加速角膜交联联合激光原位角膜磨镶术治疗亚洲人高度近视。

The Open Ophthalmology Journal Pub Date : 2018-07-23 eCollection Date: 2018-01-01 DOI:10.2174/1874364101812010143
Jin Rong Low, Li Lim, Jane Chwee Wah Koh, Daniel Kai Peng Chua, Mohamad Rosman
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引用次数: 0

摘要

背景:LASIK Xtra是一种结合LASIK和加速角膜交联(CXL)的新技术。它在亚洲高度近视患者中的长期效果尚未得到很好的描述。目的:比较LASIK Xtra与LASIK在高度近视患者中的疗效、可预测性和安全性。方法:这是一项回顾性研究,比较50只连续接受LASIK额外矫正高度近视和/或近视散光的眼睛(-6.63至-15.50 D显球当量)和50只单独接受LASIK矫正高度近视的眼睛(-6.00至-12.25 D显球当量)。LASIK Xtra的平均随访时间为5.7个月(1.5-13.3个月),仅LASIK的平均随访时间为3.6个月(1.7-4.2个月)。结果测量包括未矫正距离视力(UDVA)、矫正距离视力(CDVA)、屈光和术中及术后并发症。结果:术后3个月,所有眼UDVA均达到20/40及以上,其中80.0%的LASIK +眼UDVA达到20/20及以上,66.0%的LASIK +眼UDVA达到20/20及以上(p = 0.115)。LASIK Xtra组疗效指数为0.99±0.17,单纯LASIK组疗效指数为0.94±0.17 (p = 0.164)。术后3个月,仅LASIK组在±0.50 D内尝试矫正的眼睛比例为84%,LASIK +组为72% (p = 0.148)。LASIK +组和纯LASIK组的安全性指数分别为1.11±0.19和1.11±0.18 (p = 0.735)。结论:LASIK Xtra在高度近视患者中具有与LASIK相当的安全性、可预测性和有效性。6-12个月时获得良好的屈光稳定性。需要进一步的长期研究来确定同时进行CXL是否能够减少高危人群术后LASIK角膜扩张症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Simultaneous Accelerated Corneal Crosslinking and Laser <i>In situ</i> Keratomileusis for the Treatment of High Myopia in Asian Eyes.

Simultaneous Accelerated Corneal Crosslinking and Laser <i>In situ</i> Keratomileusis for the Treatment of High Myopia in Asian Eyes.

Simultaneous Accelerated Corneal Crosslinking and Laser <i>In situ</i> Keratomileusis for the Treatment of High Myopia in Asian Eyes.

Simultaneous Accelerated Corneal Crosslinking and Laser In situ Keratomileusis for the Treatment of High Myopia in Asian Eyes.

Background: LASIK Xtra is a recently described technique which combines LASIK and accelerated corneal cross-linking(CXL) in the same setting. Its long-term outcome in Asians with high myopia is not well described.

Objectives: To compare the efficacy, predictability and safety of LASIK Xtra with LASIK in patients with high myopia.

Method: This is a retrospective study comparing 50 consecutive eyes undergoing LASIK Xtra for the correction of high myopia and/or myopic astigmatism (-6.63 to -15.50 D manifest spherical equivalent) with a matched control group of 50 eyes undergoing LASIK alone for correction of high myopia (-6.00 to -12.25 D manifest spherical equivalent). Mean follow-up was 5.7 months (range, 1.5-13.3 months) for LASIK Xtra and 3.6 months (range, 1.7-4.2 months) for LASIK only. Outcome measures included Uncorrected Distance Visual Acuity (UDVA), Corrected Distance Visual Acuity (CDVA), refraction and intraoperative and postoperative complications.

Results: At post-operative 3 months, all eyes achieved UDVA of 20/40 or better, and 80.0% of LASIK Xtra eyes achieved UDVA of 20/20 or better, compared to 66.0% of LASIK only eyes (p = 0.115). Efficacy indices were 0.99±0.17 for LASIK Xtra and 0.94±0.17 for LASIK only (p = 0.164). The proportion of eyes within ±0.50 D of attempted correction was 84% in the LASIK only group and 72% in the LASIK Xtra group at post-operative 3 months (p = 0.148). Safety indices were 1.11±0.19 and 1.11±0.18 in the LASIK Xtra and LASIK only groups, respectively (p = 0.735).

Conclusion: LASIK Xtra achieved comparable safety, predictability and efficacy as LASIK in patients with high myopia. Good refractive stability was attained at 6-12 months. Further long term studies are required to determine whether simultaneous CXL is able to reduce postoperative LASIK keratectasia in high-risk individuals.

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