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PAH

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By Ricardo Correa Associate Professor, Medical School, Federal University OF Minas Gerais, Brazil
https://www.readbyqxmd.com/read/27434819/new-paradigm-for-pulmonary-arterial-hypertension-treatment
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Yuichi Tamura, Richard N Channick
PURPOSE OF REVIEW: Pulmonary arterial hypertension (PAH) was previously considered a uniformly fatal disease, with patients succumbing to right heart failure and death at an average of 3 years after diagnosis. The past 20 years, however, have seen the development of numerous targeted therapies that have changed the natural history of PAH. As more pharmacologic agents have been approved and utilized, further advances in the design of and endpoints for clinical trials. This study will review some of these notable developments...
September 2016: Current Opinion in Pulmonary Medicine
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