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本文引用的文献

1
Four-year outcome of aflibercept administration using a treat-and-extend regimen in eyes with recurrent neovascular age-related macular degeneration.阿柏西普治疗方案中采用“按需治疗和延长治疗间隔”方案治疗复发性新生血管性年龄相关性黄斑变性的四年疗效。
Jpn J Ophthalmol. 2021 Jan;65(1):69-76. doi: 10.1007/s10384-020-00783-8. Epub 2020 Nov 7.
2
A Trinity regimen with aflibercept for treatment-naïve neovascular age-related macular degeneration: 2-year outcomes.三联疗法联合阿柏西普治疗初治新生血管性年龄相关性黄斑变性:2 年结果。
Graefes Arch Clin Exp Ophthalmol. 2020 Aug;258(8):1663-1670. doi: 10.1007/s00417-020-04745-1. Epub 2020 May 21.
3
Two-Year Outcomes of Treat-and-Extend Intravitreal Aflibercept for Exudative Age-Related Macular Degeneration: A Prospective Study.阿柏西普玻璃体内注射治疗并延长给药方案用于湿性年龄相关性黄斑变性的两年疗效:一项前瞻性研究
Ophthalmol Retina. 2020 Aug;4(8):767-776. doi: 10.1016/j.oret.2020.03.010. Epub 2020 Mar 19.
4
Comparison of Two Different Treat-and-Extend Protocols with Aflibercept in Wet Age-Related Macular Degeneration: Two-Year Results.两种不同的阿柏西普治疗-扩展方案治疗湿性年龄相关性黄斑变性的比较:两年结果。
Adv Ther. 2020 May;37(5):2256-2266. doi: 10.1007/s12325-020-01312-2. Epub 2020 Apr 10.
5
Ranibizumab and Bevacizumab for Treatment of Neovascular Age-related Macular Degeneration: Two-Year Results.雷珠单抗和贝伐单抗治疗新生血管性年龄相关性黄斑变性:两年结果。
Ophthalmology. 2020 Apr;127(4S):S135-S145. doi: 10.1016/j.ophtha.2020.01.029.
6
Efficacy and Safety of Intravitreal Aflibercept Treat-and-Extend Regimens in Exudative Age-Related Macular Degeneration: 52- and 96-Week Findings from ALTAIR : A Randomized Controlled Trial.玻璃体内注射阿柏西普按需治疗方案治疗渗出性年龄相关性黄斑变性的疗效和安全性:ALTAIR 随机对照研究的 52 周和 96 周结果。
Adv Ther. 2020 Mar;37(3):1173-1187. doi: 10.1007/s12325-020-01236-x. Epub 2020 Feb 3.
7
Treatment Outcomes of Ranibizumab versus Aflibercept for Neovascular Age-Related Macular Degeneration: Data from the Fight Retinal Blindness! Registry.雷珠单抗与阿柏西普治疗新生血管性年龄相关性黄斑变性的疗效观察:来自 Fight Retinal Blindness! 注册研究的数据。
Ophthalmology. 2020 Mar;127(3):369-376. doi: 10.1016/j.ophtha.2019.10.006. Epub 2019 Oct 11.
8
Macular Atrophy in Neovascular Age-Related Macular Degeneration: A Randomized Clinical Trial Comparing Ranibizumab and Aflibercept (RIVAL Study).新生血管性年龄相关性黄斑变性的黄斑萎缩:比较雷珠单抗和阿柏西普的随机临床试验(RIVAL 研究)。
Ophthalmology. 2020 Feb;127(2):198-210. doi: 10.1016/j.ophtha.2019.08.023. Epub 2019 Aug 27.
9
Comparison of two different treat-and-extend protocols with aflibercept in wet age-related macular degeneration.比较湿性年龄相关性黄斑变性中两种不同的阿柏西普治疗和扩展方案。
Acta Ophthalmol. 2020 May;98(3):267-273. doi: 10.1111/aos.14231. Epub 2019 Aug 17.
10
Treat and extend versus pro re nata regimens of ranibizumab and aflibercept in neovascular age-related macular degeneration: a comparative study.雷珠单抗和阿柏西普治疗及延长给药方案与按需给药方案治疗新生血管性年龄相关性黄斑变性的比较研究
Graefes Arch Clin Exp Ophthalmol. 2019 Sep;257(9):1889-1895. doi: 10.1007/s00417-019-04404-0. Epub 2019 Jun 29.

用于评估新生血管性年龄相关性黄斑变性“治疗与延长”方案中决策制定的新型指标。

Novel metrics for evaluating decision making in a 'Treat and Extend' regimen for neovascular age related macular degeneration.

作者信息

McLeish Bethan, Morris Anna, Karpoor Meena, Babar Tehmoor, Narendran Niro, Yang Yit

机构信息

Ophthalmology Department, New Cross Hospital, Wolverhampton, WV10 0QP, UK.

School of Medicine, Cardiff University, University Hospital of Wales, Cardiff, UK.

出版信息

Eye (Lond). 2022 Oct;36(10):1994-1999. doi: 10.1038/s41433-021-01785-7. Epub 2021 Oct 12.

DOI:10.1038/s41433-021-01785-7
PMID:34642497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9500017/
Abstract

BACKGROUND

The primary aim was to investigate outcome of the decision making on duration of injection intervals between injection visits over the first 2 years of a treat and extend regimen.

METHOD

Consecutive patients receiving Aflibercept for treatment naïve neovascular age-related macular degeneration between 01.01.2016 and 15.07.2017 were identified from our departmental register. Retrospective data collected on all visits over 24 months were classified into three groups: (A) Without Interval Decision Events (IDE)" Injection only" (B) IDE resulting in injection intervals of <5 weeks and (C) IDE resulting in intervals of >5 weeks. The primary outcome was number of successful IDE relative to the total visits in Group C. Successful decision making was defined as absence of worsening of visual acuity (>5 L) or central retinal thickness (>50 microns) at the subsequent visit. Secondary visual and anatomical outcomes at 24 months were also evaluated.

RESULTS

Data from 56 eyes of 50 patients were included in the study. Visual acuity improved by +7.11 L at 24 months. Forty one patients with unilateral therapy made 721 visits: 280 visits (38.8%) were group A; 164 visits (22.8%) were group B and 277 visits (38.4%) were group C. Average interval in Group C was 8.9 weeks (range 5-15). The success rate of extension was 95.31% (264/277 visits).

CONCLUSION

These metrics for evaluating the decision making aspect of disease activity monitoring may be useful for monitoring performance and have given us a more realistic view and expectations of what can be achieved using this regime to optimise the timing of injections.

摘要

背景

主要目的是研究在治疗并延长方案的前2年中,关于注射就诊间隔时间的决策结果。

方法

从我们科室的登记册中识别出在2016年1月1日至2017年7月15日期间接受阿柏西普治疗初治新生血管性年龄相关性黄斑变性的连续患者。收集的24个月内所有就诊的回顾性数据分为三组:(A) 无间隔决策事件(IDE)“仅注射”;(B) IDE导致注射间隔小于5周;(C) IDE导致间隔大于5周。主要结局是C组中成功的IDE次数相对于总就诊次数。成功的决策定义为在随后的就诊中视力恶化不超过5行(>5 L)或中心视网膜厚度增加不超过50微米。还评估了24个月时的次要视觉和解剖学结局。

结果

研究纳入了50例患者的56只眼的数据。24个月时视力提高了7.11行。41例接受单侧治疗的患者进行了721次就诊:280次就诊(38.8%)属于A组;164次就诊(22.8%)属于B组;277次就诊(38.4%)属于C组。C组的平均间隔为8.9周(范围5 - 15周)。延长治疗的成功率为95.31%(264/277次就诊)。

结论

这些用于评估疾病活动监测决策方面的指标可能有助于监测治疗效果,并使我们对使用该方案优化注射时机所能取得的成果有更现实的认识和期望。