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首页> 外文期刊>Graefe's archive for clinical and experimental ophthalmology: Albrecht von Graefes Archiv fur klinische und experimentelle Opthalmologie >Flare levels after intravitreal injection of ranibizumab, aflibercept, or triamcinolone acetonide for diabetic macular edema
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Flare levels after intravitreal injection of ranibizumab, aflibercept, or triamcinolone acetonide for diabetic macular edema

机译:玻璃纤维素,AfliBelcept或Triamcinolone丙酮苷术治疗糖尿病性黄斑水肿的眩光水平

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Purpose To evaluate anterior flare intensity (AFI) and central retinal thickness (CRT) values after intravitreal injection of aflibercept (IVA), ranibizumab (IVR), or triamcinolone acetonide (IVTA) in patients with diabetic macular edema (DME). Methods This research was conducted as a prospective study for patients with DME. Patients with phakia received either IVA or IVR, whereas patients with pseudophakia received IVA, IVR, or IVTA. AFI and CRT were measured using a laser flare meter and spectral domain optical coherence tomography, respectively, at days 0, 1, 7, 30, and 90. Results Forty patients with phakia and 60 patients with pseudophakia were enrolled this study. In the IVTA group, AFI of pseudophakic eyes was significantly decreased at days 1 ( p ?=?0.0487), 7 ( p ?=?0.0201), and 30 ( p ?=?0.0211). In the IVA group, AFI of phakic eyes was transiently increased at day 1 ( p ?=?0.0078) and returned to baseline at day 7, whereas no significant change was observed in AFI of pseudophakic eyes. In the IVR group, there was no significant change in AFI regardless of phakic condition. All groups showed significant reduction in CRT at day 7 and later. Conclusion DME improved after treatment by IVTA, IVR, or IVA, whereas AFI was reduced only in eyes treated with IVTA. The temporal profiles of AFI are likely related to differences in the pharmacological properties of the drugs.
机译:目的在患有糖尿病黄斑水肿(DME)患者中,评估术治疗AFLiBercept(IVA),Ranibizumab(IVR)或Triamcinolone乙酮(IVTA)后的术治疗术前眩光强度(AFI)和中央视网膜厚度(CRT)值。方法采用该研究作为DME患者的前瞻性研究。 Phakia患者接受IVA或IVR,而假脂酚患者接受IVA,IVR或IVTA。使用激光闪光表和光谱域光学相干断层扫描来测量AFI和CRT,在第0,1,7,30和90天。结果患有Phakia和60名患者的尖峰患者参加了这项研究。在IVTA组中,在第1天(P?= 0.0487),7(P?= 0.0221)和30(P?= 0.0211),AFI的初级眼睛的AFI显着降低。在IVA组中,在第1天(P?= 0.0078)并在第7天返回基线,近期诊断眼睛瞬时增加,而在伪眼睛的AFI中没有显着变化。在IVR组中,无论phakic条件如何,AFI都没有显着变化。所有基团在第7天及以后显示CRT显着减少。结论DME通过IVTA,IVR或IVA治疗后改善,而AFI仅在用IVTA治疗的眼中降低。 AFI的时间谱可能与药物药理性质的差异有关。

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