Skip to main content
Log in

Quantification of the proportion of motor neurons recruited by transcranial electrical stimulation during intraoperative motor evoked potential monitoring

  • Original Research
  • Published:
Journal of Clinical Monitoring and Computing Aims and scope Submit manuscript

Abstract

Transcranial motor evoked potentials (TcMEPs) are widely used to monitor motor function during spinal surgery. However, they are much smaller and more variable in amplitude than responses evoked by maximal peripheral nerve stimulation, suggesting that a limited number of spinal motor neurons to the target muscle are excited by transcranial stimulation. The aim of this study was to quantify the proportion of motor neurons recruited during TcMEP monitoring under general anesthesia. In twenty patients who underwent thoracic and/or lumbar spinal surgery with TcMEP monitoring, the triple stimulation technique (TST) was applied to the unilateral upper arm intraoperatively. Total intravenous anesthesia was employed. Trains of four stimuli were delivered with maximal intensity and an inter-pulse interval of 1.5 ms. TST responses were recorded from the abductor digiti minimi muscle, and the negative peak amplitude and area were measured and compared between the TST test (two collisions between transcranial and proximal and distal peripheral stimulation) and control response (two collisions between two proximal and one distal peripheral stimulation). The highest degree of superimposition of the TST test and control responses was chosen from several trials per patient. The average ratios (test:control) were 17.1 % (range 1.8–38 %) for the amplitudes and 21.6 % (range 2.9–40 %) for the areas. The activity of approximately 80 % of the motor units to the target muscle cannot be detected by TcMEP monitoring. Therefore, changes in evoked potentials must be interpreted cautiously when assessing segmental motor function with TcMEP monitoring.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Jellinek D, Jewkes D, Symon L. Noninvasive intraoperative monitoring of motor evoked potentials under propofol anesthesia: effect of spinal surgery on the amplitude and latency of motor evoked potentials. Neurosurgery. 1991;29:551–7.

    Article  PubMed  CAS  Google Scholar 

  2. Keller BP, Haghighi SS, Oro JJ, Eggerrs GWN. The effect of propofol anesthesia on transcortical electric evoked potentials in the rat. Neurosurgery. 1992;30:557–60.

    Article  PubMed  CAS  Google Scholar 

  3. Taylor BA, Fennelly ME, Taylor A, Farrell J. Temporal summation—the key to motor evoked potential spinal cord monitoring in humans. J Neurol Neurosurg Psychiat. 1993;56:104–6.

    Article  PubMed  CAS  Google Scholar 

  4. Jones SJ, Harrison R, Koh KF, Mendoza N, Crockard HA. Motor evoked potential monitoring during spinal surgery: response of distal limb muscle to transcranial cortical stimulation with pulse train. Electroenceph Clin Neurophysiol. 1996;100:375–83.

    PubMed  CAS  Google Scholar 

  5. Pechstein U, Cedzich C, Nadstawek J, Schramm J. Transcranial high-frequency repetitive electrical stimulation for recording myogenic motor evoked potentials with the patient under general anesthesia. Neurosurgery. 1996;39:335–44.

    Article  PubMed  CAS  Google Scholar 

  6. Woodforth IJ, Hicks RG, Crawford MR, Stephen JP, Burke DJ. Variability of motor-evoked potentials recording during nitrous oxide anesthesia from the tibialis anterior muscle after transcranial electrical stimulation. Anesth Analg. 1996;82:744–9.

    PubMed  CAS  Google Scholar 

  7. Magistris MR, Rosler KM, Truffert A, Myers JP. Transcranial stimulation excites virtually all motor neurons supplying the target muscle. Brain. 1998;121:437–50.

    Article  PubMed  Google Scholar 

  8. Matsuda H, Shimazu A. Intraoperative spinal cord monitoring using electric responses to stimulation of caudal spinal cord or motor cortex. In: Desmedt JE, editor. Neuromonitoring in surgery. Amsterdam: Elsevier; 1989. p. 175–90.

    Google Scholar 

  9. Merton PA, Morton HB. Stimulation of the cerebral cortex in the intact human subject. Nature. 1980;285:227.

    Article  PubMed  CAS  Google Scholar 

  10. Merton PA, Morton HB. Electrical stimulation of human motor and visual cortex through the scalp. J Physiol. 1980;305:9P–10P.

    Google Scholar 

  11. Zentner J. Noninvasive motor evoked potential monitoring during neurosurgical operations on the spinal cord. Neurosurgery. 1989;24:709–12.

    Article  PubMed  CAS  Google Scholar 

  12. Calancie B, Klose KL, Baier S, Green BA. Isoflurane-induced attenuation of motor evoked potentials caused by electrical motor cortex stimulation during surgery. J Neurosurg. 1991;74:897–904.

    Article  PubMed  CAS  Google Scholar 

  13. Deletis V, Sala F. Intraoperative neurophysiological monitoring of the spinal cord during spinal cord and spine surgery: a review focus on the corticospinal tracts. Clin Neurophysiol. 2008;119:248–64.

    Article  PubMed  Google Scholar 

  14. Leppanen RE. Faces of spine care. From the electrodiagnostic lab: where transcranial stimulation, H-reflexes and F-responses monitor cord function intraoperatively. Spine J. 2004;4:601–3.

    Article  PubMed  Google Scholar 

  15. Leppanen RE. Intraoperative applications of the H-reflex and F-response: a tutorial. J Clin Monit Comput. 2006;20:267–304.

    Article  PubMed  Google Scholar 

  16. Sloan TB, Janik D, Jameson L. Multimodality monitoring of the central nervous system using motor-evoked potentials. Curr Opin Anesthesiol. 2008;21:560–4.

    Article  Google Scholar 

  17. Malhotra NR, Shaffrey CI. Intraoperative electrophysiological monitoring in spine surgery. Spine (Phila Pa 1976). 2010;35:2167–79.

    Article  Google Scholar 

  18. Taniguchi M, Cedzich C, Schramm J. Modification of cortical stimulation for motor evoked potentials under general anesthesia: technical description. Neurosurgery. 1993;32:219–26.

    Article  PubMed  CAS  Google Scholar 

  19. Iwasaki H, Tamaki T, Yoshida M, Ando M, Yamada H, Tsutsui S, Takami M. Efficacy and limitations of current methods of intraoperative spinal cord monitoring. J Orthop Sci. 2003;8:635–42.

    Article  PubMed  Google Scholar 

  20. Journee HL, Polak HE, de Kleuver M, Langeloo DD, Postma AA. Improved neuromonitoring during spinal surgery using double-train transcranial electrical stimulation. Med Biol Eng Comput. 2004;42:110–3.

    Article  PubMed  CAS  Google Scholar 

  21. Kakimoto M, Kawaguchi M, Yamamoto Y, Inoue S, Horiuchi T, Nakase H, Sakaki T, Furuya H. Tetanic stimulation of the peripheral nerve before transcranial electrical stimulation can enlarge amplitudes of myogenic motor evoked potentials during general anesthesia with neuromuscular blockade. Anesthesiology. 2005;102:733–8.

    Article  PubMed  Google Scholar 

  22. Frei FJ, Ryhult SE, Duitmann E, Hasler CC, Luetschg J, Erb TO. Intraoperative monitoring of motor evoked potentials in children undergoing spinal surgery. Spine (Phila Pa 1976). 2007;32:911–7.

    Article  Google Scholar 

Download references

Conflict of interest

No funds were received in support of this work. No benefits in any form have been or will be received from a commercial party related directly or indirectly to the subject of this manuscript.

Ethical standard

The experiments comply with the current laws of Japan.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shunji Tsutsui.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tsutsui, S., Yamada, H., Hashizume, H. et al. Quantification of the proportion of motor neurons recruited by transcranial electrical stimulation during intraoperative motor evoked potential monitoring. J Clin Monit Comput 27, 633–637 (2013). https://doi.org/10.1007/s10877-013-9480-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10877-013-9480-3

Keywords

Navigation