Hyperopia

远视
  • 文章类型: Journal Article
    目的:根据更新的2021年AAPOS视力筛查委员会关于基于仪器的儿科视力筛查验证的指南,评估Spot视力筛查。
    方法:作为IRB批准的正在进行的前瞻性研究的一部分,儿童在进行全面检查前接受了Spot筛查.
    结果:在1,090名儿童中的1,036名(95%)成功进行了斑点筛查。48%的参与者被推荐使用Spot制造商指南进行进一步筛查,通过金标准检查,发现所有儿童中有40%患有2021年弱视危险因素或视觉上明显的屈光不正。Spot建议与2021年的标准相比相当好,总体敏感性为0.88,特异性为0.78。将更新的指南应用于远视点,屈光参差,和散光产生中等至较差的敏感性(0.27-0.77),但具有出色的特异性(>0.9)。接收器工作特性分析曲线下的面积表明,对于每个诊断近视的斑点,总体上具有良好的预测性能。远视,散光,屈光参差(范围,0.87-0.97)。我们的研究结果表明,年龄较大的儿童将散光的仪器转诊标准从1.5D(本研究中使用的筛选器的制造商阈值)增加到2D。将屈光参差截止值从1D降低至0.75D将使灵敏度从0.59提高至>0.8。
    结论:在我们的研究人群中,Spot的整体预测能力良好,灵敏度为0.88,特异性为0.78。我们推荐特定的设备屈光转诊标准,以使用更新的AAPOS指南最大限度地提高筛查效果。
    To evaluate the Spot Vision Screener according to updated 2021 AAPOS Vision Screening Committee guidelines for instrument-based pediatric vision screen validation.
    As part of an IRB-approved ongoing prospective study, children were screened with the Spot prior to a complete examination.
    Spot screening was successful in 1,036 of 1,090 children (95%). Forty-eight percent of participants were referred for further screening using the Spot manufacturer guidelines, and 40% of all children were found to have a 2021 amblyopia risk factor or visually significant refractive error by gold standard examination. The Spot recommendation compared reasonably well to the 2021 criteria, with an overall sensitivity of 0.88 and a specificity of 0.78. Applying updated guidelines to the Spot for hyperopia, anisometropia, and astigmatism yielded moderate-to-poor sensitivity (0.27-0.77) but excellent specificity (>0.9). The area under the curve of the receiver operating characteristic analysis demonstrates overall good prediction performance for the Spot for each diagnosis-myopia, hyperopia, astigmatism, anisometropia (range, 0.87-0.97). Results of our study suggest increasing the instrument referral criterion for astigmatism from 1.5 D (manufacturer thresholds of the screener used in this study) to 2 D in older children. Decreasing the anisometropia cut-off from 1 D to 0.75 D would improve sensitivity from 0.59 to >0.8.
    In our study population, the overall predictive ability of the Spot is good, with a sensitivity of 0.88 and a specificity of 0.78. We recommend specific device refractive referral criteria to maximize screening effectiveness using the updated AAPOS guidelines.
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  • 文章类型: Journal Article
    该研究旨在评估两种基于屈光器械的视力筛查方法(SureSight和PlusoptiX),以检测中国学龄前儿童的屈光弱视危险因素(ARFs)和明显的屈光不正,并根据2021年AAPOS指南制定转诊标准。
    使用PlusoptiX光筛选器对61至72个月(n=1,173)的儿童进行了眼科检查,SureSight自动折射仪,和睫状肌麻痹视网膜镜检查(CR)。采用2021年AAPOS学龄前视力筛查指南的视力筛查委员会进行比较。配对t检验分析和Bland-Altman图用于评估PlusoptiX光筛选器之间的差异和一致性,SureSight自动折射仪,和CR。此外,使用受试者工作特征(ROC)曲线估算了用SureSight和PlusoptiX测得的几种ARF的截止值的有效性,并与基于年龄的2021年AAPOS检查失败水平进行了比较.
    共有1,173名儿童接受了全面的眼科检查。当根据2013年(43/3.67%)和2021年(42/3.58%)AAPOS指南的推荐数字进行比较时,散光值之间的显著差异(72.09vs.52.38%)和屈光参差(11.63vs.38.10%)被发现。PlusoptiX和CR之间的球形值和圆柱形值的95%一致性极限(LOA)分别为95.08和96.29%。SureSight和CR之间的比率分别为93.87和98.10%。考虑到屈光失败水平,ROC曲线获得了最佳截止点。然而,PlusoptiX和SureSight在远视中显示出较低的效率(Youden指数,0.60vs.0.83)和近视(尤登指数,078vs.0.93),分别。调整上述截止点后,优化的NES(南京眼科研究)近视转诊标准,远视,散光,PlusoptiX的屈光参差分别为-0.75、1.25、-1.0和0.5,SureSight的屈光参差分别为-1.25、2.75、-1.5和0.75。
    SureSight和PlusoptiX与CR表现出良好的相关性,可以有效检测屈光性ARFs和视觉上明显的屈光不正。使用SureSight检测远视和使用PlusoptiX检测近视具有明显的优势。我们根据AAPOS2021指南,为基于年龄的学龄前儿童提出了工具性转诊标准。
    The study aims to assess two refractive instrument-based methods of vision screening (SureSight and PlusoptiX) to detect refractive amblyopia risk factors (ARFs) and significant refractive errors in Chinese preschool children and to develop referral criteria according to the 2021 AAPOS guidelines.
    Eye examinations were conducted in children aged 61 to 72 months (n = 1,173) using a PlusoptiX photoscreener, SureSight autorefractor, and cycloplegic retinoscopy (CR). The Vision Screening Committee of AAPOS\'s preschool vision screening guidelines from 2021 were adopted for comparison. Paired t-test analysis and Bland-Altman plots were used to assess the differences and agreement between the PlusoptiX photoscreener, SureSight autorefractor, and CR. In addition, the validity of the cut-off values of the several ARFs measured with the SureSight and PlusoptiX was estimated using receiver operating characteristic (ROC) curves and compared to the age-based 2021 AAPOS examination failure levels.
    A total of 1,173 children were tested with comprehensive eye examinations. When the referral numbers based on the 2013 (43/3.67%) and 2021 (42/3.58%) AAPOS guidelines were compared, significant differences between the values of astigmatism (72.09 vs. 52.38%) and anisometropia (11.63 vs. 38.10%) were found. The 95% limits of agreement (LOA) of the spherical value and the cylindrical value between PlusoptiX and CR were 95.08 and 96.29%. It was 93.87 and 98.10% between SureSight and CR. Considering refractive failure levels, the ROC curves obtained the optimal cut-off points. However, the PlusoptiX and the SureSight showed lower efficiency in hyperopia (Youden index, 0.60 vs. 0.83) and myopia (Youden index, 078 vs. 0.93), respectively. After adjusting the above cut-off points, the optimized NES (Nanjing Eye Study) referral criteria for myopia, hyperopia, astigmatism, and anisometropia were -0.75, 1.25, -1.0, and 0.5 with PlusoptiX and -1.25, 2.75, -1.5, and 0.75 with SureSight.
    SureSight and PlusoptiX showed a good correlation with CR and could effectively detect refractive ARFs and visually significant refractive errors. There were obvious advantages in detecting hyperopia using SureSight and myopia using PlusoptiX. We proposed instrumental referral criteria for age-based preschool children based on AAPOS 2021 guidelines.
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  • 文章类型: Journal Article
    Myopia is a focal issue affecting the eye health of children and adolescents in China. Hyperopia reserve is the refractive state before the occurrence of myopia. As the result of dynamic matching between the axial length, cornea and lens, it is of great significance to the prevention and control of myopia. There has been a lack of the reference basis for children\'s eyeball development parameters and the influence of genetic factors, especially the changing law of the above-mentioned parameters in the process of children\'s \"emmetropization\". To promote the prevention and control of myopia in children and adolescents and to standardize population screening and clinical treatment, based on the survey data of refractive errors in children and adolescents from different regions, a consensus has been reached on the reference interval of hyperopia reserve, axial length and corneal curvature and related genetic factors of emmetropia at different ages among school-age children by the Public Health Ophthalmology Branch of the Chinese Preventive Medicine Association.
    近视眼是影响我国儿童青少年眼健康的焦点问题。远视储备是眼球发生近视前的屈光状态,是眼轴长度与角膜及晶状体等参数之间动态匹配的结果,对于近视眼防控意义重大。我国一直缺乏儿童眼球发育参数的指导依据以及遗传因素影响的参考资料,尤其针对上述参数在儿童眼球正视化过程中变化规律的总结。为了促进儿童青少年近视眼防控工作的标准化,规范人群筛查和临床治疗,使社会各界对近视眼的预防干预和评价有据可依,中华预防医学会公共卫生眼科分会基于我国不同地区儿童青少年的屈光不正调查数据,针对我国学龄儿童正视眼在不同年龄段眼球远视储备、眼轴长度和角膜曲率的参考区间及相关遗传因素达成共识性意见。.
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  • 文章类型: Journal Article
    随着基于仪器的儿科视力筛查技术的发展,美国儿科眼科和斜视协会(AAPOS)制定了统一的指南(2003年,2013年更新),旨在为能够检测特定弱视危险因素(ARFs)目标水平和视觉显著屈光不正的器械的开发提供信息.已建立的指南的临床经验表明,非弱视患者的过度转诊水平明显较高,对称散光,提示当前修订。
    修订后的指南反映了AAPOS视力筛查和研究委员会的专家共识。
    对于自动筛查设备的研究,AAPOS在2021年建议金标准验证性综合检查失败水平包括屈光参差>1.25D和远视>4.0D。任何子午线散光>3.0D,近视<-3D应在<48个月的儿童中检测到,而散光>1.75D和近视<-2D应在48个月后检测到。任何介质不透明度>1mm和明显斜视>8Δ也应被识别。除了检测ARFs和屈光不正的性能外,验证研究还应报告是否存在弱视的筛查仪器性能.建议使用仪器接收器工作特性曲线和Bland-Altman分析来提高验证研究的可比性。
    与2013年指南相比,简化了检查失败标准,提高了对称散光的阈值,而弱性屈光参差的阈值已降低。4岁以后,尽管弱视风险较低,但仍有较低幅度的对称散光和近视的目标。因为它们会影响学校的表现,并且可能需要考虑近视预防治疗。
    As instrument-based pediatric vision screening technology has evolved, the American Association for Pediatric Ophthalmology and Strabismus (AAPOS) has developed uniform guidelines (2003, updated 2013) to inform the development of devices that can detect specified target levels of amblyopia risk factors (ARFs) and visually significant refractive error. Clinical experience with the established guidelines has revealed an apparent high level of over-referral for non-amblyopic, symmetric astigmatism, prompting the current revision.
    The revised guidelines reflect the expert consensus of the AAPOS Vision Screening and Research Committees.
    For studies of automated screening devices, AAPOS in 2021 recommends that the gold-standard confirmatory comprehensive examination failure levels include anisometropia >1.25 D and hyperopia >4.0 D. Astigmatism >3.0 D in any meridian and myopia < -3 D should be detected in children <48 months, whereas astigmatism >1.75 D and myopia < -2 D should be detected after 48 months. Any media opacity >1 mm and manifest strabismus of >8Δ should also be identified. Along with performance in detecting ARFs and refractive error, validation studies should also report screening instrument performance with regard to presence or absence of amblyopia. Instrument receiver operating characteristic curves and Bland-Altman analysis are suggested to improve comparability of validation studies.
    Examination failure criteria have been simplified and the threshold for symmetric astigmatism raised compared to the 2013 guidelines, whereas the threshold for amblyogenic anisometropia has been decreased. After age 4 years, lower magnitudes of symmetric astigmatism and myopia are also targeted despite a low risk of amblyopia, because they can influence school performance and may warrant consideration of myopia prevention therapy.
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  • 文章类型: Journal Article
    2003年,美国儿科眼科和斜视视力筛查委员会提出了自动学龄前视力筛查的标准。流行病学和自然史研究的最新文献,弱视治疗的随机对照试验,为了更新这些标准,已经审查了筛查技术的现场研究。弱视危险因素(ARF)的患病率高于以前的怀疑;许多低幅度ARF的幼儿不会发展为弱视,以及那些经常独自对眼镜作出反应的人。高量级ARFs增加弱视的可能性。虽然深度随着年龄的增长而增加,弱视在60个月前仍可治疗,5岁后治疗效果下降。美国预防服务工作组预防服务工作组指南允许对36个月以上的儿童进行照片筛查。一些技术直接检测弱视而不是ARFs。使用光学筛查进行ARF检测的基于年龄的标准是谨慎的:此类仪器的转诊标准应对幼儿的ARF检测产生高度特异性,并对大龄儿童的弱视检测产生高度敏感性。对12-30个月儿童的ARFs进行屈光筛查,应检测散光>2.0D,远视>4.5D,屈光参差>2.5D;对于31-48个月的儿童,散光>2.0D,远视>4.0D,和屈光参差>2.0D。对于年龄>49个月的儿童,应使用原始标准:散光>1.5D,屈光参差>1.5D,和远视>3.5D。应在所有年龄段检测到明显的中膜混浊和明显(非间歇性)斜视。检测弱视的仪器应报告使用弱视存在作为金标准的结果。这些新的美国儿科眼科协会和斜视视力筛查委员会指南将改善结果报告和技术比较。
    In 2003 the American Association for Pediatric Ophthalmology and Strabismus Vision Screening Committee proposed criteria for automated preschool vision screening. Recent literature from epidemiologic and natural history studies, randomized controlled trials of amblyopia treatment, and field studies of screening technologies have been reviewed for the purpose of updating these criteria. The prevalence of amblyopia risk factors (ARF) is greater than previously suspected; many young children with low-magnitude ARFs do not develop amblyopia, and those who do often respond to spectacles alone. High-magnitude ARFs increase the likelihood of amblyopia. Although depth increases with age, amblyopia remains treatable until 60 months, with decline in treatment effectiveness after age 5. US Preventive Services Task Force Preventative Services Task Force guidelines allow photoscreening for children older than 36 months of age. Some technologies directly detect amblyopia rather than ARFs. Age-based criteria for ARF detection using photoscreening is prudent: referral criteria for such instruments should produce high specificity for ARF detection in young children and high sensitivity to detect amblyopia in older children. Refractive screening for ARFs for children aged 12-30 months should detect astigmatism >2.0 D, hyperopia >4.5 D, and anisometropia >2.5 D; for children aged 31-48 months, astigmatism >2.0 D, hyperopia > 4.0 D, and anisometropia >2.0 D. For children >49 months of age original criteria should be used: astigmatism >1.5 D, anisometropia>1.5 D, and hyperopia >3.5 D. Visually significant media opacities and manifest (not intermittent) strabismus should be detected at all ages. Instruments that detect amblyopia should report results using amblyopia presence as the gold standard. These new American Association for Pediatric Ophthalmology and Strabismus Vision Screening Committee guidelines will improve reporting of results and comparison of technologies.
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  • DOI:
    文章类型: Journal Article
    As the eye grows, the axial length increases while the cornea and lens flatten. High refractive errors which are common in the neonatal period, reduce rapidly during the first year of life through the process called emmetropization. The possibility that long-term full- time glasses wear may impede emmetropization must be considered. Hyperopia greater than 5.00 diopters (D) in young children is associated with an increased risk of amblyopia and strabismus, therefore optical correction should be prescribed. When hyperopia is associated with esotropia, full correction of the cycloplegic refractive error should be prescribed. Myopia greater than 8.00 D and astigmatism greater than 2.50 D are common causes of isometropic amblyopia. Patients with hyperopic anisometropia with as little as l D difference between the eyes may develop amblyopia while the difference should reach 3-4 D for myopic anisometropia to develop amblyopia. Full cycloplegic refractive difference between two eyes should be given to the anisometropic child in spite of age, strabismus and degree of anisometropia. Myopia control is the attempt to slow the rate of progression of myopia such as cycloplegic agents, plus lenses at near, and rigid contact lenses.
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