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Comparing the RETeval(®) portable ERG device with more traditional tabletop ERG systems in normal subjects and selected retinopathies

PURPOSE: Our study aimed to determine if ISCEV standard-like ERGs recorded with the LKC RETeval(®) portable ERG unit compared to those obtained using the more traditional tabletop unit. METHODS: ERGs recorded from normal subjects and patients affected with retinal ON and OFF pathway anomalies were c...

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Detalles Bibliográficos
Autores principales: You, Jia Yue, Dorfman, Allison L., Gauvin, Mathieu, Vatcher, Dylan, Polomeno, Robert C., Little, John M., Lachapelle, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082128/
https://www.ncbi.nlm.nih.gov/pubmed/36273363
http://dx.doi.org/10.1007/s10633-022-09903-w
Descripción
Sumario:PURPOSE: Our study aimed to determine if ISCEV standard-like ERGs recorded with the LKC RETeval(®) portable ERG unit compared to those obtained using the more traditional tabletop unit. METHODS: ERGs recorded from normal subjects and patients affected with retinal ON and OFF pathway anomalies were compared. Analysis included peak time and amplitude measurements as well as time–frequency domain analysis with the discrete wavelet transform of waveforms obtained with the two systems. RESULTS: Although both systems were similarly able to record reliable and highly reproducible ERG responses, there were major discrepancies in ERG responses between the portable and tabletop units, pointing toward a weaker stimulation of the retinal OFF pathway with the portable RETeval(®) unit. CONCLUSION: The portable RETeval(®) unit appears to be able to record highly reproducible and diagnostically useful clinical ERGs, albeit with some significant differences in waveform composition compared to those obtained with more standard tabletop systems. Given the unknown origin of these waveform discrepancies, if left uncorrected, these differences could potentially lead to erroneous interpretation when used in the clinical context and/or compared to ERGs recorded using more traditional table top units. Clearly, more research is warranted before handheld devices, such as the RETeval(®), can be homologated as a diagnostically sound ERG devices.