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Eisenmenger Syndrome

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  • Eisenmenger syndrome

    Eisenmenger's syndrome ( tardive cyanosis) is the process in which a left to right shunt caused by acongenital heart defect in the fetal heart causes increased flow through the pulmonary vasculature, causing pulmonary hypertension which in turn causes increased pressures in the right side of the heart and reversal of the shunt into a right-to-left shunt.

  • Eisenmenger syndrome

    45-55% of infants with a large, non-restrictive VSD or PDA develop pulmonary hypertension by early childhood.5-15% of patients with a large secundum ASD progress to pulmonary hypertension but usually not until after the third decade of life.

  • Eisenmenger syndrome

    The treatment of Eisenmenger syndrome varies widely and depends on the patient's age, degree of cyanosis, and subsequent polycythemia.Patients should avoid sudden fluid shifts or dehydration.

  • Eisenmenger syndrome

    Heart-lung transplantation and single or bilateral, sequential lung transplantation, with or without repair of relatively simple congenital cardiovascular anomalies, are viable transplant procedures and are the only surgical options for a patient with Eisenmenger syndrome.

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