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PlusoptiX与MTI视力筛查仪的比较。

Comparison between the plusoptiX and MTI Photoscreeners.

作者信息

Matta Noelle S, Arnold Robert W, Singman Eric L, Silbert David I

机构信息

CO, CRC, COT, Family Eye Group, 2110 Harrisburg Pike, Ste 215, Lancaster, PA 17601, USA.

出版信息

Arch Ophthalmol. 2009 Dec;127(12):1591-5. doi: 10.1001/archophthalmol.2009.294.

Abstract

OBJECTIVE

Both the Medical Technology and Innovations (MTI) and plusoptiX photoscreeners are used to objectively screen for amblyogenic risk factors in children. The MTI has been extensively studied, but the limited availability of film may render it obsolete. We compared the MTI with the plusoptiX, a newer digital photoscreener, for the ability to detect amblyogenic factors when compared with a comprehensive pediatric ophthalmic examination. We believe our results will help to guide community-based vision screening programs.

METHODS

One hundred fifty-one children were examined consecutively in our office. Each patient was screened with the MTI and plusoptiX devices on the same day as part of a comprehensive pediatric ophthalmic examination. Results via MTI were evaluated by an expert masked examiner (R.W.A.), and the plusoptiX results were interpreted by the incorporated software.

RESULTS

Sixty-five percent of patients were found to have amblyopia or amblyogenic risk factors during the pediatric ophthalmic examination conducted via the American Association of Pediatric Ophthalmology and Strabismus referral criteria. We found the MTI photoscreener to have a sensitivity of 83.6%, specificity of 90.5%, false- positive rate of 9.4%, false-negative rate of 16.3%, and positive predictive value of 94.2%. The plusoptiX demonstrated a sensitivity of 98.9%, specificity of 96.1%, false- positive rate of 3.7%, false-negative rate of 1.0%, and positive predictive value of 97.9%.

CONCLUSION

The MTI and plusoptiX photoscreeners proved to be effective when compared with a comprehensive cycloplegic pediatric ophthalmic examination. The plusoptiX, however, was found to have a higher sensitivity and specificity than the MTI.

摘要

目的

医学技术与创新(MTI)验光仪和plusoptiX数码验光仪均用于客观筛查儿童的致弱视危险因素。MTI已得到广泛研究,但胶片供应有限可能使其过时。我们将MTI与更新的数码验光仪plusoptiX进行比较,以评估其与全面的儿科眼科检查相比检测致弱视因素的能力。我们相信我们的结果将有助于指导社区视力筛查项目。

方法

151名儿童在我们的诊所接受了连续检查。作为全面儿科眼科检查的一部分,每位患者在同一天使用MTI和plusoptiX设备进行筛查。MTI的结果由一位不知情的专家检查人员(R.W.A.)评估,plusoptiX的结果由内置软件解读。

结果

根据美国小儿眼科与斜视协会的转诊标准进行儿科眼科检查时,65%的患者被发现患有弱视或有致弱视危险因素。我们发现MTI验光仪的敏感度为83.6%,特异度为90.5%,假阳性率为9.4%,假阴性率为16.3%,阳性预测值为94.2%。plusoptiX的敏感度为98.9%,特异度为96.1%,假阳性率为3.7%,假阴性率为1.0%,阳性预测值为97.9%。

结论

与全面的睫状肌麻痹儿科眼科检查相比,MTI和plusoptiX验光仪被证明是有效的。然而,发现plusoptiX比MTI具有更高的敏感度和特异度。

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