Fakülteler / Faculties

Permanent URI for this communityhttps://hdl.handle.net/11727/1395

Browse

Search Results

Now showing 1 - 2 of 2
  • Item
    Clinical Outcomes of Scleral Misa Lenses for Visual Rehabilitation in Patients with Pellucid Marginal Degeneration
    (2016) Asena, Leyla; Altinors, Dilek Dursun; 0000-0002-6848-203X; 0000-0001-5223-0279; 27432029; E-5914-2016; AAK-8077-2021
    Purpose: To report the clinical outcomes of scleral Misa((R)) lenses (Microlens Contactlens Technolgy, Arnhem, Netherlands) for visual rehabilitation in patients with pellucid marginal degeneration (PMD). Mehods: In this prospective interventional case series, 24 eyes of 12 PMD patients were fitted with scleral Misa((R)) lenses. Patients were followed regularly for continuous daily wearing time (CDWT), contact lens handling issues, Visual acuity, and any subjective or objective contact lens related complications. Results: The mean patient age was 35.0 +/- 13.8 years (range, 23-47 years). The average length of follow-up was 14.1 +/- 3.7 months (range, 8.5-18 months). All eyes were fit with mini Misa((R)) scleral lenses with a diameter of 16.5 or 17 mm. The mean Snellen best-corrected visual acuity (BCVA) before scleral lenses with spectacle correction was 0.42 +/- 0.15 (range, 0.2-0.6). With scleral lenses, mean BCVA was 0.75 +/- 0.15 (range, 0.5-0.9), (p = 0.003) with a mean gain of 3.3 lines of BCVA. More than half (16 eyes, 67%) reported wearing theirscleral lenses for 8 h or more on a daily basis. Three patients (6 eyes, 25%) abandoned scleral lens wear. Patients who abandoned the scleral lens wear tended to have a better spectacle corrected visual acuity and less gain of lines. Conclusions: Scleral lenses can be used succesfully in patients with PMD who are intolerant to other types of contact lenses. Patients who have a low spectacle BCVA and a higher gain of visual acuity with scleral lenses are good candidates for scleral lens use. (C) 2016 British Contact Lens Association. Published by Elsevier Ltd. All rights reserved.
  • Item
    Visual Rehabilitation After Penetrating Keratoplasty
    (2016) Asena, Leyla; Altinors, Dilek D.; 0000-0002-6848-203X; 0000-0001-5223-0279; 27805532; E-5914-2016; AAK-8077-2021
    Objectives: Here, our aim was to report our treatment strategies and their results performed for visual rehabilitation after penetrating keratoplasty. Materials and Methods: The medical records of 98 patients (54 male/44 female), with results from 104 eyes, who underwent penetrating keratoplasty between January 2013 and January 2015 at the Baskent University Faculty of Medicine, Department of Ophthalmology were reviewed. Patient age, indication for penetrating keratoplasty, interventions performed for visual rehabilitation, follow-up duration, topo graphic and refractive astigmatism at the end of follow-up, and final best corrected visual acuity results were recorded. Results: Mean age of patients was 54 +/- 23 years. Indications for penetrating keratoplasty included keratoconus, Fuchs endothelial dystrophy, pseu dophakic bullous keratopathy, and corneal scarring. The mean duration of follow-up was 23 +/- 11.5 months. Topography-guided suture adjustment and selective suture removal were performed 2 to 6 weeks and after 3 months in eyes with more than 3 diopters of corneal astigmatism in patients who had continuous and interrupted sutures. Spectacle correction was administered for 86 eyes (83%), and contact lenses including rigid gas-permeable and scleral lenses were fitted in 18 eyes (17%) in patients who were unsatisfied with spectacle correction. Relaxing corneal incisions were performed in 23 eyes (22%), and toric intraocular lens implantations were performed in 34 eyes (33%) with cataracts. The mean topographic and absolute refractive astigmatism at the end of followup was 3.4 +/- 2.6 and 3.6 +/- 1.9 diopters. Conclusions: Topography-guided suture adjustment and selective suture removal are effective for minimizing early postoperative astigmatism. If significant astigmatism remains after suture removal, which cannot be corrected by optical means, then further surgical procedures including relaxing incisions and toric intraocular lens implantation can be performed.