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Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for?standard collagen cross-linking

机译:圆锥角膜患者中标准与跨上皮胶原交联适用于标准胶原交联

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Purpose: Evaluating the clinical results of trans-epithelial collagen cross-linking (CXL) and standard CXL in patients with progressive keratoconus.Methods: This prospective study comprised 20 eyes of 20 patients with progressive keratoconus. Ten eyes were treated by standard CXL and ten by trans-epithelial cross-linking (TE-CXL, epithelium on) with 1?year of follow-up. All patients underwent complete ophthalmologic testing that included pre- and postoperative uncorrected visual acuity, corrected visual acuity, spherical error, spherical equivalent, corneal astigmatism, simulated maximum, minimum, and average keratometry, coma and spherical aberration, optical pachymetry, and endothelial cell density. Intra- and postoperative complications were recorded. The solution used for standard CXL comprised riboflavin 0.1% and dextran 20.0% (Ricrolin), while the solution for TE-CXL (Ricrolin, TE) comprised riboflavin 0.1%, dextran 15.0%, trometamol (Tris), and ethylenediaminetetraacetic acid. Ultraviolet-A treatment was performed with UV-X System at 3?mW/cm2.Results: In both the standard CXL group (ten patients, ten eyes; mean age, 30.4±7.3?years) and the TE-CXL group (ten patients, ten eyes; mean age, 28±3.8?years), uncorrected visual acuity and corrected visual acuity improved significantly after treatment. Furthermore, a significant improvement in topographic outcomes, spherical error, and spherical equivalent was observed in both groups at month 12 posttreatment. No significant variations were recorded in other parameters. No complications were noted.Conclusion: A 1-year follow-up showed stability of clinical and refractive outcomes after standard CXL and TE-CXL.
机译:目的:评估渐进性圆锥角膜患者经上皮胶原交联(CXL)和标准CXL的临床结果。方法:这项前瞻性研究包括20例渐进性圆锥形角膜患者的20只眼。随访1年,用标准CXL治疗10眼,经上皮交联(TE-CXL,上皮)治疗10眼。所有患者均接受了完整的眼科检查,包括术前和术后未矫正的视力,矫正的视力,球差,球镜当量,角膜散光,模拟的最大,最小和平均角膜曲率法,昏迷和球差,光学测厚法以及内皮细胞密度。记录术中和术后并发症。用于标准CXL的溶液包含0.1%的核黄素和20.0%的右旋糖酐(Ricrolin),而用于TE-CXL的溶液(Ricrolin,TE)包含的核黄素0.1%,右旋糖酐15.0%,曲美他莫(Tris)和乙二胺四乙酸。结果:在标准CXL组(十名患者,十只眼睛;平均年龄30.4±7.3?岁)和TE-CXL组(十名)中,UV-X系统以3?mW / cm2进行紫外线A治疗。患者,十只眼睛;平均年龄为28±3.8岁),未矫正视力和矫正视力在治疗后明显改善。此外,在治疗后的第12个月,两组患者均观察到了地形结果,球面误差和球面等效量的显着改善。其他参数没有记录到显着变化。结论:标准CXL和TE-CXL术后1年随访显示临床和屈光结果稳定。

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