Evidence map›Paper›PMID 41801663›Full record

ArticleOphthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists)2026

Tear Clearance Rate Assessment with a Modified Slit Lamp Biomicroscope.

Izabela K Garaszczuk

Abstract read
In one paragraph

Article in Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Izabela K GaraszczukVisual Optics Group, Cathedral of Optics and Photonics, Department of Fundamental Problems of Technology, Wroclaw University of Science and Technology, Wrocław, Poland. Izabela.garaszczuk@pwr.edu.pl.ORCID http://orcid.org/0000-0002-0560-7069

Funding

Narodowe Centrum Nauki 2023/07/X/NZ7/00311
6 · The paper itself

Abstract

purposeTear clearance rate (TCR) was assessed historically with fluorophotometry and used as a marker of dry eye disease (DED). Since it requires advanced tools and specialised expertise, this method has largely been confined to research settings. This study proposed a clinically accessible method for assessing TCR using a modified slit lamp biomicroscope.

methodsThis cross-sectional study included 95 subjects divided into dry eye (n = 65) and age-matched control (n = 30) groups. Five microlitres of 0.5% fluorescein solution was instilled, and tear fluorescence intensity decay was recorded over 5 min post instillation using a smartphone attached to a slit lamp biomicroscope, equipped with narrow-band filters designed to observe fluorescence. Custom-written software was used to quantify fluorescence intensity over time from the entire exposed ocular surface and calculate blinking frequency. TCR was calculated as the percentage drop in image intensity at selected intervals (0, 0.5, 1, 2, 3, 4 and 5 min) post instillation. Additionally, subjects underwent symptom assessment (ocular surface disease index (OSDI) and 5-item dry eye questionnaire (DEQ-5)), tear osmolarity, ocular surface staining, tear meniscus height, bulbar and limbal redness and noninvasive tear film break-up time (NIKBUT) assessment with the Oculus Keratograph 5M.

resultsBiomicroscope-based TCRs were lower in the DED group than controls, with TCR₀.₅₋₂ (percentage decrease in fluorescence intensity between 30 s and 2 min after instillation) showing the strongest discriminatory capacity between these two groups (TCR₀.₅₋₂: 6.9% vs. 13.8%, p < 0.01). Early-phase TCRs correlated linearly with DED severity, OSDI, DEQ-5 and ocular surface staining (r from -0.21 to -0.43, all p < 0.05) and positively with measures of NIKBUT (r from 0.27 to 0.30, all p < 0.01).

conclusionsThis study demonstrated the clinical feasibility of assessing TCR using a modified slit lamp biomicroscope. The method discriminates effectively between non-DED and DED subjects, with strong correlations with established diagnostic parameters.

Indexed as

Dry Eye SyndromesSlit Lamp MicroscopyTearsAdultAgedBlinkingCross-Sectional StudiesFemaleFluoresceinFluorophotometryHumansMaleMiddle AgedFluoresceinDry eye diseaseFluorescein imagingOcular surfaceSlit lamp biomicroscopeTear clearance rateTear film dynamics

Identifiers

PMID41801663
PMCPMC13368879

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.