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Dilated Cardiomyopathy 1hh C3151293

Published: July 22, 2026Updated: August 20, 2026

Heart condition where the main pumping chamber becomes enlarged and weakened, impairing blood flow. Can be inherited and affect both children and adults. Treatment includes medication, lifestyle changes, and in severe cases, surgery or transplant.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

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

!

Ventricular arrhythmias

Chest discomfort or palpitations

(cardiovascular)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Dyspnea (shortness of breath)

(cardiovascular)

Fatigue

(cardiovascular)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Angiotensin Receptor-Neprilysin Inhibitor

Sacubitril/valsartan combines neprilysin inhibition with ARB blockade, providing superior reduction in cardiovascular mortality compared to ACE inhibitors alone.

medication
2

Disease management and monitoring

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

SGLT2 Inhibitor Therapy

Dapagliflozin or empagliflozin provide cardiorenal benefits through glycosuric effects, reducing heart failure hospitalizations and mortality.

medication

Additional treatment options

Alcohol Abstinence

Complete avoidance of alcohol is essential, particularly in alcohol-related cardiomyopathy, to prevent further myocardial damage and support recovery.

lifestyle

Remote Hemodynamic Monitoring

Implantable pulmonary artery pressure sensors enable daily monitoring of filling pressures, allowing preemptive diuretic adjustment to prevent hospitalizations.

monitoring

Left Ventricular Assist Device

Mechanical circulatory support as bridge to transplant or destination therapy for advanced heart failure patients who fail optimal medical management.

surgical

When 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.

Q

What is Dilated Cardiomyopathy 1hh C3151293?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Dilated Cardiomyopathy 1hh C3151293. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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