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The results of intravitreal bevacizumab injections for persistent neovascularizations in proliferative diabetic retinopathy after photocoagulation therapy.

机译:玻璃体腔注射贝伐珠单抗治疗光凝治疗后增生性糖尿病视网膜病变持续性新生血管形成的结果。

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PURPOSE: The purpose of this study was to evaluate the effectiveness of intravitreal bevacizumab on persistent retinal neovascularizations in proliferative diabetic retinopathy. METHODS: Thirty-three eyes of 24 patients (mean age, 52.75 +/- 8.2 years) with proliferative diabetic retinopathy showing recurrences or no regressions in neovascularizations were evaluated in this study. After the intravitreal injection of 1.25 mg/0.05 mL of bevacizumab, the first examination was performed within 3 days and repeated at 1 week, 1 month, 3 months, and 6 months. In these examinations, localization and dimensions of neovascularizations were evaluated with red-free photographs and/or fluorescein angiography. RESULTS: All patients had type II diabetes for a period of 12 +/- 4.4 years (range, 2-20 years). After a single dose of bevacizumab, complete resolution rate of neovascularizations was 78.8% at 1 month, 63.6% at 3 months, and 45.4% at 6 months. When evaluated together with 9 eyes that had a second injection at 3 months, the complete resolution rate was 60.6% at 6 months. Mean best-corrected visual acuity and macular volume were 1.06 logarithm of the minimum angle of resolution (20/225 in Snellen) and 11.65 mm3 before treatment. Six months after treatment, these were 0.73 logarithm of the minimum angle of resolution (20/108 in Snellen) and 8.92 mm3 (P = 0.048 and 0.003, respectively). CONCLUSION: Bevacizumab can be used safely and successfully in patients with proliferative diabetic retinopathy who do not experience any resolution or experience recurrences after panretinal photocoagulation.
机译:目的:本研究的目的是评估玻璃体内贝伐单抗在增生性糖尿病视网膜病变中对持续性视网膜新血管形成的有效性。方法:本研究评估了24例增生性糖尿病视网膜病变复发或无消退的24例患者(平均年龄52.75 +/- 8.2岁)的33眼。玻璃体内注射1.25 mg / 0.05 mL贝伐单抗后,第一次检查在3天内进行,并在1周,1个月,3个月和6个月时重复进行。在这些检查中,使用无红照片和/或荧光素血管造影术评估新血管形成的位置和尺寸。结果:所有患者均患有II型糖尿病,病程为12 +/- 4.4年(2-20年)。单次服用贝伐单抗后,新血管形成的完全缓解率在1个月时为78.8%,在3个月时为63.6%,在6个月时为45.4%。与在3个月时进行第二次注射的9只眼睛一起评估时,在6个月时,完全分辨率为60.6%。最佳矫正视力和黄斑体积的平均值是治疗前最小分辨角的1.06对数(Snellen中为20/225)和11.65 mm3。治疗六个月后,它们分别是最小分辨角的0.73对数(Snellen中为20/108)和8.92 mm3(分别为P = 0.048和0.003)。结论:贝伐单抗可以安全,成功地用于全视网膜光凝后无任何缓解或复发的增生性糖尿病视网膜病变患者。

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