

Overview
Pulmonary hypertension is a progressive condition characterized by obstructive remodeling of the distal pulmonary vasculature. There are several etiologies, such as congestive heart failure, and they vary based on pathophysiological mechanisms, hemodynamic characteristics, and therapeutic management. Pulmonary arterial hypertension (PAH) is one of the most severe and aggressive forms of pulmonary hypertension. It is a severe and life-threatening condition characterized by increased resistance in the pulmonary blood vessels, which can result in right heart failure and premature death. Detecting PAH in its initial stages can be challenging since most of the symptoms often only manifest once the disease has progressed. Hence, primary care providers play a pivotal role in the early detection of PAH, facilitating referrals to specialists for diagnosis confirmation, and ensuring continuity of patient care.
This e-learning module reviews the definition and pathophysiology of PAH and discuss the role of primary healthcare providers in improving patient care and outcomes through the diagnosis, management, and monitoring of patients with PAH.
Upon completion of the educational activity, participants should be able to:
Dr. Wong Ka Lam, Michael
MBBS, MRCP, FHKAM, FRCP,
Specialist in Cardiology