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
2018-08-01
SCID: 54.1/fnc8xmmc
Discuss with AI
USA claims dataafliberceptendophthalmitisintravitreal anti-VEGF injectionsneovascular age-related macular degeneration
Figures from the paper
Abstract (AI)
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
Key Findings
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.
Research Object
Patients with neovascular age-related macular degeneration receiving intravitreal injections of aflibercept, bevacizumab, or ranibizumab
Research Subject
Rates, comparative risks, associated risk factors, and subsequent treatment of sterile or infectious endophthalmitis within 30 days after anti-VEGF injection
Publication Details
Publication Date
2018-08-01
Journal
Publisher
ISSN
Open access PDF
Access Type
Author Information
Download PDF
Subscribe to digest