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

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.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-02-06
DOI
https://doi.org/10.5281/zenodo.18503016
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
Field-Weighted Citation Impact
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article

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

Sai Charan B, K. V. Rajitha, Satyanarayana Murthy S., Ramanjaneyulu D.V. et al.
Zenodo (CERN European Organization for Nuclear Research)
Cardiomyopathy and Myosin Studies
article

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

Sai Charan B, K. V. Rajitha, Satyanarayana Murthy S., Ramanjaneyulu D.V., Kasireddy Gautam, Ramesh U., Kundara Giridhar Reddy, Muralinath E., Sainath Reddy T., Shaik Mahabooob Basha, Hari Kiran M., Mopoori Kalyan, Rahul P., Guruprasad M., Srinivas G.
article en

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.

Zenodo (CERN European Organization for Nuclear Research)
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Cardiomyopathy and Myosin Studies
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