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Dry-eye screening by using a functional visual acuity measurement system: the Osaka Study.

Minako Kaido1, Miki Uchino2, Norihiko Yokoi3

  • 1Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.

Investigative Ophthalmology & Visual Science
|May 8, 2014
PubMed
Summary

A new discriminant equation combining visual acuity and dry eye symptoms shows promise for screening visual display terminal users with unstable tear film. Further refinement is needed for optimal clinical use.

Keywords:
dry eyefunctional visual acuityscreeningtear break up timevisual display terminal user

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Area of Science:

  • Ophthalmology
  • Digital Health
  • Public Health

Background:

  • Digital screens are ubiquitous in modern life.
  • Prolonged use of visual display terminals (VDTs) is associated with digital eye strain and dry eye disease (DED).
  • Accurate prediction of DED in VDT users is crucial for early intervention.

Purpose of the Study:

  • To evaluate if functional visual acuity (VA) parameters and a dry eye symptoms questionnaire can predict DED in VDT users.
  • To assess the diagnostic performance of these parameters individually and in combination.

Main Methods:

  • A prospective study of 491 VDT users.
  • Classification into definite or probable DED groups based on symptoms, tear film stability (tear breakup time - TBUT), and corneal staining.
  • Assessment of functional VA parameters and administration of a DED symptoms questionnaire.
  • Univariate and discriminant analyses to predict DED group allocation.

Main Results:

  • The study included 320 individuals in the DED group and 171 in the non-DED group.
  • Tear breakup time (TBUT) was significantly lower in the DED group (3.1s vs. 5.9s).
  • A discriminant equation combining functional VA and questionnaire data achieved an Area Under the Curve (AUC) of 0.735, with 85.9% sensitivity and 45.6% specificity for DED prediction.

Conclusions:

  • A discriminant equation integrating functional VA measurements and a dry eye symptoms questionnaire shows potential as an initial screening tool for DED, particularly for individuals with unstable tear film.
  • The current questionnaire demonstrates suboptimal sensitivity and specificity, necessitating further improvements for effective clinical implementation.