Is dilated cardiomyopathy more serious or is myocardial ischemia more serious?

Written by Li Hai Wen
Cardiology
Updated on November 01, 2024
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This has to be judged comprehensively based on the following conditions: First, the age factor. If it occurs in young people, dilated cardiomyopathy tends to be more severe. This is because dilated cardiomyopathy is an organic heart disease, and myocardial ischemia in young people may not necessarily involve organic heart disease changes, but could also be normal physiological changes in the electrocardiogram. Second, whether there is concurrent cardiac function impairment. Dilated cardiomyopathy definitely involves impairment of the heart's pumping function, whereas myocardial ischemia does not necessarily involve such impairment. Therefore, in most cases, dilated cardiomyopathy is more serious.

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Can people with cardiomyopathy eat spicy food?

Generally speaking, patients with cardiomyopathy during stable phases may consider consuming spicy food, especially since these patients often have relatively poor appetites. Using mildly spicy food can potentially stimulate the appetite and improve nutritional status. However, from another perspective, excessive consumption of spicy food may cause patients to drink large amounts of water. Excessive intake could potentially increase the burden on cardiac function; therefore, it is not recommended for patients with cardiomyopathy to consume overly spicy foods. Patients with cardiomyopathy also have dietary restrictions, including a diet low in salt and fat, as overly salty diets can also exacerbate the burden on the heart and kidneys.

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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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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.

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Treatment of Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, due to unknown causes and often related to genetic factors, is difficult to prevent. It is important to guide patients on how to lead their lives, reminding them to avoid intense physical activities, heavy lifting, or breath-holding to reduce the incidence of sudden death. Avoid using drugs that enhance myocardial contractility and reduce cardiac capacity load, such as digoxin and nitrates, to decrease the aggravation of left ventricular outflow tract obstruction. The treatment principle for this disease is to slow down the hypertrophy of the myocardium, prevent tachycardia, and maintain normal sinus rhythm. It also aims to relieve the narrowing of the left ventricular outflow tract and counteract arrhythmias. Currently, the use of beta blockers and calcium channel blockers is advocated. For severe obstructive patients, interventional and surgical treatments can be carried out, including the implantation of a dual-chamber DTD pacemaker, and the ablation or removal of hypertrophied interventricular septum myocardium.

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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.