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Stability, Safety, and Efficacy of WaveLight Plus InnovEyes Ray-Tracing-Guided LASIK in Myopia and Myopic Astigmatism: A One-Year Prospective Study
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Stability, Safety, and Efficacy of WaveLight Plus InnovEyes Ray-Tracing-Guided LASIK in Myopia and Myopic Astigmatism: A One-Year Prospective Study

American Journal of Ophthalmology·September 10
OphthalmologyConfirms priorMyopiaMyopic AstigmatismProspective Non-Randomized Interventional StudyExcimer Laser Refractive SurgeryFemtosecond LASIKAdultWaveLight Plus InnovEyes

Summary

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What was studied

Prospective, non-randomized interventional study evaluating efficacy, safety, refractive accuracy, and stability of WaveLight Plus InnovEyes ray-tracing-guided LASIK in 800 eyes (400 patients) with myopia or myopic astigmatism, including a subgroup of 300 eyes with preoperative cylinder ≥1.50 D, followed for 12 months.

Key findings

At 12 months, 100% of eyes achieved UDVA ≥20/20 and 68% achieved ≥20/16; 96.5% were within ±0.50 D of target SE; refractive stability was strong with only 0.38% of eyes showing >0.50 D change from 1–12 months. In the high-cylinder subgroup, 91.7% had residual astigmatism ≤0.50 D and 85% of eyes had axis error within ±5°. No eyes lost ≥2 lines of CDVA.

Study limitations

- Non-randomized design with no control arm limits comparative conclusions. - Single-platform study; results may not generalize to other ray-tracing or wavefront-guided systems. - 12-month follow-up may not capture longer-term refractive drift or regression.

Clinical implications

Ray-tracing-guided LASIK with WaveLight Plus InnovEyes delivers high predictability and safety for myopia and myopic astigmatism, including eyes with cylinder ≥1.50 D — clinicians can expect precise axis alignment and low residual error with this platform. The mild systematic undercorrection (mean CI ~0.94) is worth monitoring when planning treatments for high astigmats.

Caveats

  • Age and sex distributions are not reported in the abstract; the adult age group tag is an inference based on typical LASIK eligibility criteria.
  • No randomized control arm — results reflect a single-arm interventional study, so efficacy and safety comparisons to other platforms are not directly supported by this data.
  • Sample unit is eyes (n=800), not patients (n=400); outcomes are reported per eye, which inflates effective sample size for bilateral procedures.
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  • The brand 'WaveLight Plus InnovEyes' appears to be a newer platform; clinicians should note this study may represent early commercial adoption data.

Related Questions

Explore related topics

How does ray-tracing-guided LASIK compare to wavefront-optimized LASIK for myopic astigmatism outcomes?What are the best LASIK platforms for patients with high astigmatism (≥1.50 D cylinder)?What is the Alpins vector method and how is it used to assess astigmatic correction after LASIK?

Publication Details

Year
2026
Journal
American Journal of Ophthalmology
Sample Size
n=800
Source
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