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首页> 外文期刊>International ophthalmology >Corneal endothelial safety following subconjunctival and intrastromal injection of bevacizumab for corneal neovascularization
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Corneal endothelial safety following subconjunctival and intrastromal injection of bevacizumab for corneal neovascularization

机译:结膜下和基质内注射贝伐单抗治疗角膜新生血管后的角膜内皮安全性

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摘要

The purpose of this study is to determine the effect on endothelial cell density and morphology of combined subconjunctival and intracorneal injection of bevacizumab for the treatment of corneal neovascularization (NV). The charts and specular microscopy images of ten consecutive patients with corneal NV, who received combined subconjunctival? intracorneal injections of bevacizumab were reviewed. Patients received three injections of bevacizumab 25 mg/mL (1.25 mg/0.05 mL subconjunctival and 1.25 mg/0.05 mL intrastromal) 4-6 weeks apart. Endothelial cell counts (ECCs) and morphological changes were assessed by non-contact specular microscopy performed at baseline, 1 month after each injection and at 3 and 6 months after the last injection. There were no significant changes in ECCs (p = 0.663), coefficient of variation (p = 0.076), percentage of hexagonal cells (p = 0.931) or mean corneal thickness (p = 0.462) from pre-injection values to the 6-month follow-up values. There were no intraoperative or postoperative complications. In our series, the use of combined subconjunctival and intracorneal bevacizumab did not cause any decrease in ECCs or morphological alterations up to 6 months after the last of three injections. Further studies are required to confirm long-term safety in a larger sample population with longer follow-up, as well as the ideal dose, route of administration and frequency of bevacizumab administration.
机译:这项研究的目的是确定贝伐单抗联合结膜下和角膜内注射联合治疗角膜新生血管(NV)对内皮细胞密度和形态的影响。连续10例合并结膜下结膜的NV患者的图表和镜面显微镜图像。回顾了贝伐单抗的角膜内注射。患者间隔4-6周接受三剂25 mg / mL贝伐珠单抗(结膜下1.25 mg / 0.05 mL和基质内1.25 mg / 0.05 mL)注射。在基线,每次注射后1个月以及最后一次注射后3和6个月,通过非接触式镜面显微镜评估内皮细胞计数(ECCs)和形态变化。从注射前值到6个月,ECC(p = 0.663),变异系数(p = 0.076),六角形细胞百分比(p = 0.931)或角膜平均厚度(p = 0.462)均无显着变化。后续值。没有术中或术后并发症。在我们的系列中,结膜下和角膜内贝伐单抗联合使用在最后三次注射后的6个月内并未引起ECC降低或形态学改变。需要进行进一步的研究,以确认在更大样本量中具有更长随访时间的长期安全性,以及贝伐单抗的理想剂量,给药途径和给药频率。

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