Patients with acute severe brain injury are usually admitted to the Intensive Care Unit. A substantial proportion of these patients will have disorders of consciousness (DOC) after interruption of sedation. It is difficult to reliably predict neurological outcome in these patients. Dependent on the extent of permanently damaged brain areas, DOC in patients with acute severe brain injury may improve or persist, eventually evolving into a minimal conscious state (MCS) or unresponsive wakefulness syndrome (UWS). These conditions are accompanied by long term severe disability. In current practice, the decision to withdraw life-sustaining support is made by interpreting the results of repeated bedside neurological examination and conventional CT-brain imaging. Reliable identification of patients with a possible good outcome, in whom treatment should not be withdrawn, is difficult. In this prospective observational cohort study we aim to identify patients with a good neurological outcome.
In order to identify patients with a good neurological outcome a combination of diagnostic tests is used. Clinical rating scales * Simplified evaluation of consciousness scale (SECONDs) and the full outline of unresponsiveness (FOUR) score * Once a week Blood biomarkers * Neuron specific enolase, neurofilament light, glial fibrillary acidic protein * Sampling timepoints: 24h, 72h, 7 days and 14 days after brain injury * Serum (STG-5) and plasma (EDTA-6) tubes, aliquoted (4 x 0.5ml) and stored at -80°C EEG with reactivity testing * Standard 21-electrode montage * Stimuli protocol I: a set of 5 stimuli repeated 3 times 1\. Auditory: clapping in hands, 2. Auditory: calling patients name loudly, 3. Visual: passive eye opening, 4. Tactile: nasal tickle, 5. Noxious: sternal rub Each stimuli is applied for a duration of 5 seconds and an interval between stimuli of 30 seconds * Stimuli protocol II: Cognitive-motor dissociation test MRI-scan * Sequences considered essential for patient care i.e.T1, T2, FLAIR, DWI/SWI * Preferably, performed between 4-6 weeks after hospital admission
Study Type
OBSERVATIONAL
Enrollment
160
Radboud UMC
Nijmegen, Gelderland, Netherlands
RECRUITINGAmsterdam UMC
Amsterdam, North Holland, Netherlands
RECRUITINGErasmus MC
Rotterdam, South Holland, Netherlands
NOT_YET_RECRUITINGHaaglanden MC, locatie Westeinde
The Hague, South Holland, Netherlands
RECRUITINGUMC Groningen
Groningen, Netherlands
NOT_YET_RECRUITINGGlasgow Outcome Scale Extended
Time frame: 6 months
Glasgow Outcome Scale Extended
Time frame: 12 months
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