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dc.contributor.authorGarcía Espinilla, Óscar
dc.contributor.authorSánchez Pavón, Irene 
dc.contributor.authorGallegos Cocho, Inés
dc.contributor.authorCañadas Suárez, María del Pilar 
dc.contributor.authorMartín Herranz, Raúl 
dc.date.accessioned2024-01-30T10:59:20Z
dc.date.available2024-01-30T10:59:20Z
dc.date.issued2023
dc.identifier.citationClinical and Experimental Optometry, Enero 2023, vol. 106. p. 69-74.es
dc.identifier.issn0816-4622es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/65292
dc.descriptionProducción Científicaes
dc.description.abstractClinical relevance: Ophthalmic lens adaptation requires accurate measurements of physiognomy parameters and frame angles, with a great impact on subject vision, especially when personalised progressive addition lenses are prescribed. Background: The aim of this study is to describe interdevice agreement between different methods and traditional methods (frame ruler). Methods: The agreement of the interpupillary distance, nasopupillary distance and fitting point height measured with four devices (PD-5, OptiCenter, Visioffice and a frame ruler) and of pantoscopic and frame wrap angles measured with three devices (OptiCenter, Visioffice and Essilor standard ruler) was assessed in 21 healthy volunteers, by a Bland-Altman analysis; mean difference and limits of agreement (LoA) were calculated. Results: Frame ruler nasopupillary distance measurements showed limited agreement with PD-5 [−0.38 ± 1.03 (LoA −2.40 to 1.64) and 0.44 ± 1.02 (LoA −1.72 to 2.61)] and Visioffice [0.62 ± 1.24 (LoA −1.81 to 3.05) and −0.16 ± 1.72 (LoA −3.54 to 3.22)] measurements for the right and left eyes, respectively. Poor agreement was found for interpupillary distances (PD-5 [0.21 ± 1.47 (LoA −2.67 to 3.09)], OptiCenter [−0.05 ± 1.16 (LoA −2.32 to 2.22)] and Visioffice [0.46 ± 1.95 (LoA −3.36 to 4.28)]), fitting point height (OptiCenter [−1.27 ± 2.56 (LoA −6.27 to 3.75) and −0.92 ± 2.77 (LoA −6.35 to 4.51)] and Visioffice [−5.88 ± 6.21 (LoA −18.05 to 6.29) and −5.98 ± 6.12 (LoA −17.98 to 6.02)] for the right and left eyes, respectively) and pantoscopic and frame wrap angles (OptiCenter [−4.13 ± 3.75 (LoA −11.48 to 3.22) and −1.09 ± 0.60 (LoA −2.27 to 0.09)] and Visioffice [−6.18 ± 3.53 (LoA −13.10 to 0.74) and −1.93 ± 3.49 (LoA −8.77 to 4.91)], respectively). Conclusions: These results suggest that measurements of physiognomy and frame angles are not interchangeable between assessed devices and that these differences could induce lens centration errors with a large impact on progressive addition lens prescriptions.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses
dc.subjectOptometríaes
dc.subject.classificationOphthalmic lenses adaptationes
dc.subject.classificationProgressive addition lenseses
dc.subject.classificationPresbyopia managementes
dc.titleInterdevice agreement in the measurement of physiognomy parameters and frame angles to prescribe progressive addition lenseses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1080/08164622.2021.2006042es
dc.identifier.publicationfirstpage69es
dc.identifier.publicationissue1es
dc.identifier.publicationlastpage74es
dc.identifier.publicationtitleClinical and Experimental Optometryes
dc.identifier.publicationvolume106es
dc.peerreviewedSIes
dc.identifier.essn1444-0938es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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