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Insights on sGC Stimulators in PHCME / CEDon’t miss this special episode on soluble guanylate cyclase (sGC) stimulators, as these agents are gaining traction for managing patients with pulmonary hypertension (PH).
Short Cases in Pulmonary Arterial Hypertension CMETake 10 minutes to learn the nuts and bolts of diagnosing and treating patients across the spectrum of pulmonary arterial hypertension (PAH).
Insights on sGC Stimulators in PHCME / CEDon’t miss this special episode on soluble guanylate cyclase (sGC) stimulators, as these agents are gaining traction for managing patients with pulmonary hypertension (PH).
Short Cases in Pulmonary Arterial Hypertension CMETake 10 minutes to learn the nuts and bolts of diagnosing and treating patients across the spectrum of pulmonary arterial hypertension (PAH).
Pulmonary arterial hypertension (PAH) is a rare obstructive disorder of the smallest pulmonary arteries. Progressive narrowing of these arteries increases pulmonary vascular resistance, resulting in right heart failure and death. Early diagnosis and management can improve prognosis, but diagnosis of PAH in the early stages is a clinical challenge because symptoms such as dyspnea, dizziness, and fatigue are nonspecific. PAH is therefore frequently unrecognized until in a relatively advanced stage.
