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Purpose: To evaluate the efficacy, predictability, and safety of laser in situ keratomileusis (LASIK) for the correction of myopia and myopic astigmatism using the SCHWIND Amaris 1050RS excimer laser (SCHWIND eye-tech-solutions).
Methods: This was a prospective cohort study of 1,420 eyes with myopia or myopic astigmatism that underwent LASIK in a single tertiary center between January 2017 and April 2022. The IntraLase iFS femtosecond laser (Johnson & Johnson Vision) was used for flap creation and excimer laser ablation was performed using the SCHWIND Amaris 1050RS with aspheric aberration-free ablation profile, asymmetric pupillary offset, and seven-dimensional eye tracking. Preoperative mean spherical equivalent was -5.81 ± 2.41 diopters (D) (range: -0.63 to -13.63 D).
Results: At 3 months, 95.1% and 99.6% of eyes achieved uncorrected distance visual acuity of 20/20 and 20/40 or better, respectively. The mean efficacy index was 0.99 ± 0.06 and the mean safety index was 1.0 ± 0.02. For predictability, 97.7% and 99.7% of eyes were within ±0.50 and ±1.00 D of the intended correction, respectively. The mean postoperative spherical equivalent was +0.02 ± 0.21 D, mean cylinder was 0.13 ± 0.25 D, mean vector-analyzed magnitude of cylindrical error was 0.09 ± 0.22 D, mean cylindrical angle of error was 0.64 ± 6.79 degrees, and mean cylindrical vector difference was 0.15 ± 0.26 D. None had significant surgical complications.
Conclusions: This study demonstrates excellent efficacy, predictability, and safety of the SCHWIND Amaris 1050RS excimer laser for the correction of myopic astigmatism. The seven-dimensional eye tracker was effective in compensating for eye movements intraoperatively. .
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http://dx.doi.org/10.3928/1081597X-20250130-01 | DOI Listing |
Clin Exp Optom
September 2025
School of Optometry and Vision Science, University of New South Wales, Sydney, Australia.
Clinical Relevance: Good vision is critical for childhood development and education. Pre-school vision screening is important for early detection and treatment of visual problems, and prevention of life-long vision loss.
Background: The aim of this study was to determine the prevalence of vision impairment (VI) and refractive error (RE) in rural Nepalese children under five years of age.
J Cataract Refract Surg
July 2025
Department of Ophthalmology, Santo António Local Health Unit, Porto, Portugal.
Purpose: To demonstrate the efficacy and safety of iris-claw phakic intraocular lens (pIOL) in the treatment of post keratoplasty astigmatism.
Setting: Cornea Unit, Ophthalmology Department - Unidade Local de Saúde de Santo António - Porto, Portugal.
Design: Retrospective longitudinal study.
J Ophthalmic Vis Res
September 2025
Clinical Research Development Unit, Shafa Hospital, Kerman University of Medical Sciences, Kerman, Iran.
Purpose: To evaluate the time required for refractive error (RE) stabilization after standard phacoemulsification cataract surgery and identify preoperative factors influencing this duration.
Methods: This prospective case series study enrolled patients who had undergone phacoemulsification cataract surgery. RE stabilization was defined as 0.
Clin Ophthalmol
September 2025
Department of Ophthalmology and Optometry, Medical University of Vienna, Vienna, Austria.
Purpose: To compare postoperative astigmatism and visual acuity (VA) outcomes in patients undergoing penetrating keratoplasty (PK) using a liquid-interface femtosecond laser (LI-fs) trephination and a conventional vacuum-trephine (VT) technique.
Methods: Our single-center, retrospective data analysis included 121 eyes (121 patients) treated between April 2014 and November 2022. Patients received PK either with a LI-fs or a VT system.
Clin Ophthalmol
September 2025
Faculty of Biomedical Engineering, Czech Technical University in Prague, Kladno, Czech Republic.
Aim: The objective of this study was to evaluate the efficacy of DIMS (Defocus Incorporated Multiple Segments) in comparison to control group (CTRL) in a wide age group of European progressive myopes (6-26 years).
Methods: In this prospective, non-randomised observational study, 78 myopes with progression myopia to -0.25 to -8.