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We provide our users the most up-to-date and accurate information on the treatment and prevention of cardio pathologies in accordance with current American and European clinical guidelines.
The information provided on this website is for educational purposes only and should not be considered medical advice. Always consult a licensed physician for diagnosis and treatment.
Dilated Heart (Dilated Cardiomyopathy)
Introduction
A dilated heart, medically known as dilated cardiomyopathy (DCM), is a condition where the heart's chambers (especially the left ventricle) become enlarged and weakened, reducing the heart’s ability to pump blood efficiently. This can lead to heart failure and complications such as arrhythmias and blood clots.
Causes of Dilated Cardiomyopathy
DCM can have multiple causes, including:
- Genetic factors – Inherited mutations in heart-related genes.
- Viral infections – Some viruses attack the heart muscle (myocarditis), leading to weakening.
- Toxin exposure – Alcohol abuse, chemotherapy drugs, or certain toxins.
- Metabolic disorders – Diabetes, thyroid disorders, or certain nutritional deficiencies (e.g., low thiamine).
- Hypertension – Chronic high blood pressure can lead to heart muscle enlargement and dysfunction.
- Autoimmune diseases – Conditions like lupus or sarcoidosis can lead to heart muscle inflammation.
- Idiopathic causes – In some cases, the exact cause remains unknown.
Symptoms
A patient with DCM may experience:
- Shortness of breath (especially during exertion or at night)
- Swelling in the legs and ankles
- Fatigue and weakness
- Irregular heartbeats (arrhythmias)
- Dizziness or fainting
- Chest pain (less common)
Diagnosis
The diagnosis involves several tests:
- Echocardiography (heart ultrasound) – Assesses heart chamber size and function.
- Electrocardiogram (ECG) – Detects arrhythmias or conduction problems.
- Cardiac MRI – Provides detailed images of the heart's structure.
- Blood tests – Check for biomarkers, thyroid function, or infections.
- Genetic testing – Recommended for patients with a family history of DCM.
Treatment Approaches
1. Lifestyle Modifications
- Reduce salt intake to minimize fluid overload.
- Avoid alcohol and smoking.
- Engage in light to moderate physical activity, as advised by a doctor.
2. Medications
- Beta-blockers (e.g., metoprolol, carvedilol) – Help control heart rate and reduce strain.
- ACE inhibitors / ARBs – Improve heart function and lower blood pressure.
- Diuretics – Reduce fluid buildup and swelling.
- Anticoagulants (if needed) – Prevent blood clots, especially in patients with atrial fibrillation.
- Antiarrhythmics – Help stabilize abnormal heart rhythms.
3. Device Therapy
- Implantable cardioverter defibrillator (ICD) – Prevents sudden cardiac death in high-risk patients.
- Cardiac resynchronization therapy (CRT) – Improves heart contractions and function in certain cases.
4. Advanced Therapies
- Heart transplant – Considered for end-stage DCM when other treatments fail.
- Left ventricular assist devices (LVADs) – Mechanical pumps used as a bridge to transplantation.
Conclusion
Dilated cardiomyopathy is a serious condition, but early detection and appropriate management can significantly improve a patient’s quality of life. If you experience persistent shortness of breath, fatigue, or swelling, consult a cardiologist for an evaluation.
References to Clinical Guidelines
- "American Heart Association Guidelines for Heart Failure Management"
- "European Society of Cardiology Guidelines on Cardiomyopathies"
Source recommendations
1. American Heart Association Guidelines for Heart Failure Management
- https://www.ahajournals.org/doi/10.1161/CIR.0000000000001063
- https://professional.heart.org/en/guidelines-and-statements
- https://www.heart.org/en/health-topics/heart-failure
- https://professional.heart.org/en/science-news/-/media/832EA0F4E73948848612F228F7FA2D35.ashx
- https://www.heart.org/en/professional/quality-improvement/get-with-the-guidelines/get-with-the-guidelines-heart-failure
2. European Society of Cardiology Guidelines on Cardiomyopathies
- https://www.escardio.org/Guidelines/Clinical-Practice-Guidelines/Cardiomyopathy-Guidelines
- https://academic.oup.com/eurheartj/article/44/37/3503/7246608
- https://pubmed.ncbi.nlm.nih.gov/37622657/
- https://www.acc.org/Latest-in-Cardiology/ten-points-to-remember/2023/08/30/02/53/2023-esc-guidelines-for-cardiomyopathies-esc-2023
- https://pubmed.ncbi.nlm.nih.gov/25173338/
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If you or your loved ones experience any of these symptoms, you should consult a doctor in time. Remember that self-medication can be dangerous, and timely diagnosis will preserve the quality and life expectancy.
The heart is an organ that does not know how to "keep silent" if something goes wrong. Chest pain, shortness of breath, swelling, dizziness, and rhythm disturbances are the symptoms that require our attention. The best prevention of heart disease is careful attention to your health, regular checkups with a doctor, and a healthy lifestyle. Take care of your heart, and it will serve you for many years!
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