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October 11, 2025Journal of Refractive Surgery0 citations

Visual and Refractive Outcomes of Small Incision Lenticule Extraction With VisuMax 800 in 1,500 Eyes

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SGSri GaneshSSSupriya Samak SriganeshDKDhatri Karanam

Key Points

  • At 3 months, 98% of eyes achieved uncorrected distance visual acuity of 20/20 or better, indicating the procedure's success.
  • The efficacy index recorded was 1.011, with an impressive safety index of 1.085, highlighting the procedure's reliability.
  • Postoperative spherical equivalent was within ±0.50 and ±1.00 diopters in 99% and 100% of eyes, respectively, confirming minimal refractive error.
  • Analysis revealed no substantial loss of vision, as no eyes lost two or more lines of corrected distance visual acuity in this cohort.

Abstract

Purpose: To assess visual and refractive outcomes of 1,500 eyes that underwent small incision lenticule extraction (SMILE) with the VisuMax 800 femtosecond laser (Carl Zeiss Meditec AG). Methods: This retrospective study includes 1,500 eyes of 770 patients younger than 45 years with corrected distance visual acuity (CDVA) of 20/20 or better who were treated with SMILE using the VisuMax 800. The surgery was performed by an experienced surgeon using a standard technique and 3-month follow up data were analyzed. Results: A total of 1,500 eyes of patients with a mean age of 27.25 ± 4.746 years (39.5% men and 60.52% women) were included in this study. At 3 months, 98% of eyes had uncorrected distance visual acuity (UDVA) of 20/20 or better with an efficacy index of 1.011. Mean preoperative spherical equivalent (SE) was −4.170 ± 1.860 and −0.025 ± 0.120 diopters (D) at 3 months ( P < .001). A total of 18.4% gained one line of CDVA and 9.2% lost one line with a safety index of 1.085. Postoperative SE was within ±0.50 and ±1.00 D in 99% and 100% of eyes, respectively. A total of 98.4% and 100% of eyes showed astigmatism of 0.50 and 1.00 D or less, respectively. No eyes lost two or more lines of CDVA. At 3 months, the Objective Scatter Index score was 0.844 ± 0.486, which was close to preoperative values (0.733 ± 0.871), with a mean change of 0.11. Subgroup analysis was done based on grade of myopia and age. Conclusion: The VisuMax 800, with centration guidance (CentraLign) and cyclotorsion adjustment features (OcuLign), showed safe and effective outcomes for the treatment of myopia and myopic astigmatism in a large cohort of 1,500 eyes.

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Cite This Study

Ganesh et al. (2025) studied this question.

synapsesocial.com/papers/68e9b1b5ba7d64b6fc131eb7https://doi.org/10.3928/1081597x-20250707-04
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