopathy process
- Non-familial: related to other causes as infections, toxins, drugs, and peripartum cardiomyopathy