Hypertrophic cardiomyopathy: Part 1 - Introduction, pathology and pathophysiology.
Ann Card Anaesth
;
2014 Apr; 17(2): 118-124
Article
in English
| IMSEAR
| ID: sea-150309
ABSTRACT
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease with many genotype and phenotype variations. Earlier terminologies, hypertrophic obstructive cardiomyopathy and idiopathic hypertrophic sub‑aortic stenosis are no longer used to describe this entity. Patients present with or without left ventricular outflow tract (LVOT) obstruction. Resting or provocative LVOT obstruction occurs in 70% of patients and is the most common cause of heart failure. The pathology and pathophysiology of HCM includes hypertrophy of the left ventricle with or without right ventricular hypertrophy, systolic anterior motion of mitral valve, dynamic and mechanical LVOT obstruction, mitral regurgitation, diastolic dysfunction, myocardial ischemia, and fibrosis. Thorough understanding of pathology and pathophysiology is important for anesthetic and surgical management.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Systole
/
Cardiomyopathy, Hypertrophic
/
Humans
/
Ventricular Outflow Obstruction
/
Mitral Valve Insufficiency
Language:
English
Journal:
Ann Card Anaesth
Year:
2014
Type:
Article
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