Cerebral Microdialysis Monitoring to improve individualized Neurointensive Care Therapy: An Update of Recent Clinical Data
Affiliation auteurs | Affiliation ok |
Titre | Cerebral Microdialysis Monitoring to improve individualized Neurointensive Care Therapy: An Update of Recent Clinical Data |
Type de publication | Journal Article |
Year of Publication | 2017 |
Auteurs | Carteron L, Bouzat P, Oddo M |
Journal | FRONTIERS IN NEUROLOGY |
Volume | 8 |
Pagination | 601 |
Date Published | NOV 13 |
Type of Article | Review |
ISSN | 1664-2295 |
Mots-clés | biomarkers, cerebral metabolism, hypoxia, Ischemia, microdialysis, neurointensive care, subarachnoid hemorrhage, Traumatic brain injury |
Résumé | Cerebral microdialysis (CMD) allows bedside semicontinuous monitoring of patient brain extracellular fluid. Clinical indications of CMD monitoring are focused on the management of secondary cerebral and systemic insults in acute brain injury (ABI) patients [mainly, traumatic brain injury (TBI), subarachnoid hemorrhage, and intracerebral hemorrhage (ICH)], specifically to tailor several routine interventions-such as optimization of cerebral perfusion pressure, blood transfusion, glycemic control and oxygen therapy-in the individual patient. Using CMD as clinical research tool has greatly contributed to identify and better understand important post-injury mechanisms-such as energy dysfunction, posttraumatic glycolysis, post-aneurysmal early brain injury, cortical spreading depressions, and subclinical seizures. Main CMD metabolites (namely, lactate/pyruvate ratio, and glucose) can be used to monitor the brain response to specific interventions, to assess the extent of injury, and to inform about prognosis. Recent consensus statements have provided guidelines and recommendations for CMD monitoring in neuro-critical care. Here, we summarize recent clinical investigation conducted in ABI patients, specifically focusing on the role of CMD to guide individualized intensive care therapy and to improve our understanding of the complex disease mechanisms occurring in the immediate phase following ABI. Promising brain biomarkers will also be described. |
DOI | 10.3389/fneur.2017.00601 |