Eisenmenger: Difference between revisions
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Latest revision as of 10:39, 17 March 2025
Eisenmenger's syndrome is a medical condition that affects the heart and the lungs. It is a type of congenital heart disease that results in a long-standing right-to-left heart shunt caused by a congenital heart defect. This leads to pulmonary hypertension and changes in the structure of the heart, specifically the ventricles. The syndrome is named after Victor Eisenmenger, who first described the condition in 1897.
Causes[edit]
Eisenmenger's syndrome is caused by a congenital heart defect that results in a large left-to-right shunt. This can be due to several types of heart defects, including ventricular septal defect, atrial septal defect, and patent ductus arteriosus. Over time, this shunt can cause damage to the small blood vessels in the lungs, leading to pulmonary hypertension.
Symptoms[edit]
The symptoms of Eisenmenger's syndrome can vary greatly depending on the severity of the condition. Common symptoms include shortness of breath, cyanosis (bluish coloration of the skin and lips), fatigue, and chest pain. Other symptoms can include syncope (fainting), hemoptysis (coughing up blood), and clubbing of the fingers and toes.
Diagnosis[edit]
The diagnosis of Eisenmenger's syndrome is typically made based on a combination of physical examination, medical history, and diagnostic tests. These tests can include echocardiography, cardiac catheterization, and magnetic resonance imaging (MRI) of the heart.
Treatment[edit]
The treatment of Eisenmenger's syndrome is primarily aimed at managing the symptoms and preventing complications. This can include medications to reduce pulmonary hypertension, oxygen therapy, and in some cases, heart-lung transplant.
Prognosis[edit]
The prognosis for individuals with Eisenmenger's syndrome can vary greatly. However, with proper management, many individuals with this condition can lead a relatively normal life.
