Why the study?
Recent advances in imaging, molecular understanding, and therapeutic options in HCM prompted a systematic review to identify consensus and discrepant areas across clinical practice guidelines.
Systematic Review
Contemporary guidelines for HCM show broad consensus on diagnosis and management, but notable variations remain in sudden cardiac death risk assessment and diagnostic criteria.
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Variations in sudden cardiac death risk assessment across hypertrophic cardiomyopathy guidelines may cause inconsistent stratification; challenges consensus and leaves open the need for harmonized criteria.
AIMS: In light of recent advances in imaging techniques, molecular understanding and therapeutic options in hypertrophic cardiomyopathy (HCM), we performed a systematic review of current guidelines for the diagnosis and management of HCM in order to identify consensus and discrepant areas in the clinical practice guidelines. METHODS AND RESULTS: We systematically reviewed the English language guidelines and recommendations for the management of HCM in adults. MEDLINE and EMBASE databases were searched for guidelines published in the last 10 years. Following a systematic search, three guidelines on the diagnosis and management of HCM were identified, all of which were robustly developed (AGREE rigour of development score ≥50%). These guidelines were authored by the major European (European Society of Cardiology; 2023), American (American Heart Association /American College of Cardiology/American Medical Society for Sports Medicine /Heart Rhythm Society/Pediatric and Congenital Electrophysiology Society/Society for Cardiovascular Magnetic Resonance; 2024), and Japanese [Japanese Circulation Society (JCS)/Japanese Heart Failure Society (JHFS); 2018] cardiovascular societies. There was broad consensus on echocardiographic recommendations, the medical and invasive management of HCM, the application of genetic testing and family screening, and exercise and reproductive recommendations in HCM. There were areas of variability in the definition and diagnostic criteria for HCM, cardiovascular magnetic resonance imaging recommendations, and assessment of sudden cardiac death (SCD) risk and prevention strategies. Due to the JCS/JHFS guidelines being older, there are no recommendations on the use of cardiac myosin ATPase inhibitors. CONCLUSION: Contemporary guidelines for HCM achieve consensus across a broad range of criteria and recommendations concerning diagnosis and management. However, variations in the approach towards risk assessment for SCD exist between the guidelines. There are also more subtle differences concerning diagnostic criteria and the utility of late gadolinium enhancement for risk stratification, which will likely evolve as the evidence-base broadens.
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Sanghvi et al. (2024) conducted a systematic review in Hypertrophic cardiomyopathy. Clinical practice guidelines was evaluated on Consensus and discrepant areas in the clinical practice guidelines. A systematic review of 3 major clinical practice guidelines for hypertrophic cardiomyopathy found broad consensus on management but variations in sudden cardiac death risk assessment.
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