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Published on: August 8, 2022
Prevention of sudden death in hypertrophic cardiomyopathy: bridging the gaps in knowledge
Adaya Weissler-Snir1, Arnon Adler1, Lynne Williams2
1Division of Cardiology, Peter Munk Cardiac Centre, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Insights
Sudden cardiac death (SCD) risk in hypertrophic cardiomyopathy (HCM) is low overall, but identifying high-risk patients remains challenging. This review compares international guidelines for risk stratification to aid clinical decisions.
Area of Science:
- Cardiology
- Genetics
- Preventive Medicine
Background:
- Sudden cardiac death (SCD) is a severe complication of hypertrophic cardiomyopathy (HCM).
- While the general HCM population has a low annual SCD rate (<1%), a subset faces elevated risk.
- Accurate risk stratification is crucial for timely intervention with implantable cardioverter-defibrillators (ICDs).
Purpose of the Study:
- To review current data on SCD in HCM patients.
- To compare and contrast European and American risk stratification guidelines.
- To offer balanced clinical guidance for decision-making and assess guideline implementation by experts.
Main Methods:
- Review of existing literature on SCD in HCM.
- Analysis of current European and American guidelines for risk stratification.
- Inquiry into global HCM expert perspectives on guideline implementation.
Main Results:
- Conflicting recommendations exist between European and American guidelines.
- Identifying high-risk HCM patients for ICD therapy remains a clinical challenge.
- Expert opinions on guideline implementation vary worldwide.
Conclusions:
- There is a need for harmonized risk stratification strategies for SCD in HCM.
- Clinical decision-making requires a balanced approach considering guideline differences.
- Further research and expert consensus are needed to optimize SCD prevention in HCM.
Abstract:
Sudden cardiac death (SCD) is the most devastating complication of hypertrophic cardiomyopathy (HCM). Although the annual rate of SCD in the general HCM population is <1% per year according to contemporary series, there is still a small subset of patients who are at increased risk of SCD. The greatest challenge in the management of HCM is identifying those at increased risk as an implantable cardioverter defibrillator is a potentially life-saving therapy. In this review, we sought to summarize the available data on SCD in HCM and provide a clinical perspective on the current differing and somewhat conflicting European and American recommendations on risk stratification, with balanced guidance with regards to rational clinical decision making. Additionally, we sought to learn more on the actual implementation of the guidelines by HCM experts worldwide.
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