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Published on: August 8, 2022
Single-Centre Experience of Surgical Myectomy for Hypertrophic Obstructive Cardiomyopathy
Alexander V Afanasyev1, Alexander V Bogachev-Prokophiev1, Michail A Ovcharov1
1Heart Valve Surgery Department, Meshalkin National Medical Research Center, Novosibirsk, Russian Federation.
Insights
Septal myectomy is a safe and effective treatment for hypertrophic obstructive cardiomyopathy, showing low mortality and significant improvement in patient outcomes. Long-term survival rates are comparable to the general population.
Area of Science:
- Cardiology
- Cardiac Surgery
- Medical Research
Background:
- Septal myectomy is the established gold standard for treating hypertrophic obstructive cardiomyopathy.
- This study evaluates the outcomes of patients who underwent septal myectomy.
Purpose of the Study:
- To assess the efficacy and safety of septal myectomy in patients with hypertrophic obstructive cardiomyopathy.
- To analyze clinical and hemodynamic results, mortality rates, and long-term survival post-surgery.
Main Methods:
- Prospective data collection from 345 hypertrophic cardiomyopathy patients over 7 years.
- Analysis of pre-operative and post-operative hemodynamic data, clinical outcomes, and survival rates.
- Inclusion of concomitant Cox-Maze IV procedures and prediction of atrial tachyarrhythmias.
Main Results:
- Low operative mortality (1.7%) and significant reduction in left ventricular outflow tract gradients.
- High rate of favorable functional outcomes (NYHA class I/II: 96.7%) at follow-up.
- Comparable long-term survival (95.7%) to the general population; atrial tachyarrhythmia predicted by left atrial diameter.
Conclusions:
- Septal myectomy at this center demonstrates low operative mortality and adverse event rates.
- The procedure yields acceptable intermediate-term clinical and hemodynamic results for hypertrophic obstructive cardiomyopathy.
- Septal myectomy offers a safe and effective treatment option with favorable long-term survival.
Background:
Septal myectomy is the gold standard treatment for hypertrophic obstructive cardiomyopathy. This study aimed to evaluate the results from patients with hypertrophic cardiomyopathy who had undergone septal myectomy.
Methods:
Data were analysed that has been prospectively collected over 7 years from 345 patients with hypertrophic cardiomyopathy who underwent septal myectomy at Meshalkin National Medical Research Center.
Results:
Six (6) patients (1.7%) died within 30 days of surgery. The mean (standard deviation, SD) resting left ventricular outflow tract gradients reduced from 83.4 (24.2) mmHg preoperatively to 16.2 (8.5) mmHg at discharge (p < 0.001). Of the 345 patients, 329 (95.4%) attended the most recent follow-up assessments, and of these, 254 (77.2%) were categorised as New York Heart Association (NYHA) class I, 64 (19.5%) class II, and 11 (3.3%) class III. The mean overall long-term survival rate after septal myectomy was 95.7% (SD 1.7%) (95% CI, 90.0-97.9). This did not differ from the age-matched and gender-matched general population (log-rank, p = 0.109). At the last follow-up assessments, six of 67 patients who had undergone concomitant Cox-Maze IV procedures had late atrial tachyarrhythmia recurrences. A preoperative short-axis view of left atrial diameter of 57.5 mm (hazard ratio, 1.30 (95% CI, 1.03-1.65), p < 0.001) predicted late atrial tachyarrhythmias (p < 0.002).
Conclusions:
At this hypertrophic cardiomyopathy centre, septal myectomy is associated with low operative and early mortality rates (<2%), a low risk of early adverse events, and acceptable intermediate-term clinical and haemodynamic results.
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