Effectiveness of optical treatment in amblyopia and validation of measuring spectacle compliance with the ODM.

IF 2.8 3区 医学 Q1 OPHTHALMOLOGY Ophthalmic and Physiological Optics Pub Date : 2024-07-01 Epub Date: 2024-05-17 DOI:10.1111/opo.13322
Aveen Kadhum, Emily T C Tan, Yaroslava Wenner, Maurits V Joosse, Sjoukje E Loudon
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Abstract

Purpose: The improvement in visual acuity (VA) was determined during optical treatment in children with amblyopia before their participation in a randomised clinical trial comparing the effect of dichoptic video gaming using virtual reality goggles with occlusion therapy.

Methods: Children aged 4-12 years with an interocular VA difference ≥0.20 logMAR and an amblyogenic factor: strabismus <30Δ, ≥1.00 D anisometropia, astigmatism ≥1.50 D and/or hypermetropia ≥1.50 D were eligible for 16 weeks of optical treatment. Children with previous amblyopia treatment were excluded. Compliance with spectacle wear was measured electronically over 1 week using the occlusion dose monitor (ODM). The reliability of these measurements was verified. The main outcome was an increase in amblyopic eye VA from baseline to 16 weeks.

Results: Sixty-five children entered the optical treatment period. Mean age was 6.0 ± 2.2 years (range: 4-12 years; IQR 4.5-6.7 years). Amblyopia was caused by anisometropia in 53 (82%) children, strabismus in 6 (9%) and combined mechanism in 6 (9%). After optical treatment, mean VA improved by 0.20 logMAR (SD 0.28; p < 0.001) and 0.07 in the amblyopic and fellow eye, respectively (SD 0.20; p = 0.03). This resulted in 24 children (37%) with an interocular VA difference <0.20 logMAR and in 17% of children with VA at the start of 0.30 logMAR or worse. Poor VA in the amblyopic eye at baseline (p = 0.001) and high anisometropia (p = 0.001) were associated with VA improvement. On average, spectacles were worn 9.7 ± 2.4 h/day (range: 2.3-13.6 h); mean compliance was 73% ± 18% of estimated wake time. Only ambient temperature ≥ 31°C or when spectacles were worn on top of the head prevented a reliable ODM measurement.

Conclusions: VA improved by two lines resulting in more than a third of the children being treated sufficiently with spectacles alone and no longer being classified as amblyopic. The ODM proved to be a reliable method of measuring compliance with spectacle wear.

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弱视光学治疗的效果以及用 ODM 测量眼镜依从性的验证。
目的:在弱视儿童参加随机临床试验之前,测定他们在光学治疗期间视力(VA)的改善情况,比较使用虚拟现实护目镜的二分视视频游戏与遮盖疗法的效果:方法:眼间视力差异≥0.20 logMAR且弱视因素为斜视的4-12岁儿童:65名儿童进入光学治疗期。平均年龄为 6.0 ± 2.2 岁(范围:4-12 岁;IQR:4.5-6.7 岁)。53名儿童(82%)的弱视是由内斜视引起的,6名儿童(9%)的弱视是由斜视引起的,6名儿童(9%)的弱视是由合并机制引起的。经过光学治疗后,平均视力提高了 0.20 logMAR(标准差为 0.28;P 结论:视力提高了两条线,导致视力下降:视力提高了两条线,超过三分之一的儿童只需佩戴眼镜就能得到充分治疗,不再被归类为弱视。事实证明,ODM 是测量佩戴眼镜依从性的可靠方法。
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来源期刊
CiteScore
5.10
自引率
13.80%
发文量
135
审稿时长
6-12 weeks
期刊介绍: Ophthalmic & Physiological Optics, first published in 1925, is a leading international interdisciplinary journal that addresses basic and applied questions pertinent to contemporary research in vision science and optometry. OPO publishes original research papers, technical notes, reviews and letters and will interest researchers, educators and clinicians concerned with the development, use and restoration of vision.
期刊最新文献
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