Validation of 3nethra specto, a wearable digital subjective refractor versus conventional subjective refraction for refractive error measurement in young adults: a comparative study.

IF 2.7 Q2 OPHTHALMOLOGY
Kaushik Murali, Namratha Hegde, Afia S, Varshini M, Disha Agarwal, Revathy Manthri Rangaraj, Rashmi Hullur, Kousar Sidiq, Venkatakrishnan S
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引用次数: 0

Abstract

Background: Refractive errors cause significant preventable visual impairment globally, particularly in underserved areas. Conventional subjective refraction remains the gold standard but proves examiner-dependent, time-consuming and challenging in high-volume settings. The 3nethra Specto, a wearable digital subjective refractometer, offers rapid refractive assessment. This study evaluates its accuracy and repeatability versus conventional methods.

Methods: A prospective comparative study was conducted on 135 subjects who underwent both conventional subjective refraction and 3nethra Specto assessment. Spherical (S), cylindrical (C) and axis measurements were analysed using power vector transformation (J₀, J₄₅). Primary predictive validity was assessed using univariate general linear models (GLMs) (IBM SPSS V.25.0) with age/sex as covariates. Model fit was evaluated via F-statistics, R² and residual SD. Instrument repeatability used GLM Repeated Measures, agreement assessed via Bland-Altman plots, keeping significance at p<0.05. Patient and examiner feedback on the instrument was captured using the User Experience questionnaire.

Results: Of 135 adults (mean age 31.5±8.9 years; 60% male), compound myopic astigmatism predominated (45%). 3nethra Specto measurements closely matched subjective refraction (sphere: -1.02 D vs -0.99 D; cylinder: -0.49 D vs -0.83 D; M: -1.26 D vs -1.24 D). GLM analysis showed excellent predictive validity (all p<0.001; R² 0.914 to 0.994; residual SD 0.084 D to 0.228 D). Bland-Altman plots confirmed 95% limits of agreement of -0.39 D to +0.47 D for M and -0.62 D to +0.64 D for J₀ and -0.32 D to +0.35 D for J₄₅. Device repeatability was high (all F>96, p<0.001; R²≥0.956; residual SD≤0.148 D). Patients rated subjective refraction higher for comfort/enjoyability but found 3nethra more inventive/exciting; examiners preferred 3nethra for efficiency, speed, innovation and ease of use.

Conclusions: The 3nethra Specto wearable liquid lens refractor demonstrated excellent agreement and repeatability with traditional subjective refraction across all refractive parameters, confirming clinical equivalence. Positive patient and examiner feedback highlighted its innovation, efficiency and usability. This device offers a reliable alternative for routine refractive assessment in clinical settings.

验证3nethra specto,一种可穿戴数字主观折射与传统主观折射测量年轻人屈光不正:一项比较研究。
背景:屈光不正在全球范围内造成严重的可预防的视力损害,特别是在服务不足的地区。传统的主观折射仍然是黄金标准,但在大容量环境中,它被证明依赖于考官,耗时且具有挑战性。3nethra Specto是一款可穿戴式数字主观折射仪,可提供快速的折射评估。本研究对比传统方法评估其准确性和可重复性。方法:对135例接受常规主观屈光检查和3nethra Specto检查的患者进行前瞻性比较研究。使用功率矢量变换(J 0, J₄₅)分析了球面(S),圆柱形(C)和轴向测量。以年龄/性别为协变量,采用单变量一般线性模型(GLMs) (IBM SPSS V.25.0)评估初级预测效度。通过f统计量、R²和残差SD评估模型拟合。仪器重复性采用GLM重复测量,通过Bland-Altman图评估一致性,结果保持显著性:135名成年人(平均年龄31.5±8.9岁;60%男性),复度性近视散光占主导地位(45%)。nethra Specto测量结果与主观折射密切匹配(球体:-1.02 D vs -0.99 D;圆柱体:-0.49 D vs -0.83 D; M: -1.26 D vs -1.24 D)。结论:3nethra Specto可穿戴式液体晶体屈光仪在所有屈光参数上与传统主观屈光仪表现出良好的一致性和可重复性,证实了临床等效性。病人和审查员的积极反馈突出了它的创新性、效率和可用性。该设备为临床常规屈光评估提供了可靠的替代方法。
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来源期刊
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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