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Optimizing Care for EGPA: Evidence-Based Strategies for Diagnosis, Management, and Treatment Authors: Ora Singer, MD, MS; Eileen Wang, MD, MPH; Michael E. Wechsler, MD, MMSc Patients with EGPA experience a complex and challenging journey. The rare disease is characterized by systemic vasculitis, leading to inflammation of blood vessels, often accompanied by an abnormal accumulation of eosinophils in tissues and organs. EGPA is challenging to diagnose and differentiate from other related eosinophilic disorders. This difficult disease presents healthcare providers with a challenge to effectively diagnose and provide timely interventions to prevent severe complications for patients with EGPA. In this program, a multidisciplinary expert faculty panel discusses EGPA pathophysiology, diagnostic criteria, and evidence-based management strategies to improve patient outcomes. Patient case scenarios and patient perspective video clips will illustrate challenges and management strategies for providers who treat patients with EGPA. Earn 1.0 CME by completing this free program here: https://brnw.ch/21wLcrA

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