In this online, self-learning activity:
Interstitial lung disease (ILD) is a collective term used to categorize more than 200 different types of diseases that affect the alveolar structures, the pulmonary interstitium, and small airways. The incidence and prevalence of ILD, as its own entity, are difficult to quantify because of number of different causes and the difficulty diagnosing patients. One form of ILD is associated with an overexpression of adenosine-2B receptor (A2BAR) has been linked to rapid progression of idiopathic pulmonary fibrosis (IPF), a type of IIP, and patients identified with this highly upregulated gene warrants closer monitoring of lung function and disease progression. Known as ILD with progressive lung phenotype (ILD-PF), patients with a number of diseases, such as rheumatoid arthritis and chronic hypersensitivity pneumonitis, are predisposed to this variant. This learning activity has been designed to bring HCPs’ knowledge of the strategies for treatment and management of ILD-PF up to date and to improve their competence and performance in treating it.
The following HCPs: pulmonologists, rheumatologists, primary care physicians, pathologists, dermatologists; physician assistants, nurse practitioners, nurses, and pharmacists specializing in pulmonology; and any other HCPs who have an interest in or otherwise clinically encounter patients with ILD-PF.
This program is supported by an educational grant from Boehringer Ingelheim.
Release Date: January 27, 2019 -- Expiration Date: January 27, 2021
Faculty: Terese Hammond, MD
Introduction, Disclosures |
Cursory refresher and review on ILD epidemiology and diagnosis and introduction to the PF variant
o Age, race, gender o Environmental factors o Genetics (A2BAR) o Autoimmune diseases o Immune dysfunction o Overactivation of fibroblasts
o Dyspnea on exertion o Nonproductive cough · Diagnosis o HRCT scan vs. chest radiography o Lung biopsy o Serological testing
|
Treatment of ILD-PF
o Corticosteroids o Immunomodulators o Nintedanib o Pirfenidone
|
Summary, conclusions, and best practice recap |
1 |
Introduction, Disclosures |
13 |
Cursory refresher and review on ILD epidemiology and diagnosis and introduction to the PF variant [Learning Objectives #1-3]
o Age, race, gender o Environmental factors o Genetics (A2BAR) o Autoimmune diseases o Immune dysfunction o Overactivation of fibroblasts
o Dyspnea on exertion o Nonproductive cough · Diagnosis o HRCT scan vs. chest radiography o Lung biopsy o Serological testing
|
45 |
Treatment of ILD-PF [Learning Objectives #4 & 5]
o Corticosteroids o Immunomodulators o Nintedanib o Pirfenidone
|
1 |
Summary, conclusions, and best practice recap |
By the end of the session the participant will be able to:
ACCME Activity #201220070
ACCREDITATION FOR THIS COURSE HAS EXPIRED. YOU MAY VIEW THE PROGRAM, BUT CME / CE IS NO LONGER AVAILABLE AND NO CERTIFICATE WILL BE ISSUED.
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Faculty Disclosures:
Dr. Terese C. Hammond, MD, Clinical Professor, University of Southern California, Los Angeles, CA has no relevant conflicts of interest to disclose.
Disclosures of Educational Planners: Charles Turck, PharmD has no relevant conflicts of interest to disclose.
Commercial Support Disclosure: This program is supported by an educational grant from Boehringer Ingelheim.
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