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Efficacy and safety of one intravitreal injection of bevacizumab in diabetic macular oedema

机译:一剂贝伐单抗玻璃体内注射治疗糖尿病性黄斑水肿的疗效和安全性

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Purpose: To assess the efficacy, duration of effect and safety of one intravitreal injection of bevacizumab in diabetic macular oedema (DMO). Methods: Bevacizumab (1 mg/0.04 ml) was injected intravitreally into eyes with DMO (29 with and nine without previous treatments). Best corrected visual acuity (BCVA), intraocular pressure and central retinal thickness (CRT) were measured; slit-lamp examination, macular biomicroscopy, optical coherence tomography and fluorescein angiography were performed before and at 2-4, 8 and 12 weeks post-injection. Best corrected VA and CRT were analysed in both groups.Results: In the non-pretreated group, mean BCVA improved from 0.76 +- 0.33 (baseline) to 0.57 +- 0.30 and 0.54 +- 0.27 at 2-4 weeks and 8 weeks post-injection, respectively (p = 0.02, p = 0.014, paired t-test). Mean CRT decreased from 632.4 +- 196.0 mu (baseline) to 392.3 +- 113.6 /an and 370.4 +- 141.7 mum at the same time-points, respectively (p = 0.01, p = 0.01). There was no difference in BCVA or CRT at 12 weeks. In the pretreated group, mean BCVA improved from 0.62 +- 0.30 (baseline) to 0.53 +- 0.33 at 2-4 weeks post-injection (p = 0.01), and mean CRT decreased from 583.9 +- 180.7 mum (baseline) to 404.1 +- 197.9 mum at 2-4 weeks post-injection (p < 0.001). Mean BCVA was unchanged at 8 weeks and 12 weeks post-injection, although mean CRT remained lower at 8 weeks (p = 0.004). No ocular or systemic side-effects developed during follow-up. Conclusions: One intravitreal injection of bevacizumab for DMO seems to be effective and safe in both eyes that have been treated previously and eyes that have not. The therapeutic effect is temporary and repeat treatment may be needed.
机译:目的:评估一剂贝伐单抗玻璃体内注射治疗糖尿病性黄斑水肿(DMO)的疗效,作用持续时间和安全性。方法:将贝伐单抗(1 mg / 0.04 ml)玻璃体腔注射DMO(29例有9例未经治疗)。测量最佳矫正视力(BCVA),眼压和视网膜中央厚度(CRT);在注射后和注射后2-4周,8周和12周进行裂隙灯检查,黄斑部生物显微镜检查,光学相干断层扫描和荧光素血管造影。结果:在非预处理组中,在2-4周和8周后,平均B​​CVA从0.76±0.33(基线)提高到0.57±0.30和0.54±0.27。 -注射(p = 0.02,p = 0.014,配对t检验)。在相同的时间点,平均CRT分别从632.4±196.0 mu(基线)降低到392.3±113.6 / an和370.4±141.7 m(p = 0.01,p = 0.01)。 12周时BCVA或CRT无差异。在预处理组中,平均BCVA在注射后2-4周从0.62±0.30(基线)提高到0.53±0.33(p = 0.01),平均CRT从583.9±180.7妈妈(基线)降低到404.1注射后2-4周时±197.9妈(p <0.001)。注射后第8周和第12周,平均BCVA保持不变,尽管第8周的平均CRT仍较低(p = 0.004)。随访期间未出现眼部或全身性副作用。结论:玻璃体腔注射贝伐单抗用于DMO在既往治疗过的眼睛和未曾治疗过的眼睛中似乎都是有效和安全的。治疗效果是暂时的,可能需要重复治疗。

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