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首页> 外文期刊>Retina >Intravitreous injection of bevacizumab, tissue plasminogen activator, and gas in the treatment of submacular hemorrhage in age-related macular degeneration.
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Intravitreous injection of bevacizumab, tissue plasminogen activator, and gas in the treatment of submacular hemorrhage in age-related macular degeneration.

机译:玻璃体腔注射贝伐单抗,组织纤溶酶原激活剂和气体治疗与年龄相关的黄斑变性的黄斑下出血。

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摘要

PURPOSE: To investigate the benefit of adding bevacizumab to intravitreal recombinant tissue plasminogen activator (rTPA) and gas as initial therapy in subretinal hemorrhage and choroidal neovascularization because of age-related macular degeneration. METHODS: Thirty-eight consecutive patients with recent (1-31 days) subretinal hemorrhage who were treated with intravitreal rTPA and gas (26 patients) or with intravitreal bevacizumab, rTPA, and gas (12 patients) were included in this retrospective analysis. In all patients, a standardized antivascular endothelial growth factor therapy was followed. Testing of best-corrected visual acuity, biomicroscopy, and fundus examination were performed at 4 weeks and 7 months. RESULTS: The mean pretreatment best-corrected visual acuity in the rTPA/gas group was 0.08 +/- 0.09 and 0.12 +/- 0.13 in the bevacizumab/rTPA/gas group. After 4 weeks, it was significantly higher in the bevacizumab/rTPA/gas group (0.25 +/- 0.26) than in the rTPA/gas (0.08 +/- 0.1) group (P < 0.05). Also, after 7 months, best-corrected visual acuity was significantly higher in the bevacizumab/rTPA/gas group (0.07 +/- 0.07 vs. 0.24 +/- 0.35; P < 0.05). Reading vision could be restored in 0% (rTPA/gas) versus 50% (bevacizumab/rTPA/gas). Stabilization (0 +/- 2 lines) or improvement of best-corrected visual acuity was obtained in 62% (rTPA/gas) versus 84% (bevacizumab/rTPA/gas). CONCLUSION: From our retrospective pilot study, there is a strong indication that the addition of intravitreal bevacizumab is safe and superior to the displacement of submacular hemorrhages alone with rTPA and gas.
机译:目的:探讨将贝伐单抗添加到玻璃体内重组组织纤溶酶原激活剂(rTPA)和气体中作为初期治疗因年龄相关性黄斑变性而引起的视网膜下出血和脉络膜新血管形成的益处。方法:本回顾性分析纳入了连续38例近期(1-31天)视网膜下出血的患者,这些患者接受玻璃体内rTPA和气体治疗(26例)或玻璃体内贝伐单抗,rTPA和气体治疗(12例)。在所有患者中,均遵循标准化的抗血管内皮生长因子疗法。在第4周和第7个月进行了最佳矫正视力检查,生物显微镜检查和眼底检查。结果:rTPA /气组的平均预处理最佳矫正视力为0.08 +/- 0.09,贝伐单抗/ rTPA /气组的平均视力为0.12 +/- 0.13。 4周后,贝伐单抗/ rTPA /气体组(0.25 +/- 0.26)显着高于rTPA /气体(0.08 +/- 0.1)组(P <0.05)。同样,在7个月后,贝伐单抗/ rTPA /气体组的最佳矫正视力明显更高(0.07 +/- 0.07对0.24 +/- 0.35; P <0.05)。可以将阅读视力恢复为0%(rTPA /气体)和50%(贝伐单抗/ rTPA /气体)。相对于84%(贝伐单抗/ rTPA /气体),稳定度(0 +/- 2行)或最佳矫正视敏度得到改善(62%(rTPA /气体))。结论:从我们的回顾性先导研究中,有一个强有力的迹象表明,玻璃体腔注射贝伐单抗是安全的,并且优于单纯使用rTPA和气体置换黄斑下出血。

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