Journal
CLINICS IN CHEST MEDICINE
Volume 34, Issue 4, Pages 619-+Publisher
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.ccm.2013.08.010
Keywords
Pulmonary arterial hypertension; Idiopathic pulmonary arterial hypertension; HIV infection; Portopulmonary hypertension; Systemic sclerosis; Hemolytic anemia; Pulmonary veno-occlusive disease; Anorectic drugs
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Changes in the epidemiology of pulmonary arterial hypertension (PAH) have resulted from changes in classification schemes and an increased emphasis on diagnosis because of the availability of effective therapies. The terms primary pulmonary hypertension and secondary pulmonary hypertension are considered inappropriate, confusing, and should not be used. Recent registries of patients with PAH have provided improved data regarding prognosis in the era of advanced therapies.
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