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首页> 外文期刊>Journal of Ophthalmology >Evaluation of Corneal Stromal Demarcation Line after Two Different Protocols of Accelerated Corneal Collagen Cross-Linking Procedures Using Anterior Segment Optical Coherence Tomography and Confocal Microscopy
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Evaluation of Corneal Stromal Demarcation Line after Two Different Protocols of Accelerated Corneal Collagen Cross-Linking Procedures Using Anterior Segment Optical Coherence Tomography and Confocal Microscopy

机译:使用前节光学相干断层扫描和共聚焦显微镜对两种不同协议的加速角膜胶原蛋白交联程序进行评估后的角膜基质分界线

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Purpose. To evaluate the depth of corneal stromal demarcation line using AS-OCT and confocal microscopy after two different protocols of accelerated corneal collagen cross-linking procedures (CXL).Methods. Patients with keratoconus were divided into two groups. Peschke CXL device (Peschke CCL-VARIO Meditrade GmbH) applied UVA light with an intended irradiance of 18.0 mW/cm2for 5 minutes after applying riboflavin for 20 minutes (group 1) and 30 minutes (group 2). One month postoperatively, corneal stromal demarcation line was measured using AS-OCT and confocal microscopy.Results. This study enrolled 34 eyes of 34 patients (17 eyes in group 1 and 17 eyes in group 2). The mean depth of the corneal stromal demarcation line was208.64±18.41 μm in group 1 and240.37±18.89 μm in group 2 measured with AS OCT, while it was210.29±18.66 μm in group 1 and239.37±20.07 μm in group 2 measured with confocal microscopy. Corneal stromal demarcation line depth measured with AS OCT or confocal microscopy was significantly deeper in group 2 than group 1(P<0.01).Conclusion. The group in which riboflavin was applied for 30 minutes showed significantly deeper corneal stromal demarcation line than the group in which riboflavin was applied for 20 minutes.
机译:目的。在两种不同的加速角膜胶原交联程序(CXL)协议后,使用AS-OCT和共聚焦显微镜评估角膜基质分界线的深度。圆锥角膜患者分为两组。施用核黄素20分钟(第1组)和30分钟(第2组)后,Peschke CXL装置(Peschke CCL-VARIO Meditrade GmbH)以18.0 minutesmW / cm2的预期辐照度照射UVA光5分钟。术后1个月,使用AS-OCT和共聚焦显微镜测量角膜基质分界线。这项研究招募了34例患者的34眼(第1组为17眼,第2组为17眼)。第1组角膜基质分界线的平均深度为208.64±18.41μm,第2组为240.37±18.89μm,第1组为210.29±18.66μm,第1组为239.37±20.07μm。第2组用共聚焦显微镜测量。用AS OCT或共聚焦显微镜测量的角膜基质分界线深度在第2组比第1组更深(P <0.01)。与使用核黄素20分钟的组相比,使用核黄素30分钟的组显示出更深的角膜基质分界线。

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