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Girmens, J.F., Glacet-Bernard, A., Kodjikian, L., Nghiêm-Buffet, S., Massé, H., Fourmaux, E., Wolff, B., Roquet, W., Gaucher, D., Baillif, S. and Tadayoni, R. (2015) Management of Macular Edema Secondary to Retinal Vein Occlusion. Journal Français D’Ophtalmologie, 38, 253-263.
https://doi.org/10.1016/j.jfo.2014.10.003

has been cited by the following article:

• TITLE: Intravitreal Ranibizumab Combined with Sulfotanshinone Sodium Injection in Treating Type II Optic Disc Vasculitis

  AUTHORS: Bingwen Lu, Xingwei Wu, Lei Zhang

  KEYWORDS: Intravitreal Ranibizumab, Sulfotanshinone Sodium Injection, Type II Optic Disc Vasculitis

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.5 No.11, November 22, 2016

  ABSTRACT: Objectives: To present the effect of intravitreal ranibizumab (IVR) therapy combined with sulfotanshinone sodium (SS) injection in a patient suffering from type II optic disc vasculitis (ODV). Methods: A 26-year-old female patient was diagnosed with type II ODV with macular edema (ME). The information was obtained by complete medical and ophthalmic history taking and a detailed ophthalmic examination at the initial and follow-up visits. Functional and morphological outcomes at baseline, 1 week and 1 month following IVR+SS injections, are presented. Results: Best-corrected visual acuity (BCVA) improved from 78 letters (ETDRS) at baseline to 90 letters at 1-week follow-up and maintained stable through 1-month follow-up. Central retinal thickness (CRT) measured by optical coherence tomography (OCT) decreased from 465 μm at baseline to 240 μm at 1-week follow-up and to 226 μm at 1-month follow-up. Mean deviation (MD) measured by perimetry increased from ?5.17 dB to ?4.59 dB and to ?4.29 dB, respectively. Fluorescein angiography (FFA) showed that the initial macular edema at baseline disappeared while the arm-retina circulation time (ART) was also greatly shortened when compared to the baseline. Electroretinogram (ERG) measured at 1-month follow-up demonstrated an overall improvement of the retinal function after the injection. No ocular or systemic side effects were detected. Conclusions: IVR+SS injection may lead to resolution of the associated ME and improve the retina morphologically as well as functionally. To our knowledge, this is the first case of a type II ODV benefiting from treatment with IVR+SS injection. The observed results warrant further investigation.