What causes cardiomyopathy?

Written by Zhang Yue Mei
Cardiology
Updated on September 24, 2024
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In clinical practice, the most common type of myocarditis is viral myocarditis. Due to a decrease in the body's resistance, the virus invades and damages the myocardium, causing localized and diffuse inflammatory damage to the heart muscle, which poses significant harm to the body. The early clinical symptoms of viral myocarditis often manifest primarily as respiratory and gastrointestinal symptoms, accompanied by palpitations and shortness of breath, necessitating the use of electrocardiograms and myocardial enzyme spectrum tests. Early detection, diagnosis, and treatment of viral myocarditis play a crucial role in the prognosis.

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Written by Zhang Yue Mei
Cardiology
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What should patients with cardiomyopathy pay attention to?

Patients with cardiomyopathy need to rest adequately, avoid overexerting themselves, and not get overly emotional to keep their mood calm and prevent an increased burden on the heart, which could trigger heart failure. In their diet, they should consume easily digestible foods that are high in superior protein and eat plenty of fruits and vegetables. These foods can provide the high-quality proteins, vitamins, and trace elements needed by the body, enhancing immunity and disease resistance. In the event of thrombosis and myocardial cell repair, systematic medication treatment under a doctor's guidance is essential to promote myocardial repair.

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Written by Li Hai Wen
Cardiology
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Clinical manifestations of dilated cardiomyopathy

The clinical manifestations of dilated cardiomyopathy can be summarized in two words: "three hearts," which are reflected in the following three aspects. First, heart enlargement, such as through chest X-rays or echocardiography, often reveals a notable enlargement of the patient's heart. Second, arrhythmias; dilated cardiomyopathy often accompanies a variety of arrhythmias, such as frequent ventricular premature beats, tachycardia, or atrial fibrillation. Third, heart failure. Dilated cardiomyopathy often results in symptoms of heart failure, such as exertional dyspnea and paroxysmal nocturnal dyspnea.

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Written by Liu Yong
Cardiology
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Does cardiomyopathy require surgery?

Firstly, whether myocardial disease requires surgery, we need to clarify the type of myocardial disease and the stage of myocardial disease, that is, the stage of heart function that has been affected. There are many types of myocardial diseases, including dilated cardiomyopathy, ischemic cardiomyopathy, and restrictive cardiomyopathy, for instance. The treatment plans for different types of myocardial diseases are not exactly the same. For example, dilated cardiomyopathy is generally treated with medication, and only in the very late stages of dilated cardiomyopathy, or what is known as stage IV heart function, when conventional medication is ineffective, heart transplantation might be considered if a donor is available and conditions allow. However, currently, heart donors are extremely rare, making this option quite difficult to achieve. The latest advances in clinical research have introduced artificial mechanical hearts available for transplantation, but the costs of surgery are very high, and the technology is not very mature yet. Therefore, the chances and opportunities for surgery are not very great and must be decided based on the situation. For other conditions, such as ischemic cardiomyopathy, if it is clearly caused by severe ischemia, we might consider addressing the factors causing myocardial ischemia, such as performing a coronary angiography. If there is severe coronary artery stenosis, we might consider implementing a coronary artery stent or coronary artery bypass grafting to alleviate the ischemic factors. In cases like restrictive cardiomyopathy, if there are severe restrictive factors contributing to the disease, surgical treatment might also be pursued.

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Written by Liu Ying
Cardiology
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Can dilated cardiomyopathy be inherited?

We say that dilated cardiomyopathy is a type of cardiomyopathy characterized by enlargement of the left ventricle or both ventricles, accompanied by systolic dysfunction. Some cases of dilated cardiomyopathy are familial, with the main inheritance patterns being autosomal dominant, X-linked recessive, and more rarely, mitochondrial inheritance. The cause of most dilated cardiomyopathies is unclear, but potential causes include infections, non-infectious inflammation, endocrine metabolic disorders, genetics, psychological trauma, and poisoning, including alcohol poisoning. Alcoholism is a common cause of dilated cardiomyopathy in China. Clinically, dilated cardiomyopathy presents with cardiac enlargement, heart failure, arrhythmias, thromboembolism, and sudden death.

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Written by Li Hai Wen
Cardiology
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Cardiomyopathy is divided into four types.

From a medical perspective, common cardiomyopathies are mainly divided into the following four categories: First, dilated cardiomyopathy, which refers to a type of cardiomyopathy characterized by significant enlargement of the heart, thinning of the ventricular walls, and declined heart function. Second, hypertrophic cardiomyopathy, which refers to a type of cardiomyopathy primarily characterized by thickening of the ventricular walls. Third, arrhythmogenic right ventricular dysplasia, a type of cardiomyopathy that is often clinically associated with episodes of ventricular arrhythmias. Fourth, restrictive cardiomyopathy, which is generally considered rare in clinical practice.