
Pulmonary arterial hypertension (PAH) is a rare disease causing elevated pre-capillary pulmonary hypertension. Sotatercept, recently FDA-approved, inhibits activin signaling to treat PAH. Despite clinical trial guidelines, individual patient care requires tailored decisions. This article provides a case-based discussion on clinical decisions involving diagnostic testing, first-line agents, therapy escalation, sotatercept timing, safety, practical use, and future applications for other pulmonary hypertension cohorts.
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