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dc.contributor.authorKır, Muhammet Bahattin
dc.contributor.authorTürkyılmaz, Kemal
dc.contributor.authorÖner, Veysi
dc.date.accessioned2020-12-19T19:49:38Z
dc.date.available2020-12-19T19:49:38Z
dc.date.issued2017
dc.identifier.citationKır, M. B., Türkyılmaz, K., & Öner, V. (2017). Transepithelial High-Intensity Cross-Linking for the Treatment of Progressive Keratoconus: 2-year Outcomes. Current eye research, 42(1), 28–31. https://doi.org/10.3109/02713683.2016.1148742en_US
dc.identifier.issn0271-3683
dc.identifier.issn1460-2202
dc.identifier.urihttps://doi.org/10.3109/02713683.2016.1148742
dc.identifier.urihttps://hdl.handle.net/11436/2314
dc.descriptionWOS: 000393881100004en_US
dc.descriptionPubMed: 27249007en_US
dc.description.abstractPurpose: To report 2-year outcomes of transepithelial high-intensity cross-linking (CXL) procedure in the treatment of patients with progressive keratoconus.Methods: Forty-eight eyes of 48 consecutive progressive keratoconus patients who underwent transepithelial accelerated CXL procedure were enrolled in the study. Each patient underwent pre- and postoperative comprehensive ophthalmologic examinations including determination of refractive error as spherical equivalent (SE) and corrected distant visual acuity (CDVA), slit lamp biomicroscopic examination, fundoscopy, and a detailed analysis on a Scheimplug+Placido device (Sirius, CSO, Florence, Italy). the riboflavin solution, which was composed of riboflavin 0.25% with hydroxypropyl methylcellulose (HPMC) and benzalkonium chloride (BAC) (ParaCel, Avedro), was used in the procedure. the cornea was exposed to ultraviolet A light (KXL System, Avedro Inc., Waltham, MS, USA) for 2 minutes and 40 seconds at an irradiance of 45 mW/cm(2).Results: the mean age of the patients was 25.9 4.0 (ranging from 18 to 33) years. No significant changes were observed in the mean CDVA, SE, and topographic indices at year 1 and year 2 visits compared to preoperative examination. the mean corneal thickness at the thinnest point was significantly higher at year 1 and year 2 visits than at preoperative examination (p1 = 0.014 and p2 = 0.017, respectively). No intra- or postoperative complications or adverse reactions were observed.Conclusions: Transepithelial high-intensity (irradiance of 45 mW/cm(2) for 2 minutes and 40 seconds) CXL using 0.25% riboflavin solution was a safe and effective method to halt the progression of keratoconus for a 2-year follow-up period.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCorneaen_US
dc.subjectCross-linkingen_US
dc.subjectHigh-intensityen_US
dc.subjectKeratoconusen_US
dc.subjectTransepithelialen_US
dc.titleTransepithelial high-intensity cross-linking for the treatment of progressive keratoconus: 2-year outcomesen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorTürkyılmaz, Kemal
dc.contributor.institutionauthorÖner, Veysi
dc.identifier.doi10.3109/02713683.2016.1148742
dc.identifier.volume42en_US
dc.identifier.issue1en_US
dc.identifier.startpage28en_US
dc.identifier.endpage31en_US
dc.relation.journalCurrent Eye Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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