Dilated Cardiomyopathy 1kk C3714995
A genetic heart condition where the main pumping chamber enlarges and weakens, reducing blood flow. It can run in families. Treatment includes medications, pacemakers, or heart transplant.
Key facts at a glance
- ICD-10
- B33.24
- ICD-11
- 1A00.0
- Body system
- cardiovascular
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Syncope
Chest discomfort or palpitations
(cardiovascular)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Dyspnea on exertion
(cardiovascular)Exercise intolerance
(cardiovascular)Nocturnal cough
(cardiovascular)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
ACE Inhibitors
Angiotensin-converting enzyme inhibitors are first-line medications that reduce cardiac workload by lowering blood pressure and decreasing fluid retention. They have been shown to improve survival and slow disease progression in dilated cardiomyopathy patients.
Disease management and monitoring
Active treatment with regular monitoring by a healthcare provider is recommended.
Sodium and Fluid Restriction
Strict limitation of dietary sodium intake to 2,000mg or less daily combined with fluid restriction helps prevent fluid overload and reduces cardiac strain. Patients should maintain a daily weight log to detect early fluid retention.
Additional treatment options
Implantable Cardioverter-Defibrillator
ICD placement is recommended for severe DCM patients at high risk of sudden cardiac death. The device continuously monitors heart rhythm and delivers shocks if life-threatening arrhythmias are detected.
procedureEchocardiographic Surveillance
Regular echocardiograms every 3-6 months track left ventricular ejection fraction changes and chamber dimensions. This monitoring guides medication adjustments and timing of advanced interventions.
monitoringCardiac Rehabilitation Program
Supervised exercise training improves cardiovascular fitness and endothelial function in stable DCM patients. Programs include graduated aerobic activity with continuous telemetry monitoring.
physical_therapyWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Dilated Cardiomyopathy 1kk C3714995?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalMedication Comparisons
Compare medications used to treat Dilated Cardiomyopathy 1kk C3714995. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy