Katz J, Gilbert D, Quigley H A, Sommer A
Department of International Health, Johns Hopkins School of Hygiene and Public Health, Baltimore, Maryland 21205-2103, USA.
Ophthalmology. 1997 Jun;104(6):1017-25. doi: 10.1016/s0161-6420(97)30192-4.
The authors estimated the prevalence and rates of progressive visual field loss in glaucoma patients followed annually for a median of 6.3 years.
Linear regression was used to estimate rates of progression of mean deviation, corrected pattern standard deviation (CPSD), clusters of locations based on the Glaucoma Hemifield Test (GHT), and location specific changes in C-30-2 fields of the Humphrey Analyzer.
Sixty-seven eyes of 56 patients whose first two consecutive fields were abnormal on GHT were included. Almost all patients were under treatment or had undergone surgery for glaucoma. Visual field deteriorated in 19 (28%) eyes based on worsening of one or more CPSD, GHT clusters, or individual test locations (regression slopes significantly different from zero). Corrected pattern standard deviation deteriorated in 5 eyes, at least one GHT cluster deteriorated in 17 eyes, and one or more individual test locations deteriorated in 15 eyes. For those whose visual field deteriorated, CPSD increased by 0.9 dB/year. Glaucoma Hemifield Test clusters declined by between 1.4 and 2.4 dB/year. Deterioration at individual locations ranged from 1.0 to 5.0 dB/year. Age, but not baseline visual field severity, was predictive of further visual field loss. The odds ratio for the association between progressive visual field loss and thinning of the nerve fiber layer was 1.81 (95% confidence interval: 0.52, 6.33), and 3.78 (95% confidence interval: 0.80, 18.16) for the association between progressive visual field loss and optic disc changes during follow-up based on masked photograph readings.
Less than one in three eyes of patients with glaucoma had any progressive field loss. Average changes in threshold sensitivities of less than 1 dB/year could not be detected with seven fields done over 6 years. Larger changes or increased frequency of visual field testing would need to occur before smaller changes could be detected statistically.
作者估计了青光眼患者每年随访时进行性视野缺损的患病率和发生率,随访时间中位数为6.3年。
采用线性回归估计平均偏差、校正模式标准差(CPSD)、基于青光眼半视野检测(GHT)的位置簇以及 Humphrey 分析仪C-30-2视野中特定位置变化的进展率。
纳入了56例患者的67只眼,这些患者连续前两个视野的GHT结果异常。几乎所有患者都接受了青光眼治疗或手术。基于一个或多个CPSD、GHT簇或单个检测位置的恶化情况(回归斜率显著不同于零),19只眼(28%)的视野恶化。5只眼的校正模式标准差恶化,17只眼至少一个GHT簇恶化,15只眼一个或多个单个检测位置恶化。对于视野恶化的患者,CPSD每年增加0.9 dB。青光眼半视野检测簇每年下降1.4至2.4 dB。单个位置的恶化范围为每年1.0至5.0 dB。年龄而非基线视野严重程度可预测进一步的视野缺损。进行性视野缺损与神经纤维层变薄之间关联的优势比为1.81(95%置信区间:0.52, 6.33),基于盲法照片读数,进行性视野缺损与随访期间视盘变化之间关联的优势比为3.78(95%置信区间:0.80, 18.16)。
青光眼患者中不到三分之一的眼睛有任何进行性视野缺损。在6年中进行7次视野检查无法检测到阈值敏感度每年小于1 dB的平均变化。在能够通过统计学检测到较小变化之前,需要出现更大的变化或增加视野检查的频率。