BJA Advance Access originally published online on May 12, 2006
British Journal of Anaesthesia 2006 97(1):18-25; doi:10.1093/bja/ael109
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral microdialysis: research technique or clinical tool
1 Department of Neuroanaesthesia and Neurocritical Care, The National Hospital for Neurology and Neurosurgery Queen Square, London WC1N 3BG, UK
2 Centre for Anaesthesia, University College London London, UK
*Corresponding author: Department of Neuroanaesthesia and Neurocritical Care, Box 30, The National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK. E-mail: martin.smith{at}uclh.org
Cerebral microdialysis is a well-established laboratory tool that is increasingly used as a bedside monitor to provide on-line analysis of brain tissue biochemistry during neurointensive care. This review describes the principles of cerebral microdialysis and the rationale for its use in the clinical setting, including discussion of the most commonly used microdialysis biomarkers of acute brain injury. Potential clinical applications are reviewed and future research applications identified. Microdialysis has the potential to become an established part of mainstream multi-modality monitoring during the management of acute brain injury but at present should be considered a research tool for use in specialist centres.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
C. N. Gallagher, K. L.H. Carpenter, P. Grice, D. J. Howe, A. Mason, I. Timofeev, D. K. Menon, P. J. Kirkpatrick, J. D. Pickard, G. R. Sutherland, et al. The human brain utilizes lactate via the tricarboxylic acid cycle: a 13C-labelled microdialysis and high-resolution nuclear magnetic resonance study Brain, October 1, 2009; 132(10): 2839 - 2849. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Salazar, R. Coleman, S. Griffith, J. McNeil, H. Young, J. Calhoon, F. Serrano, and R. DiGeronimo Brain preservation with selective cerebral perfusion for operations requiring circulatory arrest: protection at 25 {degrees}C is similar to 18 {degrees}C with shorter operating times Eur. J. Cardiothorac. Surg., September 1, 2009; 36(3): 524 - 531. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tyree, M. Tyree, and R. DiGeronimo Correlation of brain tissue oxygen tension with cerebral near-infrared spectroscopy and mixed venous oxygen saturation during extracorporeal membrane oxygenation Perfusion, September 1, 2009; 24(5): 325 - 331. [Abstract] [PDF] |
||||
![]() |
J. D. Salazar, R. D. Coleman, S. Griffith, J. D. McNeil, M. Steigelman, H. Young, B. Hensler, P. Dixon, J. Calhoon, F. Serrano, et al. Selective cerebral perfusion: real-time evidence of brain oxygen and energy metabolism preservation. Ann. Thorac. Surg., July 1, 2009; 88(1): 162 - 169. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Smith and R. P. Mahajan Clinical neuroscience: relevance to current practice Br. J. Anaesth., July 1, 2007; 99(1): 1 - 3. [Full Text] [PDF] |
||||
![]() |
M. M. Tisdall and M. Smith Multimodal monitoring in traumatic brain injury: current status and future directions Br. J. Anaesth., July 1, 2007; 99(1): 61 - 67. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Thompson and R. P. Mahajan Monitoring the monitors--beyond risk management. Br. J. Anaesth., July 1, 2006; 97(1): 1 - 3. [Full Text] [PDF] |
||||




