Background: Contact lenses which change the structure and color of the iris are used not only for many therapeutic situations but also for cosmetic reasons. The purpose of this study was to investigate whether such lenses cause impairment of visual functions.
Material And Methods: In healthy volunteers with an uncorrected visual acuity of 20/20 a clear soft-fitting lens and a special effect soft contact lens (Crazy lens, Bach Optic, Cologne) were tested in changing sequence. The following parameters were studied: visual acuity, contrast sensitivity (MCT 8000, VisTech Cons., Dayton, Ohio), Goldmann visual field, mesopic vision (Nyktometer, Rodenstock, Munich), and subjective wear comfort on a scale from 1 (excellent) to 10 (poor). Statistical analysis was performed using the Wilcoxon test and the Mann-Whitney U-test.
Results: Nine volunteers with a mean age of 29.9 +/- 5.1 years were analyzed. Visual acuity was reduced to 0.9 +/- 0.23 in the Crazy lens group compared to 1.2 +/- 0.13 in the clear lens group. Mesopic vision without glare was reduced from 1:2.5 to 1:7.4. Goldmann visual field displayed a significant constriction of following isopters: III/4, I/4, and I/3. Contrast sensitivity was significantly reduced in a photopic condition with and without glare and in a scotopic condition without glare; there was, however, an increase in contrast sensitivity in a scotopic condition with glare. Furthermore a decrease in wear comfort from 2.8 +/- 1.4 with the clear fitting lens to 5.7 +/- 2.1 with the print-lens was found.
Conclusion: The tested special-effect contact lenses are associated with a reduction of many visual functions, including visual acuity and contrast sensitivity. This may interfere in some wearers with the ability to drive a car.
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http://dx.doi.org/10.1007/s003470050372 | DOI Listing |
Sci Prog
January 2025
School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Purpose: The aim of this study was to evaluate the efficacy and safety of the Ahmed glaucoma valve in pediatric patients with refractory glaucoma.
Methods: A comprehensive literature search was conducted across multiple major databases, including PubMed, Embase, the Cochrane Library of Systematic Reviews, Science Direct, China's National Knowledge Infrastructure, and the Wanfang database. We retrieved studies published before December 2022 that met the inclusion criteria, including clinical controlled trials (randomized controlled trials) and clinical noncontrolled trials (non-randomized controlled trials) on the use of Ahmed glaucoma valve in pediatric patients with refractory glaucoma.
Background: Lens implantation becomes a major concern in patients lacking posterior capsular support, but various methods are available for rehabilitation. In such patients, scleral-fixated intraocular lens (SFIOL) implantation is preferred due to its fewer complications and better simulation of the natural lens position. In this non-randomized retrospective clinical study, we aimed to assess visual outcomes after sutureless SFIOL implantation in aphakic patients and factors affecting visual outcomes.
View Article and Find Full Text PDFAm J Ophthalmol Case Rep
March 2025
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangzhou, China.
Purpose: This study highlights the feasibility of femtosecond laser-assisted large-diameter lamellar corneal-limbal keratoplasty and its efficacy in the treatment of ocular surface failure caused by bilateral ocular chemical injury.
Observations: The series included 3 patients with ocular surface failure caused by bilateral ocular chemical burns. After dissection of the host cornea, a femtosecond laser-assisted large-diameter lamellar corneoscleral button, with varying thickness of 250-400 μm, was sutured to the recipient bed.
Heliyon
January 2025
Ophthalmology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Purpose: To evaluate the intermediate-term visual and safety outcomes of the small-incision second-generation implantable miniature telescope (SING IMT) in patients with late-stage age-related macular degeneration (AMD) at 6 months post-surgery.
Design: Retrospective cohort study.
Methods: Medical records of patients implanted with the SING IMT at two sites in Italy were reviewed.
Purpose: To assess the safety and efficacy of a modified suprachoroidal silicone tube (SST) shunt in patients with primary open-angle glaucoma (POAG) and pseudo-exfoliative glaucoma (PXG) in this experimental study.
Methods: In this single-center, retrospective longitudinal data analysis 66 eyes of 59 patients having POAG and PXG were included and treated with modified SST shunt in combination with cataract or as a stand-alone procedure. Pre- and postoperative intraocular pressure (IOP), best corrected visual acuity (BCVA), C/D ratio and ocular adverse events (AEs) were assessed in all participants.
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