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首页> 外文期刊>Journal of cataract and refractive surgery >One-year results of excimer laser in situ keratomileusis for hyperopia.
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One-year results of excimer laser in situ keratomileusis for hyperopia.

机译:准分子激光原位角膜磨镶术治疗远视的一年结果。

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PURPOSE: To evaluate the visual and refractive results of hyperopic LASIK. SETTING: Clinica Baviera Instituto Oftalmologico Europeo, Madrid, Spain. METHODS: This retrospective consecutive noncomparative observational study evaluated hyperopic LASIK results over 1 year. Outcomes included uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), cycloplegic refraction, and corneal topography. Surgery was performed using an MEL 80-G excimer laser. Results were analyzed by preoperative spherical equivalent (SE) (Group 1: or=+3.60 D). RESULTS: The mean UDVA improved from 0.50 +/- 0.3 (SD) to 0.90 +/- 0.2 in Group 1 and from 0.50 +/- 0.3 to 0.80 +/- 0.2 in Group 2 and the mean CDVA, from 0.86 +/- 0.2 to 0.93 +/- 0.1 and from 0.80 +/- 0.2 to 0.90 +/- 0.2, respectively. The mean cycloplegic SE improved from +2. 5+/- 0.8 to +0.1 +/- 0.5 in Group 1 and from +4.5 +/- 0.6 to +0.4 +/- 0.6 in Group 2; 70.9% of eyes and 63.3% of eyes, respectively, were within +/-0.50 D of emmetropia. Postoperatively, 92.8% of eyes in Group 1 and 87.8% in Group 2 maintained or gained 1 or more lines of CDVA; 1.7% and 4.0%, respectively, lost 2 or more lines. The safety index was 1.1 in both groups and the efficacy index, 1.01 in Group 1 and 0.98 in Group 2. The enhancement rate was 20.0% and 18.4%, respectively. CONCLUSION: Excimer laser LASIK was safe and effective for treating hyperopia up to +6.25 D with no further loss of CDVA lines after enhancement.
机译:目的:评估远视LASIK的视觉和屈光结果。地点:西班牙马德里,欧洲临床医学研究所。方法:这项回顾性连续非对照观察性研究评估了超过1年的远视LASIK结果。结果包括未矫正的远视力(UDVA),矫正的远视力(CDVA),睫状肌麻痹验光和角膜地形图。使用MEL 80-G准分子激光器进行手术。通过术前球体当量(SE)分析结果(组1:<或= + 3.50屈光度[D];组2:>或= + 3.60 D)。结果:第一组的平均UDVA从0.50 +/- 0.3(SD)改善到0.90 +/- 0.2,第二组的平均UDVA从0.50 +/- 0.3改善到0.80 +/- 0.2,平均CDVA从0.86 +/-改善0.2至0.93 +/- 0.1和0.80 +/- 0.2至0.90 +/- 0.2。平均睫状肌麻痹SE从+2提高。第1组从5 +/- 0.8到+0.1 +/- 0.5,第2组从+4.5 +/- 0.6到+0.4 +/- 0.6;分别在正视眼的+/- 0.50 D范围内有70.9%的眼睛和63.3%的眼睛。术后,第1组的92.8%的眼睛和第2组的87.8%的眼睛维持或获得了1条或更多条CDVA。 1.7%和4.0%的线丢失了2条或更多。两组的安全指数均为1.1,疗效指数为1组为1.01,第二组为0.98。增强率分别为20.0%和18.4%。结论:准分子激光LASIK手术治疗+6.25 D远视是安全有效的,而增强后CDVA不会进一步丧失。

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