Pulmonary arterial hypertension (PAH) is a relatively rare but
potentially life-threatening disease. In most forms, the disease is
likely to be diagnosed late and is associated with progressive
clinical deterioration and premature death. A Clinician's Guide to
Pulmonary Arterial Hypertension, Second Edition enhances the
overall PAH awareness of the wider clinical community and outlines
the need for more effective screening, diagnosis, and treatment.
Topics include: Disease background and epidemiology Basics of
disease pathophysiology Clinical profile and diagnosis Treatment
strategies Screening and management of PAH
General
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