Method comparison and overview of refractive measurements in children: implications for myopia management.

IF 2 Q2 OPHTHALMOLOGY BMJ Open Ophthalmology Pub Date : 2024-03-01 DOI:10.1136/bmjophth-2023-001322
Jonas Müller, Xiaoqin Chen, Arne Ohlendorf, Lihua Li, Siegfried Wahl
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Abstract

Objective: This study investigated the agreement between objective wavefront-based refraction and subjective refraction in myopic children. It also assessed the impact of cyclopentolate and refraction levels on the agreement.

Methods: A total of 84 eyes of myopic children aged 6-13 years were included in the analysis. Non-cycloplegic and cycloplegic objective wavefront-based refraction were determined and cycloplegic subjective refraction was performed for each participant. The data were converted into spherical equivalent, J0 and J45, and Bland-Altman plots were used to analyse the agreement between methods.

Results: Linear functions were used to determine the dependency between the central myopic refractive error and the difference between the method of refraction (=bias). The influence of central myopia was not clinically relevant when analysing the agreement between wavefront results with and without cyclopentolate (comparison 1). The bias for wavefront-based minus subjective spherical equivalent refraction (comparison 2) was ≤-0.50 D (95% limits of agreement -0.010 D to -1.00 D) for myopia of -4.55 D and higher when cycloplegia was used (p<0.05). When no cyclopentolate was used for the wavefront-based refraction (comparison 3), the bias of -0.50 D (95% limits of agreement -0.020 D to -0.97 D) was already reached at a myopic error of -2.97 D. Both astigmatic components showed no clinically relevant bias.

Conclusion: The spherical equivalent, measured without cycloplegic agents, led to more myopic measurements when wavefront-based refraction was used. The observed bias increased with the amount of myopic refractive error for comparisons 2 and 3, which needs to be considered when interpreting wavefront-refraction data.

Trial registration number: NCT05288335.

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儿童屈光测量方法比较和概述:对近视管理的影响。
研究目的本研究调查了近视儿童客观波前屈光度与主观屈光度之间的一致性。研究还评估了环戊丙酸和屈光度对两者一致性的影响:方法:共分析了 84 名 6-13 岁近视儿童的眼睛。方法:共有 84 名 6-13 岁的近视眼儿童参与了分析。数据被转换成球面当量、J0 和 J45,并使用 Bland-Altman 图分析不同方法之间的一致性:使用线性函数确定中心近视屈光不正与屈光方法差异(=偏差)之间的关系。在分析使用环戊丙酸和不使用环戊丙酸的波前结果的一致性时,中心近视的影响与临床无关(比较 1)。在使用环戊普利时,近视度数为-4.55 D或更高时,波前屈光度数减去主观球面等效屈光度数(对比 2)的偏差≤-0.50 D(95% 的一致性范围为-0.010 D 至-1.00 D)(p 结论:当使用波前屈光仪时,在不使用散瞳剂的情况下测量的球面等效度数会导致更多的近视度数。在比较 2 和 3 中,观察到的偏差随着近视屈光不正的增加而增加,在解释波前屈光数据时需要考虑这一点:试验注册号:NCT05288335。
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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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