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《弱视追踪器应用程序评估》

Evaluation of the Amblyopia tracker app.

机构信息

School of Health Sciences, University of Liverpool, Thompson Yates Building, Brownlow Hill, Liverpool, L69 3GB, UK.

Orthoptic Department, Manchester Royal Eye Hospital, Manchester, UK.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2024 Aug;262(8):2675-2683. doi: 10.1007/s00417-024-06413-0. Epub 2024 Feb 27.

Abstract

PURPOSE

The Amblyopia tracker app has been developed to be a tool for parents to monitor changes in vision at home during amblyopia treatment. The aims of this study were to evaluate the feasibility and repeatability of parents testing their children at home and to compare home test results to an assessment in clinic by an orthoptist.

METHODS

Children (age < 18 years) with amblyopia (interocular acuity difference of ≥ 0.2logMAR) were recruited. Parents were asked to test their child with the app three times during a two week period followed by an online questionnaire about the usability. Participants also tested within 48 h of their appointment where the measurement was repeated by an orthoptist.

RESULTS

Out of 277 potential participants contacted, 37 completed three home measurements, mean age 6.8 years (SD 2.94). Home tests comparisons were made between test two and three to ensure familiarity with the process. Paired t-tests showed no statistically significant difference for either eye or the interocular acuity difference (IAD). However, 29% had a difference in IAD of more than 0.1logMAR on repeated testing, with a maximum of 0.4logMAR difference in the IAD. Questionnaire responses from the parents who participated were predominantly positive with 97% of respondents saying they would use it if were available. Comparison of home and clinical measurements (n = 23, mean age 6.72 SD 2.60) showed no statistically significant differences for either eye or interocular acuity difference (paired t-test, p > 0.3 in all cases).

CONCLUSION

Results show no statistically significant differences for the Amblyopia tracker app when used by parents at home on repeated testing, or between the home test by a parent and the test by a clinician. However, variability in the results does indicate that further improvements are required to ensure the results can be used as a reliable clinical tool.

摘要

目的

开发弱视追踪器应用程序是为了让父母在家中监测弱视治疗期间的视力变化。本研究的目的是评估父母在家中为孩子进行测试的可行性和可重复性,并比较父母在家中测试的结果与视轴矫正专家在诊所进行评估的结果。

方法

招募患有弱视(双眼视力差异≥0.2logMAR)的儿童(年龄<18 岁)。要求父母在两周内使用该应用程序为孩子测试三次,并在线回答关于易用性的问卷。参与者也在预约后 48 小时内进行测试,由视轴矫正专家重复测量。

结果

在联系的 277 名潜在参与者中,有 37 名完成了三次家庭测试,平均年龄为 6.8 岁(标准差 2.94)。为了确保对测试过程的熟悉度,对测试二和测试三进行了比较。配对 t 检验显示,无论是单眼还是双眼视力差异,都没有统计学上的显著差异。然而,29%的人在重复测试时双眼视力差异超过 0.1logMAR,双眼视力差异最大为 0.4logMAR。参与的父母对问卷调查的回答主要是积极的,97%的受访者表示如果有可用的,他们会使用它。对 23 名在家中进行测试和在诊所进行测试的父母(平均年龄 6.72,标准差 2.60)进行比较,无论是单眼还是双眼视力差异,都没有统计学上的显著差异(配对 t 检验,所有情况下 p>0.3)。

结论

结果表明,父母在家中重复测试或父母在家中测试与视轴矫正专家在诊所进行测试时,弱视追踪器应用程序的结果没有统计学上的显著差异。然而,结果的变异性确实表明需要进一步改进,以确保结果可以作为可靠的临床工具使用。

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