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一项比较0.5%和1%托吡卡胺用于糖尿病青少年年度视网膜筛查的双盲研究。

A double-blind study comparing 0.5% and 1% tropicamide for annual retinal screening in diabetic adolescents.

作者信息

Hassler-Hurst J, Wadham C, Rayman G

机构信息

Diabetes Centre, Children and Young Adults Team, The Ipswich Hospital NHS Trust, Heath Road, Ipswich, Suffolk IP4 5PD. UK.

出版信息

Diabet Med. 2004 May;21(5):434-9. doi: 10.1111/j.1464-5491.2004.01172.x.

Abstract

AIMS

To determine whether there is any difference between 0.5% and 1% tropicamide in ocular discomfort and mydriatic efficacy in adolescents with Type 1 diabetes.

METHODS

In a double-blind study, one drop of 0.5% tropicamide was instilled in one eye and one drop of 1% instilled in the other eye of 30 subjects aged 12-18 years. Drop strengths were randomized. Pupil size was measured before instillation, at 10, 20 and 30 min. Discomfort was measured using a recognized pain scale.

RESULTS

Irrespective of the concentration of tropicamide used, all pupils dilated to at least 6 mm at 30 min, sufficient for successful ophthalmoscopy. Pain was significantly less when the lower concentration of tropicamide was used; pain score for the 0.5% group [median (interquartile range)] 1.0 (0-2) and 2.0 (1-3) for the 1.0% group, P = 0.009 (Wilcoxon rank test).

CONCLUSIONS

This minor change in practice significantly reduces the distress associated with drop instillation without compromising the clinical examination, and may thus be important in encouraging compliance at the yearly diabetic review.

摘要

目的

确定0.5%与1%托吡卡胺在1型糖尿病青少年眼部不适和散瞳效果方面是否存在差异。

方法

在一项双盲研究中,对30名年龄在12至18岁的受试者,一只眼睛滴入一滴0.5%托吡卡胺,另一只眼睛滴入一滴1%托吡卡胺。滴眼液浓度随机分配。在滴药前、滴药后10、20和30分钟测量瞳孔大小。使用公认的疼痛量表测量不适感。

结果

无论使用何种浓度的托吡卡胺,所有瞳孔在30分钟时均至少扩张至6毫米,足以成功进行眼底检查。使用较低浓度托吡卡胺时疼痛明显减轻;0.5%组的疼痛评分[中位数(四分位间距)]为1.0(0 - 2),1.0%组为2.0(1 - 3),P = 0.009(Wilcoxon秩和检验)。

结论

这种在操作上的微小改变显著减轻了滴药相关的不适,且不影响临床检查,因此在鼓励糖尿病年度复查时的依从性方面可能具有重要意义。

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