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- W1969242173 abstract "Pulmonary arterial hypertension (PAH) is a progressive disease marked by vasoconstriction and vascular remodeling within pulmonary arteries leading to right heart failure and death. Significant advances in understanding the pathobiology of the disease have identified three key pathways involved in progression of this disease, which are the endothelin pathway, the prostacyclin pathway, and the nitric oxide/cyclic guanosine monophosphate pathway. Echocardiogram is the best screening tool to obtain an estimation of the pulmonary artery systolic pressure but right heart catheterization remains the standard by which the diagnosis is made. There are currently six FDA approved therapies for PAH. The mechanistic rationale, evidence behind their use and side effect considerations in utilizing these therapies in PAH patients will be the focus of this review." @default.
- W1969242173 created "2016-06-24" @default.
- W1969242173 creator A5087034704 @default.
- W1969242173 date "2008-01-01" @default.
- W1969242173 modified "2023-09-27" @default.
- W1969242173 title "Advances in diagnosis and treatment in patients with pulmonary arterial hypertension" @default.
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- W1969242173 doi "https://doi.org/10.1002/ccd.21389" @default.
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