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On evolution of intracranial changes after severe traumatic brain injury and its impact on clinical outcome

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Institution/Department Umeå universitet/Umeå University Umeå 2016

Umeå University Medical Dissertations

On evolution of intracranial changes after severe traumatic brain injury and its impact on clinical

outcome

Lukas Bobinski

Akademisk avhandling

som med vederbörligt tillstånd av Rektor vid Umeå universitet för avläggande av medicine doktorsexamen framläggs till offentligt försvar i Sal E04, byggnad 6A, Norrlands Universitetssjukhus, fredagen den 02 september 2016, kl. 09:00.

Avhandlingen kommer att försvaras på svenska.

Fakultetsopponent: Prof. Niklas Marklund

Neurovetenskap, Neurokirurgi, Akademiska Sjukhuset, Uppsala Universitet

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Organization Document type Date of publication

Umeå University Doctoral Dissertation 15 08 2016 Department of Pharmacology

and Clinical Neuroscience, Neurosurgery

Author Lukas Bobinski

Title On evolution of intracranial changes after severe traumatic brain injury and its impact on clinical outcome

Abstract

Severe traumatic brain injury (sTBI) is a cause of death and disability worldwide and requires treatment at specialized neuro-intensive care units (NICU) with a multimodal monitoring approach.

The CT scan imaging supports the monitoring and diagnostics. The level of S100B and neuron specific enolase (NSE) reflects the severity of the injury. The therapy resistant intracranial hypertension requires decompressive craniectomy (DC). After DC, the cranium must be

reconstructed to recreate the normal intracranial physiology as well as to address cosmetic issues.

The evolution of the pathological intracranial changes was analyzed in accordance with the three CT classifications: Marshall, Rotterdam and Morris-Marshall. The Rotterdam scale was best in describing the dynamics of the pathological evolution. Both the Rotterdam score and Morris- Marshall classification showed strong correlation with the clinical outcome, a finding that suggests that they could be used for prognostication. We demonstrated a clear correlation between the CT classifications and concentrations of S100B and NSE. The results revealed a concomitant correlation between NSE and S100B and clinical outcome. We found that the interaction between the ICP, Rotterdam CT classification, and concentrations of biochemical biomarkers are all associated with DC. We found a high percentage of complications following cranioplasty. Our results call into question whether custom-made allograft should be considered the best material for cranioplasty.

It is concluded that both the Rotterdam and Morris-Marshall classification contribute to clinical evaluation of intracranial dynamics after sTBI, and might be used in combination with biochemical biomarkers for better assessment. The decision to perform DC should include a re-assesment of ICP evolution, CT scan images and concentration of the biochemical biomarkers. Furthermore, when determining whether DC treatment should be used, surgeon should also consider the risks of the following cranioplasty.

Keywords

Severe traumatic brain injury, ICP targeted therapy, ICP, decompressive craniectomy, S100B, NSE, cranioplasty

Language ISBN ISSN Number of pages

English 978-91-7601-442-4 0346-6612 131 + 4 papers

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