Key result
Hypertrophic cardiomyopathy presents a complex clinical spectrum with heterogeneous patterns and symptoms, making diagnosis and management a challenge for cardiologists.
Hypertrophic cardiomyopathy presents with a complex clinical spectrum requiring tailored management to relieve symptoms and prevent major complications like sudden cardiac death.
Phenotype-specific HCM strategies need prospective validation; leaves open tailored symptom relief and SCD prevention approaches.
The clinical spectrum of hypertrophic cardiomyopathy (HCM) is complex and includes a variety of phenotypes, which leads to different types of manifestations.Although most of the patients are asymptomatic, a significant proportion of them will develop symptoms or risk of arrhythmias and sudden cardiac death (SCD).Therefore, the objectives of HCM diagnosis and management are to relieve the patients' symptoms (chest pain, heart failure, syncope, palpitations, etc.), prevent disease progression and major cardiovascular complications and SCD.The heterogeneity of HCM patterns, their symptoms and assessment is a challenge for the cardiologist.
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A 2015 study conducted a review in Hypertrophic cardiomyopathy (HCM). Hypertrophic cardiomyopathy presents a complex clinical spectrum with heterogeneous patterns and symptoms, making diagnosis and management a challenge for cardiologists.
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