Key result
Extended myectomy in patients with hypertrophic obstructive cardiomyopathy resulted in an overall survival of 68% after 18 years, with no cases of sudden cardiac death during follow-up.
Why the study?
Does extended myectomy improve survival and prevent sudden cardiac death in patients with severely symptomatic hypertrophic obstructive cardiomyopathy?
Cohort
Does extended myectomy improve survival and prevent sudden cardiac death in patients with severely symptomatic hypertrophic obstructive cardiomyopathy?
Extended myectomy for severely symptomatic hypertrophic obstructive cardiomyopathy is associated with excellent long-term survival, symptom relief, and prevention of sudden cardiac death.
Extended myectomy experience in HOCM supports surgical rationale; leaves open need for randomized trials versus classical myectomy.
The rationale for surgical treatment of hypertrophic obstructive cardiomyopathy is based on the assumption that dynamical obstruction is mainly caused by a reduction in the left ventricular outflow tract cross-sectional area due to bulging septal myocardial tissue. In this sense, classical myotomy-myectomy is the `gold standard' therapy for patients with severely symptomatic hypertrophic obstructive cardiomyopathy. In my own experience with extended myectomy, more than three-quarters of all long-term survivors are in functional class I or II (New York Heart Association) and overall survival after 18 years (mean follow up 8.1 years) was 68%, with a linearized mortality rate of 1.9% per patient-year. Notably, there was no case of sudden cardiac death during follow up, leading to the assumption that relief from dynamical obstruction is most effective in the prevention of sudden cardiac death in these patients.
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Friedrich A. Schoendube (2001) conducted a cohort in Hypertrophic obstructive cardiomyopathy. Extended myectomy was evaluated on Overall survival after 18 years. Extended myectomy in patients with hypertrophic obstructive cardiomyopathy resulted in an overall survival of 68% after 18 years, with no cases of sudden cardiac death during follow-up.
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