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Medical Therapy For Pulmonary Arterial Hypertension*: ACCP Evidence-Based Clinical Practice Guidelines

David B. Badesch, MD, FCCP; Steve H. Abman, MD; Gregory S. Ahearn, MD; Robyn J. Barst, MD; Douglas C. McCrory, MD, MHSc; Gerald Simonneau, MD; Vallerie V. McLaughlin, MD, FCCP
Author and Funding Information

*From the University of Colorado Health Sciences Center (Dr. Badesch), Denver, CO; The Children’s Hospital (Dr. Abman), Denver, CO; Babies Hospital (Dr. Barst), Columbia-Presbyterian Medical Center, Pediatric-Cardiology Center, New York, NY; Duke University Medical Center (Drs. Ahearn and McCrory), Durham, NC; Hôpital Antoine Béclère (Dr. Simonneau), Clamart, France; and University of Michigan (Dr. McLaughlin), Ann Arbor, MI.

Correspondence to: David B. Badesch, MD, FCCP, University of Colorado Health Sciences Center, Box C-272, 4200 E Ninth Ave, Denver, CO 80262; e-mail: David.Badesch@UCHSC.edu



Chest. 2004;126(1_suppl):35S-62S. doi:10.1378/chest.126.1_suppl.35S
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Pulmonary arterial hypertension (PAH) is often difficult to diagnose and challenging to treat. Untreated, it is characterized by a progressive increase in pulmonary vascular resistance leading to right ventricular failure and death. The past decade has seen remarkable improvements in therapy, driven largely by the conduct of randomized controlled trials. Still, the selection of most appropriate therapy is complex, and requires familiarity with the disease process, evidence from treatment trials, complicated drug delivery systems, dosing regimens, side effects, and complications. This chapter will provide evidence-based treatment recommendations for physicians involved in the care of these complex patients. Due to the complexity of the diagnostic evaluation required, and the treatment options available, it is strongly recommended that consideration be given to referral of patients with PAH to a specialized center.

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