Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-19T23:45:37.162Z Has data issue: false hasContentIssue false

Bispectral index-guided administration of anaesthesia: comparison between remifentanil/propofol and remifentanil/isoflurane

Published online by Cambridge University Press:  12 July 2005

G. Schneider
Affiliation:
Emory University School of Medicine, Department of Anesthesiology, Atlanta, GA, USA
C. Elidrissi
Affiliation:
Emory University School of Medicine, Department of Anesthesiology, Atlanta, GA, USA
P. S. Sebel
Affiliation:
Emory University School of Medicine, Department of Anesthesiology, Atlanta, GA, USA
Get access

Abstract

Summary

Background and objective: The bispectral index of the electroencephalogram is a measure of the hypnotic component of anaesthesia and can be used to guide the administration of anaesthesia. This study compares bispectral index-guided anaesthesia with remifentanil and either propofol or isoflurane.

Methods: Eighty consenting patients were randomly assigned to two groups. Following induction with propofol and remifentanil, anaesthesia was maintained with remifentanil/propofol or remifentanil/isoflurane. Remifentanil infusion rates were guided by haemodynamic responses – maintaining mean arterial pressure and heart rate within 20% of baseline. Propofol and isoflurane administration was guided using the bispectral index (45–60). Thirty minutes before the end of surgery, morphine was administered (0.15 mg kg−1 intravenously). Fifteen minutes before end of surgery, propofol and isoflurane were reduced (bispectral index 60–75). At the end of surgery, the anaesthetic agents were discontinued. Groups were compared for recovery, remifentanil doses and signs of inadequate anaesthesia using the χ2-test and ANOVA (P < 0.05).

Results: The duration of surgery was longer in the propofol/remifentanil group (121 ± 53 versus 94 ± 40 min). Recovery data were not different between groups. The remifentanil infusion rate was significantly lower with additional isoflurane (0.18 ± 0.06 μg kg−1 min−1) than with additional propofol (0.31 ± 0.20 μg kg−1 min−1). The propofol infusion rate was 123 ± 48 μg kg−1 min−1; isoflurane concentration was 0.66 ± 0.13%.

Conclusions: Bispectral index-guided anaesthesia with remifentanil plus propofol or isoflurane results in the absence of postoperative recall and a fast recovery with both drug combinations. In our patients, at comparable bispectral index-levels, haemodynamic control requires higher doses of remifentanil with propofol than with isoflurane.

Type
Original Article
Copyright
2003 European Society of Anaesthesiology

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Rampil IJ. A primer for EEG signal processing in anesthesia. Anesthesiology 1998; 89: 9801002.Google Scholar
Flaishon R, Windsor A, Sigl J, Sebel PS. Recovery of consciousness after thiopental or propofol. Bispectral index and isolated forearm technique. Anesthesiology 1997; 86: 613619.Google Scholar
Liu J, Singh H, White PF. Electroencephalogram bispectral analysis predicts the depth of midazolam-induced sedation. Anesthesiology 1996; 84: 6469.Google Scholar
Sebel PS, Lang E, Rampil IJ, et al. A multicenter study of bispectral electroencephalogram analysis for monitoring anesthetic effect. Anesth Analg 1997; 84: 891899.Google Scholar
Glass PS, Bloom M, Kearse L, Rosow C, Sebel P, Manberg P. Bispectral analysis measures sedation and memory effects of propofol, midazolam, isoflurane, and alfentanil in healthy volunteers. Anesthesiology 1997; 86: 836847.Google Scholar
Liu J, Singh H, White PF. Electroencephalographic bispectral index correlates with intraoperative recall and depth of propofol-induced sedation. Anesth Analg 1997; 84: 185189.Google Scholar
Kearse LA Jr, Manberg P, DeBros F, Chamoun N, Sinai V. Bispectral analysis of the electroencephalogram during induction of anesthesia may predict hemodynamic responses to laryngoscopy and intubation. Electroencephalogr Clin Neurophysiol 1994; 90: 194200.Google Scholar
Schneider G, Sebel PS. Monitoring depth of anaesthesia. Eur J Anaesthesiol 1997; 15: 2128.Google Scholar
Johansen JW, Sebel PS, Sigl JC. Clinical impact of hypnotic-titration guidelines based on EEG bispectral index (BIS) monitoring during routine anesthetic care. J Clin Anesth 2000; 12: 433443.Google Scholar
Nelskyla KA, Yli-Hankala AM, Puro PH, Korttila KT. Sevoflurane titration using bispectral index decreases postoperative vomiting in phase II recovery after ambulatory surgery. Anesth Analg 2001; 93: 11651169.Google Scholar
Pavlin DJ, Hong JY, Freund PR, Koerschgen ME, Bower JO, Bowdle TA. The effect of bispectral index monitoring on end-tidal gas concentration and recovery duration after outpatient anesthesia. Anesth Analg 2001; 93: 613619.Google Scholar
Paventi S, Santevecchi A, Metta E, et al. Bispectral index monitoring in sevoflurane and remifentanil anesthesia. Analysis of drugs management and immediate recovery. Minerva Anestesiol 2001; 67: 435439.Google Scholar
Wong J, Song D, Blanshard H, Grady D, Chung F. Titration of isoflurane using BIS index improves early recovery of elderly patients undergoing orthopedic surgeries. Can J Anaesth 2002; 49: 1318.Google Scholar
Wuesten R, Van Aken H, Glass PS, Buerkle H. Assessment of depth of anesthesia and postoperative respiratory recovery after remifentanil- versus alfentanil-based total intravenous anesthesia in patients undergoing ear–nose–throat surgery. Anesthesiology 2001; 94: 211217.Google Scholar
Fredman B, Sheffer O, Zohar E, et al. Fast-track eligibility of geriatric patients undergoing short urologic surgery procedures. Anesth Analg 2002; 94: 560564.Google Scholar
Chen X, Zhao M, White PF, et al. The recovery of cognitive function after general anesthesia in elderly patients: a comparison of desflurane and sevoflurane. Anesth Analg 2001; 93: 14891494.Google Scholar
Aldrete JA, Kroulik D. A postanesthetic recovery score. Anesth Analg 1970; 49: 924934.Google Scholar
Liu WH, Thorp TA, Graham SG, Aitkenhead AR. Incidence of awareness with recall during general anaesthesia. Anaesthesia 1991; 46: 435437.Google Scholar
Petersen-Felix S, Arendt-Nielsen L, Bak P, Fischer M, Zbinden AM. Psychophysical and electrophysiological responses to experimental pain may be influenced by sedation: comparison of the effects of a hypnotic (propofol) and an analgesic (alfentanil). Br J Anaesth 1996; 77: 165171.Google Scholar
Savola MK, Woodley SJ, Maze M, Kendig JJ. Isoflurane and an alpha 2-adrenoceptor agonist suppress nociceptive neurotransmission in neonatal rat spinal cord. Anesthesiology 1991; 75: 489498.Google Scholar
Lawrence D, Livingston A. Opiate-like analgesic activity in general anaesthetics. Br J Pharmacol 1981; 73: 435442.Google Scholar
Housmans PR, Murat I. Comparative effects of halothane, enflurane, and isoflurane at anesthetic concentrations on isolated ventricular myocardium of the ferret. I. Contractility. Anesthesiology 1988; 69: 451463.Google Scholar
Pagel PS, Kampine JP, Schmeling WT, Warltier DC. Evaluation of myocardial contractility in the chronically instrumented dog with intact autonomic nervous system function: effects of desflurane and isoflurane. Acta Anaesthesiol Scand 1993; 37: 203210.Google Scholar
Pagel PS, Kampine JP, Schmeling WT, Warltier DC. Comparison of the systemic and coronary hemodynamic actions of desflurane, isoflurane, halothane, and enflurane in the chronically instrumented dog. Anesthesiology 1991; 74: 539551.Google Scholar
Antognini JF, Schwartz K. Exaggerated anesthetic requirements in the preferentially anesthetized brain. Anesthesiology 1993; 79: 12441249.Google Scholar
Rampil IJ, Mason P, Singh H. Anesthetic potency (MAC) is independent of forebrain structures in the rat. Anesthesiology 1993; 78: 707712.Google Scholar
Rampil IJ. Anesthetic potency is not altered after hypothermic spinal cord transection in rats. Anesthesiology 1994; 80: 606610.Google Scholar
King BS, Rampil IJ. Anesthetic depression of spinal motor neurons may contribute to lack of movement in response to noxious stimuli. Anesthesiology 1994; 81: 14841492.Google Scholar