Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review

BJ Maron, MY Desai, RA Nishimura, P Spirito… - Journal of the American …, 2022 - jacc.org
Hypertrophic cardiomyopathy (HCM) is a relatively common often inherited global heart
disease, with complex phenotypic and genetic expression and natural history, affecting both …

2020 AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: a report of the American College of Cardiology/American …

SR Ommen, S Mital, MA Burke, SM Day… - Journal of the American …, 2020 - jacc.org
The recommendations listed in this guideline are, whenever possible, evidence based. An
initial extensive evidence review, which included literature derived from research involving …

Management of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review

BJ Maron, MY Desai, RA Nishimura, P Spirito… - Journal of the American …, 2022 - jacc.org
Hypertrophic cardiomyopathy (HCM), a relatively common, globally distributed, and often
inherited primary cardiac disease, has now transformed into a contemporary highly treatable …

[HTML][HTML] Evolution of risk stratification and sudden death prevention in hypertrophic cardiomyopathy: twenty years with the implantable cardioverter-defibrillator

BJ Maron, EJ Rowin, MS Maron - Heart Rhythm, 2021 - Elsevier
Hypertrophic cardiomyopathy (HCM) is a relatively common inherited myocardial disorder,
once regarded as largely untreatable with ominous prognosis and most visibly as a common …

Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents

KC Siontis, K Liu, JM Bos, ZI Attia… - International Journal of …, 2021 - Elsevier
Background There is no established screening approach for hypertrophic cardiomyopathy
(HCM). We recently developed an artificial intelligence (AI) model for the detection of HCM …

[HTML][HTML] Gene therapy in cardiology: is a cure for hypertrophic cardiomyopathy on the horizon?

ED Paratz, J Mundisugih, SJ Rowe, E Kizana… - Canadian Journal of …, 2024 - Elsevier
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiomyopathy
worldwide, affecting approximately 1 in 500 individuals. Current therapeutic interventions …

A phase 1 dose-escalation study of the cardiac myosin inhibitor aficamten in healthy participants

FI Malik, LA Robertson, DR Armas, EP Robbie… - Basic to Translational …, 2022 - jacc.org
Summary This phase 1, randomized, double-blind, placebo-controlled study of aficamten
(formerly CK-3773274) in healthy adults identified a pharmacologically active range of …

Return-to-play for elite athletes with genetic heart diseases predisposing to sudden cardiac death

KA Martinez, JM Bos, AL Baggish, DM Phelan… - Journal of the American …, 2023 - jacc.org
Background People diagnosed with genetic heart diseases (GHDs) associated with sudden
cardiac death (SCD) have historically been restricted from competitive sports. Recent data …

[HTML][HTML] Risk factors of sudden cardiac death in hypertrophic cardiomyopathy

Y Hong, WW Su, X Li - Current Opinion in Cardiology, 2022 - journals.lww.com
The identification of independent risk factors for HCM-related SCD would likely contribute to
risk stratification. However, it is difficult to predict SCD with absolute certainty, as the annual …

Treatment strategies for cardiomyopathy in children: a scientific statement from the American Heart Association

C Bogle, SD Colan, SD Miyamoto, S Choudhry… - Circulation, 2023 - Am Heart Assoc
This scientific statement from the American Heart Association focuses on treatment
strategies and modalities for cardiomyopathy (heart muscle disease) in children and serves …