April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Prognostic Factor for Visual Outcomes Two-Years after Intravitreal ranibizumab for Myopic Choroidal Neovascularization
Author Affiliations & Notes
  • Hideo Nakanishi
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Akitaka Tsujikawa
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Kenji Yamashiro
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Akio Oishi
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Sotaro Ooto
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Hiroshi Tamura
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Nagahisa Yoshimura
    Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan
  • Footnotes
    Commercial Relationships Hideo Nakanishi, None; Akitaka Tsujikawa, None; Kenji Yamashiro, None; Akio Oishi, None; Sotaro Ooto, None; Hiroshi Tamura, None; Nagahisa Yoshimura, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 4944. doi:
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      Hideo Nakanishi, Akitaka Tsujikawa, Kenji Yamashiro, Akio Oishi, Sotaro Ooto, Hiroshi Tamura, Nagahisa Yoshimura; Prognostic Factor for Visual Outcomes Two-Years after Intravitreal ranibizumab for Myopic Choroidal Neovascularization. Invest. Ophthalmol. Vis. Sci. 2014;55(13):4944.

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

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Abstract

Purpose: To evaluate the visual outcome 24 months after intravitreal ranibizumab (IVR) for myopic choroidal neovascularization (mCNV), and to determine the effect of pre-treatment ocular factors on the visual outcome.

Methods: Twenty-three eyes of 23 patients (4 men and 16 women, the mean age [± standard deviation] was 65.6 ± 11.1 years) with treatment-naiive mCNV were treated with IVR followed by pro re nata (PRN) therapy. The efficacy of IVR was evaluated by the best-corrected visual acuity (BCVA) at 3, 6, 12, and 24 months after the initial treatment. Stepwise multiple linear regression analyses were performed to evaluate the influence of pre-treatment factors (age, duration of symptom, axial length, pre-treatment BCVA in logarithm of the minimum angle of resolution [logMAR] units, pre-treatment CNV size, and pre-treatment CNV location as subfoveal or juxtafoveal) on the BCVA and the improvement of the BCVA at 24 months.

Results: The mean pre-IVR BCVA was 0.59 ± 0.30 logMAR units and it improved to 0.36 ± 0.35 logMAR units after three month (P <0.005). The improvement was maintained at 24 months (0.35 ± 0.40 logMAR units, P <0.005). Of the 23 eyes, nine eyes (39.1 %) had IVR only once; mean number of injections was 2.2 ± 1.3 times at 24 months after the initial treatment. Stepwise regression analysis showed that the pre-IVR BCVA (standardized β =0.51, P<0.005) and CNV size (standardized β =0.46, P<0.005) significantly affected the BCVA after 24 months. The pre-IVR CNV location (juxtafoveal) was the only factor that affected the visual acuity improvement after 24 months (standardized β =0.54, P<0.05).

Conclusions: IVR with PRN therapy for mCNV led to a sustained visual improvement for 24 months after initial treatment. Good pre-IVR BCVA and smaller CNV size were significant prognostic factors that predicts better visual acuity. Patients with juxtafoveal CNV had better visual recovery than those with subfoveal CNV.

Keywords: 453 choroid: neovascularization • 605 myopia • 561 injection  
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