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Published on: March 27, 2018
Does surgical relief of obstruction improve prognosis for hypertrophic cardiomyopathy?
Ronald E Ross1, Mark V Sherrid, Mairead M Casey
1Department of Surgery, St Luke's-Roosevelt Hospital Center, Columbia University College of Physicians and Surgeons, New York, NY 10025, USA.
Insights
Surgical myectomy is a safe and effective treatment for hypertrophic cardiomyopathy (HCM). This procedure offers excellent long-term survival rates, comparable to the general population, for patients with symptomatic obstructive HCM.
Area of Science:
- Cardiology
- Genetics
- Surgical Outcomes
Background:
- Hypertrophic cardiomyopathy (HCM) presents complex prognostic challenges due to genetic heterogeneity and incomplete penetrance.
- Existing data on septal myectomy outcomes primarily originates from specialized tertiary care centers.
- Prognostic prediction in HCM is complicated by its unique genetic characteristics.
Purpose of the Study:
- To evaluate the safety and efficacy of surgical myectomy for symptomatic obstructive HCM.
- To assess long-term survival rates following septal myectomy.
- To identify potential risk factors for mortality after HCM surgery.
Main Methods:
- Retrospective review of 132 consecutive patients undergoing HCM surgery at a single institution.
- Analysis of published septal myectomy data from 1980 to 2011.
- Assessment of patient outcomes, including mortality and survival rates, at a mean follow-up of 4.2 years.
Main Results:
- No in-hospital deaths (within 30 days) were observed in the studied cohort.
- Overall survival rates at 1, 5, and 10 years were excellent: 99%, 99%, and 92%, respectively.
- Age, comorbidities, and concomitant procedures were not significant mortality risk factors.
Conclusions:
- Surgical myectomy is a safe and highly effective procedure for managing symptomatic obstructive HCM.
- The procedure confers excellent long-term survival, mirroring that of the healthy population.
- Septal myectomy provides a favorable prognosis for patients with obstructive hypertrophic cardiomyopathy.
Abstract:
Unique genetic characteristics of hypertrophic cardiomyopathy (HCM), including heterogeneity and incomplete penetrance, have made making predictions about prognosis complex. We reviewed data from septal myectomy results as published from 1980 to 2011, most of which come from specialized tertiary care centers. We also performed a retrospective review of 132 consecutive patients who underwent HCM surgery at our institution. At a mean follow-up of 4.2 ± 3.2 years (range, 3 days to 14.2 years), there were no deaths within 30 days of surgery for our cohort. Over the course of 15 years, 2 deaths occurred in older patients, both of whom had surgery for HCM along with additional cardiac procedures. Age, the presence of comorbidities, and concomitant cardiac procedures were not statistically significant risk factors for mortality. Overall survival at 1, 5, and 10 years was excellent: 99%, 99%, and 92%, respectively. Surgical myectomy has been proven to be a safe and effective procedure for symptomatic obstructive HCM, and it confers excellent survival similar to that of the healthy population.
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