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Endophthalmitis rates among patients receiving intravitreal anti-VEGF injections: a USA claims analysis.
Kiss, Szilárd; Dugel, Pravin U; Khanani, Arshad M; Broder, Michael S; Chang, Eunice; Sun, Gordon H; Turpcu, Adam.
Afiliación
  • Kiss S; Department of Ophthalmology, Weill Cornell Medical College, New York, NY, USA, szk7001@med.cornell.edu.
  • Dugel PU; Retinal Consultants of Arizona, Phoenix, AZ, USA.
  • Khanani AM; USC Roski Eye Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Broder MS; Sierra Eye Associates, Reno, NV, USA.
  • Chang E; Partnership for Health Analytic Research, LLC, Beverly Hills, CA, USA.
  • Sun GH; Partnership for Health Analytic Research, LLC, Beverly Hills, CA, USA.
  • Turpcu A; Partnership for Health Analytic Research, LLC, Beverly Hills, CA, USA.
Clin Ophthalmol ; 12: 1625-1635, 2018.
Article en En | MEDLINE | ID: mdl-30214147
ABSTRACT

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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Clin Ophthalmol Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Clin Ophthalmol Año: 2018 Tipo del documento: Article