Raman spectroscopy as a neuromonitoring tool in traumatic brain injury: a systematic review and clinical perspectives
Author
Stevens, Andrew RStickland, Clarissa A
Harris, Georgia
Ahmed, Zubair
Goldberg Oppenheimer, Pola
Belli, Antonio
Davies, David J
Affiliation
University of Birmingham; University Hospitals Birmingham NHS Foundation TrustPublication date
2022-04-05Subject
Neurology
Metadata
Show full item recordAbstract
Traumatic brain injury (TBI) is a significant global health problem, for which no disease-modifying therapeutics are currently available to improve survival and outcomes. Current neuromonitoring modalities are unable to reflect the complex and changing pathophysiological processes of the acute changes that occur after TBI. Raman spectroscopy (RS) is a powerful, label-free, optical tool which can provide detailed biochemical data in vivo. A systematic review of the literature is presented of available evidence for the use of RS in TBI. Seven research studies met the inclusion/exclusion criteria with all studies being performed in pre-clinical models. None of the studies reported the in vivo application of RS, with spectral acquisition performed ex vivo and one performed in vitro. Four further studies were included that related to the use of RS in analogous brain injury models, and a further five utilised RS in ex vivo biofluid studies for diagnosis or monitoring of TBI. RS is identified as a potential means to identify injury severity and metabolic dysfunction which may hold translational value. In relation to the available evidence, the translational potentials and barriers are discussed. This systematic review supports the further translational development of RS in TBI to fully ascertain its potential for enhancing patient care.Citation
Stevens AR, Stickland CA, Harris G, Ahmed Z, Goldberg Oppenheimer P, Belli A, Davies DJ. Raman Spectroscopy as a Neuromonitoring Tool in Traumatic Brain Injury: A Systematic Review and Clinical Perspectives. Cells. 2022 Apr 5;11(7):1227. doi: 10.3390/cells11071227.Type
ArticleAdditional Links
https://www.mdpi.com/journal/cellsPMID
35406790Journal
CellsPublisher
MDPIae974a485f413a2113503eed53cd6c53
10.3390/cells11071227