July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Twenty-four month results of intravitreal ranibizumab for macular edema after branch retinal vein occlusion in a single-center prospective study: visual prognosis and rate of complete resolution of macular edema
Author Affiliations & Notes
  • MIHO INAGAKI
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Yoshio Hirano
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Norihiro Suzuki
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Yusuke Yasuda
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Mihoko Kawamura
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Tsutomu Yasukawa
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Munenori Yoshida
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Yuichiro Ogura
    Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Sciences, Japan
  • Footnotes
    Commercial Relationships   MIHO INAGAKI, None; Yoshio Hirano, None; Norihiro Suzuki, None; Yusuke Yasuda, None; Mihoko Kawamura, None; Tsutomu Yasukawa, None; Munenori Yoshida, Novartis (F); Yuichiro Ogura, Novartis (F)
  • Footnotes
    Support  Novartis
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 4068. doi:
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      MIHO INAGAKI, Yoshio Hirano, Norihiro Suzuki, Yusuke Yasuda, Mihoko Kawamura, Tsutomu Yasukawa, Munenori Yoshida, Yuichiro Ogura; Twenty-four month results of intravitreal ranibizumab for macular edema after branch retinal vein occlusion in a single-center prospective study: visual prognosis and rate of complete resolution of macular edema. Invest. Ophthalmol. Vis. Sci. 2019;60(9):4068.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To report the 24-month results after one intravitreal ranibizumab (IVR) injection followed by pro re nata (PRN) dosing for macular edema (ME) after branch retinal vein occlusion (BRVO).

Methods : The inclusion criteria included a minimal patient age of 18 years, 20 letters or more best-corrected visual acuity (BCVA) (Early Treatment Diabetic Retinopathy Study [ETDRS] score, 77 letters or less), and central retinal thickness (CRT) of 250 microns or more. The primary outcome measure was the mean BCVA change from baseline at month 24; the secondary outcomes were mean changes in CRT, the number of IVR injections, and the rate of complete absorption of ME for longer than 6 months.

Results : Twenty patients were enrolled from March 2014 through October 2016 at Nagoya City University Hospital. The baseline mean ETDRS letters and CRT were 62.0 and 511 microns, respectively; mean time from symptom onset to initial therapy, 1.80 months; and mean ETDRS gain and CRT reduction were 19.0 letters and 240 microns, respectively. The percentages of patients with Snellen equivalent BCVAs of 20/40 (70 ETDRS letters) or better and 20/20 (85 ETDRS letters) were 95% and 70%, respectively. The mean number of IVR injections was 8.3. Forty percent of patients did not need additional IVR injections for longer than 6 months during the follow-up. No adverse side effects were observed.

Conclusions : Prompt initiation of IVR injection provided better visual prognosis at month 24. However, over 50% of the cases still had residual ME after 24 months.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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