MACULAR CHORIORETINAL ATROPHY AND VISUAL OUTCOMES IN RANIBIZUMAB- OR AFLIBERCEPT-TREATED MYOPIC CHOROIDAL NEOVASCULARIZATION

阿柏西普 血管抑制剂 医学 眼科 脉络膜新生血管 自然科学 黄斑变性 视力 萎缩 贝伐单抗 外科 内科学 化疗
作者
Yu Kawashima,Masayuki Hata,Masahiro Miyake,Mami Kusaka,Akio Oishi,Sotaro Ooto,Hiroshi Tamura,Manabu Miyata,Akihito Uji,Naoko Ueda‐Arakawa,Ayako Takahashi,Akitaka Tsujikawa
出处
期刊:Retina-the Journal of Retinal and Vitreous Diseases [Lippincott Williams & Wilkins]
标识
DOI:10.1097/iae.0000000000003930
摘要

Abstract Purpose: To investigate the predictors of macular chorioretinal atrophy (CRA), consisting of patchy atrophy (PA) at the macula and choroidal neovascularization (CNV)-related macular atrophy (CNV-MA), during treatment with either ranibizumab or aflibercept for myopic CNV (mCNV) and its impact on visual outcomes. Methods: This retrospective study included 82 eyes with treatment-naïve mCNV who were treated with pro re nata injections of either ranibizumab or aflibercept. Results: Nine eyes (11.0%) presented with macular PA at baseline (PA group), and 73 eyes (89.0%) did not (non-PA group). VA improved during the first year in the non-PA group; a similar trend was noted in the PA group until 3 months after initial treatment. This improvement was maintained until 24 months ( P <0.001) in the non-PA group, but not in the PA group. In the PA group, macular CRA progressed faster ( P <0.0001), and CNV-MA was more frequent during the 2 years of treatments ( P =0.04). Even non-PA group eyes sometimes developed CNV-MA (42% at month 24) if they had a larger CNV and thinner subfoveal CT at baseline, resulting in poorer visual prognosis ( P <0.01). Conclusion: Macular PA at baseline was a risk factor for CNV-MA development and was associated with poor visual outcomes.
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