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A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Arrhythmias in dilated cardiomyopathy
Saurabh Kumar1, William G Stevenson1, Roy M John1
1Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.
Insights
Dilated cardiomyopathies (DCM) commonly cause heart rhythm problems like conduction defects and atrial fibrillation. This review covers DCM arrhythmias, their causes, and current management strategies.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Research
Background:
- Dilated cardiomyopathies (DCM) are associated with a high incidence of cardiac arrhythmias.
- Arrhythmias in DCM range from conduction abnormalities to life-threatening ventricular arrhythmias.
- These rhythm disturbances significantly impact patient prognosis and quality of life.
Purpose of the Study:
- To summarize the common arrhythmias observed in patients with dilated cardiomyopathies.
- To review the underlying electrophysiologic mechanisms of these arrhythmias.
- To discuss current management approaches for arrhythmias in DCM.
Main Methods:
- Literature review of studies on arrhythmias in dilated cardiomyopathies.
- Analysis of electrophysiologic principles governing cardiac rhythm in DCM.
- Synthesis of clinical guidelines and evidence for arrhythmia management.
Main Results:
- Common arrhythmias include atrioventricular block, left bundle branch block, atrial fibrillation, and ventricular arrhythmias.
- Ventricular arrhythmias, particularly sustained monomorphic ventricular tachycardia, are associated with adverse outcomes.
- Sudden cardiac death is a late complication often linked to ventricular arrhythmias.
Conclusions:
- Arrhythmias are a major clinical challenge in dilated cardiomyopathies.
- Understanding the electrophysiologic basis is crucial for effective management.
- Comprehensive management strategies are essential to improve outcomes for DCM patients with arrhythmias.
Abstract:
Patients with dilated cardiomyopathies (DCM) face a significant burden of arrhythmias, including conduction defects such as atrioventricular block and interventricular delay in the form of left bundle branch block, resulting in altered electromechanical coupling that can exacerbate heart failure. Atrial fibrillation is common and carries an adverse prognosis. Ventricular arrhythmias and sudden cardiac death generally occur late in the disease course. Sustained monomorphic ventricular tachycardia accounts for most of the sustained ventricular arrhythmias in DCM. This article summarizes common forms of arrhythmias encountered in patients with DCM, and reviews the relevant electrophysiologic basis of these arrhythmias and their management.
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