Ribeiro Reis Ana Paula, Palmowski-Wolfe Anja, Beuschel Ralf
Ophthalmology, Universitätsspital Basel Augenklinik, Basel, Switzerland.
Klin Monbl Augenheilkd. 2021 Apr;238(4):437-442. doi: 10.1055/a-1440-0642. Epub 2021 Apr 30.
An estimated 49.8% of the world population will be myopic by 2050. Multifocal contact lenses (MFCLs) and orthokeratology (OK) reduce peripheral retinal hyperopic defocus, which animal studies have shown to positively impact eye growth. MFCLs are expected to slow myopic progression by 20 - 50% and OK by 30 - 60%, making them valuable therapeutic tools. In view of the guidelines for myopia management published by the International Myopia Institute in 2019, the aim of this retrospective data analysis of a tertiary care center was to review past experience with OK and MFCLs for myopia control and gain information to update current practice.
The contact lens (CL) database of the Eye Clinic of the University Hospital of Basel was searched with the label "myopia progression" between January 2012 - 2020. Patients were included if they gave informed consent, were younger than 19 years old at baseline, and had no ocular comorbidities that could potentially compromise vision. Primary outcomes were progression of spherical equivalent refraction for MFCL patients and progression of axial length (AL) for the OK group, comparing with historical data from OK trials. Secondary outcomes were the presence of risk factors for myopia, age, refractive error at baseline, follow-up duration, and adverse effects during therapy.
Twenty-one patients could be included, with a mean age of 12.80 ± 3.32 years (y) at baseline. The majority of patients were older than 12 years and already myopic (- 3.89 ± 2.30 diopters) when control treatment was started. Overall, follow-up ranged from 0.08 to 6.33 years (2.03 ± 1.66 y). In the patients treated with MFCLs, myopia control improved significantly when patients changed from spectacles to MFCLs. In the OK group, 14% dropped out during the first year and 2 patients had multiple AL measurements during therapy, which showed a slower growth of AL when compared to other OK trials and controls with spectacles. There were two cases of non-severe keratitis. Environmental risk factors had not been documented and only 48% of clinical records had a documented family risk assessment.
Patients showed a slower myopia progression under MFCLs or OK, which supports their role as a treatment option in myopia management. In this regard, AL measurement is an important additional parameter to be included in the assessment of myopia progression in clinical practice. Identification of children at risk of developing high/pathologic myopia (family history, environmental risk factors) needs to improve so that the first stages of myopic shift can be recognized and targeted. Changes in lifestyle should be actively encouraged, especially when the impact of decreases in outdoor time secondary to COVID-19 is yet to become clear.
据估计,到2050年全球将有49.8%的人口近视。多焦点隐形眼镜(MFCL)和角膜塑形术(OK)可减少周边视网膜远视性离焦,动物研究表明这对眼球生长有积极影响。预计MFCL可使近视进展减缓20%-50%,OK可使其减缓30%-60%,使其成为有价值的治疗工具。鉴于国际近视研究所2019年发布的近视管理指南,本对一家三级医疗中心的回顾性数据分析旨在回顾过去使用OK和MFCL控制近视的经验,并获取信息以更新当前的实践。
在巴塞尔大学医院眼科诊所的隐形眼镜(CL)数据库中,搜索2012年1月至2020年期间带有“近视进展”标签的记录。纳入标准为:患者签署知情同意书,基线时年龄小于19岁,且无可能损害视力的眼部合并症。主要结局指标为MFCL组患者等效球镜度的进展以及OK组眼轴长度(AL)的进展,并与OK试验的历史数据进行比较。次要结局指标包括近视危险因素的存在情况、年龄、基线屈光不正、随访时间以及治疗期间的不良反应。
共纳入21例患者,基线时平均年龄为12.80±3.32岁。大多数患者年龄超过12岁,开始控制治疗时已近视(-3.89±2.30屈光度)。总体而言,随访时间为0.08至6.33年(2.03±1.66年)。在使用MFCL治疗的患者中,当从佩戴框架眼镜改为佩戴MFCL时,近视控制有显著改善。在OK组中,14%的患者在第一年退出,2例患者在治疗期间进行了多次AL测量,与其他OK试验及框架眼镜对照组相比,其AL增长较慢。有2例非严重角膜炎病例。未记录环境危险因素,仅有48%的临床记录有家族风险评估记录。
患者在MFCL或OK治疗下近视进展较慢,这支持了它们作为近视管理治疗选择的作用。在这方面,AL测量是临床实践中评估近视进展时应纳入的重要附加参数。识别有发展为高度/病理性近视风险的儿童(家族史、环境危险因素)的工作需要改进,以便能够识别并针对近视转变的早期阶段。应积极鼓励生活方式的改变,尤其是在新冠疫情导致户外活动时间减少的影响尚不明朗的情况下。