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使用屈光仪对婴儿进行远视筛查。

Screening for hyperopia in infants using the PowerRefractor.

作者信息

Satiani Nidhi G, Mutti Donald O

机构信息

The Ohio State University College of Optometry, Columbus, Ohio, USA.

出版信息

Optom Vis Sci. 2011 Aug;88(8):905-11. doi: 10.1097/OPX.0b013e3182206df2.

DOI:10.1097/OPX.0b013e3182206df2
PMID:21602730
Abstract

PURPOSE

To determine the proportion of infants in a pediatric medical practice who have high levels of hyperopia in addition to evaluating the ability of the PowerRefractor (PR) [with and without accessory +4.50 diopter (D) spectacles] compared with cycloplegic retinoscopy to detect highly hyperopic refractive errors.

METHODS

The cycloplegic refractive error (2 drops tropicamide 1% given 5 min apart) of 200 normal birth weight infants was measured by retinoscopy and the Plusoptix PR. If initial readings were ≥ +2.00 D, PR measurement was repeated with accessory +4.50 D spectacles to extend its operating range. Examinations were conducted during well-baby visits at 2 months of age at the office of a local pediatrician group practice.

RESULTS

Of the 200 infants, 7.5% had a spherical equivalent refractive error of +5.00 D or more in both eyes. The use of +4.50 D accessory glasses during PowerRefraction significantly improved the ability to detect higher levels of hyperopia. Areas under receiver operating characteristic curves that were 0.69 to 0.51 when no glasses were worn improved to 0.87 to 0.98 when the glasses were worn (cutpoints between +3.50 and +5.00 D by retinoscopy). Significant underestimation of higher levels of hyperopia by the PR compared with retinoscopy was eliminated when +4.50 D accessory glasses were worn.

CONCLUSIONS

Accessory +4.50 diopter sphere spectacles appeared to successfully extend the operating range of the PR with cycloplegia, allowing for detection of high levels of hyperopia that occurred in a large proportion of 2-month old infants with adequate sensitivity and specificity compared with cycloplegic retinoscopy.

摘要

目的

除了评估PowerRefractor(PR)[使用和不使用附带的+4.50屈光度(D)眼镜]与睫状肌麻痹验光相比检测高度远视屈光不正的能力外,还需确定儿科医疗实践中高度远视婴儿的比例。

方法

通过检影验光和Plusoptix PR测量200名正常出生体重婴儿的睫状肌麻痹屈光不正(每隔5分钟滴入2滴1%托吡卡胺)。如果初始读数≥+2.00 D,则使用附带的+4.50 D眼镜重复PR测量以扩大其操作范围。在当地儿科医生团体诊所对2个月大的婴儿进行健康检查时进行检查。

结果

在200名婴儿中,7.5%的婴儿双眼等效球镜屈光不正为+5.00 D或更高。在屈光检查期间使用+4.50 D附带眼镜显著提高了检测更高程度远视的能力。不戴眼镜时受试者工作特征曲线下面积为0.69至0.51,戴眼镜时提高到0.87至0.98(检影验光的切点在+3.50和+5.00 D之间)。当佩戴+4.50 D附带眼镜时,与检影验光相比,PR对更高程度远视的显著低估得以消除。

结论

附带的+4.50屈光度球镜眼镜似乎成功地扩大了PR在睫状肌麻痹情况下的操作范围,与睫状肌麻痹检影验光相比,能够以足够的敏感性和特异性检测出很大比例的2个月大婴儿中出现的高度远视。

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