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高危眼压升高和早期青光眼患者的多焦视觉诱发电位与标准自动视野计比较

Comparing multifocal VEP and standard automated perimetry in high-risk ocular hypertension and early glaucoma.

作者信息

Fortune Brad, Demirel Shaban, Zhang Xian, Hood Donald C, Patterson Emily, Jamil Annisa, Mansberger Steven L, Cioffi George A, Johnson Chris A

机构信息

Discoveries in Sight, Devers Eye Institute, Portland, Oregon, USA.

出版信息

Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1173-80. doi: 10.1167/iovs.06-0561.

DOI:10.1167/iovs.06-0561
PMID:17325161
Abstract

PURPOSE

To compare the diagnostic performance of multifocal visual evoked potential (mfVEP) and standard automated perimetry (SAP), in eyes with high-risk ocular hypertension or early glaucoma.

METHODS

Both eyes of 185 individuals with high-risk ocular hypertension or early glaucoma were evaluated. Subjects ranged in age from 37 to 87 (mean +/- SD: 61 +/- 11 years). Pattern-reversal mfVEPs were obtained by using VERIS (Electro-Diagnostic Imaging, San Mateo, CA) with a four-electrode array and were analyzed with custom software. SAP visual fields (SITA-standard; Carl Zeiss Meditec, Inc., Dublin, CA) were obtained within 22.3 +/- 27.0 days of the mfVEP. Stereo disc photographs and Heidelberg Retina Tomograph (HRT) images were obtained during one visit, which was within 24.8 +/- 50.4 days of the mfVEP and 33.1 +/- 62.9 days of the SAP visual field. Abnormalities on the mfVEP were defined by using a variety of cluster criteria: SAP with pattern standard deviation (PSD) P </= 0.05 or glaucoma hemifield test (GHT) outside normal limits, according to OHTS criteria (SAP-OHTS). In separate analyses cluster criteria were used to determine SAP abnormalities. Disc photographs were graded as either glaucomatous optic neuropathy (GON) or normal by two independent masked experts, and disagreements were adjudicated by a third masked expert. The overall Moorfields regression analysis (MRA) result from the HRT was used as a separate diagnostic classification. All eyes classified as "borderline" by the MRA were assigned to the normal category (i.e., "within normal limits"). Sensitivity for mfVEP or SAP was defined as the percentage of GON eyes that had an abnormality on the functional test. Specificity for mfVEP or SAP was defined as the percentage of eyes with normal optic disc structure that had normal functional test

RESULTS

results. Disc photographs from 50% of eyes were graded GON. Both eyes were graded GON in 71 (38%) of the 185 subjects. Exactly half as many eyes were abnormal by HRT MRA. The average SAP mean deviation (MD) was +0.3 +/- 2.1 dB; average PSD was 2.3 +/- 1.9 dB. By OHTS criteria, 83 (22%) of the 370 eyes had an abnormal SAP. Depending on the cluster criterion used, the proportion of eyes with an abnormal SAP ranged from 8% to 26% and with an abnormal mfVEP, from 14% to 45%. A criterion with an estimated specificity in normal subjects of 91% resulted in 102 (28%) eyes with an abnormal mfVEP. For criteria with estimated specificities of 95% and 99%, respectively, 88 (24%) eyes and 52 (14%) eyes had an abnormal mfVEP. Agreement between SAP and mfVEP ranged from 75% to 81%. The sensitivity of SAP-OHTS to detect GON (using the disc photograph as diagnostic standard) was 29%, whereas specificity was 84%. Sensitivity of the mfVEP to detect GON, for cluster criteria with disc structure specificity between 84% and 87%, ranged from 28% to 32%. When the HRT MRA was used as the diagnostic standard, sensitivities of both functional tests to detect GON increased to 42%.

CONCLUSIONS

The diagnostic performance of mfVEP was similar to that of SAP. However, the two modalities agreed in only approximately 80% of eyes, suggesting that they may detect slightly different functional deficits.

摘要

目的

比较多焦视觉诱发电位(mfVEP)和标准自动视野计(SAP)在高危眼压升高或早期青光眼患者眼中的诊断性能。

方法

对185例高危眼压升高或早期青光眼患者的双眼进行评估。受试者年龄在37至87岁之间(平均±标准差:61±11岁)。使用VERIS(Electro-Diagnostic Imaging,加利福尼亚州圣马特奥)通过四电极阵列获得图形翻转mfVEP,并使用定制软件进行分析。在mfVEP检查后的22.3±27.0天内进行SAP视野检查(SITA标准;Carl Zeiss Meditec公司,加利福尼亚州都柏林)。在一次就诊期间获取立体视盘照片和海德堡视网膜断层扫描(HRT)图像,此次就诊在mfVEP检查后的24.8±50.4天内,且在SAP视野检查后的33.1±62.9天内。根据OHTS标准(SAP - OHTS),使用多种聚类标准定义mfVEP异常:SAP的模式标准差(PSD)P≤0.05或青光眼半视野检测(GHT)超出正常范围。在单独分析中,使用聚类标准确定SAP异常。两名独立的盲法专家将视盘照片分级为青光眼性视神经病变(GON)或正常,如有分歧则由第三位盲法专家裁决。将HRT的总体摩尔菲尔德回归分析(MRA)结果用作单独的诊断分类。所有被MRA分类为“临界”的眼睛均归入正常类别(即“在正常范围内”)。mfVEP或SAP的敏感性定义为在功能测试中出现异常的GON眼睛的百分比。mfVEP或SAP的特异性定义为视神经盘结构正常且功能测试正常的眼睛的百分比。

结果

50%的眼睛视盘照片被分级为GON。在185名受试者中,71名(38%)的双眼被分级为GON。HRT MRA显示异常的眼睛数量恰好是前者的一半。SAP的平均偏差(MD)平均值为+0.3±2.1 dB;平均PSD为2.3±1.9 dB。根据OHTS标准,370只眼中有83只(22%)的SAP异常。根据所使用的聚类标准,SAP异常的眼睛比例在8%至26%之间,mfVEP异常的眼睛比例在14%至45%之间。在正常受试者中估计特异性为91%的一项标准导致102只(28%)眼睛的mfVEP异常。对于估计特异性分别为95%和99%的标准,mfVEP异常的眼睛分别为88只(24%)和52只(14%)。SAP和mfVEP之间的一致性在75%至81%之间。SAP - OHTS检测GON(以视盘照片作为诊断标准)的敏感性为29%,而特异性为84%。对于视盘结构特异性在84%至87%之间的聚类标准,mfVEP检测GON的敏感性在28%至32%之间。当以HRT MRA作为诊断标准时,两种功能测试检测GON的敏感性均提高到42%。

结论

mfVEP的诊断性能与SAP相似。然而,这两种方法仅在约80%的眼睛中结果一致,这表明它们可能检测到略有不同的功能缺陷。

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