Chen Eric, Benz Matthew S, Fish Richard H, Brown David M, Wong Tien P, Kim Rosa Y, Major James C
Retina Consultants of Houston, The Methodist Hospital, Houston, TX, USA.
Clin Ophthalmol. 2010 Oct 28;4:1249-52. doi: 10.2147/OPTH.S14092.
The purpose of this study is to determine the efficacy of combining topical nepafenac with monthly intravitreal injections of ranibizumab or bevacizumab in the treatment of recalcitrant exudative macular degeneration.
This was a retrospective, consecutive case series of patients with exudative macular degeneration requiring maintenance therapy of antivascular endothelial growth factor ( anti-VEGF) injections at least every 6 weeks, who were started on topical nepafenac. Despite frequent anti-VEGF dosing, all patients included in the study had persistence of any combination of the following: intraretinal cysts, subretinal fluid, and/or pigment epithelial detachment. Patients underwent pinhole visual acuity, clinical exam, and optical coherence tomography (OCT) at baseline and every follow-up visit. Response to therapy was graded by reviewing quantitative and qualitative OCT data, and statistical analysis was done with paired Student's t-test.
Twenty-five patients (average age 77; 14 male and 11 female) were reviewed; the mean number of previous injections was 17.4 (range 3-31). Baseline mean visual acuity was 20/55, and final mean visual acuity after 3 months of treatment was 20/51 (P = 0.13). Monthly mean central foveal thickness measurements were 248, 250, 257, and 247 μm (P = 0.53) at baseline, 1, 2, and 3 months, respectively. By the end of the 3-month time point, qualitative OCT findings on 13 patients treated with nepafenac were classified as stable, 10 as better, and 2 as worse.
There was no significant change in visual acuity or quantitative OCT measurements, but there appeared to be a mild trend toward improved anatomy and qualitative OCT findings when topical nepafenac was added to monthly anti-VEGF injections in patients with persistent intraretinal cysts, subretinal fluid, and/or pigment epithelial detachment. Further prospective studies with longer follow-up may be warranted.
本研究旨在确定局部使用奈帕芬酸联合每月玻璃体内注射雷珠单抗或贝伐单抗治疗顽固性渗出性黄斑变性的疗效。
这是一项回顾性、连续性病例系列研究,研究对象为患有渗出性黄斑变性且需要至少每6周进行一次抗血管内皮生长因子(抗VEGF)注射维持治疗的患者,这些患者开始局部使用奈帕芬酸治疗。尽管频繁进行抗VEGF给药,但纳入研究的所有患者均存在以下任意组合情况:视网膜内囊肿、视网膜下液和/或色素上皮脱离。患者在基线时以及每次随访时均接受针孔视力、临床检查和光学相干断层扫描(OCT)。通过回顾定量和定性OCT数据对治疗反应进行分级,并采用配对学生t检验进行统计分析。
共纳入25例患者(平均年龄77岁;男性14例,女性11例);既往平均注射次数为17.4次(范围3 - 31次)。基线平均视力为20/55,治疗3个月后的最终平均视力为20/51(P = 0.13)。基线、1个月、2个月和3个月时中央凹平均厚度测量值分别为248、250、257和247μm(P = 0.53)。在3个月时间点结束时,接受奈帕芬酸治疗的13例患者的定性OCT检查结果分类为稳定,10例为改善,2例为恶化。
视力或定量OCT测量值无显著变化,但在患有持续性视网膜内囊肿、视网膜下液和/或色素上皮脱离的患者中,每月抗VEGF注射联合局部使用奈帕芬酸时,解剖结构和定性OCT检查结果似乎有轻微改善趋势。可能需要进行进一步的长期前瞻性研究。