An Indispensible Parameters of Dilated Cardio Myopathy Include Etiology Include Etiology, Epidemiology, Patho Physiology, Diagnosis, Differential Diagnosis, Treatment, Prognosis, Complications and Health Care Outcomes

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Authors: Srinivas G., Ramanjaneyulu D.V., Satyanarayana Murthy S., Muralinath E., Guruprasad M., Hari Kiran M., Shaik Mahabooob Basha, Kundara Giridhar Reddy, Kasireddy Gautam, Mopoori Kalyan, Sai Charan B, Sainath Reddy T.
+3 more Ramesh U., Rahul P., K. V. Rajitha
Cited by: 0

Abstract

Dilated Cardiomyopathy (DCM) is a disease of heart muscle manifested by enlargement and dilation of one or both of the ventricles along with impaired contractility narrated as left ventricular ejection fraction (LVEF) less than 40%. Patients may or may not have overt signs of heart failure, but they are by definition exhibiting systolic dysfunction. There are two types of DCM for this disease process: primary and secondary. Since primary DCM is thought to be idiopathic, secondary causes must be ruled out before the diagnosis can be made. This exercise describes the causes, symptoms, and importance of the interprofessional team in managing dilated cardiomyopathy.

Fields of Study & Subjects

Cardiomyopathy and Myosin Studies Heart Failure Treatment and Management Viral Infections and Immunology Research

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
6 February 2026
Language
EN