Title
Intravitreal infliximab for refractory pseudophakic cystoid macular edema: Results of the Pan-American Collaborative Retina Study Group
Date Issued
01 June 2012
Access level
metadata only access
Resource Type
journal article
Author(s)
Wu L.
Fernando Arevalo J.
Hernandez-Bogantes E.
Abstract
Inflammation is themajor etiologic factor in the development of pseudophakic cystoid macular edema (CME). Several soluble mediators of inflammation such as tumor necrosis factor alpha (TNF-α) have been implicated in the pathogenesis of ocular inflammation. The purpose of this study is to report the shortterm visual and anatomic outcomes following intravitreal injections of infliximab in eyes with refractory CME secondary to cataract surgery. An interventional, retrospective study of 7 eyes with refractory CME that were injected with 1 mg of infliximab. The main outcome measures were best-corrected visual acuity (BCVA) and central macular thickness (CMT) at 6-month follow-up. At the 6 month follow-up, BCVA improved from 1.14 ± 0.59 logMAR at baseline to 0.51 ± 0.35 logMAR (p = 0.0156). CMT also improved from 584 ± 159 lm at baseline to 327 ± 127 lmat 6 months (p = 0.0111).Nosystemic adverse events were reported in these patients. There was a single episode of uveitis that responded to topical steroids. Inhibition of TNF-a may be beneficial in the treatment of refractory pseudophakic CME. © Springer Science+Business Media B.V. 2012.
Start page
235
End page
243
Volume
32
Issue
3
Language
English
OCDE Knowledge area
Oftalmología
Scopus EID
2-s2.0-84864290002
PubMed ID
Source
International Ophthalmology
Resource of which it is part
International Ophthalmology
ISSN of the container
01655701
Sponsor(s)
Fig. 4 OCT horizontal and vertical scans through the fovea showing intraretinal cystoid changes 2 months after an intravitreal injection of 4 mg of triamcinolone acetate. CMT was 640 µm; BCVA was 20/100 Fig. 5 OCT horizontal and vertical scans showing that most of the intraretinal cystoid changes have resolved after three consecutive monthly injections of 1 mg of intravitreal infliximab. The macular architecture has been restored. CMT was 295 µm; BCVA improved to 20/25 Acknowledgments Supported in part by the Arevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela. J.G. Sanchez, Clinica Oftalmologica Centro Caracas and the Arevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela; M. Farah (PI), M. Maia, Universidade Federal de São Paulo, De-partamento de Oftalmologia, Instituto da Visão, Sao Paulo, Brazil; V. Morales-Canton (PI), H. Quiroz-Mercado, J. Fromow-Guerra, J.L. Guerrero-Naranjo, J. Dalma-Weiszhausz, Asociación para Evitar la Ceguera en México, Mexico City, Mexico; F.J. Rodriguez (PI), R. Infante, D. Medina, Fundacion Oftalmologica Nacional, Universidad del Rosario, Bogota, Colombia; M.H. Berrocal (PI), V. Cruz-
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