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2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
by , Bernard J. Gersh, Barry J. Maron, Robert O. Bonow, Joseph A. Dearani, Michael A. Fifer, Mark S. Link, Srihari S. Naidu, Rick A. Nishimura, Steve R. Ommen, Harry Rakowski, Christine E. Seidman, Jeffrey A. Towbin, James E. Udelson, and Clyde
W. Yancy
CirculationVolume 124(24):e783-e831
December 13, 2011
Copyright © American Heart Association, Inc. All rights reserved.
Applying Classification of Recommendation and Level of Evidence.
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
Summary of the nomenclature that distinguishes HCM from other genetic diseases associated with LV hypertrophy. *At this time the overwhelming evidence links the clinical diagnosis of HCM
with a variety of genes encoding protein components of the cardiac sarcomere.
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
Prognosis profiles for HCM and targets for therapy.
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
Treatment algorithm.
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
Indications for ICDs in HCM. *SCD risk modifiers include established risk factors and emerging risk modifiers (Section 6.3.1.2).
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
Management of AF in HCM. AF indicates atrial fibrillation; AV, atrioventricular; INR, international normalized ratio; PPM, permanent pacemaker; and PVI, pulmonary vein isolation.
Writing Committee Members et al. Circulation. 2011;124:e783-e831
Copyright © American Heart Association, Inc. All rights reserved.
