From the Department of Ophthalmology (Torky), Faculty of Medicine, Mansoura University, Mansoura, Egypt; Department of Ophthalmology (Alzafiri), Dar Al-Shifa Hospital, Hawally, Kuwait.
From the Department of Ophthalmology (Torky), Faculty of Medicine, Mansoura University, Mansoura, Egypt; Department of Ophthalmology (Alzafiri), Dar Al-Shifa Hospital, Hawally, Kuwait.
J Cataract Refract Surg. 2017 Apr;43(4):459-465. doi: 10.1016/j.jcrs.2017.01.015.
To evaluate the efficacy, safety, predictability, and stability of small-incision lenticule extraction in low, moderate, and high myopia.
Prospective case series.
Eyes were divided into a low myopia group (spherical equivalent [SE] refraction -1.00 to -3.00 diopters [D]), moderate myopia group (SE refraction of -3.25 to -6.00 D), and high myopia group (SE refraction -6.25 to -10.00 D). Small-incision lenticule extraction surgery was performed, and outcomes were reported 6 months postoperatively.
The low myopia group comprised 94 eyes; the moderate myopia group, 95 eyes; and the high myopia group, 85 eyes. There was significant improvement in uncorrected (UDVA) and corrected (CDVA) distance visual acuities, sphere, cylinder, and SE in all groups 6 months postoperatively. The difference in postoperative UDVA, sphere, and SE was statistically significant between the low and moderate myopia groups and the high myopia group; however, there was no difference in the CDVA, cylinder, efficacy, or safety indices. The difference between the attempted SE and achieved SE correction was 0.12 D ± 0.14 (SD) in the low myopia group, -0.18 ± 0.02 D in the moderate myopia group, and -0.60 ± 0.03 D in the high myopia group. There was no statistically significant change in the postoperative SE in any group at 3 months or 6 months.
Small-incision lenticule extraction showed acceptable efficacy, safety, predictability, and stability in low, moderate, and high myopia. The tendency toward undercorrection in the high myopia group suggests the need to modify the nomograms of small-incision lenticule extraction in highly myopic patients.
评估小切口微透镜提取术在低度、中度和高度近视中的疗效、安全性、可预测性和稳定性。
前瞻性病例系列。
将眼分为低度近视组(等效球镜[SE]屈光度-1.00 至-3.00 屈光度[D])、中度近视组(SE 屈光度为-3.25 至-6.00 D)和高度近视组(SE 屈光度-6.25 至-10.00 D)。行小切口微透镜提取术,术后 6 个月报告结果。
低度近视组 94 眼;中度近视组 95 眼;高度近视组 85 眼。术后 6 个月,所有组的未矫正(UDVA)和矫正(CDVA)远视力、球镜、柱镜和 SE 均有显著改善。术后 UDVA、球镜和 SE 在低度和中度近视组与高度近视组之间差异有统计学意义,但 CDVA、柱镜、疗效和安全性指标之间差异无统计学意义。低度近视组的目标 SE 与实际 SE 矫正差值为 0.12 D±0.14(SD),中度近视组为-0.18±0.02 D,高度近视组为-0.60±0.03 D。术后 3 个月和 6 个月,各组 SE 均无统计学意义变化。
小切口微透镜提取术在低度、中度和高度近视中显示出可接受的疗效、安全性、可预测性和稳定性。高度近视组存在明显欠矫趋势,提示需要对高度近视患者的小切口微透镜提取图进行修改。