A Clinician's Guide to Pulmonary Arterial Hypertension
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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
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