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dc.contributor.authorCoco Martín, Rosa María 
dc.contributor.authorPichel Mouzo, María Dolores
dc.contributor.authorFernández Martínez, Itziar 
dc.contributor.authorPlata Cordero, María
dc.contributor.authorLópez Miguel, Alberto 
dc.date.accessioned2024-07-22T08:33:53Z
dc.date.available2024-07-22T08:33:53Z
dc.date.issued2020-11
dc.identifier.citationEur J Ophthalmol, Nov, 2020; vol.30, n. 6 p.1480-1486.es
dc.identifier.issn1120-6721es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/68936
dc.descriptionProducción Científicaes
dc.description.abstractABSTRACT: BACKGROUND: The aim of this study was to determine the intra-session repeatability and inter-examiner reproducibility of the colour perimetry technique when assessing in vivo macular pigment optical density in age-related macular degeneration patients. METHODS: Age-related macular degeneration patients were classified into four groups: early age-related macular degeneration, intermediate age-related macular degeneration, atrophic age-related macular degeneration and neovascular age-related macular degeneration after undergoing fundus photography (TRC 50DX type IA) and spectral-domain optical coherence tomography analysis (Topcon 3D-2000). Central fixation was confirmed in all patients using the MP-1 microperimeter (Nidek, Padua, Italy). To analyse repeatability, one examiner obtained three consecutive macular pigment optical density measures with MonCV3 device (Metrovision, Perenchies, France). To study agreement between two observers, a second examiner performed another macular pigment optical density measurement in random order. Within-subject standard deviation, coefficient of variation, and intraclass correlation coefficient data were obtained. RESULTS: Fifty two (32 females and 20 males) consecutive age-related macular degeneration patients having a mean age of 71.5 ± 8.2 years were recruited. Six had early age-related macular degeneration, 25 had intermediate age-related macular degeneration, 10 had atrophic age-related macular degeneration and 11 had neovascular age-related macular degeneration. For repeatability, coefficient of variation values ranged from 22.3% (neovascular age-related macular degeneration) to 41.0% (atrophic age-related macular degeneration) and intraclass correlation coefficient values from 0.52 (intermediate age-related macular degeneration) to 0.79 (neovascular age-related macular degeneration). For agreement between two examiners, coefficient of variation values ranged from 20.1% (intermediate age-related macular degeneration) to 37.8% (neovascular age-related macular degeneration) and intraclass correlation coefficient values from 0.61 (neovascular age-related macular degeneration) to 0.80 (atrophic age-related macular degeneration). CONCLUSION: The reliability (intra-session repeatability and inter-examiner reproducibility) of colour perimetry technique to assess macular pigment optical density in age-related macular degeneration patients is only moderate. Thus, it cannot be recommended to be performed when evaluating and monitoring age-related macular degeneration patients in the daily clinic.es
dc.format.mimetypeapplication/mswordes
dc.language.isoenges
dc.publisherSAGE Publications LTDes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationAge-related Macular Degeneration, macular pigment optical density, color perimetry technique, intra-session repeatability, inter-examiner reproducibility.es
dc.titleReliability of colour perimetry to assess macular pigment optical density in age-related macular degenerationes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holderSAGEes
dc.identifier.doi10.1177/1120672119870362es
dc.relation.publisherversionhttps://journals.sagepub.com/doi/10.1177/1120672119870362?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmedes
dc.identifier.publicationfirstpage1480es
dc.identifier.publicationissue6es
dc.identifier.publicationlastpage1486es
dc.identifier.publicationtitleEuropean Journal of Ophthalmologyes
dc.identifier.publicationvolume30es
dc.peerreviewedSIes
dc.identifier.essn1724-6016es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones
dc.subject.unesco3201.09 Oftalmologíaes


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