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Ischemic Dilated Cardiomyopathy

Definition and Pathophysiological Mechanisms

Ischemic dilated cardiomyopathy is a condition characterized by **left ventricular dilation and systolic dysfunction** secondary to chronic myocardial ischemia.
It is one of the most common causes of **heart failure with reduced ejection fraction (HFrEF)**. The primary pathophysiological mechanism is **ventricular remodeling** induced by repeated episodes of ischemia, myocardial necrosis, and fibrosis.

The main contributing factors are:


Ischemic dilated cardiomyopathy is one of the leading causes of heart failure in patients with pre-existing **coronary artery disease**. The main risk factor is a **previous myocardial infarction**, which causes **irreversible myocardial necrosis and ventricular remodeling**. Additional risk factors include **hypertension, dyslipidemia, diabetes mellitus, and metabolic syndrome**.

Clinical Presentation and Diagnosis

The primary symptoms result from **left ventricular dysfunction and heart failure**.

Patients may experience:
Diagnostic tools include:

Treatment of Ischemic Dilated Cardiomyopathy

The treatment aims to **improve ventricular function, reduce symptoms, and prevent disease progression**.

Lifestyle Modifications: A low-sodium diet, controlled physical activity, smoking cessation, and blood pressure management improve prognosis.

Pharmacological Therapy:
Myocardial Revascularization: In patients with significant ischemia, **coronary revascularization** through **percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)** may improve ventricular function.

Advanced Therapy: In patients with **advanced heart failure**, additional interventions may be required:

Prognosis and Complications

Ischemic dilated cardiomyopathy is a **progressive condition** with a high risk of **refractory heart failure, ventricular arrhythmias, and sudden cardiac death**. However, **optimized treatment can significantly improve quality of life and survival**.
    References
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