4.4 Article

Myopic LASIK Outcomes: Comparison of Three Different Femtosecond Lasers and a Mechanical Microkeratome Using the Same Excimer Laser

Journal

OPHTHALMOLOGY AND THERAPY
Volume 11, Issue 3, Pages 1047-1066

Publisher

SPRINGER INT PUBL AG
DOI: 10.1007/s40123-022-00486-y

Keywords

Femtosecond LASIK; LASIK; Mechanical LASIK; Myopia

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The study compares the outcomes of myopic LASIK with one microkeratome and three femtosecond lasers. It found that visual restoration may be slightly delayed for patients who underwent FS200 LASIK surgery, with significant differences observed at 1 day and 1 week postoperatively but no differences after 1 month. Additionally, significant differences were found among devices in terms of safety index and refractive results, although these differences were not clinically significant.
Introduction: To compare the influence of one microkeratome and three femtosecond lasers on myopic laser in situ keratomileusis (LASIK) outcomes. Methods: Retrospective, observational cohort study. We compared 134 eyes treated with the IntraLase 60 kHz, 112 eyes treated with the Femto LDV Z6, 206 eyes treated with the FS200, and 98 eyes treated with the Hansatome zero compression microkeratome. All eyes were operated on using the same surgical protocol with the same excimer laser (Wavelight Allegretto) and were allocated to refraction-matched groups. Results: One day and one week postoperatively, uncorrected distance visual acuity was significantly lower in the FS200 group compared to others (P = 0.0001). This difference disappeared at the 1- and 3-month postoperative visits. Significant differences were found among groups in terms of safety index (P = 0.0001), residual sphere (P = 0.0001), and residual cylinder (P = 0.02) at the 3-month postoperative visit. No significant differences were found in corrected distance visual acuity or efficacy index. Conclusion: According to our results, a slight delay in visual restoration after FS200 LASIK surgery might be expected. This delay was statistically significant at 1 day and 1 week postoperatively, but there were no differences from the 1-month visit onwards. Additionally, significant differences were found among devices in terms of safety index and the refractive results, which were found not to be clinically relevant.

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