Key result
Advances in diagnostic tools, disease-specific therapy, and defibrillator technology are improving outcomes and risk stratification for sudden cardiac death.
Why the study?
Increasing knowledge about molecular mechanisms and genetic drivers of malignant arrhythmias is needed to optimise risk stratification and personalise care in sudden cardiac death.
This review highlights the importance of uncovering definitive causes of sudden cardiac death to optimize risk stratification and personalize care for surviving relatives.
Advances in SCD diagnostics and therapies may refine risk stratification; leaves open prospective validation for personalized family screening.
Sudden cardiac death (SCD) is a devastating and all too common result of both acquired and genetic heart diseases. The profound sadness endured by families is compounded by the risk many of these deaths confer upon surviving relatives. For those with known cardiac disease, disease-specific therapy and risk stratification are key to reducing sudden death. For families of a SCD victim, uncovering a definitive cause of death can help relieve the agonising uncertainty and is a vital first step in screening surviving relatives and instituting therapy to reduce SCD risk. Increasing knowledge about the molecular mechanisms and genetic drivers of malignant arrhythmias in the diverse clinical entities that can cause SCD is vital if we are to optimise risk stratification and personalise patient care. Advances in diagnostic tools, disease-specific therapy and defibrillator technology are improving outcomes for patients and their families but there is still much progress to be made.
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Isbister et al. (2019) conducted a review in Sudden cardiac death. Advances in diagnostic tools, disease-specific therapy, and defibrillator technology are improving outcomes and risk stratification for sudden cardiac death.
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