Main description:

Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease, but has been under–recognized and often misrepresented. However, more recently, the understanding of HCM has evolved and options for diagnosis and treatment have advanced considerably. HCM can now be regarded as a contemporary and treatable disease, compatible with normal or extended longevity.

This book was written by Dr. Barry J. Maron, an authority on HCM, and Ms. Lisa Salberg, Founder of the Hypertrophic Cardiomyopathy Association (HCMA), and herself an HCM patient. This new 3rd edition provides an important update on advances in diagnosis, emerging treatment options, and advice for patients. It is a unique resource and cornerstone of current educational efforts making practical information about HCM accessible to a wide range of patients and physicians.

Back cover:

Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease, but has been under–recognized and often misrepresented. However, more recently, the understanding of HCM has evolved and options for diagnosis and treatment have advanced considerably. HCM can now be regarded as a contemporary and treatable disease, compatible with normal or extended longevity.

This book was written by Dr. Barry J. Maron, an authority on HCM, and Ms. Lisa Salberg, Founder of the Hypertrophic Cardiomyopathy Association (HCMA), and herself an HCM patient. This new 3rd edition provides an important update on advances in diagnosis, emerging treatment options, and advice for patients. It is a unique resource and cornerstone of current educational efforts making practical information about HCM accessible to a wide range of patients and physicians.

Contents:

Acknowledgments and Dedications vii

Foreword viii

Introduction: Tips for using this book x

What is hypertrophic cardiomyopathy (HCM) 1

Historical perspective and names 3

How common is HCM? 5

What is the cause of HCM? 8

Structure of the heart 14

Heart function in HCM 21

Left ventricular outflow obstruction 22

When does HCM develop? 25

Gender and race 27

What are the symptoms of HCM? 28

How is HCM diagnosed and what tests are used? 31

 Other tests that may be useful in assessing HCM in selected patients 38

Inaccurate diagnosis 40

General outlook for patients with HCM 40

Complications of HCM 43

Special considerations: athletes and sports activities 53

Treatments for HCM 55

Special considerations for implantable defibrillators 65

Obstructive sleep apnea and HCM 78

Gene therapy and stem cells 78

Automated external defibrillators (AEDs) 79

HCM as a chronic disease: Is a cure available? 80

Are you newly diagnosed? 82

Adapting psychologically to HCM 84

Family screening 87

What about having children? pregnancy and delivery 89

Routine medical care 91

Community screening for HCM 96

Community outreach 97

Driving 98

Traveling 99

Military service 100

Social security benefits 101

Family and Medical Leave Act 103

Health insurance 103

Life insurance 105

Students 105

HCM centers 106

Support and advocacy groups (HCMA) 107

What research is being conducted? 110

The 36 most frequently asked questions about HCM that are addressed to the HCMA by patients, caregivers, and family members 112

Glossary 123

Further reading 130

HCMA membership application 135

Index 137