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Updated: Mar 2, 2026

Isolation and Functional Characterization of Human Ventricular Cardiomyocytes from Fresh Surgical Samples
Published on: April 21, 2014
Surgery for hypertrophic cardiomyopathy
James J Wu1,2,3, Michael Seco1,2,3, Caroline Medi4,5
1Sydney Medical School, The University of Sydney, Sydney, Australia.
Insights
Septal myectomy effectively treats hypertrophic cardiomyopathy (HCM) by relieving left ventricular outflow tract obstruction. This surgery offers excellent long-term survival and symptom relief for HCM patients.
Area of Science:
- Cardiology
- Cardiac Surgery
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is a genetic heart condition causing unexplained left ventricular hypertrophy.
- HCM is a leading cause of sudden cardiac death in young adults, often due to arrhythmias.
- Left ventricular outflow tract obstruction can occur in HCM patients.
Purpose of the Study:
- To evaluate the efficacy and outcomes of septal myectomy for treating symptomatic hypertrophic cardiomyopathy with outflow tract obstruction.
- To assess the safety, long-term survival, and symptom relief provided by surgical intervention in HCM patients.
Main Methods:
- Septal myectomy involves surgically removing a portion of the hypertrophied interventricular septum.
- Surgical access is achieved through transaortic, transapical, or transmitral approaches.
- Data from large, contemporary series of experienced centers were analyzed.
Main Results:
- Septal myectomy demonstrated a low early mortality rate of less than 2%.
- Patients experienced excellent long-term survival, comparable to the general population.
- The procedure provided durable relief of symptoms associated with outflow tract obstruction.
Conclusions:
- Septal myectomy is a safe and effective surgical treatment for hypertrophic cardiomyopathy with moderate to severe outflow tract obstruction.
- The procedure offers significant long-term benefits, including improved survival and sustained symptom resolution.
- It is indicated for patients with severe symptoms unresponsive to medical management.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a genetically determined cardiac disease characterised by otherwise unexplained myocardial hypertrophy of the left ventricle, and may result in left ventricular outflow tract obstruction. It is the most common cause of sudden cardiac death in young adults due to arrhythmias. Septal myectomy is a surgical treatment for HCM with moderate to severe outflow tract obstruction, and is indicated for patients with severe symptoms refractory to medical therapy. The surgical approach involves obtaining access to the interventricular septum via transaortic, transapical or transmitral approaches, and excising a portion of the hypertrophied myocardium to relieve the outflow tract obstruction. Large, contemporary series from centres experienced in septal myectomy patients have demonstrated a low early mortality of <2 %, excellent long-term survival that matches the general population, and durable relief of symptoms.
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