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Heart 2004;90:707-712; doi:10.1136/hrt.2003.024778
Copyright © 2004 BMJ Publishing Group Ltd & British Cardiovascular Society
Heart 2004;90:707-712
© 2004 by BMJ Publishing Group & British Cardiac Society

EDUCATION IN HEART

Cardiomyopathy

Utility of echocardiography in the evaluation of individuals with cardiomyopathy

Malissa J Wood, Michael H Picard

Cardiac Ultrasound Laboratory, Cardiology Division and Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA

Correspondence to:
Correspondence to:
Malissa J Wood MD
Cardiac Ultrasound Laboratory VBK 508, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USA; mjwood@partners.org

Keywords: cardiomyopathy; dilated cardiomyopathy; hypertrophic cardiomyopathy; amyloid; echocardiography

The first 150 words of the full text of this article appear below.

Cardiomyopathies and their resultant systolic and diastolic heart failure remain a major cause of cardiovascular morbidity and mortality. The prevalence of heart failure continues to increase and it remains a major public health threat, particularly in the elderly.1 The overall annual healthcare expenditure for heart failure continues to increase. While a new diagnosis of heart failure is associated with substantial risk of death within one year, the institution of appropriately guided pharmacologic treatment has led to substantial reductions in cardiovascular mortality.2 Identification of potential candidates for such treatment can be facilitated through use of echocardiography.

In many patients the diagnosis of a cardiomyopathy is made after the onset of heart failure symptoms, atrial or ventricular arrhythmias, or a stroke. These complications of the underlying cardiomyopathy represent major causes of cardiovascular morbidity and mortality and frequently result in referral for echocardiography. Echocardiography provides an assessment of systolic and diastolic function . . . [Full text of this article]


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  • Mourad, G., Delabre, J.-P., Garrigue, V. (2008). Cardiac Amyloidosis with the E526V Mutation of the Fibrinogen A {alpha}-Chain. NEJM 359: 2847-2848 [Full Text]  
  • Chumnanvej, S., Wood, M. J., MacGillivray, T. E., Melo, M. F. V. (2007). Perioperative Echocardiographic Examination for Ventricular Assist Device Implantation. Anesth. Analg. 105: 583-601 [Abstract] [Full Text]  

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