Endophthalmitis rates among patients receiving intravitreal anti-VEGF injections: a USA claims analysis

Частота эндофтальмита у пациентов, получающих интравитреальные инъекции анти-VEGF-препаратов: анализ страховых требований в США
Szilárd Kiss, Pravin U. Dugel, Arshad M. Khanani, Michael S. Broder, Eunice Chang, Gordon H. Sun, Adam Turpcu
2018-08-01

USA claims dataafliberceptendophthalmitisintravitreal anti-VEGF injectionsneovascular age-related macular degeneration
Purpose: Intravitreal (IVT) injections of the anti-vascular endothelial growth factor (VEGF) agents aflibercept, bevacizumab, and ranibizumab are commonly prescribed to treat neovascular age-related macular degeneration (nAMD). Studies comparing inflammation rates in large populations of patients receiving these agents and the treatment of ocular inflammation post-IVT anti-VEGF injections are scarce. In this study, we compared rates of endophthalmitis claims (sterile and infectious) following IVT anti-VEGF injections to determine the risk factors associated with developing endophthalmitis, and examined the claims for subsequent treatment. Patients and methods: This retrospective cohort study of USA claims data examined the risk of developing endophthalmitis following IVT injection of aflibercept, bevacizumab, or ranibizumab in patients with nAMD between 11/18/2011 and 5/31/2013. The primary study outcome was occurrence of endophthalmitis within 30 days of a claim for an IVT anti-VEGF injection. Endophthalmitis rates were calculated separately for aflibercept, bevacizumab, and ranibizumab, followed by pairwise comparisons of endophthalmitis frequencies among the 3 treatments. Results: This analysis included 818,558 injections from 156,594 patients with nAMD. The rates (% [n/N]) of endophthalmitis following aflibercept, bevacizumab, and ranibizumab IVT injections were 0.100% (136/135,973), 0.056% (268/481,572), and 0.047% (94/201,013), respectively. In a multivariate analysis, aflibercept was associated with a significantly higher risk of endophthalmitis vs ranibizumab (adjusted odds ratio, 2.19; 95% CI: 1.68–2.85; P <0.0001). The risk of endophthalmitis was similar for bevacizumab and ranibizumab. Within 14 days after endophthalmitis, 38.6% of cases received injectable antibiotics, 15.3% received injectable steroids, and 30.3% underwent vitrectomy. Conclusion: The rate of endophthalmitis was very low, but higher following IVT injection with aflibercept compared with both bevacizumab and ranibizumab in patients with nAMD. Keywords: ranibizumab, aflibercept, bevacizumab, regression analysis
1
A USA claims analysis included 818,558 anti-VEGF injections from 156,594 patients with neovascular age-related macular degeneration.
2
Aflibercept was associated with significantly higher endophthalmitis risk than ranibizumab, with an adjusted odds ratio of 2.19 (95% CI, 1.68–2.85).
3
Endophthalmitis rates were 0.100% after aflibercept, 0.056% after bevacizumab, and 0.047% after ranibizumab injections.
4
Endophthalmitis risk was similar between bevacizumab and ranibizumab injections.
5
Within 14 days of endophthalmitis, 38.6% of cases received injectable antibiotics, 15.3% injectable steroids, and 30.3% underwent vitrectomy.

Patients with neovascular age-related macular degeneration receiving intravitreal injections of aflibercept, bevacizumab, or ranibizumab

Rates, comparative risks, associated risk factors, and subsequent treatment of sterile or infectious endophthalmitis within 30 days after anti-VEGF injection

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2018-08-01
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Szilárd Kiss
Pravin U. Dugel
Arshad M. Khanani
Michael S. Broder
Eunice Chang
Gordon H. Sun
Adam Turpcu
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