Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Retinal vasculitis with or without retinal vascular occlusion among eyes with nAMD or DME treated with IVT agents as recorded in the Vestrum database
Author Affiliations & Notes
  • Shriji Patel
    Genentech Inc, South San Francisco, California, United States
  • Gloria Chi
    Genentech Inc, South San Francisco, California, United States
  • Vaibhavi Patel
    Roche Products Ltd, Welwyn Garden City, United Kingdom
  • Nick Boucher
    Vestrum Health, Waltham, Massachusetts, United States
  • Nitika Aggarwal
    Vestrum Health, Ottawa, Ontario, Canada
  • Shih-Chen Chang
    Genentech Inc, South San Francisco, California, United States
  • Sumit Sharma
    Cleveland Clinic, Cleveland, Ohio, United States
  • Manuel Amador
    Genentech Inc, South San Francisco, California, United States
  • Marco A Zarbin
    Rutgers New Jersey Medical School, Newark, New Jersey, United States
  • Footnotes
    Commercial Relationships   Shriji Patel Genentech, Inc., Code E (Employment); Gloria Chi Genentech, Inc., Code E (Employment); Vaibhavi Patel Roche Products Ltd., Code E (Employment); Nick Boucher None; Nitika Aggarwal None; Shih-Chen Chang Genentech, Inc., Code E (Employment); Sumit Sharma Allergan, Genentech/Roche, Gilead, IONIS, Santen, AbbVie, ClearSide, 51 Bausch, EyePoint, Regenxbio, Code C (Consultant/Contractor); Manuel Amador Genentech, Inc., Code E (Employment); Marco Zarbin Apellis, Boehringer Ingelheim, EdiGene, Genentech, Inc./Roche, Illuminare, Life Biosciences, Novartis, Perfuse Therapeutics, Seeing Medicines, Smile Biotech, Tamarix Pharmaceuticals, Tenpoint, Code C (Consultant/Contractor), NVasc, Code I (Personal Financial Interest)
  • Footnotes
    Support  Financial support was provided by Genentech, Inc., a member of the Roche Group (South San Francisco, California). The sponsor participated in the design of the study; collection, management, analysis, and interpretation of the data; and preparation, review, and approval of the abstract. Third-party writing assistance, provided by Adam Dagnall, DPhil, of Envision Pharma Group, was funded by Genentech, Inc.
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 5672. doi:
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    • Get Citation

      Shriji Patel, Gloria Chi, Vaibhavi Patel, Nick Boucher, Nitika Aggarwal, Shih-Chen Chang, Sumit Sharma, Manuel Amador, Marco A Zarbin; Retinal vasculitis with or without retinal vascular occlusion among eyes with nAMD or DME treated with IVT agents as recorded in the Vestrum database. Invest. Ophthalmol. Vis. Sci. 2024;65(7):5672.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To assess incidence of retinal vasculitis (RV) with or without retinal vascular occlusion (RO) among eyes with neovascular age-related macular degeneration (nAMD) or diabetic macular edema (DME) treated with intravitreal (IVT) agents as recorded by individual clinicians in routine clinical practice in the US.

Methods : This was a retrospective observational study of eyes in patients (≥ 18 years) with nAMD or DME, that received ≥ 1 IVT treatment from 01/01/2014–31/03/2023 following initial diagnosis, from the Vestrum database. Eyes with no visits following the index injection; or eyes that had diagnoses of IOI, RV, or RO on or prior to index injection were excluded. Incidence of the first event of RV, RV and RO, and intraocular inflammation (IOI; including RV) and RO, recorded as occurring within 180 days of an IVT injection were identified using ICD-9/10-CM diagnosis codes through the end of the study period (30/09/2023). Eyes were not followed for additional events after the first instance. Event incidence by approved IVT agents for nAMD or DME of interest, including faricimab (FAR), aflibercept (AFL), ranibizumab (RAN), and brolucizumab (BRO) were recorded. Events were attributed to the IVT agent immediately prior to (but not on) the date of the event.

Results : 302,334 eyes, receiving over 4 million injections, were included in the analysis. The incidence of RV, RV with RO, and IOIs with RO were low across IVT agents. The percentage (%, 95% CI) of exposed eyes with recorded IOI (including RV) with RO events were broadly comparable between FAR (0.013; 0.004–0.037), AFL (0.025; 0.019–0.033), and RAN (0.011; 0.007–0.018), but was higher for BRO (0.148; 0.072–0.306). Similarly, for RV, and RV with RO, event incidence (%) among exposed eyes were low and generally comparable between FAR (0.008/0), AFL (0.005/0.001), and RAN (0.002/0.001). However, the percentages of eyes with RV, and RV with RO, events were highest for BRO (0.339/0.064), respectively (Table).

Conclusions : Incidence of first RV, RV and RO, and IOI and RO events are similar among eyes treated with FAR, AFL, and RAN. Eyes treated with BRO had a higher incidence than other approved IVT agents.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Table: Overview of events by IVT agent

Table: Overview of events by IVT agent

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