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Original Research

Choroidal thickness after intravitreal ranibizumab injections for choroidal neovascularization

, , , , , & show all
Pages 837-844 | Published online: 30 May 2012
 

Abstract

Purpose

To study changes in choroidal thickness with ranibizumab treatment for choroidal neovascularization (CNV).

Design

Prospective case series.

Methods

This prospective study consisted of 60 CNV-affected eyes of 60 patients treated with intravitreal injections of ranibizumab using an on-demand protocol after an initial loading phase. The eyes studied included 20 with age-related macular degeneration (AMD), 20 with polypoidal choroidal vasculopathy (PCV), and 20 with myopic CNV. In the eyes with AMD and PCV, choroidal thickness at the fovea was measured with optical coherence tomography using enhanced depth imaging. In eyes with myopic CNV, the choroidal thickness was measured using standard optical coherence tomography without the enhanced depth imaging technique.

Results

With ranibizumab treatment, central retinal thickness decreased significantly (P < 0.001) and visual acuity improved significantly (P < 0.001). However, central choroidal thickness (167.2 ± 108.3 μm) showed no significant change at 1 month after the loading phase (165.2 ± 107.8 μm, P = 0.120) or at final examination (164.8 ± 107.7 μm, P = 0.115). At baseline, central retinal thickness in eyes with AMD was significantly greater that those with PCV (P = 0.005) or high myopia (P = 0.029). However, central choroidal thickness in eyes with myopic CNV was significantly thinner than in eyes with AMD (P < 0.001) or PCV (P < 0.001). In each type of disease, there was no significant change in central choroidal thickness with ranibizumab treatment.

Conclusion

The effect of ranibizumab on the choroidal thickness is minimal, if any.

Acknowledgements

This study was supported in part by the Japan Society for the Promotion of Science (JSPS), Tokyo, Japan (Grant-in-Aid for Scientific Research, no 21592256), and by the Japan National Society for the Prevention of Blindness, Tokyo, Japan.

Contributions of the authors were as follows: Conception and design of the study (AAE, AT, NY); analysis and interpretation (AAE, AT, KO, SO, KY, AO, NY); writing of the article (AAE, AT); critical revision of the article (KO, SO, KY, AO, NY); final approval of the article (AAE, AT, KO, SO, KY, AO, NY); and data collection (AAE, AT, KO, SO, KY, AO).

The Institutional Review Board and Ethics Committee of Kyoto University approved this study, which adhered to the tenets of the Declaration of Helsinki. Written informed consent was obtained from each subject before examination.

Disclosure

The authors report no conflicts of interest in this work.