Visual results and subjective satisfaction after implantation of two different trifocal diffractive intraocular lenses models (AcrySof IQ PanOptix and AT LISA tri 839 MP)

Author:

Boris Malyugin12ORCID,Olga Fomina1,Nikolay Sobolev1,Alexander Belokopytov3ORCID,Eliya Levinger4,Boris Knyazer5,Krauthammer Mark4,Yahalomi Tal6ORCID,Asaf Achiron4ORCID

Affiliation:

1. The S. Fyodorov Eye Microsurgery Federal State Institution, Moscow, Russian Federation

2. Yevdokimov Moscow State University of Medicine and Dentistry, Department of Eye Diseases, Moscow, Russian Federation

3. Institute for Information Transmission Problems (Kharkevich Institute), Russian Academy of Sciences, Moscow, Russian Federation

4. Souraski Medical Center and School of Medicine, Tel Aviv University, Tel Aviv, Israel

5. Soroka University Medical Center and Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel

6. Samson Assuta Ashdod Hospital and the faculty of Health Sciences, Ben-Gurion University of the Negev, Israel

Abstract

Background This study aimed to compare visual results following the implantation of two distinct diffractive trifocal IOLs utilizing various vision evaluation techniques and subjective satisfaction. Methods The study included 32 eyes receiving AcrySof IQ PanOptix implantation and 32 receiving AT LISA tri 839 MP. Post-operative examination at one year included uncorrected visual acuity (UCVA), distance-corrected visual acuity (DCVA) at 4 m, 80 cm, 60 cm, and 40 cm, Contrast sensitivity under photopic and mesopic conditions, and a questionnaire on subjective quality of vision, optical phenomena, and spectacle independence. Results The two groups were similar in baseline demographics, pre-operative visual, biometric data (except for axial length), and surgical paraments. The PanOptix outperformed the AT LISA tri in the intermediate range when using the standard visual acuity testing (UCVA: 0.23 ± 0.14 logMAR vs. 0.31 ± 0.17 logMAR, p = 0.04; BCVA: 0.21 ± 0.12 vs. 0.28 ± 0.14, p = 0.03) and in the intermediate and far range when using the interactive computer program (intermediate: UNVA “E” optotype test: 0.05 ± 0.12 vs. 0.12 ± 0.13, p = 0.03; Far: UNVA “E” optotype: 0.07 ± 0.12 vs. 0.13 ± 0.10, p = 0.05). In addition, the PanOptix group had higher contrast sensitivity under photopic and mesopic conditions with and without glare at all spatial frequencies. There was no difference in subjective outcomes between the groups. Conclusions Patients who received PanOptix IOL had better visual outcomes for intermediate and far with higher contrast sensitivity under various conditions. Based on patients ‘ needs and demands, these results could support discussion when tailoring the optimal multifocal IOl.

Publisher

SAGE Publications

Subject

Ophthalmology,General Medicine

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