Diagnosis and Management of Hypertrophic Cardiomyopathy
Sudden Death Prevention
Edited by Barry J. Maron
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Diagnosis and Management of Hypertrophic Cardiomyopathy by Barry J. Maron
Book Description"Diagnosis and Management of Hypertrophic Cardiomyopathy" is a unique, multi-authored compendium of information regarding the complexities of clinical and genetic diagnosis, natural history, and management of hypertrophic cardiomyopathy (HCM) - the most common and important of the genetic cardiovascular diseases - as well as related issues impacting the health of trained athletes. Edited by Dr. Barry J. Maron, a world authority on HCM, and with major contributions from all of the international experts in this field, this book provides a single comprehensive source of information concerning HCM.Recent advances in the field are discussed, including the importance of left ventricular outflow tract obstruction, the use of implantable defibrillators for the prevention of sudden death in young people, definition of the genetic basis for HCM and its role in clinical diagnosis and risk stratification, the development of more precise strategies for assessing the level of risk for sudden death among all patients with HCM, and the evolution of invasive interventions for heart failure symptoms, such as surgical management and its alternatives (alcohol septal ablation and dual-chamber pacing). It features contributions from all experts in the field, representing diverse viewpoints regarding this heterogeneous disease and related issues in athletes. It has information to dispel misunderstandings regarding issues associated with HCM and cardiovascular disease in athletes. This is the only comprehensive source of information available on the topic.
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Book DetailsISBN: 9781405117326
(235mm x 161mm x 33mm)
Imprint: Blackwell Futura
Publisher: John Wiley and Sons Ltd
Publish Date: 27-Feb-2004
Country of Publication: United Kingdom
Books By Author Barry J. Maron
Hypertrophic Cardiomyopathy, Paperback (November 2006)
When there is a diagnosis of HCM in a family, this complete, easy-to-read guide is your essential resource for finding the answers to your many questions.
Guide to Hypertrophic Cardiomyopathy, Paperback (February 1982)» View all books by Barry J. Maron
Written by the world's 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.
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Author Biography - Barry J. Maron
A unique, multi-authored compendium of information (edited by Dr. Barry J. Maron) regarding the complexities of clinical and genetic diagnosis, natural history and management of hypertrophic cardiomyopathy (HCM) - - - the most common and important of the genetic cardiovascular diseases, as well as related issues impacting the health of trained athletes. The contributions are from all of the international experts in this field. Major purpose To provide a single comprehensive source of information, including differing viewpoints, concerning HCM as well as cardiovascular disease in athletes - - - for clinical and research cardiologists, primary care physicians, and basic scientists, and written and assembled by all the experts in the field. 3 features 1. The book literally includes the contributions of all experts in the field and therefore can be regarded as truly comprehensive, taking into account sometimes diverse viewpoints regarding this heterogeneous disease (i.e., HCM) and related issues in athletes. 2. There is no other available source that comes remotely close...so it is a novel undertaking. 3. Because there is so much misunderstanding regarding the aforementioned issues in the physician community...and because these are not clinical problems necessarily encountered on a daily basis by most practicing physicians...this book becomes a particularly important source to interested parties - - - i.e., information they may not be able to assemble easily in any other way. Recent advances of note 1. Use of implantable defibrillator in HCM for prevention of sudden death in young people. 2. Introduction of catheter-based alcohol septal ablation to reduce obstruction and symptoms as a treatment alternative to surgery for some HCM patients. 3. Definition of the genetic basis for HCM and its role in clinical diagnosis and risk stratification. 4. Development of more precise strategies for assessing the level of risk for sudden death among all patients with HCM. 5. More precise definition of the relatively high frequency with which HCM occurs in the general population. Special emphasis All of the above, plus: the septal myectomy operation remains the gold standard for the severely symptomatic patient with obstruction, refractory to medications.
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