How to recover from decreased physical fitness due to dilated cardiomyopathy?

Written by Xie Zhi Hong
Cardiology
Updated on November 05, 2024
00:00
00:00

Dilated cardiomyopathy is diagnosed after excluding conditions such as hyperthyroidism, hypertension, coronary heart disease, cardiac hypertrophy, or myocarditis as underlying causes. Generally, the exact cause of dilated cardiomyopathy is unknown, rendering causal treatment impossible. Once diagnosed with dilated cardiomyopathy, it is impossible to completely cure the condition. The only approach is to manage symptoms and prevent further progression of the disease. Typically, this involves the use of beta-blockers, ACE inhibitors, and diuretics. If the patient has severe cardiac dysfunction, drugs like digoxin, which strengthen heart function, may be considered. If medication does not adequately control the condition, other treatments like CRT might be considered, as well as the use of phosphodiesterase inhibitors, diuretics, or intravenous cardiotonic glycosides.

Other Voices

doctor image
home-news-image
Written by Zhang Yue Mei
Cardiology
39sec home-news-image

Can people with cardiomyopathy run?

Whether a person with myocardial disease can run or not depends on the extent of myocardial damage and clinical symptoms. If the myocardial damage is severe and there are significant clinical symptoms of heart failure and arrhythmia, this group should not run and needs bed rest. If strenuous activity would worsen heart failure, the myocardial damage is mild, with no typical clinical symptoms, and does not affect daily activities, this group can engage in appropriate exercises like walking or running, but the duration should not be too long, about 20 to 30 minutes each time.

doctor image
home-news-image
Written by Liu Ying
Cardiology
1min 4sec home-news-image

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.

doctor image
home-news-image
Written by Xie Zhi Hong
Cardiology
1min 4sec home-news-image

How to recover from decreased physical fitness due to dilated cardiomyopathy?

Dilated cardiomyopathy is diagnosed after excluding conditions such as hyperthyroidism, hypertension, coronary heart disease, cardiac hypertrophy, or myocarditis as underlying causes. Generally, the exact cause of dilated cardiomyopathy is unknown, rendering causal treatment impossible. Once diagnosed with dilated cardiomyopathy, it is impossible to completely cure the condition. The only approach is to manage symptoms and prevent further progression of the disease. Typically, this involves the use of beta-blockers, ACE inhibitors, and diuretics. If the patient has severe cardiac dysfunction, drugs like digoxin, which strengthen heart function, may be considered. If medication does not adequately control the condition, other treatments like CRT might be considered, as well as the use of phosphodiesterase inhibitors, diuretics, or intravenous cardiotonic glycosides.

doctor image
home-news-image
Written by Li Hai Wen
Cardiology
44sec home-news-image

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.

doctor image
home-news-image
Written by Li Hai Wen
Cardiology
56sec home-news-image

What is dilated cardiomyopathy?

Dilated cardiomyopathy is a relatively common disease in our daily lives. So, what is dilated cardiomyopathy? It refers to a disease characterized primarily by an enlarged heart and a severe reduction in the heart's pumping function. The cause of dilated cardiomyopathy is often unclear. Its clinical symptoms typically present as symptoms of heart failure, such as exertional dyspnea, or severe orthopnea and profuse sweating. Additionally, arrhythmias are also a common manifestation of dilated cardiomyopathy, such as atrial fibrillation, frequent premature ventricular contractions, and ventricular tachycardia. If diagnosed with dilated cardiomyopathy, it is essential to visit the department of cardiology at a hospital for specialized treatment and to take medication as prescribed. (The use of medication should be under the guidance of a professional doctor.)