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Long-term follow-up for type 1 (subretinal pigment epithelium) neovascularization using a modified 'treat and extend' dosing regimen of intravitreal antivascular endothelial growth factor therapy.

机译:使用改良的玻璃体腔内抗血管内皮生长因子治疗的“治疗和扩展”给药方案对1型(视网膜下色素上皮)新血​​管形成进行长期随访。

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PURPOSE: The purpose of the study was to analyze long-term outcomes for the treatment of type 1 (subretinal pigment epithelium) neovascularization using a modified "treat and extend" antivascular endothelial growth factor dosing regimen. METHODS: We performed a retrospective, noncomparative analysis of visual acuity, funduscopic, and optical coherence tomography data for 18 eyes of 16 consecutive patients with newly diagnosed type 1 neovascularization treated with intravitreal bevaci-zumab and/or ranibizumab with at least 24-month follow-up. Three monthly injections were followed by continued treatment at intervals increasing by 2 weeks per visit to a maximum of 10 weeks. The interval was shortened if clinical or optical coherence tomography evidence of recurrent fluid at the foveola or increased extrafoveolar fluid was detected. RESULTS: Median baseline logarithm of the minimum angle of resolution visual acuity was 0.53 (20/69 Snellen equivalent) and remained stable at 24 months (logarithm of the minimum angle of resolution 0.52, P = 0.84) after an average of 12 injections (range, 8-19 injections) and at 36 months (logarithm of the minimum angle of resolution 0.52, P = 0.68) after an average of 20 injections (range, 18-25 injections). Although most eyes (15 of 18 [83%]) continued to manifest extrafoveolar subretinal fluid throughout the course of treatment, only 1 eye developed geographic atrophy overlying the areas of choroidal neovascularization. During a cumulative observation period of 540 months, no eyes developed a sight-threatening submacular hemorrhage. CONCLUSION: A modified "treat and extend" dosing regimen of intravitreal antivascular endothelial growth factor therapy reduces the need for monthly visits and imaging and allows for stable long-term visual acuity in eyes with type 1 neovascularization.
机译:目的:本研究的目的是使用改良的“治疗和扩展”抗血管内皮生长因子给药方案来分析治疗1型(视网膜下色素上皮)新血​​管形成的长期结果。方法:我们对玻璃体腔注射贝伐单抗和/或兰尼单抗治疗的连续16例新诊断为1型新生血管的连续患者的18眼进行了回顾性,非对比性视力,眼底镜和光学相干断层扫描数据,随访至少24个月-向上。每月进行3次注射,然后以每次就诊增加2周的间隔持续治疗,最多10周。如果临床或光学相干断层扫描的证据表明黄斑中心凹处复发性液体或黄斑中心凹液增多,则可缩短间隔。结果:平均12次注射(范围)后,最小分辨力视敏度的中位数基线对数为0.53(20/69 Snellen当量),并在24个月(最小分辨力对角数的对数0.52,P = 0.84)保持稳定,8-19次注射)和平均20次注射(18-25次注射)后36个月(最小分辨角0.52的对数,P = 0.68)。尽管在整个治疗过程中,大多数眼睛(18只中的15只[83%])在整个治疗过程中均继续表现为视网膜中央凹,但只有1只眼出现了覆盖于脉络膜新血管形成区域的地理萎缩。在540个月的累积观察期内,没有眼睛出现威胁视力的黄斑下出血。结论:改良的玻璃体腔内抗血管内皮生长因子治疗的“治疗和扩展”给药方案减少了每月检查和影像检查的需要,并为1型新血管形成的眼睛提供了稳定的长期视力。

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