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改善非新生血管性年龄相关性黄斑变性的初步研究的患者选择标准。

Patient selection criteria for pilot studies on amelioration of non-neovascular age-related macular degeneration.

机构信息

Laboratory of Ocular Sciences, Senju Pharmaceutical Corporation Ltd ., Beaverton, Oregon, USA.

出版信息

J Ocul Pharmacol Ther. 2010 Aug;26(4):367-71. doi: 10.1089/jop.2010.0042.

DOI:10.1089/jop.2010.0042
PMID:20653480
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2928702/
Abstract

PURPOSES

Non-neovascular age-related macular degeneration (AMD) is characterized by accumulation of macular drusen, changes in pigmentation of the retinal pigment epithelium, and geographic atrophy. The purposes of this study were to (1) measure the rate of progression of non-neovascular AMD and (2) from the rate data, to propose patient selection criteria for testing drugs to prevent progression of non-neovascular AMD.

METHODS

Medical charts were searched for all AMD billing codes, consecutively reviewed, and 51 patients with a median age of 76 years were mined for severity of AMD using a standardized worsening scale from 0 to 6, visual acuity (VA, Snellen), medications or procedures to treat eye diseases, date of eye examinations, age, and sex. Individual eyes, excluding those with cataract, were grouped and compared.

RESULTS

Using all grades, VA (logMAR) was positively correlated with AMD scores (P < 0.0001, n = 66). The median length of time to progress from AMD grade 3 or 4 to the next grade was 1.0 (n = 14) and 1.7 years (n = 7), respectively. Statistical analyses predicted that drug-treated and nontreated groups, each containing 409 grade 3 and 4 AMD eyes, could detect 50% drug inhibition (P = 0.05) in a 2-year trial.

CONCLUSIONS

VA measurements and structural AMD grades would be useful markers in clinical trials on non-neovascular AMD. Recruiting only grade 3 and 4 patients may be ideal for time- and cost-efficient pilot drug efficacy studies on moderately progressing non-neovascular AMD.

摘要

目的

非新生血管性年龄相关性黄斑变性(AMD)的特征是黄斑玻璃膜疣积聚、视网膜色素上皮色素变化和地图状萎缩。本研究的目的是:(1) 测量非新生血管性 AMD 的进展速度;(2) 根据这些数据,提出用于测试预防非新生血管性 AMD 进展药物的患者选择标准。

方法

搜索所有 AMD 计费代码的医疗记录,连续进行审查,并对 51 名年龄中位数为 76 岁的患者进行 AMD 严重程度的挖掘,使用 0 到 6 的标准化加重量表进行评估,视力(VA,Snellen)、治疗眼病的药物或程序、眼部检查日期、年龄和性别。排除白内障的个体眼睛被分组并进行比较。

结果

使用所有级别,VA(logMAR)与 AMD 评分呈正相关(P<0.0001,n=66)。从中度 AMD 3 级或 4 级进展到下一级的中位时间分别为 1.0 年(n=14)和 1.7 年(n=7)。统计分析预测,每个包含 409 只 AMD 3 级和 4 级眼睛的药物治疗组和未治疗组,在 2 年试验中可以检测到 50%的药物抑制(P=0.05)。

结论

VA 测量和结构 AMD 分级将是评估非新生血管性 AMD 的临床试验中的有用标志物。仅招募 AMD 3 级和 4 级患者,可能是评估中度进展的非新生血管性 AMD 药物疗效的高效、经济的初步研究的理想选择。

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