The repeatability of tests for dry eye signs and symptoms in the dry eye assessment and management (DREAM) study.

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Tác giả: Penny Asbell, Patrick Augello, Anna Chen, Gui-Shuang Ying

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : Contact lens & anterior eye : the journal of the British Contact Lens Association , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 715784

 PURPOSE: To assess the repeatability of measures for dry eye disease (DED) symptoms and signs in the DREAM study. METHODS: At screening and baseline visits approximately 2 weeks apart, participants were assessed for symptoms by Ocular Surface Disease Index (OSDI) and Brief Ocular Discomfort Index (BODI), and signs by the same physician in the same order: tear break-up time (TBUT), corneal staining, conjunctival staining, Meibomian gland evaluation, and the Schirmer test. The repeatability of DED symptoms and signs was assessed by interclass correlation coefficient (ICC), 95 % limits of agreement, and the percent of eyes with inter-visit difference above the clinically significant threshold. RESULTS: Among 1046 eyes (523 participants), ICC for signs ranged from 0.53 (TBUT) to 0.73 (corneal staining). A substantial percentage of eyes showed clinically significant inter-visit differences: ≥2 points in 17.8 % of eyes for conjunctival staining
  ≥3 points in 18.8 % for corneal staining
  >
 2 s in 14.1 % for TBUT
  ≥5 mm/5 min in 29.9 % for the Schirmer test, and ≥ 2 points in 27.5 % for Meibomian gland plugging and lid secretion. The OSDI and BODI had ICC of 0.64 and 0.63 respectively, and nearly 40 % of participants had inter-visit score differences ≥ 10 points. CONCLUSION: In DREAM participants with moderate-to-severe DED, DED signs and symptoms had moderate repeatability, with ocular surface staining scores being the most repeatable and TBUT the least repeatable. A notable percentage of participants had inter-visit differences above the clinically meaningful threshold. These test-retest variabilities in DED signs and symptoms should be considered for designing clinical trials and monitoring disease progression.
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