Pulmonary arterial hypertension (PAH) is a chronic and progressive condition that affects the pulmonary vasculature, resulting in elevated pulmonary vascular resistance, right ventricular dysfunction, and eventually, right heart failure. It is essential to identify and manage PAH early to improve patient outcomes. This necessitates comprehensive knowledge of the diagnostic criteria and classification of PAH, as well as a care approach based on evidence that incorporates the latest guidelines, advancements, and recommendations from leading professional organizations. In addition, due to the inadequacies of current therapies, it is necessary to critically evaluate novel treatment pathways and new/emerging therapeutic targets for PAH.
In this clinical discussion, you'll hear from two leading experts who will discuss patient cases and discuss how you can optimize PAH treatment plans based on risk stratification and comorbidities and integrate the evidence-based recommendations and treatments in your practice.
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