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Prognosis and Management

  • Chapter
Cardiomyopathies

Abstract

Dilated cardiomyopathy is a disease of unknown etiology that principally affects the myocardium [1]. The diagnosis of dilated cardiomyopathy is established by the presence of left ventricular dilatation and systolic dysfunction in the absence of congenital, coronary, valvular, or pericardial heart disease [2]. In some patients the development of dilated cardiomyopathy is associated with clinical factors such as alcoholism, pregnancy or a family history of cardiomyopathy [1,2]. However, dilated cardiomyopathy is distinct from specific heart muscle disease (“secondary myocardial disease”), which occurs with a specific systemic disorder that may be metabolic, collagen-vascular, infiltrative, neuromuscular, inflammatory, or neoplastic in origin [1, 2] (see Chap. 1). There are currently no specific gross anatomic, histologic, or ultrastructural morphologic features which can differentiate dilated cardiomyopathy from other causes of heart failure [3]. Since dilated cardiomyopathy is defined clinically, it is likely that several specific etiologies are responsible for this condition. It is therefore not surprising that patients with dilated cardiomyopathy have a heterogeneous clinical presentation and prognosis.

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Gilbert, E.M., Di Lenarda, A., O’Connell, J.B. (1993). Prognosis and Management. In: Goodwin, J.F., Olsen, E.G.J. (eds) Cardiomyopathies. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77598-7_5

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  • DOI: https://doi.org/10.1007/978-3-642-77598-7_5

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-77600-7

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