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Ultrasonic Assessment of Myocardial Microstructure
Published on: January 14, 2014
Non-compacted cardiomyopathy: clinical-echocardiographic study
Nilda Espinola-Zavaleta1, M Elena Soto, Luis Muñóz Castellanos
1Echocardiography in Outpatient Clinic, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano No. 1, Colonia Sección XVI Tlalpan, 14080 México, D.F., Mexico. niesza2001@hotmail.com
Insights
Ventricular noncompaction, a congenital heart condition, often presents in isolation and is diagnosed via echocardiography. A ratio of noncompacted to compacted myocardium over 3 indicates a poor prognosis.
Area of Science:
- Cardiology
- Medical Diagnostics
- Congenital Heart Disease
Background:
- Ventricular noncompaction is a rare congenital cardiomyopathy.
- It can occur as an isolated finding or be associated with other cardiac anomalies.
- Clinical presentation varies, necessitating reliable diagnostic tools.
Purpose of the Study:
- To elucidate the clinical and echocardiographic features of ventricular noncompaction in adult patients.
- To identify prognostic indicators associated with this condition.
Main Methods:
- A cohort of 53 adult patients with ventricular noncompaction was studied.
- Methods included clinical evaluation, electrocardiogram, Holter monitoring, and transthoracic echocardiography.
Main Results:
- Ventricular noncompaction was isolated in 74% of cases and associated with other congenital heart disease in 26%.
- The left ventricle was involved in 62% of patients; both ventricles in 38%.
- A ratio of noncompacted to compacted myocardium >3 and involvement of >3 segments correlated with poorer functional class and increased ventricular arrhythmias (p < 0.003).
Conclusions:
- Noncompaction cardiomyopathy is a congenital condition, often isolated, and can affect one or both ventricles.
- Echocardiography is crucial for diagnosis and identifying prognostic factors.
- A high noncompacted to compacted myocardium ratio and multi-segment involvement signal a poor prognosis.
Unlabelled:
The aim of the present study was to describe the clinical and echocardiographic findings of ventricular noncompaction in adult patients. Fifty-three patients underwent complete clinical history, electrocardiogram, Holter and transthoracic echocardiogram. Forty patients (75%) were in class I/II of the New York Heart Association, and 13 (25%) in class III/IV. Ventricular and supraventricular escape beats were found in 40% and 26.4%, respectively. Holter showed premature ventricular contractions in 32% and sustained ventricular tachycardia in 7.5%. Ventricular noncompaction was an isolated finding in 74% of cases and was associated with other congenital heart disease in 26%. Noncompacted ventricular myocardium involved only left ventricle in 62% of the patients and both ventricles in 38%. The mean ratio of noncompacted to compacted myocardial layers at the site of maximal wall thickness was 3.4 +/- 0.87 mm (range 2.2-7.5). The presence of ventricular noncompaction in more than three segments was associated with a functional class greater than II and ventricular arrhythmia with demonstrable statistical significance by chi2(p < 0.003).
Conclusion:
a) Noncompacted cardiomyopathy is a congenital pathological entity that can occur in isolated form or associated with other heart disease and often involves both ventricles. b) A ratio of noncompacted to compacted myocardium greater than 3 and involvement of three or more segments are indicators of poor prognosis. c) Since the clinical manifestations are not sufficient to establish diagnosis, echocardiography is the diagnostic tool that makes it possible to document ventricular noncompaction and establish prognostic factors.
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