Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111748
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dc.contributorSchool of Optometry-
dc.creatorSantodomingo-Rubido, J-
dc.creatorCheung, SW-
dc.creatorVilla-Collar, C-
dc.date.accessioned2025-03-14T03:56:50Z-
dc.date.available2025-03-14T03:56:50Z-
dc.identifier.issn1367-0484-
dc.identifier.urihttp://hdl.handle.net/10397/111748-
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.rights© 2024 The Author(s). Published by Elsevier Ltd on behalf of British Contact Lens Association. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Santodomingo-Rubido, J., Cheung, S.-W., & Villa-Collar, C. (2025). The safety of orthokeratology contact lens wear in slowing the axial elongation of the eye in children. Contact Lens and Anterior Eye, 48(1), 102258 is available at https://doi.org/10.1016/j.clae.2024.102258.en_US
dc.subjectAdverse eventen_US
dc.subjectComplicationen_US
dc.subjectDiscontinuationen_US
dc.subjectDropouten_US
dc.subjectMyopia controlen_US
dc.subjectMyopia managementen_US
dc.subjectMyopia progressionen_US
dc.titleThe safety of orthokeratology contact lens wear in slowing the axial elongation of the eye in childrenen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume48-
dc.identifier.issue1-
dc.identifier.doi10.1016/j.clae.2024.102258-
dcterms.abstractPurpose: To evaluate the safety of orthokeratology contact lens wear in slowing the axial elongation of the eye in myopic children.-
dcterms.abstractMethods: Safety data from three prospective studies, which evaluated the use of orthokeratology for slowing myopia progression in children in comparison to a parallel control group of single-vision spectacle lens wearers over a 2-year period, were pooled together for analysis. The primary and secondary safety endpoints are the comparisons of adverse events and slit-lamp findings grades ≥ 2 between orthokeratology and control groups, respectively.-
dcterms.abstractResults: Collectively, data from 125 orthokeratology and 118 control subjects were analyzed in this study. Of these, 101 (81 %) and 88 (75 %) orthokeratology and control subjects completed the 2-year follow-up period, respectively. Nineteen orthokeratology subjects experienced 28 adverse events, of which 6 were significant, whereas just one adverse event was found in the control group; this difference was statistically significant (p < 0.001). Most adverse events found in the orthokeratology group were corneal in nature, primarily corneal abrasion/staining, accounting for around 40 % of all adverse events. Of the 28 adverse events, only 18 (3 significant) are likely to be contact lens-related, leading to incidence rates of total and device-related adverse events per 100 patient years of lens wear (95 % confidence intervals) of 13.1 (9.2–18.2) and 8.4 (5.4–10.7), respectively. No significant differences were found between groups in the total number of silt-lamps findings with grades ≥ 2 (p > 0.05).-
dcterms.abstractConclusion: Around 13% of eyes wearing overnight orthokeratology contact lenses are likely to experience an adverse event over one year of lens wear, with this figure being lower when considering device-related adverse events alone. No serious adverse events were found, with most being non-significant. These results inform eye care practitioners on the safety of orthokeratology lenses when prescribed for slowing myopia progression to myopic children.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationContact lens and anterior eye, Feb. 2025, v. 48, no. 1, 102258-
dcterms.isPartOfContact lens and anterior eye-
dcterms.issued2025-02-
dc.identifier.scopus2-s2.0-85198373573-
dc.identifier.eissn1476-5411-
dc.identifier.artn102258-
dc.description.validate202503 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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