Pulmonary Hypertension Treatment
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Pulmonary hypertension - In medicine, pulmonary hypertension (PH) or pulmonary artery hypertension (PAH) is an increase in blood pressure in the pulmonary artery or lung vasculature. Depending on the cause, it can be a severe disease with a markedly decreased exercise tolerance and right-sided heart failure.
Bosentan - Bosentan is an endothelin receptor antagonist important in the treatment of pulmonary artery hypertension.
Eisenmenger's syndrome - Eisenmenger's syndrome or Eisenmenger's reaction is defined as the process in which a left-to-right shunt in the 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.
Secondary hypertension - While most forms of hypertension have no known underlying cause (and are thus known as "essential hypertension" or "primary hypertension", in about 10% of the cases, there is a known cause, and thus the hypertension is secondary hypertension (or, less commonly, inessential hypertension).
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