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First European results of a new refractive lenticular extraction procedure—SmartSight by SCHWIND eye-tech-solutions

Abstract

Background

To evaluate vision 3 months after SmartSight lenticule extraction treatments.

Design

Case series.

Methods

This case series of patients were treated at Specialty Eye Hospital Svjetlost in Zagreb, Croatia. Sixty eyes of 31 patients consecutively treated with SmartSight lenticule extraction were assessed. The mean age of the patients was 33 ± 6 years (range 23–45 years) at the time of treatment with a mean spherical equivalent refraction of −5.10 ± 1.35 D and mean astigmatism of 0.46 ± 0.36 D. Monocular corrected distance visual acuity (CDVA), uncorrected distance visual acuity (UDVA) were assessed pre- and post-operatively. Ocular and corneal wavefront aberrations have been postoperatively compared to the preoperative baseline values. Changes in ocular wavefront refraction, as well as changes in keratometric readings are reported.

Results

At 3 months post-operatively, mean UDVA was 20/20 ± 2. Spherical equivalent showed a low myopic residual refraction of −0.37 ± 0.58 D with refractive astigmatism of 0.46 ± 0.26 D postoperatively. There was a slight improvement of 0.1 Snellen lines at 3-months follow-up. Compared to the preoperative status, ocular aberrations (at 6 mm diameter) did not change at 3 months follow-up; whereas corneal aberrations increased (+0.22 ± 0.21 µm for coma; +0.17 ± 0.19 µm for spherical aberration; and +0.32 ± 0.26 µm for HOA-RMS). The same correction was determined using changes in ocular wavefront refraction, as well as changes in keratometric readings.

Conclusion

Lenticule extraction after SmartSight is safe and efficacious in the first 3 months postoperatively. The post-operative outcomes indicate improvements in vision.

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Fig. 1: Standard graphs for reporting outcomes in laser vision correction.
Fig. 2: Wavefront refraction.
Fig. 3: Wavefront refraction vs topographic changes.
Fig. 4: Change in high order aberrations.

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Data availability

Data are available upon request.

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Funding

The study was self-financed.

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Authors and Affiliations

Authors

Contributions

The authors confirm their contribution to the paper as follows: IG—study conception and design, data collection, analysis and interpretation of results, draft manuscript preparation. MB—study conception and design, data collection, analysis and interpretation of results, draft manuscript preparation. KG—study conception and design, data collection, analysis and interpretation of results. SAM—study conception and design, data collection, analysis and interpretation of results, draft manuscript preparation. All authors reviewed the results and approved the final version of the manuscript.

Corresponding author

Correspondence to Maja Bohac.

Ethics declarations

Competing interests

SAM is an employee at and inventor in several patents owned by SCHWIND eye-tech-solutions. None of the other authors has financial or proprietary interests in materials or methods presented herein.

Ethical approval and consent to participate

The study was conducted according to the guidelines of the Declaration of Helsinki. The study was retrospective with anonymized data. Ethics approval was not required due to the retrospective nature of the review chart. The purpose of this clinical research does not represent a clinical investigation. The medical device was used within its intended purpose without any additional invasive or patient-burdensome procedures used. Informed consent was obtained from all subjects involved in the study.

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Gabric, I., Bohac, M., Gabric, K. et al. First European results of a new refractive lenticular extraction procedure—SmartSight by SCHWIND eye-tech-solutions. Eye 37, 3768–3775 (2023). https://doi.org/10.1038/s41433-023-02601-0

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