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Outcomes of LASIK for Myopia or Myopic Astigmatism Correction with the FS200 Femtosecond Laser and EX500 Excimer Laser Platform

机译:FS200飞秒激光和EX500准分子激光平台用于近视或近视散光矫正的LASIK结果

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Purpose:To evaluate the efficacy, predictability, stability and safety of laser in situ keratomileusis (LASIK) using the FS200 femtosecond laser and EX500 excimer laser platform.Methods:The outcomes of 254 eyes of 129 consecutive patients with myopia or myopic astigmatism who underwent full correction femtosecond laser-assisted LASIK at CMU LASIK Center were assessed. Pre-operative and post-operative parameters including manifest refraction, Uncorrected Distance Visual Acuity (UDVA), Best Corrected Distance Visual Acuity (BDVA), corneal topography and tomography were analyzed. The results between low to moderate myopia and high myopia were compared up to 12 months.Results:Mean pre-operative Spherical Equivalent (SE) was -5.15±2.41 Diopters (D) (range -0.50 to -11.50 D) and -0.13±0.28 D, -0.13±0.27 D, -0.13±0.28 D and -0.14±0.30 D at 1, 3, 6, and 12 months, post-operatively. At 12 months, the propor?tion of eyes achieving UDVA ≥ 20/20 was 90.0% and ≥20/40 was 98.8%. The proportion of eyes achieving post-operative mean SE ±0.5 D, and ±1 D was 91.3%, and 98.5%. No eyes lost more than two lines of BDVA. The low to moderate myopic group had a statistically significant better UDVA at one (p=0.017) and three months (p=0.014) but no difference at six (p=0.061) and 12 months (p=0.091). The mean post-operative SE was better in low to moderate myopic group at every follow-up visit (p=0.001, 0.007, 0.001 and 0.001).Conclusion:One-year clinical results of LASIK with the FS200 femtosecond laser and EX500 excimer laser showed high efficacy, predictability, stability and safety.
机译:目的:通过FS200飞秒激光和EX500准分子激光平台评估激光原位角膜磨镶术(LASIK)的疗效,可预测性,稳定性和安全性。评估了CMU LASIK中心的飞秒激光辅助LASIK矫正。分析了术前和术后参数,包括明显屈光度,未矫正远视力(UDVA),最佳矫正远视力(BDVA),角膜地形图和断层扫描。比较了中低度近视和高度近视之间长达12个月的结果。结果:术前平均球镜当量(SE)为-5.15±2.41屈光度(D)(范围-0.50至-11.50 D)和-0.13±术后1、3、6和12个月分别为0.28 D,-0.13±0.27 D,-0.13±0.28 D和-0.14±0.30D。在12个月时,达到UDVA≥20/20的眼睛比例为90.0%,≥20/ 40的眼睛比例为98.8%。达到术后平均SE±0.5 D和±1 D的眼睛比例分别为91.3%和98.5%。没有眼睛损失超过两行BDVA。低度至中度近视组的UDVA在一个月(p = 0.017)和三个月(p = 0.014)时有统计学上的显着改善,但在六个月(p = 0.061)和12个月(p = 0.091)时无差异。低至中度近视组的每次术后随访平均SE较好(p = 0.001、0.007,<0.001和<0.001)。结论:FS200飞秒激光和EX500 LASIK的一年临床结果准分子激光显示出高功效,可预测性,稳定性和安全性。

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