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Intravitreal injection of bevacizumab combined with verteporfin photodynamic therapy for choroidal neovascularization in age-related macular degeneration.

机译:玻璃体内注射贝伐单抗联合维替泊芬光动力疗法治疗年龄相关性黄斑变性中的脉络膜新生血管。

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PURPOSE: To report the outcome for eyes treated with intravitreal injection of bevacizumab combined with verteporfin photodynamic therapy (PDT) for choroidal neovascularization (CNV) in age-related macular degeneration (AMD). STUDY DESIGN AND PARTICIPANTS: Interventional, consecutive, retrospective case series including 40 eyes of 40 patients with newly diagnosed juxtafoveal or subfoveal CNV secondary to AMD. METHODS: The charts of patients treated with a 1.25-mg intravitreal injection of bevacizumab followed by PDT within a 2-week period were reviewed. Main outcome measures were visual acuity stabilization (defined as no change or a gain in visual acuity) and need for retreatment. RESULTS: Thirty-three (83%) of 40 eyes had stabilization of visual acuity. Mean improvement in visual acuity was 1.73 lines. Twenty-six eyes (65%) required only a single intravitreal injection of bevacizumab combined with PDT. Of the 23 eyes with 12 months of follow-up, 17 (74%) had stabilization of visual acuity, while 9 (40%) had improvement in visual acuity (mean, 1.22 Snellen lines). Eleven eyes (48%) required only a single combined treatment for CNV resolution at the 12-month follow-up. Fifteen (88%) of 17 eyes with only 6 months of follow-up required only a single combined treatment. There were no complications such as endophthalmitis, uveitis, or ocular hypertension. CONCLUSION: These findings suggest that eyes treated with both intravitreal injection of bevacizumab and PDT require none to a minimal number of re-treatments to have stabilization of vision, even at 12 months of follow-up. Further investigation with large controlled trials is warranted to outline the appropriate treatment paradigm for combination therapy.
机译:目的:报告玻璃体腔注射贝伐单抗联合维替泊芬光动力疗法(PDT)治疗年龄相关性黄斑变性(AMD)的脉络膜新生血管(CNV)的结果。研究设计和参与者:介入性,连续性,回顾性病例系列,包括40例40眼新诊断为继发于AMD的近凹或凹下CNV的患者。方法:回顾了在两周内接受1.25 mg玻璃体腔注射贝伐单抗治疗并随后进行PDT治疗的患者图表。主要结局指标为视力稳定(定义为视力无变化或增加)和需要再次治疗。结果:40眼中有33眼(83%)的视力稳定。视力的平均改善为1.73线。二十六只眼睛(65%)仅需玻璃体腔注射贝伐单抗联合PDT。在随访12个月的23眼中,有17眼(74%)的视力稳定,而9眼(40%)的视力得到了改善(平均数为1.22 Snellen线)。在12个月的随访中,仅11眼(48%)仅需接受一次联合治疗即可解决CNV。仅进行了6个月的随访,在17只眼中有15只(88%)仅需要一次联合治疗。没有并发症,如眼内炎,葡萄膜炎或高眼压。结论:这些发现表明,玻璃体腔注射贝伐单抗和PDT治疗的眼睛,即使在随访的12个月内,也几乎不需要重新治疗即可恢复视力。有必要通过大型对照试验进行进一步研究,以概述适合联合治疗的治疗方案。

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