DISEASE SCANNER
Global Incurable Diseases Tracker
Dilated Cardiomyopathy (DCM)
A condition in which the heart's main pumping chamber (left ventricle) becomes enlarged and weakened, reducing the heart's ability to pump blood effectively. Can lead to heart failure and sudden cardiac death.
2.0M
16
Symptoms
Treatment Options
Risk Factors
Diagnostic Methods
- 1Echocardiogram (dilated LV, reduced EF)
- 2ECG
- 3Chest X-ray
- 4Cardiac MRI
- 5Coronary angiography (exclude ischemia)
- 6Genetic testing
- 7BNP/NT-proBNP
Prognosis
Variable; 5-year mortality 20-50% without transplant. Modern medical therapy significantly improves outcomes. ICD reduces sudden death risk. Transplant offers best survival for refractory cases.
Prevention
- Genetic counseling for familial cases
- Avoid alcohol excess
- Cardiac monitoring during chemotherapy
- Treatment of underlying conditions
- Family screening
Research Status
Medical therapy with ACE inhibitors, beta-blockers, MRAs, SGLT2 inhibitors improves survival. Cardiac resynchronization therapy (CRT), ICDs for arrhythmias. Ventricular assist devices and transplant for end-stage.
Affected Countries
Sources
- https://www.heart.org/en/health-topics/cardiomyopathy/what-is-cardiomyopathy-in-adults/dilated-cardiomyopathy-dcm
- https://www.hematology.org/education/patients
- https://www.ncbi.nlm.nih.gov/books
- https://rarediseases.org/rare-diseases
Medical Disclaimer
This information is for educational purposes only. Always consult healthcare professionals for medical advice, diagnosis, and treatment.