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首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >The combination of intravitreal bevacizumab and phacoemulsification surgery in patients with cataract and coexisting diabetic macular edema.
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The combination of intravitreal bevacizumab and phacoemulsification surgery in patients with cataract and coexisting diabetic macular edema.

机译:玻璃体腔注射贝伐单抗联合超声乳化术治疗白内障合并糖尿病性黄斑水肿的患者。

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PURPOSE: The aim of this study was to assess the efficacy of phacoemulsification combined with intravitreal (i.v.t.) bevacizumab injection in diabetics with clinically significant macular edema (CSME) and cataract. METHODS: This retrospective study included diabetic patients with cataract and CSME who underwent phacoemulsification and intraocular lens implantation with a 2.5-mg bevacizumab i.v.t injection (ivBe) (15 eyes) or without ivBe (controls, 14 eyes). Best-corrected visual acuity (BCVA), central macular thickness (CMT) measured by optic coherence tomography (OCT), and adverse events were recorded. RESULTS: In the ivBe group, the OCT images demonstrated that CMT (mean +/- standard deviation [SD]) decreased significantly from 466 +/- 105 at baseline to 333 +/- 107, 313 +/- 138 and 333 +/- 111 microm at 4, 8, and 12 weeks, respectively, after treatment (P < 0.05). The visual acuity in logMAR (mean +/- SD) improved significantly from 1.66 +/- 0.39 at baseline to 1.30 +/- 0.50, 1.15 +/- 0.42, 0.99 +/- 0.48, and 1.03+/- 0.44 at 1, 4, 8, and 12 weeks, respectively, after treatment (P < 0.05). However, in the control group, the CMT changed insignificantly from 443 +/- 109 at baseline to 463 +/- 106, 425 +/- 128, and 421 +/- 119 microm at 4, 8 and 12 weeks, respectively after treatment (P > 0.05). The visual acuity in logMAR improved insignificantly from 1.63 +/- 0.42 at baseline to 1.43 +/- 0.53, and 1.39 +/- 0.43 at 1, and 4 weeks (P > 0.05) and significantly to 1.24 +/- 0.45 and 1.18 +/- 0.44 at 8 and 12 weeks, respectively, after treatment (P < 0.05). None of the patients in both groups experienced injection- or surgery-related complications or any obvious systemic adverse events. CONCLUSIONS: The short-term results suggest that phacoemulsification with i.v.t. bevacizumab safely reduces macular edema and improves visual acuity for cataract and CSME in diabetics.
机译:目的:本研究的目的是评估超声乳化联合玻璃体内(i.v.t.)贝伐单抗注射液对具有临床意义的黄斑水肿(CSME)和白内障的糖尿病患者的疗效。方法:这项回顾性研究包括患有白内障和CSME的糖尿病患者,这些患者接受了2.5毫克贝伐单抗静脉注射(ivBe)(15眼)或无ivBe(对照组,14眼)的超声乳化和人工晶状体植入。记录最佳矫正视力(BCVA),通过光学相干断层扫描(OCT)测量的中央黄斑厚度(CMT)和不良事件。结果:在ivBe组中,OCT图像显示CMT(平均+/-标准偏差[SD])从基线的466 +/- 105显着降低至333 +/- 107、313 +/- 138和333 + / -治疗后第4、8和12周分别为111微米(P <0.05)。 logMAR的视敏度(平均值+/- SD)从基线时的1.66 +/- 0.39显着提高到1时的1.30 +/- 0.50、1.15 +/- 0.42、0.99 +/- 0.48和1.03 +/- 0.44治疗后第4、8和12周(P <0.05)。然而,在对照组中,CMT在治疗后第4、8和12周分别从基线的443 +/- 109微小变化到463 +/- 106、425 +/- 128和421 +/- 119微米,变化不明显。 (P> 0.05)。 logMAR的视敏度从基线时的1.63 +/- 0.42显着提高至第1周和第4周的1.43 +/- 0.53和1.39 +/- 0.43(P> 0.05)并显着提高至1.24 +/- 0.45和1.18 +治疗后第8周和第12周分别为0.44(P <0.05)。两组患者均未出现与注射或手术相关的并发症或任何明显的全身性不良事件。结论:短期结果提示超声乳化术在静脉内。贝伐单抗可安全地减轻黄斑水肿,并改善糖尿病患者白内障和CSME的视力。

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