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Published on: August 8, 2022
Surgical management of hypertrophic cardiomyopathy
Chandrasekaran Ananthanarayanan1, SriKrishna Reddy Modugula1, Vincent Chauvette1
1Department of Thoracic and Cardiovascular Surgery, Heart Vascular and Thoracic Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195 USA.
Insights
Surgical myectomy offers a curative solution for symptomatic hypertrophic cardiomyopathy (HCM) patients unresponsive to medication. This procedure safely reduces left ventricular outflow tract obstruction, improving long-term survival and quality of life.
Area of Science:
- Cardiology
- Cardiac Surgery
- Medical Research
Background:
- Hypertrophic cardiomyopathy (HCM) presents a wide clinical spectrum, from incidental findings to sudden cardiac death.
- Medical management is the initial approach for symptomatic patients, with new drugs under investigation.
- Invasive therapy, specifically surgical myectomy, is indicated for patients with persistent symptoms despite maximal medical therapy and offers better long-term survival.
Purpose of the Study:
- To analyze the outcomes of surgical myectomy for hypertrophic cardiomyopathy (HCM) performed between 2005 and 2015.
- To evaluate the effectiveness of septal myectomy in reducing left ventricular outflow tract (LVOT) obstruction.
- To assess the safety and complication rates associated with surgical myectomy in a large patient cohort.
Main Methods:
- Retrospective analysis of 1549 patients who underwent surgical myectomy for HCM.
- Evaluation of pre- and post-operative left ventricular outflow tract (LVOT) gradients.
- Assessment of operative parameters including aortic cross-clamp time and muscle resection mass.
- Review of complication rates, operative mortality, hospital stay, and post-operative functional status (NYHA class).
Main Results:
- Surgical myectomy significantly reduced the mean LVOT gradient from 63 mmHg pre-operatively to 15 mmHg post-operatively.
- The mean aortic cross-clamp time was 28 minutes, with an average of 8.1 g of muscle resected.
- Low complication rates were observed, including 4.2% pacemaker insertion, two iatrogenic ventricular septal defects, and an operative mortality of 0.38%.
- Mean hospital stay was 6 days, with most patients achieving New York Heart Association (NYHA) class I post-operatively.
Conclusions:
- Septal myectomy is a curative treatment for symptomatic HCM patients refractory to medical management.
- A thorough understanding of individual septal anatomy and LVOT obstruction mechanisms is crucial for successful surgical outcomes.
- Surgical myectomy can be performed safely, yielding excellent long-term results and significantly improving patient functional status.
Background:
Hypertrophic cardiomyopathy (HCM) is a dynamic disease with a spectrum of clinical presentations ranging from incidental diagnosis to sudden cardiac death. Symptomatic patients are initially managed medically, and newer drugs are currently under investigation. Invasive therapy is needed for patients with intractable symptoms despite maximal medical therapy, and surgical myectomy is the gold standard treatment with better long-term survival.
Results:
Over three decades, more than 4000 patients underwent surgical myectomy at the Cleveland Clinic. We conducted a detailed analysis of patients who underwent surgery for HCM between 2005 and 2015. Within this study period, 1549 patients underwent surgical myectomy. Their mean pre-operative peak left ventricular outflow tract (LVOT) gradient was 63 ± 4.6 mmHg, and it reduced to 15 ± 8.9 mmHg after surgery. Mean aortic cross-clamp time was 28 ± 10 min for isolated septal myectomy, and the mean mass of muscle resected was 8.1 ± 3.7 g. Complications include new incidences of pacemaker insertion in 4.2% of the patients, iatrogenic ventricular septal defects in two patients, and the overall operative mortality was 0.38%. Mean hospital stay was 6 days, and the majority of the patients are in New York Heart Association (NYHA) class I in their post-operative follow-up.
Conclusion:
Septal myectomy is a curative therapy for most patients of HCM who are symptomatic despite maximal medical management. Clear understanding of individual septal anatomy and mechanisms of LVOT obstruction are key to successful surgical outcomes. Septal myectomy can be done safely with excellent long-term results.
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