Hypertrophic Cardiomyopathy

This extensively updated edition provides a comprehensive review of hypertrophic cardiomyopathy, the most common genetic disorder of the heart characterized by dysfunctional contractility at the sarcomere level. The disease produces abnormal and oftentimes focal hypertrophy on a macroscopic level that further impairs cardiac performance and may lead to life-threatening arrhythmias. This edition provides a practical approach, establishing evidence-based best practice for all scenarios. Hypertrophic Cardiomyopathy provides readers with key points and critical clinical pearls to assist them in managing patients. New chapters have been included on managing hypertension, sleep apnea, coronary artery disease, structural and congenital disease, nutrition and pharmacotherapies. All aspects of treatment are covered – medications, pacemakers and defibrillators, and invasive septal reduction therapy (both surgical myectomy and alcohol septal ablation) – in addition to genetics, family screening, lifestyle concerns, and athletic screening. The practical approach has been reinforced with an expanded emphasis on creating a Center of Excellence, how to facilitate the multi-disciplinary approach, and on case-based reviews and discussions, with each chapter ending with a post-test. This book is an essential text for cardiology professionals from trainee to board-certified physician, and includes important information for interventional cardiologists, cardiac surgeons, cardiac imagers, critical care physicians, sports medicine physicians, genetic counsellors, and electrophysiologists.

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

When there is a diagnosis of HCM in a family, this complete,easy-to-read guide is your essential resource for finding theanswers to your many questions. In clear and straightforwardlanguage, it explains what hypertrophic cardiomyopathy is, what thesymptoms are, and how it can be treated, as well as reviewing thegenetic implications and offering candid lifestyle advice. Drawing on the expertise of Dr. Barry Maron, an internationallyrecognized authority on HCM, the book addresses major questions andconcerns of both patients and families. Fully revised to reflectthe latest developments, Hypertrophic Cardiomyopathy: Forpatients, their families and interested physicians, SecondEdition, is a valuable source of straightforward advice anddependable information for everyone who is affected by HCM.

The Social Security Administration (SSA) uses a screening tool called the Listing of Impairments to identify claimants who are so severely impaired that they cannot work at all and thus immediately qualify for benefits. In this report, the IOM makes several recommendations for improving SSA's capacity to determine disability benefits more quickly and efficiently using the Listings.

Cardiovascular Hemodynamics for the Clinician, 2nd Edition, provides a useful, succinct and understandable guide to the practical application of hemodynamics in clinical medicine for all trainees and clinicians in the field. Concise handbook to help both practicing and prospective clinicians better understand and interpret the hemodynamic data used to make specific diagnoses and monitor ongoing therapy Numerous pressure tracings throughout the book reinforce the text by demonstrating what will be seen in daily practice Topics include coronary artery disease; cardiomyopathies; valvular heart disease; arrhythmias; hemodynamic support devices and pericardial disease New chapters on TAVR, ventricular assist devices, and pulmonic valve disease, expanded coverage of pulmonary hypertension, fractional flow reserve, heart failure with preserved ejection fraction and valvular heart disease Provides a basic overview of circulatory physiology and cardiac function followed by detailed discussion of pathophysiological changes in various disease states

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