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Three treatments for macular edema because of branch retinal vein occlusion: Intravitreous bevacizumab or tissue plasminogen activator, and vitrectomy

机译:因视网膜分支静脉阻塞而引起的黄斑水肿的三种治疗方法:玻璃体内贝伐单抗或组织纤溶酶原激活剂和玻璃体切割术

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Purpose: To evaluate the effectiveness of intravitreous bevacizumab (Avastin), intravitreous tissue plasminogen activator, and vitrectomy for the macular edema secondary to branch retinal vein occlusion. Methods: Retrospective, interventional case series. We studied 228 eyes of 228 patients. Forty-one eyes received 1.25 mg of intravitreous bevacizumab, 71 eyes received tissue plasminogen activator, and 116 eyes underwent vitrectomy. A reinjection of 1.25 mg of bevacizumab was based on the morphologic and functional findings. The main outcome measures were the best-corrected visual acuity and optical coherence tomography-determined foveal thickness. Results: The mean postoperative follow-up period was 32.2 months with a range of 12 months to 69 months. The mean number of intravitreous bevacizumab was 2.8 with a range of 1 to 5. The mean best-corrected visual acuity and foveal thickness significantly improved after all 3 treatments, and the differences in the best-corrected visual acuity between the 3 groups were not significant at 12 months. Fourteen eyes (34%) in the intravitreous bevacizumab group and 21 eyes (30%) in the tissue plasminogen activator group required additional surgeries. Conclusion: The 3 treatments appear to provide similar visual outcomes at 12 months. However, in some eyes treated with intravitreous bevacizumab or tissue plasminogen activator, additional surgeries were required, and a longer follow-up period was required to determine the final outcome.
机译:目的:评估玻璃体内贝伐单抗(Avastin),玻璃体内组织纤溶酶原激活剂和玻璃体切除术对继发于视网膜分支静脉阻塞的黄斑水肿的疗效。方法:回顾性,介入性病例系列。我们研究了228例患者的228眼。 41只眼接受了1.25mg玻璃体内贝伐单抗治疗,71只眼接受了组织纤溶酶原激活剂,116眼接受了玻璃体切割术。根据形态和功能发现,再注射1.25 mg贝伐单抗。主要结局指标为最佳矫正视力和光学相干断层扫描确定的中央凹厚度。结果:术后平均随访时间为32.2个月,范围为12个月至69个月。玻璃体内贝伐单抗的平均数为2.8,范围为1到5。在全部3种治疗后,平均最佳矫正视力和中央凹厚度均显着改善,而3组之间的最佳矫正视力差异不显着在12个月时。玻璃体内贝伐单抗组有14眼(34%),组织纤溶酶原激活剂组有21眼(30%)需要额外的手术。结论:这三种治疗在12个月时似乎提供相似的视觉效果。但是,在某些接受玻璃体内贝伐单抗或组织纤溶酶原激活剂治疗的眼睛中,需要进行其他手术,并且需要更长的随访时间才能确定最终结果。

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