Diagnosis and Management of Hypertrophic Cardiomyopathy is aunique, multi-authored compendium of information regarding thecomplexities of clinical and genetic diagnosis, natural history,and management of hypertrophic cardiomyopathy (HCM)—the mostcommon and important of the genetic cardiovasculardiseases—as well as related issues impacting the health oftrained athletes. Edited by Dr. Barry J. Maron, a world authority on HCM, and withmajor contributions from all of the international experts in thisfield, this book provides a single comprehensive source ofinformation concerning HCM. Recent advances in the field arediscussed, including the importance of left ventricular outflowtract obstruction, the use of implantable defibrillators for theprevention of sudden death in young people, definition of thegenetic basis for HCM and its role in clinical diagnosis and riskstratification, the development of more precise strategies forassessing the level of risk for sudden death among all patientswith HCM, and the evolution of invasive interventions for heartfailure symptoms, such as surgical management and its alternatives(alcohol septal ablation and dual-chamber pacing). Key Features: Contributions from all experts in the field,representing diverse viewpoints regarding this heterogeneousdisease and related issues in athletes Information to dispel misunderstandings regarding issuesassociated with HCM and cardiovascular disease in athletes The only comprehensive source of information available on thetopic

Hypertrophic cardiomyopathy is a disease of the cardiac muscle leading to severe debilitating symptoms with relentless progression. Medical options in treating this disease are limited to its early stages, with the disease often becoming resistant to pharmacological interventions. Hypertrophic Cardiomyopathy: A Practical Guide to Diagnosis and Management describes the various sub-types of this condition, including its unique anatomic features, with an emphasis on a therapeutic approach, encapsulating several techniques. Surgical myectomy has become the gold standard of effective treatment. This book also throws light on patient selection, newer surgical techniques, and novel image-based pre-operative planning modalities for surgical myectomy. Key Features Explores the surgical aspects along with the clinical coverage of hypertrophic cardiomyopathy Provides ready resource for practicing cardiologists, practitioners, trainees, and fellows Covers anatomical variants, mitral valve pathology, and non-invasive pre-surgical planning with a detailed surgical video and intra-operative pictures

An illustrated guide for anesthesia providers for congenital heart disease patients, with a focus on non-cardiac operating room settings.

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.

Cardiomyopathies are diseases of the heart muscle with diverse etiologies ranging from myocarditis to gene mutations. They are classified according to morphology and function, and then further categorized based on whether they are familial or non-familial and based on specific etiologies. This book examines the various cardiomyopathies, including arrhythmogenic cardiomyopathy, hypertrophic cardiomyopathy, and dilated cardiomyopathy, as well as their genetic basis.

Written by the authority on hypertrophic cardiomyopathy (HCM) and an HCM patient, and fully endorsed by the Hypertrophic Cardiomyopathy Association (HCMA), the leading advocacy and support organization, the 3rd Edition of this best-selling guide offers unparalleled insight into all aspects of living with and treating HCM. Accessible and practical, A Guide to Hypertrophic Cardiomyopathy For Patients, Their Families and Interested Physicians 3rd Edition: Answers the most pressing questions posed by patients, their families, and non-specialists health professionals involved in their care Covers everything from what is HCM and initial diagnosis of this increasingly prevalent condition to the latest treatment options Reflects the first-ever HCM guidelines published by the American Heart Association in 2011

This issue of Cardiology Clinics, guest edited by Drs. Srihari S. Naidu and Julio A. Panza, will focus on Hypertrophic Cardiomyopathy. Articles in this issue include: Historical Perspective and the Diagnostic Dilemma, Echocardiography for Diagnosis and Management, Cardiac Magnetic Resonance for Diagnosis and Risk Stratification, Genetic Testing and Counseling, Role of Advanced Testing: Invasive Hemodynamics, Biopsies and CPET, Lifestyle Modification and Medical Management, Arrhythmia Evaluation and Management, Sudden Cardiac Death Risk Stratification and the Role of the ICD, Choice of Septal Reduction Therapies and Alcohol Septal Ablation, Surgical Myectomy: Sub-aortic, Mid-ventricular and Apical, Advanced Heart Failure Management and Transplantation, Novel Pharmacotherapy, and Unresolved Issues and Future Directions.