Key result
Adult patients diagnosed with hypertrophic cardiomyopathy and asymmetric septal hypertrophy generally have a benign clinical course, with sudden death occurring in only 3.6% of cases.
Why the study?
What is the prognosis and clinical course of older adult patients diagnosed with hypertrophic cardiomyopathy with asymmetric septal hypertrophy?
Cohort
What is the prognosis and clinical course of older adult patients diagnosed with hypertrophic cardiomyopathy with asymmetric septal hypertrophy?
Hypertrophic cardiomyopathy with asymmetric septal hypertrophy diagnosed in older adults generally follows a benign clinical course with a low incidence of sudden death.
Answers are grounded in this paper and cite their sources.
Supports benign prognosis in older HCM patients with ASH; leaves open prospective validation.
Summary Hypertrophic cardiomyopathy with asymmetric septal hypertrophy is not an uncommon disorder in the older adult population, and frequently masquerades as coronary artery disease. Most symptomatic patients with hypertrophic cardiomyopathy diagnosed as adults have a benign course with mild disability lasting for many years. Associated significant obstructive coronary artery disease was present in 22% of our patients and probably represents the cause of symptoms and, therefore, investigation in some of our patients rather than a high incidence of coronary disease in patients with asymmetric septal hypertrophy. Sudden death was not common in our patients (3.6%) and occurred at 11 years after diagnosis in a patient with associated coronary artery disease and 4 years after diagnostic study in a patient with uncomplicated hypertrophic cardiomyopathy.
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Wadehra et al. (1985) conducted a cohort in Hypertrophic cardiomyopathy with asymmetric septal hypertrophy. Adult patients diagnosed with hypertrophic cardiomyopathy and asymmetric septal hypertrophy generally have a benign clinical course, with sudden death occurring in only 3.6% of cases.
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