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Title: [Treatment of pulmonary artery hypertensions]. Author: Philip-Joet F, Saadjian A, Reynaud-Gaubert M, Arnaud A. Journal: Rev Prat; 1991 Jun 11; 41(17):1573-6. PubMed ID: 1853127. Abstract: The pulmonary hypertension (PAH) in chronic obstructive lung disease include therapy of the respiratory disease i.e. bronchodilator, kinesitherapy. Long-term oxygen therapy (more than 15 h/day) reverse the course of PAH and increase survey. Long-term efficiency of vasodilators is not well demonstrated. Primary PAH could benefit from vasodilators, especially waiting lung or heart-lung transplantation. Patients with PAH secondary to respiratory insufficiency could also be successfully transplanted. In post embolic PAH, antithrombotic agents are useful. Thrombectomy or transplantation are sometimes proposed.[Abstract] [Full Text] [Related] [New Search]