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暗适应瞳孔直径的六个月变异性。

Six-month variability of the dark-adapted pupil diameter.

作者信息

Khanani Arshad M, Brown Sandra M, Xu Ke Tom

机构信息

Department of Ophthalmology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

出版信息

J Cataract Refract Surg. 2005 May;31(5):987-90. doi: 10.1016/j.jcrs.2004.09.057.

Abstract

PURPOSE

To determine the individual variability of the dark-adapted pupil diameter over 6 months using a standardized dark-adaptation protocol.

SETTING

Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

METHODS

This prospective observational cohort study comprised volunteers with no history of ocular disease, surgery, or injury other than requirement for refractive correction. The right eye was tested. A standardized dark-adaptation protocol was used that controlled for accommodation and patient alertness. Infrared, still digital photographs were taken after 10 minutes of dark adaptation at 1 lux and were analyzed using digital image software. Testing was performed at baseline in the afternoon, at 3 months in the afternoon, and at 6 months in the morning. Lifestyle factors such as diet and exercise were not controlled.

RESULTS

Mean intersession differences were 0.04 mm (95% confidence interval [CI]: -0.68-0.146), 0.15 mm (95% CI: -0.001-0.297), and 0.09 mm (95% CI: -0.048-0.236) for baseline-3 month, baseline-6 month, and 3 month-6 month comparisons, respectively. None of these differences was significantly different from zero (P>.05, 2-tailed Student t tests). The likelihood that the mean intersession difference was >.25 mm was negligible for all comparisons (P=.9996, .9099, and .9829 respectively, 1-tailed Student t tests).

CONCLUSION

When a consistent dark-adaptation protocol that controls for alertness and accommodation is used, normal young individuals showed no significant variation in the dark-adapted pupil diameter over a 6-month period.

摘要

目的

使用标准化暗适应方案确定6个月内暗适应瞳孔直径的个体变异性。

设置

美国得克萨斯州拉伯克市的得克萨斯理工大学健康科学中心。

方法

这项前瞻性观察性队列研究纳入了除屈光不正矫正需求外无眼部疾病、手术或损伤史的志愿者。对右眼进行测试。使用标准化暗适应方案,该方案可控制调节和患者警觉性。在暗适应10分钟后,于1勒克斯光照条件下拍摄红外静态数码照片,并使用数字图像软件进行分析。测试在下午的基线期、3个月后的下午以及6个月后的上午进行。饮食和运动等生活方式因素未得到控制。

结果

基线至3个月、基线至6个月以及3个月至6个月比较的平均时段间差异分别为0.04毫米(95%置信区间[CI]:-0.68 - 0.146)、0.15毫米(95%CI:-0.001 - 0.297)和0.09毫米(95%CI:-0.048 - 0.236)。这些差异均无显著不同于零(P>.05,双侧学生t检验)。所有比较中,平均时段间差异>.25毫米的可能性可忽略不计(分别为P = 0.9996、0.9099和0.9829,单侧学生t检验)。

结论

当使用控制警觉性和调节的一致暗适应方案时,正常年轻个体在6个月期间暗适应瞳孔直径无显著变化。

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