Traumatic brain injury (TBI) is a major cause of death and severe prolonged disability. Intracranial hypertension (ICH) is a critical risk factor of bad outcomes after TBI. Continuous infusion of hyperosmolar therapy has been proposed for the prevention or the treatment of ICH. Whether an early administration of continuous hyperosmolar therapy improves long term outcomes is uncertain. The aim of the current study is to assess the efficiency and the safety of continuous hyperosmolar therapy in TBI patients. The COBI trial is the first randomized controlled trial powered to investigate whether continuous hyperosmolar therapy in TBI patients improve long term recovery. Hypothesis Patients treated with early continuous hyperosmolar therapy have reduced morbidity and mortality rates compared to those receiving standard care alone after traumatic brain injury. Research Questions 1. Does early continuous hyperosmolar therapy reduce morbidity and mortality rates at 3 and 6 months after TBI assessed by the GOSE questionnaire? 2. Does early continuous hyperosmolar therapy prevent intracranial hypertension?
Background Traumatic brain injury (TBI) is a major cause of death and severe prolonged disability. Intracranial hypertension (ICH) is a critical risk factor of bad outcomes after TBI. Continuous infusion of hyperosmolar therapy has been proposed for the prevention or the treatment of ICH. Whether an early administration of continuous hyperosmolar therapy improves long term outcomes is uncertain. The aim of the current study is to assess the efficiency and the safety of continuous hyperosmolar therapy in TBI patients. Methods The COBI (Continuous hyperosmolar therapy in traumatic brain-injured patients) trial is a multicenter, randomized, controlled, open-label, two-arms study with blinded adjudication of primary outcome. Three hundred and seventy patients hospitalized in Intensive Care Unit with a traumatic brain injury (Glasgow Coma Scale ≤ 12 and abnormal brain CT-scan) are randomized in the first 24 hours following trauma to standard care or continuous hyperosmolar therapy (NaCl 20%) plus standard care. Continuous hyperosmolar therapy is maintained for at least 48 hours in the treatment group and continued for as long as is necessary to prevent intracranial hypertension. The primary outcome is the score on the Extended Glasgow Outcome Scale (GOS-E) at 6 months. The treatment effect is estimated with ordinal logistic regression adjusted for pre-specified prognostic factors and expressed as a common odds ratio. Discussion The COBI trial is the first randomized controlled trial powered to investigate whether continuous hyperosmolar therapy in TBI patients improve long term recovery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
370
Early intravenous administration (\<24 hours after traumatic brain injury) of NaCl20% for a minimal duration of 48 hours (continued for as long as is necessary to prevent intracranial hypertension) 1-hour bolus (15 g if Na+ \< 145 mmol/L; 7.5 g if 145 \< Na+ \< 150 mmol/L; or no bolus) followed by 1 g/hour as long as Na+\< 150 mmol/L, reduced to 0.5 g/L if 150 \< Na+ \< 155 mmol/L, Discontinuation when 155 mmol/L\<Na+
CHU Angers
Angers, France
CHU Brest Hopital La Cavale Blanche
Brest, France
AP-HP Beaujon
Clichy, France
CHU Montpellier
Montpellier, France
CHU de Nantes
Nantes, France
Centre Hospitalier Sainte-Anne
Paris, France
CHU Poitiers
Poitiers, France
CHU Rennes-Hopital Pontchaillou
Rennes, France
CHU Toulouse Hôpital Pierre-Paul Riquet
Toulouse, France
CHU Tours
Tours, France
Score on the Extended Glasgow Outcome Scale (GOS-E) at 6 months
The GOS-E is a scale measuring the neurological recovery after traumatic brain injuries
Time frame: 6 months
Mortality rate in ICU
Time frame: 3 months
Mortality rate in ICU
Time frame: 6 months
GOS-E
The GOS-E is a scale measuring the neurological recovery after traumatic brain injuries
Time frame: 3 months
functional independence measure : ADL (Activities of Daily Living) of Katz
Scale measuring the autonomy of patient
Time frame: 3 months
functional independence measure : ADL (Activities of Daily Living) of Katz
Scale measuring the autonomy of patient
Time frame: 6 months
Short Form 36
Scale measuring the quality of life
Time frame: 3 months
Short Form 36
Scale measuring the quality of life
Time frame: 6 months
Rate of patients with anterograde amnesia
Time frame: 3 months
Rate of patients with anterograde amnesia
Time frame: 6 months
Intracranial pressure control
Time frame: 7 Days
Blood level of sodium
Time frame: 7 Days
blood osmolality
Time frame: 7 Days
Rate of thrombo-embolic events
Time frame: 28 days
Rate of acute kidney injury
KDIGO 3
Time frame: 28 days
Rate of centropontine myelinolysis
Diagnosis on MRI realized in case of clinical suspicion
Time frame: 28 days
Blood level of chlore
Time frame: 7 Days
Blood level of potassium
Time frame: 5 Days
Blood level of pH (Hydrogen Potention)
Time frame: 5 Days
brain oxygenation (PtiO2)
Time frame: 5 Days
blood level of creatinine
Time frame: 5 Days
Diuresis
Time frame: 5 Days
weight
Time frame: 5 Days
Ancillary study: questionnaire HADS (Hospital Anxiety and Depression Scale) in patient's relative
Scale measuring the quality of life
Time frame: 6 months
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