Comparative Evaluation of Clinical Methods of Tear Film Stability Assessment: A Randomized Crossover Trial.

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dc.contributor.author Wang, Michael en
dc.contributor.author Craig, Jennifer en
dc.date.accessioned 2018-10-14T22:23:25Z en
dc.date.issued 2018-03 en
dc.identifier.issn 2168-6165 en
dc.identifier.uri http://hdl.handle.net/2292/41359 en
dc.description.abstract Importance:Tear film breakup time assessment is an integral component of dry eye evaluation. To our knowledge, the comparative discriminative ability of the noninvasive Keratograph (Oculus) vs conventional fluorescein method in detecting dry eye is unknown. Objective:To compare tear film stability measurements obtained with an automated noninvasive corneal topographer vs conventional fluorescein methods and evaluate their respective discriminative ability in detecting dry eye. Design, Setting, and Participants:This investigator-masked randomized crossover trial was conducted at a single-center university clinic between May 26, 2016, and October 3, 2016, and included 74 participants 18 years or older. Participants were recruited into 2 equally sized age, sex, and race/ethnicity-matched groups, with and without symptomatic dry eye (Ocular Surface Disease Index ≥13). Interventions:Participants were assigned to receive a noninvasive keratograph evaluation and topical fluorescein instillation in a randomized order. Main Outcomes and Measures:Noninvasive keratograph breakup time (NIKBUT) and fluorescein breakup time (TBUT). Area under the receiver operating characteristic curve, Youden-optimal diagnostic cutoff sensitivity, and specificity of NIKBUT and TBUT in detecting dry eye. Results:Seventy-four participants (74 eyes; 43 women [58.1%]) with a mean (SD) age of 24 (4) years were randomized. Noninvasive keratograph breakup time was significantly longer than TBUT in participants with dry eye (median, 6.3 seconds vs 4.3 seconds [difference, 2.0 seconds]; 95% CI, 1.1-3.4 seconds; P = .003), and healthy participants (median, 11.9 seconds vs 5.0 seconds [difference, 6.9 seconds]; 95% CI, 4.7-7.6 seconds; P < .001). Fluorescein breakup time measurements were more narrowly distributed in both the dry eye (variance, 188 seconds2 vs 27.9 seconds2; P < .001) and control groups (variance, 113 seconds2 vs 13.4 seconds2; P < .001). The discriminative ability of NIKBUT in detecting dry eye (area under the receiver operating characteristic curve, 0.68; 95% CI, 0.56-0.81; P = .007) was greater than that of TBUT (area under the receiver operating characteristic curve, 0.57; 95% CI, 0.44-0.70; P = .31). The optimal diagnostic cutoff for NIKBUT was 9 seconds or less with a sensitivity of 68% (95% CI, 50%-82%), specificity of 70% (95% CI, 53%-84%), positive likelihood ratio of 2.27 (95% CI, 1.32-3.91), and negative likelihood ratio of 0.46 (95% CI, 0.28-0.77). The optimal threshold for TBUT was 5 seconds or less with a sensitivity of 54% (95% CI, 37%-71%), specificity of 68% (95% CI, 50%-82%), positive likelihood ratio of 1.67 (95% CI, 0.96-2.89), and negative likelihood ratio of 0.68 (95% CI, 0.45-1.03). Conclusions and Relevance:Conventional fluorescein tear film breakup time measurements were significantly shorter with narrower distributions, while automated noninvasive keratograph readings displayed superior discriminative ability in detecting dry eye. Trial Registration:anzctr.org.au Identifier: ACTRN12617001428358. en
dc.format.medium Print en
dc.language eng en
dc.relation.ispartofseries JAMA ophthalmology en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Tears en
dc.subject Humans en
dc.subject Dry Eye Syndromes en
dc.subject Fluorescein en
dc.subject Fluorescent Dyes en
dc.subject False Positive Reactions en
dc.subject Corneal Topography en
dc.subject Likelihood Functions en
dc.subject Sensitivity and Specificity en
dc.subject Prospective Studies en
dc.subject Cross-Over Studies en
dc.subject Double-Blind Method en
dc.subject Predictive Value of Tests en
dc.subject ROC Curve en
dc.subject Adult en
dc.subject Female en
dc.subject Male en
dc.subject Young Adult en
dc.title Comparative Evaluation of Clinical Methods of Tear Film Stability Assessment: A Randomized Crossover Trial. en
dc.type Journal Article en
dc.identifier.doi 10.1001/jamaophthalmol.2017.6489 en
pubs.issue 3 en
pubs.begin-page 291 en
pubs.volume 136 en
dc.rights.holder Copyright: The author en
dc.identifier.pmid 29392287 en
pubs.end-page 294 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Comparative Study en
pubs.subtype brief-report en
pubs.subtype Research Support, Non-U.S. Gov't en
pubs.subtype Randomized Controlled Trial en
pubs.subtype Journal Article en
pubs.elements-id 723021 en
pubs.org-id Medical and Health Sciences en
pubs.org-id School of Medicine en
pubs.org-id Ophthalmology Department en
dc.identifier.eissn 2168-6173 en
pubs.record-created-at-source-date 2018-02-03 en
pubs.dimensions-id 29392287 en


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