TY - JOUR
T1 - Exploring the methods of data analysis in multifocal visual evoked potentials
AU - Malmqvist, Lasse
AU - Santiago de Abreu, Lucimar
AU - Fraser, C.
AU - Klistorner, Alexander
AU - Hamann, S.
PY - 2016
Y1 - 2016
N2 - Purpose: The multifocal visual evoked potential (mfVEP) provides a topographical assessment of visual function, which has already shown potential for use in patients with glaucoma and multiple sclerosis. However, the variability in mfVEP measurements has limited its broader application. The purpose of this study was to compare several methods of data analysis to decrease mfVEP variability. Methods: Twenty-three normal subjects underwent mfVEP testing. Monocular and interocular asymmetry data were analyzed. Coefficients of variability in amplitude were examined using peak-to-peak, root mean square (RMS), signal-to-noise ratio (SNR) and logSNR techniques. Coefficients of variability in latency were examined using second peak and cross-correlation methods. Results: LogSNR and peak-to-peak methods had significantly lower intra-subject variability when compared with RMS and SNR methods. LogSNR had the lowest inter-subject amplitude variability when compared with peak-to-peak, RMS and SNR. Average latency asymmetry values for the cross-correlation analysis were 1.7 ms (CI 95 % 1.2–2.3 ms) and for the second peak analysis 2.5 ms (CI 95 % 1.7–3.3 ms). A significant difference was found between cross-correlation and second peak analysis for both intra-subject variability (p < 0.001) and inter-subject variability (p < 0.001). Conclusions: For a comparison of amplitude data between groups of patients, the logSNR or SNR methods are preferred because of the smaller inter-subject variability. LogSNR or peak-to-peak methods have lower intra-subject variability, so are recommended for comparing an individual mfVEP to previous published normative data. This study establishes that the choice of mfVEP data analysis method can be used to decrease variability of the mfVEP results.
AB - Purpose: The multifocal visual evoked potential (mfVEP) provides a topographical assessment of visual function, which has already shown potential for use in patients with glaucoma and multiple sclerosis. However, the variability in mfVEP measurements has limited its broader application. The purpose of this study was to compare several methods of data analysis to decrease mfVEP variability. Methods: Twenty-three normal subjects underwent mfVEP testing. Monocular and interocular asymmetry data were analyzed. Coefficients of variability in amplitude were examined using peak-to-peak, root mean square (RMS), signal-to-noise ratio (SNR) and logSNR techniques. Coefficients of variability in latency were examined using second peak and cross-correlation methods. Results: LogSNR and peak-to-peak methods had significantly lower intra-subject variability when compared with RMS and SNR methods. LogSNR had the lowest inter-subject amplitude variability when compared with peak-to-peak, RMS and SNR. Average latency asymmetry values for the cross-correlation analysis were 1.7 ms (CI 95 % 1.2–2.3 ms) and for the second peak analysis 2.5 ms (CI 95 % 1.7–3.3 ms). A significant difference was found between cross-correlation and second peak analysis for both intra-subject variability (p < 0.001) and inter-subject variability (p < 0.001). Conclusions: For a comparison of amplitude data between groups of patients, the logSNR or SNR methods are preferred because of the smaller inter-subject variability. LogSNR or peak-to-peak methods have lower intra-subject variability, so are recommended for comparing an individual mfVEP to previous published normative data. This study establishes that the choice of mfVEP data analysis method can be used to decrease variability of the mfVEP results.
KW - Coefficient of variability
KW - Data analysis
KW - Inter-subject variability
KW - Intra-subject variability
KW - Multifocal visual evoked potentials
U2 - 10.1007/s10633-016-9546-x
DO - 10.1007/s10633-016-9546-x
M3 - Journal article
C2 - 27312134
AN - SCOPUS:84975167738
SN - 0012-4486
VL - 133
SP - 41
EP - 48
JO - Documenta Ophthalmologica
JF - Documenta Ophthalmologica
IS - 1
ER -