Brunson Phillip B, Mann Ii Paul M, Mann Paul Michael, Potvin Richard
Mann Eye Institute and Laser Centers, Houston, TX, USA.
Science in Vision, Bend, OR, USA.
Clin Ophthalmol. 2020 Nov 17;14:3983-3990. doi: 10.2147/OPTH.S280818. eCollection 2020.
To compare the clinical outcomes from laser refractive surgery performed with the same laser with and without incorporating iris registration technology to compensate for ocular cyclotorsion.
Single-site, two-arm, retrospective chart review.
Clinical outcomes at a single site after wavefront-optimized LASIK using the Wavelight excimer laser with and without the Vario imaging system for iris registration (IR) were evaluated. Eligible subjects were those that received on-label wavefront-optimized treatment of myopia with astigmatism >1.5 D. Measures of interest were the amount of residual refractive cylinder after surgery, the refractive error, and the best-corrected (BCVA) and uncorrected (UCVA) visual acuities, with a target follow-up of around 90 days.
A total of 112 eligible eyes that were treated with IR and 126 similar eyes treated without IR (NO IR) were included. The refractive sphere and spherical equivalent refractions were statistically significantly different between groups (p < 0.05), but the mean differences were <0.1 D in both cases. Refractive cylinder averaged around 0.12 D and was not statistically significantly different between groups. The number of eyes with residual cylinder >0.50 D was higher in the NO IR group vs the IR group (6% vs 1%, respectively, p = 0.04). The mean logMAR UCVA and BCVA were statistically significantly better in the IR group, with a difference of 1.5 letters for UCVA and 1.0 letters for BCVA (p < 0.001 for both). Significantly more eyes in the IR group had a UCVA (p = 0.01) and a BCVA of 20/15 or better (p = 0.003). Overall, 96% of eyes in the IR group and 91% of eyes in the NO IR group had uncorrected visual acuity of 20/20 or better.
Iris registration with the VARIO imaging device demonstrably reduced the overall variability in clinical outcomes.
比较使用同一台激光设备进行激光屈光手术时,采用和不采用虹膜配准技术来补偿眼球旋转所产生的临床效果。
单中心、双臂、回顾性病历审查。
评估在使用Wavelight准分子激光进行波前优化的LASIK手术时,采用和不采用Vario成像系统进行虹膜配准(IR)的单中心临床效果。符合条件的受试者为接受近视且散光>1.5 D的标签上标注的波前优化治疗的患者。感兴趣的测量指标为术后残余屈光柱镜量、屈光不正、最佳矫正视力(BCVA)和未矫正视力(UCVA),目标随访时间约为90天。
共纳入112只接受IR治疗的符合条件的眼睛和126只未接受IR治疗(无IR)的类似眼睛。两组之间的屈光球镜和等效球镜屈光在统计学上有显著差异(p < 0.05),但两种情况下的平均差异均<0.1 D。屈光柱镜平均约为0.12 D,两组之间在统计学上无显著差异。无IR组残余柱镜>0.50 D的眼睛数量高于IR组(分别为6%和1%,p = 0.04)。IR组的平均logMAR UCVA和BCVA在统计学上显著更好,UCVA相差1.5个字母,BCVA相差1.0个字母(两者p < 0.001)。IR组中UCVA(p = 0.01)和BCVA为20/15或更好(p = 0.003)的眼睛明显更多。总体而言,IR组96%的眼睛和无IR组91%的眼睛未矫正视力达到20/20或更好。
使用VARIO成像设备进行虹膜配准明显降低了临床效果的总体变异性。