Abstract
Purpose
To evaluate the early findings of new monofocal intraocular lens (Tecnis® Eyhance) in comparison with standard monofocal intraocular lens (Tecnis® 1-piece) in patients who underwent cataract surgery.
Methods
Sixty-four eyes of thirty-two patients (each intraocular lens model was implanted bilaterally in 16 patients) were included in this retrospective study. Preoperative and postoperative (at one month) manifest refraction, spherical equivalent (SE) values, monocular and binocular uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), uncorrected intermediate visual acuity (UCIVA), distance-corrected intermediate visual acuity (DCIVA), distance-corrected near visual acuity (DCNVA), binocular defocus curve, photopic contrast-sensitivity, spectacle independence, photic phenomena, tolerance to residual refractive errors and complications were recorded.
Results
The mean monocular postoperative UDVA, CDVA, DCNVA, spherical equivalent and cylinder values were comparable between each group (p > 0.05). Monocular and binocular DCIVA and UCIVA were significantly higher in Tecnis® Eyhance group than Tecnis® 1-piece group (p = 0.033, p = 0.038, respectively). No statistically significant difference was detected between groups regarding the photopic contrast sensitivities for any spatial frequency (p > 0.05). Spectacle independence was significantly higher in Tecnis® Eyhance group than Tecnis® 1-piece group. Tecnis® Eyhance IOL revealed a good tolerance to unexpected residual refractive errors than Tecnis® 1-piece IOL.
Conclusion
Tecnis® Eyhance appears to be an effective option for both patients and surgeons regarding better intermediate visual acuities and more forgiving for residual refractive errors relative to the standard monofocal intraocular lenses. However, longer follow-up studies with larger group of patients are needed to evaluate the effectiveness of Tecnis® Eyhance intraocular lens.
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Availability of data and material
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
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The authors obtained no commercial provider for the investigation, authorship, and broadcasting of the study.
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UU conceived the idea. UU performed surgeries and HS collected the data. UU analyzed the data and HS wrote the manuscript. All authors approved the final version.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of Faculty of Medicine, Bakırcay University/Izmir. All procedures conformed to the tenets of the Declaration of Helsinki. Written informed consent was obtained from all individual participants included in the study.
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Unsal, U., Sabur, H. Comparison of new monofocal innovative and standard monofocal intraocular lens after phacoemulsification. Int Ophthalmol 41, 273–282 (2021). https://doi.org/10.1007/s10792-020-01579-y
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DOI: https://doi.org/10.1007/s10792-020-01579-y