A Lighting Facility For Objective Assessment Of Visual Performance Of Presbyopic Patients In A Series Of Activities Of Daily Living: Development And Validation
Published 2022
- 40th Congress of the ESCRS
Reference: PO132
| Type: ESCRS 2022 - Posters
| DOI:
10.82333/3y3h-3285
Authors:
Eirini-Kanella Panagiotopoulou* 1
, Ioannis Seimenis 2
, Kostas Boboridis 3
, Georgios Labiris 1
1Department of Ophthalmology,University Hospital of Alexandroupolis,Alexandroupolis,Greece, 2Μedical Physics Laboratory, School of Medicine,National and Kapodistrian University of Athens,Athens,Greece, 3Department of Ophthalmology,Aristotle University of Thessaloniki,Thessaloniki,Greece
Purpose
The primary objective of this study is to develop and validate an experimental lighting facility that allows the evaluation of near and intermediate vision in different user-defined illuminance levels.
Setting
Department of Ophthalmology, University Hospital of Alexandroupolis, Alexandroupolis, Greece
Methods
This is a prospective, randomized, controlled study. Normophakic patients populated three validation groups (VGs) according to their binocular uncorrected near visual acuity (UNVA): a) VG1: 0.0 to 0.1 logMAR, b) VG2: 0.4 logMAR, and, c) VG3: 0.7 logMAR. All participants addressed 10 near and intermediate activities of daily life (ADLs) in the three following lighting settings: 1) 25fc/3000K, 2) 50fc/4000K, 3) 75fc/6000K
Results
Thirty patients in each group performed all ADLs in the three lighting settings. VG1 demonstrated the best ADL scores in all ADLs and lighting settings, followed by the VG2. VG3 presented the worst scores. ADLs using printed material showed significant differences among the three lighting settings for all study groups, while ADLs using screens or needing manual dexterity demonstrated no significant differences except for ST in VG1. All ADL scores demonstrated high correlation with UNVA in all lighting settings (p < 0.001).
Conclusions
This is the first study that validates a lighting facility for comparative studies in patients with different near vision capacity performing a series of ADLs. This facility could be used in future studies for the evaluation of near and intermediate vision, in different illuminance levels, of presbyopic patients and of patients following lens extraction surgery with implantation of premium intraocular lenses.