Retina Service, Wills Eye Institute, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Am J Ophthalmol. 2012 Mar;153(3):468-473.e1. doi: 10.1016/j.ajo.2011.08.011. Epub 2011 Oct 11.
To evaluate the visual outcomes, number of injections, and direct medical cost of a treat-and-extend regimen in managing neovascular age-related macular degeneration with intravitreal bevacizumab.
Retrospective, interventional, consecutive case series.
Seventy-four eyes of 73 patients with treatment-naïve neovascular age-related macular degeneration from a single clinical practice were treated monthly with intravitreal bevacizumab until no intraretinal or subretinal fluid was observed on optical coherence tomography. The treatment intervals then were lengthened sequentially by 2 weeks until signs of exudation recurred and then were reduced accordingly to maintain an exudation-free macula. Main outcomes measured included mean change from baseline visual acuity, proportion of eyes losing fewer than 3 and gaining 3 or more Snellen visual acuity lines at 1 year of follow-up, annual mean number of injections, optical coherence tomography mean central retinal thickness change from baseline, mean maximum period of extension, adverse events, and mean direct annual medical cost.
The mean follow-up period was 1.41 years. Mean Snellen visual acuity improved from 20/230 at baseline to 20/109 at 12 months (P < .001) and 20/106 at 24 months (P < .001). The mean number of injections over the first year was 7.94. The mean optical coherence tomography central retinal thickness decreased from 316 to 239 μm at 12 months (P < .001). The mean direct medical cost over the first year was $3493.85.
Eyes with neovascular age-related macular degeneration experienced significant visual improvements on average when managed with intravitreal bevacizumab using a treat-and-extend regimen with fewer patient visits and injections along with lower costs compared with a fixed, monthly dosing regimen.
评估玻璃体内注射贝伐单抗治疗新生血管性年龄相关性黄斑变性的治疗方案,包括视力结果、注射次数和直接医疗成本。
回顾性、干预性、连续病例系列。
73 例初治新生血管性年龄相关性黄斑变性患者 74 只眼,每月接受玻璃体内注射贝伐单抗治疗,直至光学相干断层扫描(OCT)显示无视网膜内或视网膜下积液。然后,治疗间隔按每 2 周延长一次,直到出现渗出迹象,然后相应减少,以保持黄斑无渗出。主要观察指标包括:从基线视力的平均变化、1 年随访时视力丧失少于 3 行和增加 3 行或以上的眼比例、每年平均注射次数、从基线开始的 OCT 平均中央视网膜厚度变化、最长延长期的平均值、不良事件和每年的直接医疗成本。
平均随访时间为 1.41 年。平均 Snellen 视力从基线时的 20/230 提高到 12 个月时的 20/109(P<0.001)和 24 个月时的 20/106(P<0.001)。第一年的平均注射次数为 7.94 次。OCT 中央视网膜厚度从基线时的 316 μm 下降到 12 个月时的 239 μm(P<0.001)。第一年的直接医疗费用为 3493.85 美元。
与固定的每月剂量方案相比,使用玻璃体内注射贝伐单抗的治疗和延长方案治疗新生血管性年龄相关性黄斑变性可减少患者就诊次数和注射次数,降低成本,平均视力提高显著。