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
Effect on Intraocular Pressure Following Intravitreal Triamcinolone Acetonide Injection
Author Affiliations & Notes
  • Casey Scroggins
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Varun Natarajan
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Avanthia Terovolas
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Sofia Yarosh
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Aidan Oliss
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Alexander Merheb
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Harrison Dean Sciulli
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • David G Miller
    Retina Associates of Cleveland Inc, Beachwood, Ohio, United States
  • Footnotes
    Commercial Relationships   Casey Scroggins None; Varun Natarajan None; Avanthia Terovolas None; Sofia Yarosh None; Aidan Oliss None; Alexander Merheb None; Harrison Sciulli None; David Miller None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 3133. doi:
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      Casey Scroggins, Varun Natarajan, Avanthia Terovolas, Sofia Yarosh, Aidan Oliss, Alexander Merheb, Harrison Dean Sciulli, David G Miller; Effect on Intraocular Pressure Following Intravitreal Triamcinolone Acetonide Injection. Invest. Ophthalmol. Vis. Sci. 2024;65(7):3133.

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

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Abstract

Purpose : Ocular steroid therapy is often used for its anti-inflammatory mechanism of action, but often resulting in an undesirable increase in the intraocular pressure (IOP) of the treated eye. This study sought to analyze the effects on IOP following intravitreal delivery of triamcinolone acetonide (TRI) injections.

Methods : The practice management system at Retina Associates of Cleveland was used to gather patients receiving a series of 2 or 3 intravitreal injections of TRI between 2011 and 2023. Using a retrospective cohort analysis, the IOP measurements were collected and analyzed for both treated and fellow eyes. The mean and median baseline visit was compared to the mean and median IOP at the final visit. Likewise, the number of glaucoma medications for both treated and fellow eyes was measured at baseline and compared to the number at the final visit. The mean and median IOP and number of glaucoma medications at the baseline and final visit were calculated and compared using a t-test. The Institutional Review Board granted this study a waiver of authorization.

Results : A total of 146 patients with a mean age of 69.8 received 2 or 3 treatments of TRI. Data collected showed the mean IOP at baseline was 15.3 mmHg (median 14 mmHg) for the treated eye and 16.7 mmHg (median 16 mmHg) for the fellow eye. At the final visit, the mean IOP was 14.5 mmHg (median 14.5 mmHg) for the treated eye and 16.8 mmHg (median 17.5 mmHg) for the fellow eye. These IOP changes were found to be insignificant (p = 0.71 and 0.92 for treated and fellow eye, respectively). The mean number of glaucoma medications at baseline was 0.26 for the treated eye and 0.21 for the fellow eye which was insignificant (p = 0.3). At the final visit, the mean number of glaucoma medications was 0.21 for the treated eye and 0.12 for the untreated eye which was a statistically significant difference (p = 0.03).

Conclusions : In this limited analysis, TRI does not appear to cause significant steroid related elevation of IOP. However, a partial explanation for this lack of elevation in IOP can be explained by the significant increase in IOP-lowering medications for treated eyes at the final visit. It is unclear if clinicians were prophylactically treating eyes treated with TRI, but this is also plausible. Further study with longer follow up periods or additional injections could be enlightening.

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

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