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Intravitreal bevacizumab (Avastin) treatment of proliferative diabetic retinopathy complicated by vitreous hemorrhage.

机译:玻璃体内贝伐单抗(Avastin)治疗并发玻璃体出血的增生性糖尿病视网膜病变。

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PURPOSE: To report the short-term anatomic and visual acuity response after intravitreal injection of bevacizumab (Avastin, Genentech) in patients with proliferative diabetic retinopathy complicated by vitreous hemorrhage. METHODS: Two patients with vitreous hemorrhage due to proliferative diabetic retinopathy were treated with at least one intravitreal injection of bevacizumab 1.25 mg in 0.05 mL. The patients underwent Snellen visual acuity testing, ophthalmoscopic examination, and fluorescein angiography at baseline and follow-up visits. RESULTS: Both patients had proliferative diabetic retinopathy with vitreous hemorrhage extensive enough to preclude panretinal photocoagulation. Following intravitreal injection of bevacizumab both patients experienced improvement in visual acuity starting within the first week. At 1 month of follow-up one patient had 2 lines of improvement in visual acuity and the other 5 lines. Each patient had regression of retinal neovascularization at 1 month of follow-up. Repeat injection was given to one patient at the 1-month follow-up because of slight leakage from neovascularization on the nerve, and to the other patient at 3 months because the retinal neovascularization showed early signs of reperfusion. The vitreous hemorrhage in each patient showed partial resolution at 1 week and nearly complete regression at 1 month. No adverse events were observed in either patient. CONCLUSIONS: Initial treatment results of patients with vitreous hemorrhage and proliferative diabetic retinopathy did not reveal any short-term safety concerns. Intravitreal bevacizumab resulted in marked regression of neovascularization and rapid resolution of vitreous hemorrhage. The favorable short-term results suggest further study is needed in a larger group of patients.
机译:目的:报道玻璃体腔内注射贝伐单抗(Avastin,Genentech)对增生性糖尿病视网膜病变并发玻璃体出血的患者的短期解剖和视敏度反应。方法:对两名因增生性糖尿病性视网膜病变而引起的玻璃体出血的患者,至少用一次玻璃体内注射0.05毫克贝伐单抗1.25 mg治疗。患者在基线和随访时接受了Snellen视力测试,检眼镜检查和荧光素血管造影。结果:两名患者均患有增生性糖尿病视网膜病变,并伴有玻璃体出血,足以阻止全视网膜光凝。玻璃体内注射贝伐单抗后,两个患者在第一周内均开始改善视力。随访1个月时,一名患者的视敏度改善了2线,其他5线。每例患者在随访1个月时视网膜新生血管消退。在1个月的随访中,由于神经新生血管轻微渗漏,对一名患者进行了重复注射;而在3个月,由于视网膜新生血管显示出早期的再灌注迹象,因此对另一名患者进行了重复注射。每例患者的玻璃体出血在1周时显示部分消退,在1月时几乎完全消退。两名患者均未观察到不良事件。结论:玻璃体出血和增生性糖尿病视网膜病变患者的初步治疗结果未显示任何短期安全性问题。玻璃体内贝伐单抗可导致新血管形成的明显消退和玻璃体出血的快速解决。短期的有利结果表明,需要对大量患者进行进一步研究。

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