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首页> 外文期刊>International ophthalmology >The effect of combined treatment of bevacizumab and triamcinolone for diabetic macular edema refractory to previous intravitreal mono-injections
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The effect of combined treatment of bevacizumab and triamcinolone for diabetic macular edema refractory to previous intravitreal mono-injections

机译:贝伐单抗联合曲安奈德联合治疗对先前玻璃体内单次注射治疗难治的糖尿病性黄斑水肿的作用

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摘要

The purpose of this study is to evaluate the efficiency of combined treatment of bevacizumab and triamcinolone in refractory diffuse DME (DDME). Twenty-five pseudophakic eyes with DDME refractory to previous successive intravitreal bevacizumab (IVB, 1.25 and 2.5 mg/0.1 ml) and triamcinolone (IVT, 4 mg and 10 mg/0.1 ml) injections were included. The average number of injections was two (1–4). The mean best corrected visual acuity (BCVA) was 0.8 (0.3–1.5) logMAR before enrollment, 0.6 (0.0–1.5) logMAR at 6 months and 0.6 (0–1.8) logMAR at 12 months (p = 0.0001, p = 0.003). The median central macular thickness (CMT) of all the eyes was 575 (502–1049) μm at baseline, 370 (179–983) μm at 6 months, and 410 (198–929) μm at 12 months (p = 0.0001; p = 0.0001). At 6 months, the VA of 13 (52 %) patients was stabilized (± 0.2 logMAR of initial BCVA) and 12 (48 %) patients showed visual improvement (>0.2 logMAR). At 12 months, 10 (40 %) patients had stabilized vision, 13 (52 %) showed visual improvement and 2 (8 %) showed visual loss. At 6 months, 18 (72 %) patients showed anatomic stabilization (a decrease of 10 % to 50 % in initial CMT) and 7 (28 %) anatomical success (a decrease in CMT more than 50 % or ≤250 μm at final visit). At 12 months, 13 (52 %) patients showed anatomic stabilization, 10 (40 %) anatomic success, and 2 (8 %) anatomical failure (decrease in CMT less than 10 %). The combined application of IVB and triamcinolone may improve vision and decrease CMT in severe DDME cases refractory to previous monotherapies.
机译:这项研究的目的是评估贝伐单抗和曲安西龙联合治疗难治性弥漫性DME(DDME)的效率。包括二十五只具有前继连续玻璃体内贝伐珠单抗(IVB,1.25和2.5 mg / 0.1 ml)和曲安西龙(IVT,4 mg和10 mg / 0.1 ml)注射剂不能耐受的DDME的假晶状体眼。平均注射次数为两次(1-4)。入选前的平均最佳矫正视力(BCVA)为0.8(0.3–1.5)logMAR,6个月时为0.6(0.0–1.5)logMAR,而12个月时为0.6(0–1.8)logMAR(p = 0.0001,p = 0.003) 。基线时所有眼睛的中央黄斑中心厚度(CMT)为575(502–1049)μm,6个月时为370(179–983)μm,12个月时为410(198–929)μm(p = 0.0001; p = 0.0001)。在6个月时,13例(52%)患者的VA稳定(初始BCVA的±0.2 logMAR),12例(48%)患者的视力得到改善(> 0.2 logMAR)。在12个月时,有10位(40%)的患者视力稳定,有13位(52%)的患者视力得到改善,有2位(8%)的患者视力下降。在6个月时,有18名(72%)的患者表现出解剖学稳定(初始CMT下降10%至5​​0%)和7名(28%)的解剖学成功(最终访视时CMT下降超过50%或≤250μm) )。在12个月时,有13位(52%)的患者表现出解剖学稳定,10位(40%)的解剖学成功,2位(8%)的解剖学失败(CMT的下降小于10%)。 IVB和曲安奈德的联合应用可改善严重的DDME病例的视力,并降低CMT,而这些病例在以前的单药治疗中均无效。

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