De Moraes Carlos Gustavo, Liebmann Jeffrey M, Ritch Robert, Hood Donald C
Department of Ophthalmology, Einhorn Clinical Research Center, New York Eye and Ear Infirmary, 310 East 14th Street, New York, NY 10003, USA.
Doc Ophthalmol. 2012 Aug;125(1):1-9. doi: 10.1007/s10633-012-9324-3. Epub 2012 Apr 5.
To test a framework that describes how the multifocal visual-evoked potential (mfVEP) technique is used in a particular glaucoma practice.
In this prospective, descriptive study, glaucoma suspects, ocular hypertensives and glaucoma patients were referred for mfVEP testing by a single glaucoma specialist over a 2-year period. All patients underwent standard automated perimetry (SAP) and mfVEP testing within 3 months. Two hundred and ten patients (420 eyes) were referred for mfVEP testing for the following reasons: (1) normal SAP tests suspected of early functional loss (ocular hypertensives, n = 43; and glaucoma suspects on the basis of suspicious optic disks, n = 52); (2) normal-tension glaucoma patients with suspected central SAP defects (n = 33); and (3) SAP abnormalities needing confirmation (n = 82).
All the glaucoma suspects with normal SAP and mfVEP results remained untreated. Of those with abnormal mfVEP results, 68 % (15/22) were treated because the abnormal regions on the mfVEP were consistent with the abnormal regions seen during clinical examination of the optic disk. The mfVEP was abnormal in 86 % (69/80) of eyes with glaucomatous optic neuropathy and SAP damage, even though it did not result in an altered treatment regimen. In NTG patients, the mfVEP showed central defects in 44 % (12 of 27) of the eyes with apparently normal central fields and confirmed central scotomata in 92 % (36 of 39), leading to more rigorous surveillance of these patients.
In a clinical practice, the mfVEP was used when clinical examination and subjective visual fields provided insufficient or conflicting information. This information influenced clinical management.
测试一个描述多焦视觉诱发电位(mfVEP)技术在特定青光眼诊疗实践中如何应用的框架。
在这项前瞻性描述性研究中,青光眼可疑患者、高眼压症患者和青光眼患者在两年时间内由一位青光眼专科医生转介进行mfVEP检测。所有患者在3个月内均接受了标准自动视野计(SAP)检查和mfVEP检测。210名患者(420只眼)因以下原因被转介进行mfVEP检测:(1)SAP检测正常但怀疑有早期功能丧失(高眼压症患者,n = 43;基于可疑视盘的青光眼可疑患者,n = 52);(2)怀疑有中央SAP缺陷的正常眼压性青光眼患者(n = 33);(3)需要确认的SAP异常(n = 82)。
所有SAP和mfVEP结果正常的青光眼可疑患者均未接受治疗。mfVEP结果异常的患者中,68%(15/22)接受了治疗,因为mfVEP上的异常区域与视盘临床检查中所见的异常区域一致。86%(69/80)患有青光眼性视神经病变和SAP损害的眼睛mfVEP异常,尽管这并未导致治疗方案改变。在正常眼压性青光眼患者中,mfVEP在44%(27只眼中的12只)中央视野明显正常的眼睛中显示中央缺陷,在92%(39只眼中的36只)确诊有中央暗点的眼睛中显示中央缺陷,从而导致对这些患者进行更严格的监测。
在临床实践中,当临床检查和主观视野提供的信息不足或相互矛盾时,会使用mfVEP。这些信息影响了临床管理。