Analysis of somatosensory evoked potentials in peroneal nerve palsy

The peroneal nerve SEPs over the CZ' of the scalp were studied in patients with peroneal nerve palsy. The initial positive peak latencies of P27 (to popliteal fossa stimulation), P30 (to fibular neck stimulation) and P37 (to dorsum of the foot stimulation) were measured. The latency difference P30-P27 was prolonged in all patients with the fibular head lesions. In patients with the superficial peroneal nerve lesions at the foreleg, P37-P27 was prolonged whereas P30-P27 was normal. Clinical application of peroneal nerve SEPs was useful in deciding the site of the lesion causing the peroneal nerve palsy.     

三叉神经体感诱发电位检测的改进

本文对正常80人采用上下唇表面电刺激记录了三叉神经诱发电位。记录电极安放在C_5’/C_6’(10～20系统Cz至外耳孔的中间点),参考电极安放在Fz点,刺激强度为感觉阈的3～4倍。其结果:刺激上唇在C_5’/C_6’点可记录到P_3、N_9、P_(20)、N_(25)、P_(35)、N_(45)各波,刺激下唇时在C_5’/C_6’,可记录到N_3、P_9、N_(13)、P_(20)、N_(25)、P_(35)、N_(45)各波。其记录方法简单,准确,易使被检者接受并在临床应用。     

Recovery functions of common peroneal, posterior tibial and sural nerve somatosensory evoked potentials.

We studied recovery functions of the somatosensory evoked potentials (SEPs) of common peroneal (CPN), posterior tibial (PTN) and sural nerves (SN) using a paired conditioning-test paradigm. The interstimulus interval (ISI) of paired stimuli ranged from 2 to 400 msec. In all SEPs with ISIs of 12-20 msec, the amplitude recovery was close to or beyond 100% of the control response, though their latencies and wave forms were not the same as the control. Further increases of the ISI resulted in significant depression of SEP (late phase suppression), most markedly in CPN, and less prominently in SN-SEP. With a longer than 50 msec ISI there was progressive recovery of SEP, but full recovery differed depending on the nerve stimulated; 400 msec ISI was required for CPN-, 250 msec for PTN- and 100 msec for SN-SEP. The peroneal nerve block by local anesthetic injected just distal to the stimulus electrodes abolished the late phase SEP suppression observed before the nerve block. These findings suggest that the late phase SEP suppression is attributable to the "secondary" afferents as a result of activation of peripheral receptors (muscle, joint and/or cutaneous) by the efferent volley initiated from the stimulus point. The greater and longer duration of peripheral receptor activation in CPN than in PTN or SN stimulation could explain the more pronounced and the longer duration of late phase suppression in CPN-SEP.     

Sensory and motor interfering influences on somatosensory evoked potentials.

The interfering influences by which the different components of the early somatosensory evoked potentials are modified are reviewed from both neurophysiologic and clinical perspectives. Special consideration is given to the specific differences between sensory and motor interferences. In this context, the specific effect of the mental movement simulation task on the frontal N30 component is discussed in relation to the involvement of this evoked wave as a physiologic index of the dopaminergic motor pathways. Relevant interfering approaches, including concurrent events ranging from tactile stimulation to locomotion, are reviewed and discussed insofar as these data provide insights into the neurophysiologic processes of interaction between competing internal models controlling motor acts and sensory information.     

Short latency somatosensory evoked potentials to peroneal nerve stimulation in normal Japanese children

Short latency somatosensory evoked potentials (SSEP) were elicited by stimulation of the peroneal nerve in 68 normal children of 39 weeks to 15 years old. In all subjects, three positive potentials (P1, P2 and P3) and one negative potential (N1) were consistently recorded. A further positive potential (P4) after N1 was not always observed. There was no change of wave form with development. P1, P2, P3 and N1 might be generated in subcortical structures; caudal cervical spine, brainstem, thalamus and thalamocortical pathway, respectively. The latency of each peak per one meter body length decreased with age until 5 or 6 years of age. Moreover, the latency between peaks per one meter body length also decreased with age until 5 to 6 years of age. These findings are consistent with the development of SSEP on median nerve stimulation and with the developmental phenomenon of spinal conduction velocity, and might be related to the increase in the diameter and the progressive myelination of nerve fibers.     

N10 potential as an antidromic motor evoked potential in a median nerve short-latency somatosensory evoked potential study.

When stimulating the mixed nerve to record evoked potential, both sensory and motor fibers are activated before entering the spinal cord. The N10 potential has been described as an antidromic motor evoked potential based on results obtained by recording at the anterior midneck. In the present study, we examined the changes in latencies of Erb's potential, N10, and N13 by stimulating the median nerve distally at the wrist and proximally at the elbow. The conduction velocity of N10 calculated by the difference between N10 latencies at the two stimulation points was consistent with motor conduction velocity, although N13 conduction velocity estimated by the same method reflected a sensory conduction velocity. A positive relation was also observed between the indirect latency from the stimulation point to the anterior root as calculated using the equation (F - M - 1) / 2 (ms) and the direct latency to the negative peak of the N10 potential. Our data support the notion that N10 represents antidromic motor potential originating in the spinal entry zone of the anterior root.     

The effect of stimulus rate upon common peroneal, posterior tibial, and sural nerve somatosensory evoked potentials.

We examined the effect of stimulus rate on somatosensory evoked potentials (SEPs) following stimulation of the common peroneal nerve (CPN) at the knee, and the posterior tibial nerve (PTN) and sural nerve (SN) at the ankle. We measured the amplitude of P40-N50 and N50-P60 in the PTN-SEP and corresponding amplitude of CPN-SEP and SN-SEP at the rate of 2.3, 3.4, 4.1, and 5.1 Hz. When the stimulation rate was increased from 2.3 to 5.1 Hz, the P40-N50 amplitude decreased by 50% for the CPN-SEP and 20% for the PTN-SEP. Also, the N50-P60 amplitude was reduced by 30% in the CPN-SEP and 20% in the PTN-SEP. In contrast, this change in stimulus rate produced no significant amplitude decline in the SN-SEP. Blocking the peroneal nerve with lidocaine just distal to the stimulating electrodes eliminated the descending peroneal nerve volley and abolished the amplitude attenuation observed with the faster stimulus rate. The findings suggest that at higher rates of stimulation, the afferent volleys induced by the movements that follow mixed nerve stimulation interfere with the SEP produced by electrical activation of the sensory afferents. The interference is greater when the more proximal site of the mixed nerve is stimulated.     

Cervical synapse-dependent somatosensory evoked potential following posterior tibial nerve stimulation

We have demonstrated the presence of a localized, synapse-dependent negativity (N29) recorded over the upper cervical spine after bilateral stimulation of the posterior tibial nerves at the ankle. The amplitude of N29 is maximal at the level of the second cervical spine and decreases at more rostral and caudal levels. The peak latency of N29 remains constant at all levels. N29 has a long refractory period when compared with the refractory period of the afferent volley recorded at either the sacral or thoracic level. N29 is most likely generated by activation of the nucleus gracilis by the afferent volley. The cervical N13 after median nerve stimulation probably has multiple generator sites, including the nucleus cuneatus.     

Dermatomal somatosensory evoked potential demonstration of nerve root decompression after VAX-D therapy.

Reductions in low back pain and referred leg pain associated with a diagnosis of herniated disc, degenerative disc disease or facet syndrome have previously been reported after treatment with a VAX-D table, which intermittently distracts the spine. The object of this study was to use dermatomal somatosensory evoked potentials (DSSEPs) to demonstrate lumbar root decompression following VAX-D therapy. Seven consecutive patients with a diagnosis of low back pain and unilateral or bilateral L5 or S1 radiculopathy were studied at our center. Disc herniation at the L5-S1 level was documented by MRI or CT in all patients. All patients were studied bilaterally by DSSEPs at L5 and S1 before and after VAX-D therapy. All patients had at least 50% improvement in radicular symptoms and low back pain and three of them experienced complete resolution of all symptoms. The average pain reduction was 77%. The number of treatment sessions varied from 12 to 35. DSSEPs were considered to show improvement if triphasic characteristics returned or a 50% or greater increase in the P1-P2 amplitude was seen. All patients showed improvement in DSSEPs after VAX-D therapy either ipsilateral or contralateral to the symptomatic leg. Two patients showed deterioration in DSSEPs in the symptomatic leg despite clinically significant improvement in pain and radicular symptoms. Overall, 28 nerve roots were studied before and after VAX-D therapy. Seventeen nerve root responses were improved, eight remained unchanged and three deteriorated. The significance of DSSEP improvement contralateral to the symptomatic leg is emphasized. Direct compression of a nerve root by a disc herniation is probably not the sole explanation for referred leg pain.     

Abnormalities of nerve conduction and somatosensory evoked potential in Poland's syndrome

We report a case of Poland's dyndrome with associated primary generalized tonic-clonic epilepsy. Somatosensory evoked potentials at median nerve stimulation showed delayed latencies and reduced amplitudes of the evoked response from the hypoplastic right upper limb. Nerve conduction studies showed reduced mixed nerve conduction velocity in the right ulnar nerve and decrease in amplitudes of the compound nerve action potentials in the right median and ulnar nerves. We postulate a congenital hypoplasea of the above nerves and brachial plexus in the present case.     

Conduction characteristics of somatosensory evoked potentials to peroneal, tibial and sural nerve stimulation in man

Lumbar spine and scalp short latency somatosensory evoked potentials (SSEPs) to stimulation of the posterior tibial, peroneal and sural nerves at the ankle (PTN-A, PN-A, SN-A) and common peroneal nerve at the knee (CPN-K) were obtained in 8 normal subjects. Peripheral nerve conduction velocities and lumbar spine to cerebral cortex propagation velocities were determined and compared. These values were similar with stimulation of the 3 nerves at the ankle but were significantly greater with CPN-K stimulation. CPN-K and PTN-A SSEPs were recorded from the L3, T12, T6 and C7 spines and the scalp in 6 normal subjects. Conduction velocities were determined over peripheral nerve-cauda equina (stimulus-L3), caudal spinal cord (T12-T6) and rostral spinal cord (T6-C7). Propagation velocities were determined from each spinal level to the cerebral cortex. With both CPN-K and PTN-A stimulation the speed of conduction over peripheral nerve and spinal cord was non-linear. It was greater over peripheral nerve-cauda equina and rostral spinal cord than over caudal cord segments. The CPN-K response was conducted significantly faster than the PTN-A response over peripheral nerve-cauda equina and rostral spinal cord but these values were similar over caudal cord. Spine to cerebral cortex propagation velocities were significantly greater from all spine levels with CPN-K stimulation. These data show that the conduction characteristics of SSEPs over peripheral nerve, spinal cord and from spine to cerebral cortex are dependent on the peripheral nerve stimulated.     

Dermatomal somatosensory evoked potential demonstration of nerve root decompression after VAX-D therapy

Abstract

Reductions in low back pain and referred leg pain associated with a diagnosis of herniated disc, degenerative disc disease or facet syndrome have previously been reported after treatment with a VAX-D table, which intermittently distracts the spine. The object of this study was to use dermatomal somatosensory evoked potentials (DSSEPs) to demonstrate lumbar root decompression following VAX-D therapy. Seven consecutive patients with a diagnosis of low back pain and unilateral or bilateral L5 or S1 radiculopathy were studied at our center. Disc herniation at the L5-S1 level was documented by MRI or CT in all patients. All patients were studied bilaterally by DSSEPs at L5 and S1 before and after VAX-D therapy. All patients had at least 50% improvement in radicular symptoms and low back pain and three of them experienced complete resolution of all symptoms. The average pain reduction was 77%. The number of treatment sessions varied from 12 to 35. DSSEPs were considered to show improvement if triphasic characteristics returned or a 50% or greater increase in the P1-P2 amplitude was seen. All patients showed improvement in DSSEPs after VAX-D therapy either ipsilateral or contralateral to the symptomatic leg. Two patients showed deterioration in DSSEPs in the symptomatic leg despite clinically significant improvement in pain and radicular symptoms. Overall, 28 nerve roots were studied before and after VAX-D therapy. Seventeen nerve root responses were improved, eight remained unchanged and three deteriorated. The significance of DSSEP improvement contralateral to the symptomatic leg is emphasized. Direct compression of a nerve root by a disc herniation is probably not the sole explanation for referred leg pain. [Neurol Res 2001; 23: 706-714]     

Interside amplitude asymmetries in the median nerve somatosensory evoked potential: normative data

Short latency median nerve somatosensory evoked potentials (SEPs) were recorded from a group of 31 adults in order to establish the boundaries between normal and abnormal interside amplitude asymmetries. The potentials studied were the cervical SEP (N13) and the primary cortical response (N20). In order to more accurately analyse and compare intersubject data, the amplitude of the lesser potential was expressed as a percentage of the greater potential. The limit for normality was defined as 1 SD (of the mean amplitude asymmetry) below the lowest individual value observed among normal subjects. It is concluded that if a cervical potential from one side is no more than 60% of the potential from the other side, then this represents a significantly abnormal amplitude asymmetry. In contrast, a cortical potential must have an amplitude which is less than 36% of the larger potential in order to be considered significantly abnormal.     

Peripheral nerve fiber and spinal cord pathway contributions to the somatosensory evoked potential

In monkeys anesthetized with 70% N₂O-30% O₂, alterations in the configuration of the somatosensory evoked potential (SEP) were observed to follow specific spinal cord lesions. The SEPs were recorded in response to stimulation of the exposed superficial peroneal nerve after bilateral dorsal or anterolateral column transection, right or left hemisection, or central cord lesions. Stimulus intensities were sufficient to stimulate large nerve fibers or all nerve fibers. Small nerve fibers were selectively stimulated by blocking large fibers, using a combination of cooling and electrical polarization, while applying maximal stimulus intensities. The results indicate that large-diameter peripheral nerve fibers and the dorsal columns contribute primarily to early wave components (less than 40 ms). Small-diameter peripheral nerve fibers and the anterolateral columns appear to contribute primarily to later wave components (greater than 70 ms). Both large- and small-diameter peripheral nerve fibers and both dorsal and anterolateral columns appear to contribute to components with latencies between 35 and 70 ms.     

Impact of somatosensory evoked potential monitoring on cervical surgery.

Controversy still exists about the necessity of somatosensory evoked potential (SSEP) monitoring during cervical surgery. The purpose of this prospective study is to determine the impact of SSEP monitoring on anterior cervical surgery. Intraoperative SSEP monitoring was performed in 100 patients treated by an anterior cervical approach. The patients were divided into three groups according to their preoperative clinical condition. Somatosensory evoked potential monitoring was performed during five stages of the procedure: M1, after the induction of anesthesia; M2, during positioning; M3, during distraction of the intervertebral space; M4, throughout decompression; and M5, during graft placement. Normal SSEPs were obtained during M1 from all the patients in group 2. Pathologic SSEPs were recorded at M1 in 45 patients from group 1. No SSEPs were recorded at M1 in six patients in group 3. A deterioration of the SSEPs was observed in 35 patients during M2. Deteriorated SSEPs were observed during M3 in 14 patients. No deterioration of the SSEPs was recorded during M4. Intraoperative SSEP monitoring is easy to perform and helps to increase safety during anterior cervical surgery. Critical phases of the surgical procedure were identified and the surgical strategy was modified as a result of this study.     

Frontal component of the somatosensory evoked potential

Electric stimulation of the median nerve at the wrist evokes a series of electric potentials that can be recorded from the scalp or directly from the cortex. These somatosensory evoked potentials (SEP) include a parietal negativity with a maximum 20 ms after the stimulus, which originates in the somatosensory cortex, probably area 3b (Allison et al. [1991a], Brain 114:2465–2503 and Desmedt et al. [1987], Electroenceph Clin Neurophysiol 68:1–19). Thirty milliseconds after the stimulus, a negative potential (N30) occurs at frontal recording sites. Recently it was observed that the amplitude of this potential is altered in patients with dystonia, Parkinson's disease, and Huntington's chorea. It has been argued that the N30 potential stems from cortical areas other than the somatosensory cortex, for example, the supplementary motor area. We used multichannel recordings to investigate the scalp distribution of the N20 and the N30 potentials in healthy subjects. We found that the N20 as well as the N30 potentials were accompanied by a corresponding positivity at frontal and parietal recording sites, respectively. The N20/P20 and the N30/P30 potential fields had a mirrorlike appearance, and both showed a polarity reversal near the central sulcus. This and the results of correlation analyses led us to the conclusion that the N30 generator is located near the central sulcus. © 1995 Wiley-Liss, Inc.     

State-dependent changes in the N20 component of the median nerve somatosensory evoked potential

Short-latency components of median nerve somatosensory evoked potentials are generally assumed to be unaffected by sleep and level of arousal. We found that sleep prolongs the latency and alters the morphology of the N20 component in normal subjects. These changes may represent differential effects of sleep on various elements contributing to generation of the N20. Failure to control for patient state may degrade the reliability of clinical somatosensory evoked potential testing.     

Multichannel recording of median nerve somatosensory evoked potentials.

OBJECTIVES: Clinical applications of multichannel (>or=64 electrodes) electroencephalography (EEG) have been limited so far. Amplitude variability of evoked potentials in healthy subjects is large, which limits their diagnostic applicability. This amplitude variability may be partially due to spatial undersampling of anatomical variations in cortical generators. In the present study, we therefore investigated whether 128-channel recordings of somatosensory evoked potentials (SEPs) can reduce this amplitude variability in healthy subjects. Additionally, we explored the relation between amplitude and age. METHODS: We recorded median nerve SEPs using a 128-channel EEG system in 50 healthy subjects (20-70 years) and compared N20, P27, and P45 amplitude as obtained with a 128-channel analysis method - based on butterfly plots and spatial topographies - and as obtained using a conventional one-cortical-channel configuration and analysis. Scalp and earlobe references were compared. RESULTS: Although amplitude variability itself was not reduced, a reduced coefficient of variation was obtained with the 128-channel method due to higher SEP amplitudes, compared to the conventional one-channel method, independent of reference. CONCLUSION: These results suggest that at the cost of some additional preparation time, the 128-channel method can measure SEP amplitude more accurately and might therefore be more sensitive to physiological and pathological changes. For optimal amplitude estimation, we recommend to increase the number of centroparietal electrodes or, preferably, to perform at least a 64-channel recording.