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).
Key Features:
Contributions from all experts in the field, representing diverse viewpoints regarding this heterogeneous disease and related issues in athletes
Information to dispel misunderstandings regarding issues associated with HCM and cardiovascular disease in athletes
The only comprehensive source of information available on the topic
Diagnosis and Management of Hypertrophic Cardiomyopathy
RRP:
$368.00
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).
Key Features:
Contributions from all experts in the field, representing diverse viewpoints regarding this heterogeneous disease and related issues in athletes
Information to dispel misunderstandings regarding issues associated with HCM and cardiovascular disease in athletes
The only comprehensive source of information available on the topic
First described in 1907 by Schicke but recognized as a clinical entity only as recently as 1958, when Teare published the pathologic findings in patients with hypertrophic cardiomyopathy (HeM), an...
Hypertrophic cardiomyopathy (HCM) is a myocardial disorder characterized by left ventricular hypertrophy, which cannot be entirely attributed to loading conditions such as valve or congenital heart...
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