There are many diseases and illnesses in this world. Some are easy to cure/fix and others are not. Yet, others cannot be cured nor are they completely life threatening. This is the case when it come to cardiomyopathy because cardiomyopathy is neither curable but neither is it completely life threatening. What this paper will do below, will be to discuss in some length an accurate pathophysiology description of cardiomyopathy from viral infection, diagnostics tests, assessment findings, expected progression, treatment and living with cardiomyopathy. Pathophysiology
The only way to truly understand a disease is to understand all of its properties. What is an accurate pathophysiology of cardiomyopathy from a viral infection? In general, "the cardiomyopathies are diseases of the heart muscle that cause cardiac dysfunction resulting in heart failure, dysrhythmias, or sudden death" (Morton & Fontaine, 2009). There is a variety of cardiomyopathy types. The distinct categories are "dilated, hypertrophic, restrictive, arrhythmogenic right ventricular cardiomyopathy, and unclassified" ( Morton & Fontaine, 2009). Viral cardiomyopathy in particular, is a form of disorder due to an attack on the cardiac heart muscles. As mentioned above, one of the types of cardiomyopathy is dilated cardiomyopathy, this type of cardiomyopathy is distinguished by an increased myocardial cavity. The cavity size gets bigger and thus produces a reduction in the left ventricular wall. There is a thickness of the wall and an impaired systolic function. In these circumstances, the heart takes on a new shape. The heart takes on the shape of a glob. There is also dilation in the ventricular chamber. Basically speaking, with dilated cardiomyopathy, the left ventricular walls of the chamber thicken. There is also Hypertrophic forms of cardiomyopathy. Here, "diastolic dysfunction marked hypertrophy of left ventricle, occasionally also of right ventricle, and usually (but no always) disproportionate...
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