Repeatability and Reproducibility of an Automated Image-Processing Software for Quantitative Conjunctival Hyperemia Analysis: A Pilot Study
Keywords:
repeatability, reproducibility, conjunctival hyperemia, automated, softwareAbstract
Objective Conjunctival hyperemia reflects the severity of various ocular conditions and is a common side effect of glaucoma medications, posing a significant concern for affected patients. Most existing clinical grading systems are subjective and rely heavily on individual physician interpretation, making interobserver comparison difficult. We developed an automated grading software to objectively and quantitatively assess conjunctival hyperemia. This study aimed to evaluate the repeatability and reproducibility of a newly developed automated software for quantitative assessment of conjunctival hyperemia in glaucoma patients in a pilot validation study.
Methods In this pilot study, glaucoma patients using at least one topical anti-glaucoma medication and exhibiting conjunctival hyperemia were enrolled. Each patient’s conjunctival hyperemia was assessed using the automated software, which segmented images into four regions: blood vessel area, strong red area, weak red area, and non-red area. An automatic region of interest (ROI) registration function was incorporated to enhance measurement consistency. Repeatability was assessed using two measurements from the same image, and reproducibility was tested using separate images of the same eye.
Results Eighty images from twenty glaucoma patients were analyzed (collected between December 1, 2016, and December 31, 2018). Following administration of 10% phenylephrine ophthalmic solution, the percentage
of conjunctival hyperemia decreased significantly in all regions (p < 0.001). Spearman correlation coefficients for repeated measurements on the same image were 0.884 (blood vessel), 0.982 (strong red), and 0.932 (weak red). Corresponding values for repeated images of the same eye were 0.988, 0.992, and 0.995, respectively. The intraclass correlation coefficient (ICC) for clinical grading by ten ophthalmologists was 0.969 (95% CI: 0.952–0.981).
Conclusion This pilot study demonstrates that the proposed automated software provides an objective and quantitative assessment of conjunctival hyperemia with excellent repeatability and reproducibility. The system shows high correlation with clinical grading and may serve as a reliable tool for monitoring conjunctival hyperemia changes in clinical practice.
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