CJA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Submit a scholarly reply
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Modica, P. A.
Right arrow Articles by Tempelhoff, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Modica, P. A.
Right arrow Articles by Tempelhoff, R.

Canadian Journal of Anesthesia, Vol 39, 236-241, Copyright © 1992 by Canadian Anesthesiologists' Society


ARTICLES

Intracranial pressure during induction of anaesthesia and tracheal intubation with etomidate-induced EEG burst suppression

PA Modica and R Tempelhoff
Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110.

This study was designed to determine if induction of anaesthesia with etomidate titrated to an early EEG burst suppression pattern would produce minimal changes in cerebral perfusion pressure, and prevent increases in intracranial pressure (ICP) associated with tracheal intubation. Eight patients, 18-71 yr, with intracranial space-occupying lesions, were studied. In each patient ICP was monitored via a lateral ventriculostomy catheter placed preoperatively. In the operating room, an ECG, a radial arterial line, and a two-channel computerized EEG were placed. Control (awake) measurements of MAP (mmHg), ICP (mmHg), CPP (mmHg), heart rate (HR-bpm), EEG power (picowatts-pW), and spectral edge frequency (SEF, Hz) were obtained. Anaesthesia was induced with etomidate, 0.2 mg.kg-1 iv, followed immediately by an etomidate infusion, 20 mg.min-1, iv, and vecuronium 0.2 mg.kg-1 iv. When early burst suppression was achieved, the etomidate infusion was stopped and tracheal intubation performed. The etomidate dose (bolus plus infusion) required to reach burst suppression was 1.28 +/- 0.11 mg.kg-1. Compared with awake control values (mean +/- SE), the period from induction to burst suppression was associated with a 50% decrease in ICP (22 +/- 1 vs 11 +/- 1 mmHg, P less than 0.01), but there were no changes in MAP, CPP, or HR. The decrease in ICP was maintained during the first 30 sec and the following 60 sec after intubation as MAP and HR remained unchanged. Our results suggest that when etomidate was administered to early burst suppression pattern on EEG, minimal changes in CPP occurred during induction of anaesthesia and a marked reduction in ICP was maintained following tracheal intubation.


This article has been cited by other articles:


Home page
JWatch Emergency Med.Home page
Special Report: Should Etomidate Be Used as an Induction Agent for Patients with Sepsis?
Journal Watch Emergency Medicine, February 1, 2008; 2008(201): 5 - 5.
[Full Text]


Home page
Anesth. Analg.Home page
W. J. Kox, C. von Heymann, J. Heinze, L. S. Prichep, E. R. John, and I. Rundshagen
Electroencephalographic mapping during routine clinical practice: cortical arousal during tracheal intubation?
Anesth. Analg., March 1, 2006; 102(3): 825 - 831.
[Abstract] [Full Text] [PDF]


Home page
Canadian J. AnesthesiaHome page
I.-W. Shin, J.-T. Sohn, H.-J. Kim, C. Kim, H.-K. Lee, K. C. Chang, and Y.-K. Chung
Etomidate attenuates phenylephrine-induced contraction in isolated rat aorta: [L'etomidate attenue la contraction induite par la phenylephrine dans des aortes isolees de rats]
Can J Anesth, November 1, 2005; 52(9): 927 - 934.
[Abstract] [Full Text] [PDF]


Home page
Crit Care NurseHome page
M. K. Bader, L. R. Littlejohns, and K. March
Brain Tissue Oxygen Monitoring in Severe Brain Injury, II: Implications for Critical Care Teams and Case Study
Crit. Care Nurse, August 1, 2003; 23(4): 29 - 44.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by the Canadian Anesthesiologists' Society.