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Understanding and diagnosing eosinophilic granulomatosis with polyangiitis (EGPA)

  • Overview

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Description

EGPA is a rare immune-mediated disease characterized[1] by adult-onset asthma , blood and tissue eosinophilia, and small-vessel vasculitis thought to contribute to organ damage[2]. In this programme, divided into four segments, viewers will learn about the pathophysiology, diagnosis, clinical complications associated with EGPA, and multidisciplinary assessment of EGPA. References: 1. Trivioli G, et al. Rheumatology (Oxford). 2020;59(Suppl 3):iii84-iii94; 2. Greco A, et al. Autoimmun Rev. 2015;14:341-348. PSE-US-0717; 02/2022. This program is limited to Health Care Professionals (HCP) only. This is a non-CME event. The industry program content and views expressed therein do not necessarily reflect the views, policies or position of the American Thoracic Society.

This program is sponsored by GSK.  

By registering for this webinar, you agree your information will be shared with the sponsor.

No CME or MOC credits are available for this program.

Opinions expressed and resources shared may not have been reviewed by the ATS prior to distribution through ATS channels, or reflect official positions of the ATS, unless it is explicitly noted as a result of official ATS approval. References to specific commercial entities (companies) or products do not reflect review or endorsement by the ATS unless it is explicitly noted as a result of official ATS approval.

Contributors

  • Peter Howarth BSc, MBBS, DM

    Professor Emeritus in Allergy and Respiratory Medicine; Global Scientific Lead for Biologics.
    University of Southampton; GSK

  • Benjamin Terrier MD

    Professor of Internal Medicine
    Cochin Hospital

  • Michael Wechsler MD, PhD

    Professor of Medicine
    National Jewish Health

  • David Jayne MD

    Professor of Clinical Autoimmunity.
    University of Cambridge

March 28, 2022
Mon 12:00 PM EDT

Duration 1H 0M

This live web event has ended.

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