Abstract
The role of the anesthesiologist during procedures where intraoperative electrophysiological monitoring (IOM) is being performed involves anesthetic titration, attaining physiological homeostasis, and medical management of the patient. Further, the anesthesiologist participates in mitigating neural injury when the monitoring indicates that the nervous system may be at risk for injury. More specifically, the choice of anesthetic agents directly impacts the ability to reliably record IOM responses, and the physiological management (e.g., blood pressure) impacts on the reserve of the nervous system to tolerate procedural trespass. When altered responses indicate the health of the nervous system may be compromised, the insights of the anesthesiologist and the ability to improve the physiological reserve are keys to reducing neurological risk. This chapter is written to discuss these aspects to improve integration of the anesthesiologist into the IOM monitoring team effort.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
Alkire MT, Hudetz AG, Tononi G. Consciousness and anesthesia. Science. 2008;322(5903):876–80.
Lyon R, Feiner J, Lieberman JA. Progressive suppression of motor evoked potentials during general anesthesia: the phenomenon of “anesthetic fade”. J Neurosurg Anesthesiol. 2005;17(1):13–9.
Nickalls RW, Mapleson WW. Age-related iso-MAC charts for isoflurane, sevoflurane and desflurane in man. Br J Anaesth. 2003;91(2):170–4.
Miller RD, et al., editors. Miller’s anesthesia. 7th ed. Philadelphia: Churchill-Livingstone Elsevier; 2010.
John ER, Prichep LS. The anesthetic cascade: a theory of how anesthesia suppresses consciousness. Anesthesiology. 2005;102(2):447–71.
Mavroudakis N, et al. Spinal and brain-stem SEPs and H reflex during enflurane anesthesia. Electroencephalogr Clin Neurophysiol. 1994;92(1):82–5.
Ohara A, et al. A comparative study of the antinociceptive action of xenon and nitrous oxide in rats. Anesth Analg. 1997;85(4):931–6.
Sloan TB. Evoked potentials. In: Albin MA, editor. Textbook of neuroanesthesia with neurosurgical and neuroscience perspectives. New York: McGraw-Hill; 1997. p. 221–76.
van Dongen EP, et al. The influence of nitrous oxide to supplement fentanyl/low-dose propofol anesthesia on transcranial myogenic motor-evoked potentials during thoracic aortic surgery. J Cardiothorac Vasc Anesth. 1999;13(1):30–4.
van Dongen EP, et al. Effect of nitrous oxide on myogenic motor potentials evoked by a six pulse train of transcranial electrical stimuli: a possible monitor for aortic surgery. Br J Anaesth. 1999;82(3):323–8.
Sakamoto T, et al. Suppressive effect of nitrous oxide on motor evoked potentials can be reversed by train stimulation in rabbits under ketamine/fentanyl anaesthesia, but not with additional propofol. Br J Anaesth. 2001;86(3):395–402.
Sloan T, Sloan H, Rogers J. Nitrous oxide and isoflurane are synergistic with respect to amplitude and latency effects on sensory evoked potentials. J Clin Monit Comput. 2010;24(2):113–23.
Logginidou HG, et al. Propofol suppresses the cortical somatosensory evoked potential in rats. Anesth Analg. 2003;97(6):1784–8.
Kawaguchi M, Furuya H. Intraoperative spinal cord monitoring of motor function with myogenic motor evoked potentials: a consideration in anesthesia. J Anesth. 2004;18(1):18–28.
Altermatt FR, et al. Evaluation of the effect of intravenous lidocaine on propofol requirements during total intravenous anaesthesia as measured by bispectral index. Br J Anaesth. 2012;108(6):979–83.
Cassuto J, et al. Inhibition of postoperative pain by continuous low-dose intravenous infusion of lidocaine. Anesth Analg. 1985;64(10):971–4.
Sneyd JR, Rigby-Jones AE. New drugs and technologies, intravenous anaesthesia is on the move (again). Br J Anaesth. 2010;105(3):246–54.
Jones AE. The etomidate debate. Ann Emerg Med. 2010;56(5):490–1.
Cherfan AJ, et al. Advantages and disadvantages of etomidate use for intubation of patients with sepsis. Pharmacotherapy. 2012;32(5):475–82.
Kochs E, Treede RD, Schulte am Esch J. [Increase in somatosensory evoked potentials during anesthesia induction with etomidate]. Anaesthesist. 1986;35(6):359–64.
Sloan TB, et al. Improvement of intraoperative somatosensory evoked potentials by etomidate. Anesth Analg. 1988;67(6):582–5.
McPherson RW, Sell B, Traystman RJ. Effects of thiopental, fentanyl, and etomidate on upper extremity somatosensory evoked potentials in humans. Anesthesiology. 1986;65(6):584–9.
Russ W, et al. [Somatosensory evoked potentials under thiopental and etomidate]. Anaesthesist. 1986;35(11):679–85.
Koht A, et al. Effects of etomidate, midazolam, and thiopental on median nerve somatosensory evoked potentials and the additive effects of fentanyl and nitrous oxide. Anesth Analg. 1988;67(5):435–41.
Langeron O, et al. Comparison of the effects of ketamine-midazolam with those of fentanyl-midazolam on cortical somatosensory evoked potentials during major spine surgery. Br J Anaesth. 1997;78(6):701–6.
Rampil IJ. Electroencephalogram. In: Albin MA, editor. Textbook of neuroanesthesia with neurosurgical and neuroscience perspectives. New York: McGraw-Hill; 1997. p. 193–220.
Sloan TB, Fugina ML, Toleikis JR. Effects of midazolam on median nerve somatosensory evoked potentials. Br J Anaesth. 1990;64(5):590–3.
Kalkman CJ, et al. Effects of propofol, etomidate, midazolam, and fentanyl on motor evoked responses to transcranial electrical or magnetic stimulation in humans. Anesthesiology. 1992;76(4):502–9.
Scheufler K-M, Zentner J. Total intravenous anesthesia for intraoperative monitoring of the motor pathways: an integral view combining clinical and experimental data. J Neurosurg. 2002;96(3):571–9.
Zentner J. Motor evoked potential monitoring in operations of the brainstem and posterior fossa. In: Schramm J, Moller AR, editors. Intraop neurophysiol monitoring. Berlin: Springer; 1991. p. 95–105.
Ghaly RF, et al. The effect of an anesthetic induction dose of midazolam on motor potentials evoked by transcranial magnetic stimulation in the monkey. J Neurosurg Anesthesiol. 1991;3:20–5.
Schonle PW, et al. Changes of transcranially evoked motor responses in man by midazolam, a short acting benzodiazepine. Neurosci Lett. 1989;101(3):321–4.
Crawford ME, et al. Direct spinal effect of intrathecal and extradural midazolam on visceral noxius stimulation in rabbits. Br J Anaesth. 1993;70:642–6.
Faull RL, Villiger JW. Benzodiazepine receptors in the human spinal cord: a detailed anatomical and pharmacological study. Neuroscience. 1986;17(3):791–802.
Tobias JD, et al. Effects of dexmedetomidine on intraoperative motor and somatosensory evoked potential monitoring during spinal surgery in adolescents. Paediatr Anaesth. 2008;18(11):1082–8.
Yamamoto Y, et al. The effects of dexmedetomidine on myogenic motor evoked potentials in rabbits. Anesth Analg. 2007;104(6):1488–92.
Mahmoud M, et al. Susceptibility of transcranial electric motor-evoked potentials to varying targeted blood levels of dexmedetomidine during spine surgery. Anesthesiology. 2010;112(6):1364–73. doi:10.1097/ALN.0b013e3181d74f55.
Lauretti GR. Mechanisms of analgesia of intravenous lidocaine. Rev Bras Anestesiol. 2008;58(3):280–6.
Asouhido I, et al. Somatosensory evoked potentials suppression due to remifentanil during spinal operations; a prospective clinical study. Scoliosis. 2010;5:8–13.
Schubert A, Licina MG, Lineberry PJ. The effect of ketamine on human somatosensory evoked potentials and its modification by nitrous oxide. Anesthesiology. 1990;72(1):33–9 [erratum appears in Anesthesiology 1990 Jun;72(6):1104].
Schwender D, et al. Mid-latency auditory evoked potentials during ketamine anaesthesia in humans. Br J Anaesth. 1993;71(5):629–32.
Kano T, Shimoji K. The effects of ketamine and neuroleptanalgesia on the evoked electrospinogram and electromyogram in man. Anesthesiology. 1974;40(3):241–6.
Glassman SD, et al. Anesthetic effects on motor evoked potentials in dogs. Spine. 1993;18(8):1083–9.
Taniguchi M, et al. Effects of four intravenous anesthetic agents on motor evoked potentials elicited by magnetic transcranial stimulation. Neurosurgery. 1993;33(3):407–15. Discussion 415.
Kaba A, et al. Intravenous lidocaine infusion facilitates acute rehabilitation after laparoscopic colectomy. Anesthesiology. 2007;106(1):11–8. Discussion 5–6.
Lauwick S, et al. Intraoperative infusion of lidocaine reduces postoperative fentanyl requirements in patients undergoing laparoscopic cholecystectomy. Can J Anaesth. 2008;55(11):754–60.
Kuo CP, et al. Comparison of the effects of thoracic epidural analgesia and i.v. infusion with lidocaine on cytokine response, postoperative pain and bowel function in patients undergoing colonic surgery. Br J Anaesth. 2006;97(5):640–6.
Sugimoto M, Uchida I, Mashimo T. Local anaesthetics have different mechanisms and sites of action at the recombinant N-methyl-D-aspartate (NMDA) receptors. Br J Pharmacol. 2003;138(5):876–82.
Gottschalk A, et al. Systemic lidocaine decreases the Bispectral Index in the presence of midazolam, but not its absence. J Clin Anesth. 2012;24(2):121–5.
Senturk M, et al. Effects of intramuscular administration of lidocaine or bupivacaine on induction and maintenance doses of propofol evaluated by bispectral index. Br J Anaesth. 2002;89(6):849–52.
Borges LF. Motor evoked potentials. Int Anesthesiol Clin. 1990;28:170–3.
Kothbauer K. Motor evoked potential monitoring for intramedullary spinal cord surgery. In: Deletis V, Shills J, editors. Neurophysiology in neurosurgery: a modern approach. Amsterdam: Academic; 2002. p. 73–92.
Fagerlund MJ, Eriksson LI. Current concepts in neuromuscular transmission. Br J Anaesth. 2009;103(1):108–14.
Ghai B, Makkar JK, Wig J. Neuromuscular monitoring: a review. J Anesthesiol Clin Pharmacol. 2006;22(4):347–56.
Davis L, Britten JJ, Morgan M. Cholinesterase. Its significance in anaesthetic practice. Anaesthesia. 1997;52:244–60.
Jonsson M, et al. Distinct pharmacologic properties of neuromuscular blocking agents on human neuronal nicotinic acetylcholine receptors: a possible explanation for the train-of-four fade. Anesthesiology. 2006;105(3):521–33.
Bowman WC. Prejunctional and postjunctional cholinoceptors at the neuromuscular junction. Anesth Analg. 1980;59(12):935–43.
Fodale V, Santamaria LB. Laudanosine, an atracurium and cisatracurium metabolite. Eur J Anaesthesiol. 2002;19(7):466–73.
Bevan DR, Donati F, Kopman AF. Reversal of neuromuscular blockade. Anesthesiology. 1992;77(4):785–805.
Lee C, Katz RL. Fade of neurally evoked compound electromyogram during neuromuscular block by d-tubocurarine. Anesth Analg. 1977;56(2):271–5.
Sloan TB. Muscle relaxant use during intraoperative neurophysiologic monitoring. J Clin Monit Comput. 2013;27:35–46.
Sloan TB, Heyer EJ. Anesthesia for intraoperative neurophysiologic monitoring of the spinal cord. J Clin Neurophysiol. 2002;19(5):430–43.
May DM, Jones SJ, Crockard HA. Somatosensory evoked potential monitoring in cervical surgery: identification of pre- and intraoperative risk factors associated with neurological deterioration. J Neurosurg. 1996;85(4):566–73.
Drummond JC. The lower limit of autoregulation: time to revise our thinking? Anesthesiology. 1997;86(6):1431–3.
Seyal M, Mull B. Mechanisms of signal change during intraoperative somatosensory evoked potential monitoring of the spinal cord. J Clin Neurophysiol. 2002;19(5):409–15.
Wiedemayer H, et al. The impact of neurophysiological intraoperative monitoring on surgical decisions: a critical analysis of 423 cases. J Neurosurg. 2002;96(2):255–62.
Brodkey JS, et al. Reversible spinal cord trauma in cats: additive effects of direct pressure and ischemia. J Neurosurg. 1972;37:591–3.
Dolan EJ, et al. The effect of spinal distraction on regional blood flow in cats. J Neurosurg. 1980;53:756–64.
Griffiths IR, Trench JG, Crawford RA. Spinal cord blood flow and conduction during experimental cord compression in normotensive and hypotensive dogs. J Neurosurg. 1979;50(3):353–60.
Sloan T. General anesthesia for monitoring. In: Koht A, Sloan T, Toleikis JR, editors. Monitoring for the anesthesiologist and other health professionals. New York: Springer; 2012. p. 319–35.
Manninen PH, Lam AM, Nicholas JF. The effects of isoflurane and isoflurane-nitrous oxide anesthesia on brainstem auditory evoked potentials in humans. Anesth Analg. 1985;64(1):43–7.
Sloan T, Jameson LC. Monitoring anesthetic effect. In: Koht A, Sloan T, Toleikis JR, editors. Monitoring the nervous system for anesthesiologists and other health professionals. New York: Springer; 2012. p. 337–60.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2014 Springer Science+Business Media New York
About this chapter
Cite this chapter
Sloan, T.B., Kaye, A.D. (2014). Anesthesiology and Intraoperative Electrophysiological Monitoring. In: Kaye, A., Davis, S. (eds) Principles of Neurophysiological Assessment, Mapping, and Monitoring. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-8942-9_5
Download citation
DOI: https://doi.org/10.1007/978-1-4614-8942-9_5
Published:
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-8941-2
Online ISBN: 978-1-4614-8942-9
eBook Packages: MedicineMedicine (R0)