Diagnostic Power and Reproducibility of Objective Perimetry in Glaucoma

dc.contributor.authorMaddess, Teden
dc.contributor.authorCarle, Corinne F.en
dc.contributor.authorKolic, Mariaen
dc.contributor.authorSaraç, Özgeen
dc.contributor.authorEssex, Rohan W.en
dc.contributor.authorRohan, Emilie M.F.en
dc.contributor.authorSabeti, Faranen
dc.contributor.authorvan Kleef, Josh P.en
dc.date.accessioned2026-01-12T08:41:31Z
dc.date.available2026-01-12T08:41:31Z
dc.date.issued2024-12-01en
dc.description.abstractPrécis: An objective perimetry method provides four 30-2 style reports in 8 minutes.These comprise sensitivity and delay reports for both eyes.A combined report format shows comparable diagnostic power to 2 forms of automated perimetry.Purpose: To compare objective perimetry with 2 forms of standard automated perimetry (SAP) in glaucoma.Methods: The study cohort contained 40 persons with glaucoma (PwG) and 94 normal control subjects.The PwG had both perimetric and preperimetric eyes.Multifocal pupillographic objective perimetry was performed with the objectiveField Analyser (OFA), which independently assesses the visual fields of both eyes concurrently.Its OFA30 test assessed the central ± 30 degrees, and the OFA15 test assessed the central ± 15 degrees, both providing 30-2 style reports.The OFA tests were repeated 2 weeks apart to assess test-retest variability (TRV).OFA was compared with Matrix and HFA-SITA fast 24-2 threshold testing.Diagnostic power was quantified as the area under the receiver operating characteristic curves (AUROC).Test durations, mean defects, and pattern standard deviations of the 4 tests were compared.Results: At a median of 4.09 ± 0.02 minutes/eye the OFA tests were quicker than SAP (all P ≤ 0.0001), 2 minutes/eye if OFA per-region sensitivities and delays are considered separately.The %AUROCs for OFA, Matrix, and HFA were not significantly different, averaging 93 ± 3% (mean ± SD) in perimetric eyes, and 73 ± 6% in preperimetric eyes.For moderate to severe fields, OFA TRV was less than the published results for SAP.OFA30 mean defects were significantly correlated between repeats (r = 0.91) and with OFA15 (r = 0.93, both P < 0.0001).Conclusions: OFA provides extra functional measures in the form of per-region delays and between-eye asymmetries.Both the OFA wide-field and macular tests provided comparable diagnostic power to SAP and better TRV in damaged eyes.en
dc.description.sponsorshipThis research was supported by the Australian Research Council through the ARC Centre of Excellence in Vision Science (CE0561903) and the Our Health in Our Hands (OHIOH) ANU intramural grant.The authors are grateful to Associate Professor Andrew James for helping to develop the initial mfPOP methods. Conflict of Interest Statement: Prof Ted Maddess has received grant support from Konan Medical USA. Prof Ted Maddess, Dr Corinne F Carle, and Dr Joshua van Kleef could be paid royalties for the sale of the OFA. The other authors have no conflicts to disclose. Funding: This research was supported by the Australian Research Council through the ARC Centre of Excellence in Vision Science (CE0561903) and the Our Health in Our Hands (OHIOH) ANU intramural grant.en
dc.description.statusPeer-revieweden
dc.format.extent11en
dc.identifier.issn1057-0829en
dc.identifier.otherPubMed:39171974en
dc.identifier.otherORCID:/0000-0003-4591-3658/work/201881598en
dc.identifier.otherORCID:/0000-0003-2167-0348/work/201882188en
dc.identifier.otherORCID:/0000-0002-3309-9073/work/201884058en
dc.identifier.scopus85202155966en
dc.identifier.urihttps://hdl.handle.net/1885/733804164
dc.language.isoenen
dc.provenanceThis is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.en
dc.rights© 2024 The Authors en
dc.sourceJournal of Glaucomaen
dc.subject30-2 reporten
dc.subjectautomated perimetryen
dc.subjectglaucomaen
dc.subjectobjective perimetryen
dc.subjectper-region delaysen
dc.subjecttest-retest variabilityen
dc.titleDiagnostic Power and Reproducibility of Objective Perimetry in Glaucomaen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage950en
local.bibliographicCitation.startpage940en
local.contributor.affiliationMaddess, Ted; John Curtin School of Medical Research, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationCarle, Corinne F.; John Curtin School of Medical Research, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationKolic, Maria; University of Melbourneen
local.contributor.affiliationSaraç, Özge; Wills Eye Hospitalen
local.contributor.affiliationEssex, Rohan W.; Canberra Hospitalen
local.contributor.affiliationRohan, Emilie M.F.; John Curtin School of Medical Research, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationSabeti, Faran; John Curtin School of Medical Research, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationvan Kleef, Josh P.; John Curtin School of Medical Research, ANU College of Science and Medicine, The Australian National Universityen
local.identifier.citationvolume33en
local.identifier.doi10.1097/IJG.0000000000002485en
local.identifier.pured5b3fc89-99b1-40cf-911e-68b4c4fdf006en
local.identifier.urlhttps://www.scopus.com/pages/publications/85202155966en
local.type.statusPublisheden

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