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首页> 外文期刊>Cornea >Comparison of implantable collamer lens (ICL) and laser-assisted in situ keratomileusis (LASIK) for low myopia.
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Comparison of implantable collamer lens (ICL) and laser-assisted in situ keratomileusis (LASIK) for low myopia.

机译:植入式护目镜(ICL)和激光辅助原位角膜磨镶术(LASIK)用于近视度数的比较。

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摘要

PURPOSE: To compare the results of laser-assisted in situ keratomileusis (LASIK) and implantable collamer lenses (ICL) in the correction of myopia -4 to -7.88 D. METHODS: A total of 1678 LASIK eyes from the Davis Duehr Eye Center, Madison, WI, and 144 ICL eyes from the 14-site US FDA Clinical Trial for ICL for Myopia were compared. Both series were concurrently operated on with 4 to 7.88 D of preoperative spherical equivalent of the manifest refraction and were examined at 1 day, 1 week, 1 month, and 6 months postoperatively. The mean baseline myopia was slightly higher in the ICL group (ICL: -6.4 +/- 1.1 D; LASIK: -5.6 +/- 1.1 D). Best spectacle-corrected visual acuity (BSCVA), uncorrected visual acuity (UCVA), and refractions were collected prospectively in both series. RESULTS: BSCVA loss of at least 2 lines was significantly higher in the LASIK series in the early healing period (1 week: 6% vs. 0.7%; P = 0.008), whereas a BSCVA gain of at least 2 lines was statistically better with the ICL at 1 (5%vs. 0.9%, P = 0.001) and 6 months (4% vs. 0.8%, P = 0.013). Proportion of cases seeing 20/15 or better uncorrected (21.6% vs. 7.8%, P < 0.001) and 20/20 or better (67% vs. 57%, P = 0.027) at 6 months postoperatively was better in the ICL group. The ICL was statistically more predictable (attempted vs. achieved) at 6 months; +/-0.50 D (79% ICL vs. 70% LASIK, P = 0.034) and +/-1.0 D (97% ICL vs. 88% LASIK, P < 0.001). Stability was achieved (95% < or = 1.0 D) at the 1-week to 1-month interval for both groups (95% LASIK; 98% ICL). The stability of refraction (< or =0.5 D change) was significantly better in the ICL group than the LASIK group through 6 months. No serious complications occurred in either series. CONCLUSIONS: The ICL was safer and more effective than LASIK and seems to be a viable alternative to corneal refractive excimer surgery in the treatment of low myopia.
机译:目的:为了比较激光辅助原位角膜磨镶术(LASIK)和植入式角膜晶状体(ICL)矫正近视-4至-7.88D的方法。方法:戴维斯·杜尔眼中心的共计1678副LASIK眼,比较了美国FDA在14个站点针对近视ICL进行的ICL临床试验中的Madison,WI和144个ICL眼睛。两组均在术前等效于明显屈光度的术前球镜上进行4至7.88 D的手术,并在术后1天,1周,1个月和6个月进行检查。 ICL组的平均基线近视略高(ICL:-6.4 +/- 1.1 D; LASIK:-5.6 +/- 1.1 D)。在这两个系列中,前瞻性地收集了最佳的眼镜矫正视力(BSCVA),未矫正视力(UCVA)和折射。结果:LASIK系列的BSCVA损失在康复早期至少显着高于2行(1周:6%对0.7%; P = 0.008),而BSCVA的至少2行在统计学上好于ICL为1(5%对0.9%,P = 0.001)和6个月(4%对0.8%,P = 0.013)。在ICL组中,术后6个月未矫正为20/15或更高(21.6%vs. 7.8%,P <0.001)和20/20或更高(67%vs. 57%,P = 0.027)的病例比例更好。在6个月时,ICL在统计上更可预测(尝试与实现); +/- 0.50 D(79%ICL vs.70%LASIK,P = 0.034)和+/- 1.0 D(97%ICL vs. 88%LASIK,P <0.001)。两组(95%LASIK; 98%ICL)在1周至1个月的间隔内达到了稳定性(95%<或= 1.0 D)。在6个月内,ICL组的屈光稳定性(<或= 0.5 D变化)明显优于LASIK组。两组均未发生严重并发症。结论:ICL比LASIK更安全,更有效,并且在角膜屈光不正准分子手术中是治疗近视度数的可行替代方法。

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