...
首页> 外文期刊>Journal of refractive surgery >Bioptics in phakic and pseudophakic intraocular lens with the Nidek EC-5000 excimer laser.
【24h】

Bioptics in phakic and pseudophakic intraocular lens with the Nidek EC-5000 excimer laser.

机译:Nidek EC-5000受激准分子激光在有晶状和假晶状体人工晶状体中的活检。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

PURPOSE: To evaluate predictability, safety, stability, and complications related to bioptics in patients that received phakic and those that received pseudophakic intraocular lenses. Both groups had LASIK with the Nidek EC-5000 excimer laser following IOL implantation. METHODS: We evaluated retrospectively 281 eyes of 196 patients with posterior chamber phakic implantation (ICL) and 64 pseudophakic eyes of 55 patients. All patients had LASIK 1 month or more after the first surgery. We used a treatment zone of 5.5 mm with a 7.00-mm transition zone. The flap was made with the Automated Corneal Shaper (ACS). RESULTS: In the group of phakic ICL eyes with bioptics, preoperative mean spherical equivalent refraction was -5.50 D (range, -1.37 to -16.00 D). The first day after LASIK, mean spherical equivalent refraction was -0.06 D, and at 1 month, -0.40 D. In pseudophakic bioptics eyes, preoperative mean spherical equivalent refraction was -2.61 D (range, +0.50 to -5.50 D). The first day after LASIK it was +0.27 D, and 1 month after LASIK it was +0.09 D. The incidence of complications was similar in both groups of patients. The most frequent complication was keratitis sicca (approximately 10% in each group). Interstitial edema (2.1%) was present only in phakic bioptics eyes. No retinal complications were observed. Refraction was stable 4 years after surgery. Target achieved refraction was +/- 0.50 D, showing the predictability of the procedure. CONCLUSIONS: Predictability and safety were demonstrated according to results and absence of severe complications related with this technique. Older patients did not develop more complications than younger people; dry eye incidence was similar in both groups. In extreme myopia patients did not present retinal complications related to surgical procedures.
机译:目的:评估接受晶状体切除术的患者和接受假晶状体人工晶状体的患者的与活检相关的可预测性,安全性,稳定性和并发症。两组均在IOL植入后使用Nidek EC-5000准分子激光进行LASIK手术。方法:我们回顾性评估了196例后房性晶状体植入术(ICL)的281眼和55例的64假晶状体眼。所有患者在第一次手术后1个月或更长时间都患有LASIK。我们使用5.5毫米的治疗区域和7.00毫米的过渡区域。皮瓣由自动角膜塑形器(ACS)制成。结果:在有晶状体眼的有晶状体眼的ICL眼组中,术前平均球面等效屈光度为-5.50 D(范围-1.37至-16.00 D)。 LASIK手术后的第一天,平均球镜等效屈光度为-0.06 D,在1个月时为-0.40D。在伪晶状体活检眼中,术前平均球镜等效屈光度为-2.61 D(范围为+0.50至-5.50 D)。 LASIK术后第一天为+0.27 D,LASIK术后1个月为+0.09D。两组患者的并发症发生率相似。最常见的并发症是干燥性角膜炎(每组约10%)。间质性水肿(2.1%)仅存在于有晶状体的活检眼中。没有观察到视网膜并发症。术后4年屈光稳定。目标获得的屈光度为+/- 0.50 D,表明该过程的可预测性。结论:根据结果证明了可预测性和安全性,并且没有与该技术相关的严重并发症。年龄较大的患者没有比年轻人更多的并发症。两组的干眼症发病率相似。在极端近视眼中,患者未出现与手术程序有关的视网膜并发症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号