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Image courtesy of UCL Institute of Cardiovascular Science / James Tye milla1cf Tue, 12/19/2023 - 18:19 December 19, 2023 — A vest that can map the electrical activity of the heart in fine detail could potentially be used to better identify people at high risk of suddencardiacdeath , suggests a new study led by UCL researchers.
Hypertrophic cardiomyopathy (HCM) has a prevalence of 1 in 500 people and highly increases the risk of suddencardiacdeath (SCD). Diagnosis is typically based on the Echocardiogram, while cardiac MRI is used for detection of myocardial scarring through Late Gadolinium Enhancement (LGE), an important risk marker for SCD.
Whether you’re gearing up for your Family Medicine or Cardiology Board Exam, you’ll need to master the topic of Hypertrophic Cardiomyopathy (HCM). Explanation: Shown electrocardiogram suggests left ventricular hypertrophy. Hypertrophic cardiomyopathy is one of them. Hypertrophic cardiomyopathy is one of them.
Dilated cardiomyopathy with arrhythmic phenotype. Abstract Aims Dilated cardiomyopathy (DCM) with arrhythmic phenotype combines phenotypical aspects of DCM and predisposition to ventricular arrhythmias, typical of arrhythmogenic cardiomyopathy.
Since its identification in 1981 its diagnosis has increased due to the advancements in cardiac imaging. It’s association with ventricular arrythmia (VA) and suddencardiacdeath (SCD) underscores the importance of its identification. Electrocardiogram (ECG) showed sustained monomorphic VT at a rate of 160 bpm.
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