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Published on: June 21, 2016
Progression of hypertrophic cardiomyopathy. A cross sectional echocardiographic study
Insights
Septal myotomy-myectomy effectively prevented hypertrophy progression in hypertrophic cardiomyopathy patients. Echocardiography accurately detected this progression, highlighting the surgical intervention
Area of Science:
- Cardiology
- Medical Imaging
Background:
- Hypertrophic cardiomyopathy (HCM) is characterized by left ventricular hypertrophy.
- Understanding hypertrophy progression is crucial for patient management.
- Echocardiography is a key diagnostic tool in cardiology.
Purpose of the Study:
- To investigate the progression of hypertrophy in patients with hypertrophic cardiomyopathy.
- To evaluate the efficacy of medical treatment (propranolol) versus surgical intervention (septal myotomy-myectomy) in preventing hypertrophy progression.
- To assess the role of echocardiography in detecting hypertrophy progression.
Main Methods:
- Echocardiography was used to study hypertrophy progression in 39 HCM patients over a mean follow-up of 42 months.
- Patients were divided into two groups: 32 treated medically (propranolol) and 11 treated with septal myotomy-myectomy.
- Electrocardiogram (ECG) changes were also monitored in patients with documented hypertrophy progression.
Main Results:
- Progression of hypertrophy was observed in four patients treated with propranolol.
- These four patients showed significant ECG changes, including increased QRS voltages and Romhilt-Estes scores, or developed left bundle branch block.
- None of the 11 patients who underwent septal myotomy-myectomy showed progression of hypertrophy.
Conclusions:
- Echocardiography is a reliable method for detecting hypertrophy progression in hypertrophic cardiomyopathy.
- Septal myotomy-myectomy appears to prevent the progression of hypertrophy.
- Medical management with propranolol did not prevent hypertrophy progression in this cohort.
Abstract:
The progression of hypertrophy was studied in 39 patients with hypertrophic cardiomyopathy by echocardiography at follow up from January 1979 to September 1983 (mean follow up 42 months). Thirty two patients were treated medically and 11 had had a septal myotomy-myectomy. Progression of the hypertrophy was noted in four patients treated with propranolol. An additional region in the left ventricular long axis plane was affected in two, extending to the apical region in one and to the basal region in the other, and an additional segment in the left ventricular short axis plane in two extending from the septum into the free wall. The electrocardiograms of these four patients showed a significant increase in QRS voltages (Sokolow-Lyon index increase greater than 10 mm) and of the Romhilt-Estes score (increase greater than or equal to 3 points) in two, development of a left bundle branch block in one, and no change in one. Progression of hypertrophy was seen in none of the 11 patients treated with myotomy-myectomy. Thus echocardiography accurately detects the progression of hypertrophy in patients with hypertrophic cardiomyopathy, which may be prevented by septal myotomy-myectomy.
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