Steady-state analysis of somatosensory evoked potentials

We report the development of a new method for frequency domain analysis of steady-state somatosensory evoked potentials (SEPs) to amplitude-modulated electrical stimulation, which can be recorded in significantly less time than traditional SEPs. Resampling techniques were used to compare the steady-...

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Published inElectroencephalography and clinical neurophysiology Vol. 100; no. 5; pp. 453 - 461
Main Authors Noss, Roger S., Boles, Colby D., Yingling, Charles D.
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 01.09.1996
Amsterdam Elsevier
Subjects
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ISSN0168-5597
0013-4694
DOI10.1016/0168-5597(96)96011-6

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Abstract We report the development of a new method for frequency domain analysis of steady-state somatosensory evoked potentials (SEPs) to amplitude-modulated electrical stimulation, which can be recorded in significantly less time than traditional SEPs. Resampling techniques were used to compare the steady-state SEP to traditional SEP recordings, which are based on signal averaging in the time domain of cortical responses to repetitive transient stimulation and take 1–2 min or more to obtain a satisfactory signal/noise ratio. Median nerves of 3 subjects were stimulated continuously with electrical alternating current at several modulation frequencies from 7 to 41 Hz. Amplitude modulation was used to concentrate the power in higher frequencies, away from the modulation frequency, to reduce the amount of stimulus artifact recorded. Data were tested for signal detectability in the frequency domain using the T circ 2 statistic. A reliable steady-state response can be recorded from scalp electrodes overlying somatosensory cortex in only a few seconds. In contrast, no signal was statistically discriminable from noise in the transient SEP from as much as 20 s of data. This dramatic time savings accompanying steady-state somatosensory stimulation may prove useful for monitoring in the operating room or intensive care unit.
AbstractList We report the development of a new method for frequency domain analysis of steady-state somatosensory evoked potentials (SEPs) to amplitude-modulated electrical stimulation, which can be recorded in significantly less time than traditional SEPs. Resampling techniques were used to compare the steady-state SEP to traditional SEP recordings, which are based on signal averaging in the time domain of cortical responses to repetitive transient stimulation and take 1-2 min or more to obtain a satisfactory signal/noise ratio. Median nerves of 3 subjects were stimulated continuously with electrical alternating current at several modulation frequencies from 7 to 41 Hz. Amplitude modulation was used to concentrate the power in higher frequencies, away from the modulation frequency, to reduce the amount of stimulus artifact recorded. Data were tested for signal detectability in the frequency domain using the T(circ)2 statistic. A reliable steady-state response can be recorded from scalp electrodes overlying somatosensory cortex in only a few seconds. In contrast, no signal was statistically discriminable from noise in the transient SEP from as much as 20 s of data. This dramatic time savings accompanying steady-state somatosensory stimulation may prove useful for monitoring in the operating room or intensive care unit.
We report the development of a new method for frequency domain analysis of steady-state somatosensory evoked potentials (SEPs) to amplitude-modulated electrical stimulation, which can be recorded in significantly less time than traditional SEPs. Resampling techniques were used to compare the steady-state SEP to traditional SEP recordings, which are based on signal averaging in the time domain of cortical responses to repetitive transient stimulation and take 1–2 min or more to obtain a satisfactory signal/noise ratio. Median nerves of 3 subjects were stimulated continuously with electrical alternating current at several modulation frequencies from 7 to 41 Hz. Amplitude modulation was used to concentrate the power in higher frequencies, away from the modulation frequency, to reduce the amount of stimulus artifact recorded. Data were tested for signal detectability in the frequency domain using the T circ 2 statistic. A reliable steady-state response can be recorded from scalp electrodes overlying somatosensory cortex in only a few seconds. In contrast, no signal was statistically discriminable from noise in the transient SEP from as much as 20 s of data. This dramatic time savings accompanying steady-state somatosensory stimulation may prove useful for monitoring in the operating room or intensive care unit.
Author Boles, Colby D.
Yingling, Charles D.
Noss, Roger S.
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  organization: Departments of Anesthesia, Neurological Surgery, and Otolaryngology, School of Medicine, University of California, San Francisco, CA 94143-0648, USA
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10.1016/0168-5597(92)90007-X
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10.1016/0168-5597(95)00048-W
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Issue 5
Keywords Amplitude modulation
Fourier analysis
Intraoperative monitoring
Median nerve stimulation
Somatosensory evoked potentials
Peripheral nervous system
Human
Spinal cord
Methodology
Electrical stimulus
Central nervous system
Electrophysiology
Frequency domain method
Wrist
Analysis method
Surgery
Median nerve
Somatosensory evoked potential
Monitoring
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PublicationTitle Electroencephalography and clinical neurophysiology
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Snippet We report the development of a new method for frequency domain analysis of steady-state somatosensory evoked potentials (SEPs) to amplitude-modulated...
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elsevier
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Enrichment Source
Publisher
StartPage 453
SubjectTerms Adult
Amplitude modulation
Biological and medical sciences
Cerebrospinal fluid. Spinal cord. Spinal roots. Spinal nerves
Electric Stimulation
Evoked Potentials, Somatosensory - physiology
Fourier analysis
Humans
Intraoperative monitoring
Male
Median Nerve - physiology
Median nerve stimulation
Medical sciences
Middle Aged
Neurosurgery
Somatosensory evoked potentials
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Title Steady-state analysis of somatosensory evoked potentials
URI https://dx.doi.org/10.1016/0168-5597(96)96011-6
https://www.ncbi.nlm.nih.gov/pubmed/8893664
Volume 100
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