激光导航联合抗血管生成治疗视网膜分支静脉闭塞性黄斑水肿的疗效及安全性评价

P. L. Volodin, E. V. Ivanova, Yuliya I. Kukharskaya
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The combined method for the treatment of ME due to BRVO included the initial intravitreal injection of ranibizumab. 2 weeks after the injection, the patients carry out OCT, in the presence of central retinal thickness (CRT) more than 350 μm, 1 month after injection, one or more injections of ranibizumab were performed until the CRT reached 350 μm or less, when the «target» level was reached, combined navigation laser treatment was performed. Results. 1 month after the combined laser treatment, the best corrected visual acuity (BCVA) was 0.67±0.14 (on average), the CRT, on the average for the group, was 311.9 114.5 μm, the central retinal sensitivity was 22.3±1.6 dB. After 3 months, BCVA was 0.71±0.14, CRT was 289.9±110.5 μm, central retinal sensitivity was 22.8±1.6 dB. After 6 months, BCVA was 0.74±0.14, CRT was 236.5±107.6 μm, central retinal sensitivity was 23.1±1.5 dB. 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目的。目的:探讨抗血管生成治疗联合导航激光治疗BRVO合并MO的方法。材料和方法。本研究纳入99例BRVO所致ME患者,主组(n=54)采用联合治疗,对照组(n=45)采用雷尼单抗单药治疗。治疗BRVO所致ME的联合方法包括初始玻璃体内注射雷尼单抗。注射后2周,患者进行OCT检查,在视网膜中央厚度(CRT)大于350 μm的情况下,注射后1个月,进行1次或多次雷尼单抗注射,直到CRT达到350 μm以下,当达到“目标”水平时,进行联合导航激光治疗。结果:激光联合治疗1个月后,患者最佳矫正视力(BCVA)平均值为0.67±0.14,CRT平均值为311.9 114.5 μm,视网膜中央灵敏度为22.3±1.6 dB。3个月后,BCVA为0.71±0.14,CRT为289.9±110.5 μm,视网膜中央灵敏度为22.8±1.6 dB。6个月后,BCVA为0.74±0.14,CRT为236.5±107.6 μm,视网膜中央灵敏度为23.1±1.5 dB。在随访1年时,主组平均需要注射3.47±1.58针,对照组平均需要注射4.36±1.58针,BCVA和CRT的平均指标无显著差异。结论。导航联合激光治疗联合抗血管生成治疗视网膜分支静脉闭塞所致黄斑水肿的有效性和安全性已得到证实。组合激光技术的有效性在所有功能和形态计量参数中表现为正动态。该技术的安全性体现在没有明显的临床内、术后并发症。关键词:导航激光技术,微脉冲模式,视网膜静脉阻塞,黄斑水肿,抗血管生成治疗
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Evaluation of the efficacy and safety of navigational combined laser treatment in combination with antiangiogenic therapy in macular edema due to the branch retinal vein occlusion
Purpose. To study methods of using antiangiogenic therapy in combination with combined navigational laser treatment in patients with MO due to BRVO. Material and methods. The study included 99 patients with ME due to BRVO, the main group (n=54) consisted of patients treated using the combined technique, the control group – patients treated with ranibizumab monotherapy (n=45). The combined method for the treatment of ME due to BRVO included the initial intravitreal injection of ranibizumab. 2 weeks after the injection, the patients carry out OCT, in the presence of central retinal thickness (CRT) more than 350 μm, 1 month after injection, one or more injections of ranibizumab were performed until the CRT reached 350 μm or less, when the «target» level was reached, combined navigation laser treatment was performed. Results. 1 month after the combined laser treatment, the best corrected visual acuity (BCVA) was 0.67±0.14 (on average), the CRT, on the average for the group, was 311.9 114.5 μm, the central retinal sensitivity was 22.3±1.6 dB. After 3 months, BCVA was 0.71±0.14, CRT was 289.9±110.5 μm, central retinal sensitivity was 22.8±1.6 dB. After 6 months, BCVA was 0.74±0.14, CRT was 236.5±107.6 μm, central retinal sensitivity was 23.1±1.5 dB. At follow-up period of 1 year in the main group was required on average, 3.47±1.58 injections of ranibizumab for stabilization, in the control group, on average, 4.36±1.58 injections were required, the average indicators of BCVA and CRT significantly did not differ. Conclusion. Navigational combined laser treatment in combination with antiangiogenic therapy has shown its effectiveness and safety in the treatment of macular edema due to the branch retinal vein occlusion. The effectiveness of the combined laser technology is expressed in positive dynamics in all functional and morphometric parameters. The safety of the proposed technology is expressed in the absence of clinically significant intra- and postoperative complications. Key words: navigation laser technology, micropulse mode, retinal vein occlusion, macular edema, antiangiogenic therapy
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