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Historical Terminology, Classifications, and Present Definition of DCM
Pages 1-9
This open access book presents a comprehensive overview of dilated cardiomyopathy, providing readers with practical guidelines for its clinical management. The first part of the book analyzes in detail the disease’s pathophysiology, its diagnostic work up as well as the prognostic stratification, and illustrates the role of genetics and gene-environment interaction. The second part presents current and future treatment options, highlighting the importance of long-term and individualized treatments and follow-up.
Furthermore, it discusses open issues, such as the apparent healing phenomenon, the early prognosis of arrhythmic events or the use of genetic testing in clinical practice.
Offering a multidisciplinary approach for optimizing the clinical management of DCM, this book is an invaluable aid not only for the clinical cardiologists, but for all physicians involved in the care of this challenging disease.
Historical Terminology, Classifications, and Present Definition of DCM
Pages 1-9
Epidemiology
Pages 11-16
Pathophysiology
Pages 17-25
Etiological Definition and Diagnostic Work-Up
Pages 27-43
Genetics of Dilated Cardiomyopathy: Current Knowledge and Future Perspectives
Pages 45-69
Clinical Presentation, Spectrum of Disease, and Natural History
Pages 71-82
Role of Cardiac Imaging: Echocardiography
Pages 83-111
Role of Cardiac Imaging: Cardiac Magnetic Resonance and Cardiac Computed Tomography
Pages 113-133
Endomyocardial Biopsy
Pages 135-147
Arrhythmias in Dilated Cardiomyopathy: Diagnosis and Treatment
Pages 149-171
Regenerative Medicine and Biomarkers for Dilated Cardiomyopathy
Pages 173-185
Prognostic Stratification and Importance of Follow-Up
Pages 187-198
Current Management and Treatment
Pages 199-215
Unresolved Issues and Future Perspectives
Pages 217-227
Dilated Cardiomyopathy at the Crossroad: Multidisciplinary Approach
Pages 229-241
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