Retina Mythbusters: Dispelling Common Myths About the Use of Dual Inhibition Therapy Versus Anti-VEGF in Retinal Vascular Diseases
This activity is supported by an educational grant from Genentech, a member of the Roche Group.
Release Date: March 25, 2024
Expiration Date: March 25, 2025
Time to Complete Activity: 1.0 hour
Faculty
Jennifer I. Lim, MD, FARVO
Marion H. Schenk Esq. Chair and UIC Distinguished Professor of Ophthalmology
Director of Retina Service
Vice Chair for Diversity and Inclusion
University of Illinois at Chicago
Chicago, IL
Christina Y. Weng, MD, MBA, FASRS
Professor of Ophthalmology
Fellowship Program Director, Vitreoretinal Diseases & Surgery
Baylor College of Medicine, Cullen Eye Institute
Houston, TX
Target Audience
This activity has been designed to address the educational needs of retina specialists and comprehensive ophthalmologists. It may also benefit other clinicians involved in the care of patients with retinal vascular diseases.
Educational Provider
This activity is provided by Paradigm Medical Communications, LLC.
Supporter Acknowledgement
This activity is supported by an educational grant from Genentech, a member of the Roche Group.
Program Overview
Uncertain about the role of novel therapies in retinal vascular diseases? Who you gonna call? Mythbusters! Join our expert faculty as they dispel common myths and misconceptions about dual inhibition therapy and high-dose anti-vascular endothelial growth factor (VEGF) therapy, including those surrounding their durability, effects on disease activity, patient selection, retreatment criteria, and more.
Learning Objectives
Upon completion of this activity, participants should be able to:
- Differentiate dual inhibition therapy from anti-VEGF therapy based on key anatomic outcomes that demonstrate direct effects on the pathophysiology of retinal vascular diseases
- Describe the significance of retreatment criteria used in recent clinical trials of dual inhibition therapy and high-dose anti-VEGF therapy
- Personalize treatment decisions for patients with retinal vascular diseases that demonstrate application of the latest evidence to inform appropriate selection and dosing of therapy
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Physician Credit Designation Statement
Paradigm Medical Communications, LLC designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
PA Continuing Education
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Instructions for Participation
To receive a certificate of participation, participants must:
- Follow instructions to register or log in with your professional information and complete the preassessment
- View the online activity in its entirety
- Complete and submit the online postassessment and evaluation. You must answer 70% of the postassessment questions correctly to earn credit. You will have unlimited opportunities to successfully complete the postassessment
A certificate of participation will be available for download/printing immediately following your successful completion of the postassessment and evaluation.
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Disclosures of Relevant Financial Relationships
In accordance with the ACCME’s Standards for Integrity and Independence in Accredited Continuing Education, Paradigm requires that all planners, faculty, and others who are in a position to control the content of this activity disclose all financial relationships with ineligible companies during the past 24 months.
All relevant relationships are identified and mitigated according to Paradigm policy prior to individuals assuming their roles, and are disclosed prior to learners’ engagement in the activity. Paradigm is committed to providing learners with high-quality accredited continuing education that promotes improvements or quality in healthcare and not a specific proprietary business interest of an ineligible company.
The content of this activity was independently reviewed to ensure that it is fair and balanced, scientifically rigorous, evidence based, and aligned with the public interest. All relevant relationships have been mitigated.
Jennifer I. Lim, MD, FARVO
Advisor: Alimera Sciences; Bausch & Lomb; EyePoint Pharmaceuticals, Inc; IVERIC bio, Inc; Regeneron Pharmaceuticals Inc
Consultant: AbbVie Inc.; Aura Biosciences, Inc.; Cognition Therapeutics; Eyenuk, Inc.; Genentech, Inc.; Luxa Biotechnology, LLC; Quark Pharmaceuticals Inc.; Santen Pharmaceutical Co., Ltd.; UNITY Biotechnology; Viridian Therapeutics Inc.
Research Funding: Adverum Biotechnologies, Inc; Aldeyra Therapeutics, Inc; Chengdu Kanghong Pharmaceutical Group Co, LTD; Genentech, Inc.; Graybug Vision Inc (expired 12/2022); Janssen Pharmaceuticals, Inc; NGM Biopharmaceuticals; Regeneron Pharmaceuticals Inc; REGENXBIO Inc; Spring Vision LTD; Stealth BioTherapeutics Inc (expired 12/2022)
Christina Y. Weng, MD, MBA, FASRS
Consultant: AbbVie Inc.; Alcon; Alimera Sciences; Apellis Pharmaceuticals, Inc; DORC; EyePoint Pharmaceuticals, Inc; Genentech, Inc.; IVERIC bio, Inc; Novartis AG; Regeneron Pharmaceuticals Inc; REGENXBIO Inc
Independent Contractor: agtc; Alimera Sciences
Peer Reviewer
Stock: Medtronic (expired 3/24); Pfizer Inc. (expired 3/24); F. Hoffmann-La Roche Ltd (expired 3/24)
Paradigm Medical Communications, LLC staff members have no relevant financial relationships with ineligible companies to disclose.
Disclosure of Unlabeled Use
This educational activity may contain discussion of published and/or investigational uses of agents that are not approved by the FDA.
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