This issue of Cardiac Electrophysiology Clinics examines Arrhythmias in Cardiomyopathies. Articles include Atrial and Ventricular Arrhythmias in Hypertrophic Cardiomyopathy and Its Variants; Role of Cardiac MRI in Risk Stratification of Hypertrophic Cardiomyopathy; Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy; Exercise-Induced Right Ventricular Cardiomyopathy; Dilated Cardiomyopathy; Sarcoidosis; Amyloidosis; Chagas Disease; Fabry Disease; Left Ventricular Hypertrophy: Ventricular Arrhythmias and SCD; Left Ventricular Non-compaction; Mitochondrial Cardiomyopathy and Related Arrhythmias; Arrhythmias in Viral Myocarditis and Pericarditis Cardiomyopathy; Takotsubo Cardiomyopathy; Post-partum Cardiomyopathy; Arrhythmias in Alcohol- and Drug-Associated Cardiomyopathies; Arrhythmias in Neuromuscular Dystrophies; Cardiomyopathies Related to Anti-cancer Therapy– and Radiation- Induced Heart Disease; Arrhythmias After Myocardial Stem Cell Therapy; and more.

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.

This book provides a comprehensive review of the ECG findings of inherited arrhythmias and cardiomyopathies. Despite new forms of medical imaging, electrocardiography (ECG) remains the cornerstone of diagnosis, risk-stratification, and prognosis for these conditions. It is extremely important for clinicians to develop the skills required to interpret the ECG correctly as both overdiagnosis and underdiagnosis of these conditions can have a deleterious effect on patients and their families. Each chapter covers a specific condition and highlights typical or critically important ECG findings. Chapters include detailed descriptions of these findings along with pathophysiological mechanisms and clinical vignettes. In addition, the book reviews some normal ECG findings in athletes in order to differentiate some ECG findings from those which may be found in inherited arrhythmia or cardiomyopathy conditions. Electrocardiography of Inherited Arrhythmias and Cardiomyopathies: From Basic Science to Clinical Practice is an essential resource for physicians, residents, fellows, and medical students in cardiology, cardiac electrophysiology, emergency medicine, sports medicine, and primary care.

This issue of Cardiac Electrophysiology Clinics covers arrhythmias in athletes, which can be a cause of morbidity and mortality. Expert authors review the most current information available about management of ventricular arrhythmias, atrial fibrillation, bradyarrhythmias, syncope and other conditions. Preparticipation screening, defibrillator use, and prevention are also discussed. Keep up-to-the-minute with the latest developments in this important aspect of cardiac electrophysiology practice.

This issue of Cardiac Electrophysiology Clinics, guest edited by Mohammad Shenasa and Amin Al-Ahmad, is the second part of ourAdvances in Cardiac Mapping and Catheter Ablation issue. Article topics will include, but are not limited to,New Findings in Atrial Fibrillation Mechanisms; Mapping and Ablation of Neuraxial in Patients with Ventricular Arrhythmias; How to Map and Ablate Rotors in Atrial Fibrillation; Post-ablation Atrial Arrhythmias; Substrate Mapping in Atrial Arrhythmias; Substrate Mapping in Ventricular Arrhythmias; Challenges in Ablation of Complex Congenital Heart Disease; Mapping and Ablation of Ventricular Arrhythmias from the RV and LV Outflow Tract; Novel Insights on Idiopathic VF and Early Repolarization; Novel Observations in Mapping and Ablation in Brugada Syndrome; Ablations of Ventricular Arrhythmias; Mapping and Ablation of Arrhythmias from uncommon sites; Mapping and Ablation of VT in Patients with HF and Cardiomyopathies; Mapping and Ablation of Unmappable VT, VT Storm, and Those in Acute Myocardial Infarction; Mapping and Ablation of Ventricle Arrhythmia in patients of LVAD; Fluoroless Catheter Ablation of Cardiac Arrhythmias; Toward a Uniform Ablation Protocol for Paroxysmal; Persistent and Permanent AF; and The Ideal Mapping System.

This special case-based issue of Cardiac Electrophysiology Clinics features a selection of cases on the following topics: Use of the Surface ECG to Define the Nature of Challenging Arrhythmias; Diagnostic and Prognostic Implications of Surface Recordings from Patients with A-V Block; Supraventricular Tachycardia; Ventricular Tachycardia; Atrial Fibrillation and Flutter; Troubleshooting Device Function; Adult Congenital Cardiac Disease; and Arrhythmias in Patients with Genetic Arrhythmia Syndromes.

In this issue of Cardiac Electrophysiology Clinics, guest editors Drs. Rafik Tadros, Julia Cadrin-Tourigny, and Jason D. Roberts bring their considerable expertise to the topic of Inherited Cardiac Diseases Predisposing to Sudden Death. Top experts in the field cover key topics such as genetic counseling and genetic testing in inherited heart disease; implantable devices in genetic heart disease; gene-based therapy in inherited arrythmias and cardiomyopathies; personalized care in long QT syndrome; and more. - Contains 16 relevant, practice-oriented topics including novelties in Brugada syndrome: complex genetics, risk stratification and catheter ablation; novel approaches to treatment of catecholaminergic polymorphic ventricular tachycardia; investigation of unexplained cardiac arrest: phenotyping and genetic testing; impact of imaging to arrhythmic risk stratification in non-ischemic cardiomyopathy; and more. - Provides in-depth clinical reviews on inherited cardiac diseases predisposing to sudden death, offering actionable insights for clinical practice. - Presents the latest information on this timely, focused topic under the leadership of experienced editors in the field. Authors synthesize and distill the latest research and practice guidelines to create clinically significant, topic-based reviews.