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从其他抗血管内皮生长因子(VEGF)药物转换为玻璃体内注射阿柏西普治疗的新生血管性年龄相关性黄斑变性患者的长期结果

Long term results of patients with neovascular age-related macular degeneration switched from other anti-VEGF agents to intravitreal Aflibercept.

作者信息

Adrean Sean D, Knight Darren, Chaili Siyang, Ramkumar Hema L, Pirouz Ash, Grant Scott

机构信息

Retina Consultants of Orange County, 301 W. Bastanchury Ave #285, Fullerton, CA, 92835, USA.

University of California San Diego, Shiley Eye Institute, La Jolla, CA, 92093, USA.

出版信息

Int J Retina Vitreous. 2022 Feb 10;8(1):11. doi: 10.1186/s40942-022-00361-9.

DOI:10.1186/s40942-022-00361-9
PMID:35144686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8832635/
Abstract

BACKGROUND

This study explores the long term anatomic and functional results of patients who were switched to intravitreal aflibercept injections (IAI) after being initially managed with other anti-VEGF agents for neovascular age-related macular degeneration (nAMD).

METHODS

Patients with nAMD were included if they started with another anti-VEGF agent and were switched to IAI. Subjects had at least 3 years of consistent therapy with IAI and at least 1 injection quarterly.

RESULTS

Eighty-eight patients had at least 3 years of treatment while 58 of those patients, had at least 4 years of IAI. Average treatment time with other anti-VEGF agents was 32 months prior to switching. Baseline best corrected vision (VA) was 59.4 letters (20/70 + 2). At time of switch, VA increased significantly to 66.7 letters (20/50 + 2). At 3 months after switch, VA increased significantly to 69.0 (20/40-) letters. After 3 years of consistent IAI, vision was 67.5 letters (20/40-2), and for those patients that completed 4 years of therapy, the average VA was 66.0 letters (20/50 + 2), with a gain of 6.6 letters over baseline vision. 32.1% of patients gained 3 or more lines of vision. Initial central macular thickness (CMT) was 369 µm, which improved to 347 µm at time of switch, and further improved at 3 months to 301 µm and was maintained over time.

CONCLUSION

Patients switched to IAI can maintain vision over the long term. Patients treated on average for 5.7 years, had a visual gain of 8.1 letters after 3 years and 6.6 letters after 4 years of IAI therapy. CMT significantly improved following the switch and was maintained.

摘要

背景

本研究探讨了在最初使用其他抗血管内皮生长因子(VEGF)药物治疗新生血管性年龄相关性黄斑变性(nAMD)后转而接受玻璃体内注射阿柏西普(IAI)治疗的患者的长期解剖学和功能结果。

方法

纳入最初使用其他抗VEGF药物治疗后转而接受IAI治疗的nAMD患者。受试者接受IAI持续治疗至少3年,且每季度至少注射1次。

结果

88例患者接受治疗至少3年,其中58例患者接受IAI治疗至少4年。转而接受IAI治疗前,使用其他抗VEGF药物的平均治疗时间为32个月。基线最佳矫正视力(VA)为59.4个字母(20/70 +2)。转而接受IAI治疗时,VA显著提高至66.7个字母(20/50 +2)。转而接受IAI治疗3个月后,VA显著提高至69.0(20/40-)个字母。经过3年持续的IAI治疗后,视力为67.5个字母(20/40-2),对于完成4年治疗的患者,平均VA为66.0个字母(20/50 +2),比基线视力提高了6.6个字母。32.1%的患者视力提高了3行或更多行。初始中心黄斑厚度(CMT)为369μm,转而接受IAI治疗时改善至347μm,3个月时进一步改善至301μm,并随时间维持。

结论

转而接受IAI治疗的患者可长期维持视力。平均接受5.7年治疗的患者,在接受IAI治疗3年后视力提高了8.1个字母,4年后提高了6.6个字母。转而接受IAI治疗后CMT显著改善并维持。

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本文引用的文献

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Recurrence Rate of Choroidal Neovascularization in Neovascular Age-Related Macular Degeneration Managed with a Treat-Extend-Stop Protocol.采用治疗-延长-停药方案治疗的新生血管性年龄相关性黄斑变性中脉络膜新生血管的复发率
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Long-term outcomes of switching to aflibercept for treatment-resistant neovascular age-related macular degeneration.治疗抵抗性新生血管性年龄相关性黄斑变性患者转换为阿柏西普治疗的长期疗效。
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