Clinician's Guide to Pulmonary Arterial Hypertension

<p>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. <strong>A Clinician's Guide to Pulmonary Arterial Hypertension Second Edition</strong> enhances the overall PAH awareness of the wider clinical community and outlines the need for more effective screening diagnosis and treatment. Topics include:</p><ul> <li>Disease background and epidemiology </li> <li>Basics of disease pathophysiology </li> <li>Clinical profile and diagnosis </li> <li>Treatment strategies </li> <li>Screening and management of PAH </li> </ul>