Gillespie Brenda W, Musch David C, Guire Kenneth E, Mills Richard P, Lichter Paul R, Janz Nancy K, Wren Patricia A
Department of Biostatistics, Epidemiology, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2613-20. doi: 10.1167/iovs.02-0543.
To compare the baseline Collaborative Initial Glaucoma Treatment Study (CIGTS) visual field (VF) score and mean deviation (MD), investigate test-retest variability, and identify variables associated with VF loss and VF measurement variability.
Baseline data from a randomized clinical trial of 607 patients with newly diagnosed open-angle glaucoma were collected at 14 clinical centers. The CIGTS VF score and MD were obtained from 24-2 VF tests (Zeiss-Humphrey Systems, Dublin, CA) at two visits approximately 2 weeks apart.
Although most baseline CIGTS VF scores showed limited field loss, 15% (91/607) of patients showed a substantial deficit (VF score >10 on a 0-20 scale). A small but significant learning effect was seen over the two baseline measures for CIGTS VF score and MD. CIGTS VF score and MD correlate highly (r = -0.93); both have high test-retest correlation (0.83 and 0.91, respectively). Variables associated with greater baseline VF loss for both CIGTS VF score and MD include (probabilities for VF only): male sex (P = 0.018), black race (P <or= 0.0001), lower visual acuity (P <or= 0.0001), higher intraocular pressure if more than 30 mm Hg (P = 0.0034), poor field reliability score (P <or= 0.0001), cardiovascular disease (P = 0.015), reduced patient-reported alertness (P = 0.023), and CIGTS clinical center (P <or= 0.0001). Predictors of increased CIGTS VF score variability include a midrange VF score (P <or= 0.0001), first-tested eye (P = 0.0027), reduced patient-reported alertness (P = 0.0177), increasing age (P = 0.0040), current smoker (P = 0.0014), and CIGTS clinical center (P = 0.0215).
The CIGTS VF score provides a measure of VF strikingly similar to the MD. Variables associated with VF loss and VF variability may help identify patients who need greater clinical scrutiny.
比较青光眼联合初始治疗研究(CIGTS)的基线视野(VF)评分和平均偏差(MD),研究重测变异性,并确定与VF丧失和VF测量变异性相关的变量。
在14个临床中心收集了607例新诊断开角型青光眼患者的随机临床试验基线数据。CIGTS VF评分和MD来自相隔约2周的两次就诊时的24-2视野测试(蔡司-汉弗莱系统,加利福尼亚州都柏林)。
尽管大多数CIGTS基线VF评分显示视野丧失有限,但15%(91/607)的患者存在严重缺陷(0-20分制下VF评分>10)。在CIGTS VF评分和MD的两次基线测量中观察到小但显著的学习效应。CIGTS VF评分和MD高度相关(r = -0.93);两者的重测相关性都很高(分别为0.83和0.91)。与CIGTS VF评分和MD的更大基线VF丧失相关的变量包括(仅针对VF的概率):男性(P = 0.018)、黑人种族(P≤0.0001)、较低的视力(P≤0.0001)、眼压高于30 mmHg时较高的眼压(P = 0.0034)、较差的视野可靠性评分(P≤0.0001)、心血管疾病(P = 0.015)、患者报告的警觉性降低(P = 0.023)以及CIGTS临床中心(P≤0.0001)。CIGTS VF评分变异性增加的预测因素包括中等范围的VF评分(P≤0.0001)、首次测试的眼睛(P = 0.0027)、患者报告的警觉性降低(P = 0.0177)、年龄增加(P = 0.0040)、当前吸烟者(P = 0.0014)以及CIGTS临床中心(P = 0.0215)。
CIGTS VF评分提供了一种与MD惊人相似的VF测量方法。与VF丧失和VF变异性相关的变量可能有助于识别需要更严格临床检查的患者。