Abstract

Hypertrophic cardiomyopathy (HCM) is a relatively common inherited myocardial disorder, once regarded as largely untreatable with ominous prognosis and most visibly as a common cause of sudden death (SD) in the young. Over the last several years, HCM has been transformed into a contemporary treatable disease with management options that significantly alter clinical course. With the use of implantable cardioverter-defibrillators (ICDs) in the HCM patient population, a new paradigm has emerged, with primary prevention device therapy reliably terminating potentially lethal ventricular tachyarrhythmias (3%-4% per year) and being largely responsible for a >10-fold decrease in disease-related mortality (to 0.5% per year), independent of age. An evidenced-based and guideline directed clinical risk stratification algorithm has evolved, including variables identified with cardiac magnetic resonance. One or more risk markers judged major and relevant within a patient's clinical profile can be considered sufficient to recommend a primary prevention implant (associated with a measure of physician judgment and shared decision-making). ICD decisions using the prospective individual risk marker strategy have been associated with 95% sensitivity for identifying patients who subsequently experienced appropriate ICD therapy, (albeit often delayed substantially for >5 or >10 years after implant), but without heart failure deterioration or HCM death following device intervention. A rigid mathematically derived statistical risk model proposed by the European Society of Cardiology is associated with low sensitivity (ie, 33%) for predicting SD events. Introduction of prophylactically inserted ICDs to HCM 20 years ago has significantly altered the clinical course and landscape of this disease. SD prevention has reduced HCM mortality significantly, making preservation of life and the potential for normal longevity a reality for most patients.

Highlights

  • Introduction of prophylactically inserted implantable cardioverter-defibrillators (ICDs) toHypertrophic cardiomyopathy (HCM) 20 years ago has significantly altered the clinical course and landscape of this disease

  • Left ventricular (LV) apical aneurysms represent a novel mechanism of re-entry (Figures 1 and 2), with ventricular tachycardia (VT)/ventricular fibrillation (VF) emanating from discrete fibrosis at the intersection of aneurysmal rim and contiguous myocardium,[44,45] providing a unique opportunity to ablate refractory arrhythmias.[46,47,48]

  • The evolving risk algorithm began with asymptomatic bursts of nonsustained ventricular tachycardia (NSVT) on ambulatory electrocardiography (ECG)50,52,S-8 and thereafter family history of sudden death (SD) based on pedigrees with clustered malignant events.[55]

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Summary

CONTEMPORARY REVIEW

Evolution of risk stratification and sudden death prevention in hypertrophic cardiomyopathy: Twenty years with the implantable cardioverter-defibrillator. With the use of implantable cardioverter-defibrillators (ICDs) in the HCM patient population, a new paradigm has emerged, with primary prevention device therapy reliably terminating potentially lethal ventricular tachyarrhythmias (3%–4% per year) and being largely responsible for a .10-fold decrease in disease-related mortality (to 0.5% per year), independent of age. ICD decisions using the prospective individual risk marker strategy have been associated with 95% sensitivity for identifying patients who subsequently experienced appropriate ICD therapy, (albeit often delayed substantially for .5 or .10 years after implant), but without heart failure deterioration or HCM death following device intervention. SD prevention has reduced HCM mortality significantly, making preservation of life and the potential for normal longevity a reality for most patients.

Introduction
Principles of risk prediction Evolution of risk algorithm
ECHO with contrast
Year Study
No SD events
Risk scores
Findings
Conclusion and future perspectives
Full Text
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