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Pulmonary Vascular Disease Journals

Pulmonary arterial hypertension of variable degree is usually related to adult congenital heart condition. Depending on size and site of the underlying cardiac defect also as on repair status, pulmonary arterial hypertension may present with or without reversed shunting and associated cyanosis (ie, Eisenmenger syndrome). We review available data on etiology, clinical presentation, prognosis, and management strategies of pulmonary arterial hypertension in adult patients with congenital heart condition . In addition, we discuss the various complications related to Eisenmenger syndrome, representing a multisystem disorder. Finally, we present general management strategies and emerging disease-targeting therapies. It is a chronic condition which affects those blood vessels which are related to lungs or from the lungs. Causes of pulmonary vascular diseases are varies according to lungs blood vessels are affected. Adults with congenital heart disease represent an expanding patient population requiring life-long tertiary medical care. Approximately 5% to 10% of them develop pulmonary arterial hypertension (PAH) of variable severity that affects quality of life, morbidity, and mortality 

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