Abstract
Objective
Determine the association between initial treatment method (tap and inject [T/I] or pars plana vitrectomy [PPV]) and microbiology findings on post-treatment visual acuity (VA) in endophthalmitis patients.
Methods
This retrospective study evaluated patients treated for endophthalmitis in Toronto, Canada. The association between treatment, microbiology, and VA at 1-, 3-, 6-, and 12-months post-treatment was analysed using linear regression, adjusted for age, sex, time to treatment, and baseline VA.
Results
A total of 111 patients were treated with initial T/I (n = 93, 84%) or PPV (n = 18, 16%) between 2011 and 2023. Microbiology identified 69 (62%) culture-negative, 36 (32%) bacterial, and 6 (5%) fungal cases. Adjusted VA improvement did not differ between bacterial and culture-negative groups at all timepoints, including 1 month (–0.68 ± 0.86 vs. –0.69 ± 0.87 logMAR, p = 0.98, n = 102) and last measured follow-up (–1.01 ± 0.90 vs. –0.84 ± 0.83 logMAR, p = 0.35, n = 105). VA improvement also did not differ between T/I and PPV at all timepoints, including at 1 month (–0.66 ± 0.87 vs. –0.50 ± 0.78 logMAR, p = 0.55, n = 108) and last measured follow-up (–0.91 ± 0.86 vs. -0.60 ± 0.80 logMAR, p = 0.20, n = 111). Last measured follow-up time did not differ between T/I and PPV (6.0 vs. 3.8 months, p = 0.05) or between bacterial and culture-negative groups (6.1 vs. 5.6 months, p = 0.85). Retreatment rates were similar between T/I and PPV (35% vs. 33%, OR = 0.95, p = 0.93), but higher in bacterial vs. culture-negative cases (56% vs. 22%, OR = 4.80, p < 0.01).
Conclusions
Visual outcomes did not differ by treatment or microbiology. Bacterial cases had higher retreatment rates than culture-negative cases.
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Data availability
The dataset analysed during the current study is not publicly available due patient privacy but is available from the corresponding author in a deidentified format upon reasonable request.
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Study Details | Endophthalmitis Post Intravitreal Injections | ClinicalTrials.gov [Internet]. [cited 2024 Jul 11]. Available from: https://clinicaltrials.gov/study/NCT04035369.
Acknowledgements
Dr. Rajeev H. Muni’s research is supported by the Silber TARGET Fund.
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Shayaan Kaleem, AM, AG, AL, CJ, and Sameen Kaleem were responsible for designing the study, extracting the data, and analysing the data. MMP, PJK, RHM, and DTW were responsible for interpreting results and overseeing the project. All authors contributed to the writing and review of the manuscript and have approved the final version.
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MMP: Financial support (to institution) – PSI Foundation, Fighting Blindness Canada. PJK: Honoraria: Novartis, Bayer, Roche, Boehringer Ingelheim, RegenxBio, Apellis; Advisory board – Novartis, Bayer, Roche, Apellis, Novelty Nobility, Viatris, Biogen, AdMare, Kriya Therapeutics; Financial support (to institution) – Roche, Novartis, Bayer, RegenxBio. DTW: Consultant – AbbVie, Alcon, Apellis, Bayer, Bausch Health, Biogen, Boehringer Ingelheim, Novartis, Ripple Therapeutics, Roche, Topcon, Zeiss. Research grants from Novartis, Roche. RHM: Consultant- Alcon,Apellis, AbbVie, Bayer, Bausch Health, Roche; Financial Support (to institution) - Alcon, AbbVie, Bayer, Novartis, Roche.
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Kaleem, S., Mihalache, A., Golrokhian-Sani, AA. et al. The association between treatment method, microbiological findings, and visual acuity in endophthalmitis patients: A retrospective, multi-centred study. Eye 40, 406–411 (2026). https://doi.org/10.1038/s41433-025-04125-1
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DOI: https://doi.org/10.1038/s41433-025-04125-1


