TFOS DEWS III: Diagnostic Methodology

医学 计算机科学 验光服务
作者
James S. Wolffsohn,José M. Benítez-Del-Castillo,Denise Loya-García,Takenori Inomata,Geetha Iyer,Lingyi Liang,Heiko Pult,Alfonso L. Sabater,Christopher E. Starr,Jelle Vehof,Michael T.M. Wang,Wei Chen,Jennifer P. Craig,Murat Doğru,Victor L Perez Quinones,Fiona Stapleton,David A. Sullivan,Lyndon Jones
出处
期刊:American Journal of Ophthalmology [Elsevier BV]
卷期号:279: 387-450 被引量:125
标识
DOI:10.1016/j.ajo.2025.05.033
摘要

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 either eye or an interocular difference >8mOsm/L) or alternatively >5 corneal fluorescein and/or >9 conjunctival lissamine green punctate spots and/or lid margin lissamine green staining of ≥2mm length & ≥25 % width, gives a diagnosis of dry eye. Subclassification was separated into tear film deficiencies (lipid, aqueous and mucin/glycocalyx), eyelid anomalies (blink/lid closure and lid margin) and ocular surface abnormalities (anatomical misalignment, 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.
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