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首页> 外文期刊>International ophthalmology >Six-month visual outcome after pars plana vitrectomy in proliferative diabetic retinopathy with or without a single preoperative injection of intravitreal bevacizumab.
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Six-month visual outcome after pars plana vitrectomy in proliferative diabetic retinopathy with or without a single preoperative injection of intravitreal bevacizumab.

机译:在有或无术前单次注射玻璃体内贝伐单抗的增生性糖尿病视网膜病变中,经平板玻璃体切除术后六个月的视觉结果。

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摘要

The purpose of this study is to evaluate the effect of a single preoperative injection of intravitreal bevacizumab (IVB) on visual outcome in patients undergoing pars plana vitrectomy (PPV) for proliferative diabetic retinopathy (PDR). Retrospective chart review of patients who underwent PPV for PDR and followed for at least 6 months after surgery. Patients who received a single IVB injection (1.25 mg in 0.05 ml) preoperatively were assigned to group A. Those who did not receive IVB were assigned to group B. The primary outcome measure was visual outcome at 6-month follow-up. The secondary outcomes were postoperative complications. At 6 months, visual acuity improved by at least 0.3 logMAR units in 70 (74.5 %) of the 94 eyes in group A versus 46 (52.9 %) of the 87 eyes in group B (p = 0.002). Postoperative vitreous hemorrhage occurred significantly less frequently in group A (6 eyes, 6.4 %) than in group B (14 eyes, 16.1 %; p = 0.037). The incidence of other postoperative complications did not differ significantly between the two groups. Preoperative use of bevacizumab improved the 6-month visual outcome in patients undergoing PPV for PDR and significantly reduced the occurrence of postoperative vitreous hemorrhage.
机译:这项研究的目的是评估术前单次玻璃体内贝伐单抗(IVB)注射对接受增殖性糖尿病性视网膜病变(PDR)的人行平板玻璃体切除术(PPV)的患者视觉效果的影响。回顾性图表回顾了接受PPV进行PDR且术后至少随访6个月的患者。术前接受单次IVB注射(1.25 mg在0.05 ml中)的患者被分配到A组。未接受IVB的患者被分配到B组。主要结局指标是随访6个月时的视觉结局。次要结果是术后并发症。在6个月时,A组94只眼中的70只(74.5%)的视敏度至少提高了0.3 logMAR单位,而B组87只眼中有46只(52.9%)的视敏度提高了(p = 0.002)。 A组(6眼,6.4%)的术后玻璃体出血发生率明显低于B组(14眼,16.1%; p = 0.037)。两组之间其他术后并发症的发生率无显着差异。术前使用贝伐单抗可改善接受PPV进行PDR的患者的6个月视觉效果,并显着减少术后玻璃体出血的发生。

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