A Randomized Pilot Study of Low-Fluence Photodynamic Therapy Versus Intravitreal Ranibizumab for Chronic Central Serous Chorioretinopathy

被引:81
作者
Bae, So Hyun [1 ,2 ]
Heo, Jang Won [1 ,2 ]
Kim, Cinoo [2 ,3 ]
Kim, Tae Wan [1 ,4 ]
Lee, Joo Yong [5 ]
Song, Su Jeong [6 ]
Park, Tae Kwann [7 ]
Moon, Sang Woong [8 ]
Chung, Hum [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Ophthalmol, Seoul 110744, South Korea
[2] Seoul Natl Univ Hosp, Dept Ophthalmol, Seoul 110744, South Korea
[3] Incheon Med Ctr, Dept Ophthalmol, Inchon, South Korea
[4] Seoul Natl Univ, Boramae Med Ctr, Dept Ophthalmol, Seoul 110744, South Korea
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Ophthalmol, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Dept Ophthalmol, Kangbuk Samsung Hosp, Seoul, South Korea
[7] Soonchunhyang Univ, Coll Med, Dept Ophthalmol, Puchon, South Korea
[8] Kyung Hee Univ, Sch Med, Dept Ophthalmol, Seoul, South Korea
关键词
HALF-DOSE VERTEPORFIN; MACULAR THICKNESS MEASUREMENTS; INDOCYANINE GREEN ANGIOGRAPHY; FOLLOW-UP; BEVACIZUMAB; PATHOGENESIS;
D O I
10.1016/j.ajo.2011.04.008
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To report 6-month outcomes of a prospective, randomized study comparing the efficacy and safety between low-fluence photodynamic therapy (PDT) and intravitreal injections of ranibizumab in the treatment of chronic central serous chorioretinopathy. DESIGN: Prospective, randomized, single-center pilot study. METHODS: Sixteen eyes with chronic central serous chorioretinopathy were randomized to receive either low-fluence PDT or intravitreal injections of ranibizumab: 8 eyes in the low-fluence PDT group and 8 in the ranibizumab group. Rescue treatment was considered if subretinal fluid was sustained after completion of primary treatment: low-fluence PDT for the ranibizumab group and ranibizumab injection for the low-fluence PDT group. Main outcome measures were excess foveal thickness, resolution of subretinal fluid, choroidal perfusion on indocyanine green angiography, and best-corrected visual acuity. RESULTS: At 3 months, the mean excess foveal thickness was reduced from 74.1 +/- 56.0 mu m to -35.4 +/- 44.5 pm in the low-fluence PDT group (P = .017) and from 26.3 +/- 50.6 mu m to -23.1 +/- 56.5 mu m in the ranibizumab group (P = .058). After a single session of PDT, 6 eyes (75%) in the low-fluence PDT group achieved complete resolution of subretinal fluid and reduction of choroidal hyperpermeability, whereas 2 (25%) eyes in the ranibizumab group achieved this after consecutive ranibizumab injections. Four eyes (50%) in the ranibizumab group underwent additional low-fluence PDT and accomplished complete resolution. At 3 months, significant improvement of best-corrected visual acuity was not demonstrated in the low-fluence PDT group (P = .075), whereas it was observed in the ranibizumab group (P = .012). However, the tendency toward improvement of best-corrected visual acuity was not maintained. CONCLUSIONS: In terms of anatomic outcomes, the effect of ranibizumab injections was not promising compared with that of low-fluence PDT. (Am J Ophthalmol 2011;152:784-792. (C) 2011 by Elsevier Inc. All rights reserved.)
引用
收藏
页码:784 / 792
页数:9
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