首页> 外文期刊>Japanese Journal of Ophthalmology >Cycloplegic effect of 0.5% tropicamide and 0.5% phenylephrine mixed eye drops: objective assessment in Japanese schoolchildren with myopia.
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Cycloplegic effect of 0.5% tropicamide and 0.5% phenylephrine mixed eye drops: objective assessment in Japanese schoolchildren with myopia.

机译:0.5%托吡卡胺和0.5%苯肾上腺素混合滴眼液的致盲效果:对日本近视小学生的客观评估。

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摘要

PURPOSE: To evaluate the cycloplegic effect of mixed eye drops containing 0.5% tropicamide and 0.5% phenylephrine in myopic children, and to determine whether their efficacy was associated with their clinical characteristics. METHODS: Eighty-one myopic children (age, mean +/- SD, 11.0 +/- 1.5 years; mean spherical equivalent refractive error, -4.27 +/- 1.41 D; range, -1.57 to -8.66 D) were recruited. One drop of Mydrin-P was administered to each eye twice, with an interval of 5 min between. Twenty-five minutes after the second drop, accommodative responses were measured with an open-view autorefractometer, while the subject was encouraged to accommodate by binocularly looking at a Maltese cross located at a distance of 33 cm. The difference between the refractive reading and that obtained with a Maltese cross at 500 cm was regarded as residual accommodation (RA). The repeatability of this measurement was also evaluated. RESULTS: The mean RA was 0.21 +/- 0.29 D (range, -0.31 to 0.99 D). There was no association in RA between the right and left eyes, between RA and age, or between RA and sex, but RA was weakly correlated with refractive error (r = 0.274, P = 0.019). The intersubject difference found in RA can be explained mostly by the extent of repeatability (+/-0.71 D). CONCLUSION: The insignificant magnitude of RA indicated that the mixed eye drop is an acceptable and useful cycloplegic agent in Japanese schoolchildren with a wide range of myopic refractive errors.
机译:目的:评估含有0.5%托吡卡胺和0.5%苯肾上腺素的混合滴眼剂在近视儿童中的睫状肌麻痹效果,并确定其功效是否与其临床特征有关。方法:招募了81名近视儿童(年龄,平均+/- SD,11.0 +/- 1.5岁;平均球面等效屈光不正,-4.27 +/- 1.41 D;范围,-1.57至-8.66 D)。将一滴Mydrin-P滴眼两次,每次间隔5分钟。第二次下降后的25分钟,用开放式自动折光仪测量调节反应,同时通过双目观察位于33厘米处的马耳他十字鼓励受试者适应。屈光度读数与在500厘米处的马耳他十字屈光度读数之间的差异被认为是残差调节(RA)。还评估了该测量的可重复性。结果:平均RA为0.21 +/- 0.29 D(范围-0.31至0.99 D)。右眼和左眼之间,RA与年龄之间或RA与性别之间没有RA相关性,但RA与屈光不正的相关性很弱(r = 0.274,P = 0.019)。 RA中发现的受试者间差异主要可以通过重复性(+/- 0.71 D)的程度来解释。结论:RA的微不足道的大小表明混合眼药水是日本小学生可接受的和有用的睫状肌麻痹剂,其近视屈光不正范围广泛。

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