TFOS DEWS III Diagnostic Methodology

James S. Wolffsohn*, Jose Benitez-Del-Castillo, Denise Loya-Garcia, Takenori Inomata, Geetha Iyar, Lingyi Liang, Heiko Pult, Alfonso L. Sabater, Christopher E. Starr, Jelle Vehof, Michael TM Wang, Wei Chen, Jennifer P. Craig, Murat Dogru, Victor L. Perez Quinones, Fiona Stapleton, David A. Sullivan, Lyndon Jones, TFOS collaborator group

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

A standard approach to the diagnosis of dry eye disease across eye care practitioners is critical to reassuring the patient, providing consistency between practitioners and informing governments as to the true prevalence and resulting healthcare needs. The Tear Film & Ocular Surface Society (TFOS) Dry Eye Workshop (DEWS) III has reviewed the evidence-base since their previous reports published in 2017 and revised the definition to “Dry eye is a multifactorial, symptomatic disease characterized by a loss of homeostasis of the tear film and/or ocular surface, in which tear film instability and hyperosmolarity, ocular surface inflammation and damage, and neurosensory abnormalities are etiological factors.” Key features from the definition include that dry eye disease is multifactorial, is a disease and not a syndrome and is always symptomatic. Differential diagnosis and ocular examination guidance is given along with the risk factors that should be discussed with the patient. The recommended screening questionnaire is the OSDI-6 with a cut-off score ≥4. A positive result together with a non-invasive breakup time <10s or alternatively tear film hyperosmolarity (≥308mOsm/L in higher eye or an interocular difference >8mOsm/L) gives a diagnosis of dry eye. In addition, the ocular surface should be stained and positive symptomology together with >5 corneal fluorescein and/or >9 conjunctival lissamine green punctate spots and/or lid margin lissamine green staining of ≥2mm length & ≥25 %width also gives a diagnosis of dry eye. Subclassification was separated into tear film (lipid, aqueous and mucin/glycocalyx) and ocular surface and adnexa (anatomical misalignment, blink/lid closure, lid margin, neural dysfunction, ocular surface cell damage/disruption and primary inflammation/oxidative stress) components, with appropriate clinical tests and cut-offs provided to identify these etiological drivers in an individual, to inform appropriate management and therapy.
Original languageEnglish
Number of pages101
JournalAmerican Journal of Ophthalmology
Early online date30 May 2025
DOIs
Publication statusE-pub ahead of print - 30 May 2025

Bibliographical note

Copyright © 2025 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/)

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