Thananjeyan Akshaya L, Bala Chandra
PersonalEyes, Sydney, NSW, Australia.
Emergency Department, Sydney Hand and Eye Hospital, Sydney, NSW, Australia.
Clin Ophthalmol. 2025 Jul 3;19:2079-2089. doi: 10.2147/OPTH.S524774. eCollection 2025.
To assess factors affecting successful data acquisition for InnovEyes guided ray trace LASIK.
Single-site ophthalmology practice.
Retrospective review.
A total of 1283 eyes with myopia and myopic astigmatism were assessed over 18-months for ray trace-based LASIK planning. Preoperative measurements were acquired using the InnovEyes Sightmap (Wavelight Plus, Alcon). Scan time per eye, number of scans, pupil size, calculated refraction and manifest spherical equivalent (SEQ) refraction were assessed. In a subset of eyes with significant accommodation, aberrometry-based refraction was adjusted prior to treatment, or cycloplegic measurement was used for treatment planning. In these subsets, 3-month post-operative refractive outcomes were analysed.
Mean noncycloplegic scanning time (11.10±14.11 minutes/eye to 8.10±3.17 minutes/eye) and number of noncycloplegic scans per eye (6.28±2.97 scans to 5.23±2.12 scans) decreased over time. In nine eyes where the wavefront SEQ (4 mm) was less myopic (by 0.5D or more) than the manifest SEQ and no adjustment was made, all achieved uncorrected distance visual acuity (UDVA) of 20/20 or better. In 274 eyes (21.4%), wavefront SEQ (4mm) was more myopic (by > 0.5D) than manifest SEQ. Surgeon adjusted treatment in 95 eyes to within 0.5D of manifest SEQ resulted in 98% achieving UDVA of 20/20 or greater. In 23 eyes treated using cycloplegic wavefront data, 96% achieved UDVA of 20/20 or greater.
Use of the InnovEyes Sightmap system for ray trace LASIK is feasible in a clinical environment but demonstrates an operator learning curve. Accommodation during wavefront measurement can occur; this can be managed through surgeon adjustment of treatment or the use of cycloplegic wavefront data.
评估影响InnovEyes引导的光线追踪准分子原位角膜磨镶术(LASIK)成功获取数据的因素。
单中心眼科诊所。
回顾性研究。
在18个月内对1283例近视和近视散光患者的眼睛进行基于光线追踪的LASIK手术规划评估。术前使用InnovEyes Sightmap(爱尔康Wavelight Plus)进行测量。评估每只眼睛的扫描时间、扫描次数、瞳孔大小、计算的屈光度和明显球镜等效(SEQ)屈光度。在一部分有明显调节的眼睛中,在治疗前对基于像差仪的屈光度进行调整,或使用睫状肌麻痹测量进行治疗规划。在这些亚组中,分析术后3个月的屈光结果。
平均非睫状肌麻痹扫描时间(从每只眼睛11.10±14.11分钟降至8.10±3.17分钟)和每只眼睛的非睫状肌麻痹扫描次数(从6.28±2.97次降至5.23±2.12次)随时间减少。在9只眼睛中,波前SEQ(4毫米)比明显SEQ近视程度低(相差0.5D或更多)且未进行调整,所有眼睛的裸眼远视力(UDVA)均达到20/20或更好。在274只眼睛(21.4%)中,波前SEQ(4毫米)比明显SEQ近视程度高(相差>0.5D)。外科医生对95只眼睛的治疗进行调整,使其与明显SEQ相差在0.5D以内,98%的眼睛UDVA达到20/20或更高。在23只使用睫状肌麻痹波前数据治疗的眼睛中,96%的眼睛UDVA达到20/20或更高。
在临床环境中,使用InnovEyes Sightmap系统进行光线追踪LASIK是可行的,但显示出操作者的学习曲线。波前测量期间可能会发生调节;这可以通过外科医生调整治疗或使用睫状肌麻痹波前数据来处理。