Brain Injuries, Subarachnoid Hemorrhage
Conditions
Keywords
traumatic brain injury, subarachnoid hemorrhage, secondary brain ischemia, microdialysis, modified Lund concept, cerebral perfusion pressure, intracranial pressure
Brief summary
Secondary brain ischaemia (SBI) usually develops after aneurysmal subarachnoid haemorrhage (SAH) and severe traumatic brain injury (TBI). The current management strategies are based on intracranial pressure-targeted therapy (ICP-targeted) with cerebral microdialysis monitoring (modified Lund concept) or cerebral perfusion pressure-targeted therapy (CPP-targeted). We present a randomised controlled study to compare the two management strategies. The hypotheses of the study were: * SBI developed after aneurysmal SAH and severe TBI share the same crucial characteristics and any treatment applied will essentially treat the same underlying pathophysiology. * ICP-targeted therapy with cerebral microdialysis monitoring according to the modified Lund concept is superior to CPP-targeted therapy in managing comatose patients with SBI after aneurysmal SAH and severe TBI. Sixty comatose operated patients with SBI following aneurysmal SAH and severe TBI were randomized into ICP-targeted therapy with cerebral microdialysis monitoring and CPP-targeted therapy groups. Mortality rates in both groups were calculated and biochemical signs of cerebral ischaemia were analysed using cerebral microdialysis. Outcome for cerebral microdialysis was measured as poor outcome (Glasgow Outcome Scale score 1, 2 and 3) or good outcome (Glasgow Outcome Scale score 4 and 5).
Interventions
PROCEDUREModified Lund concept
After surgical evacuation of intracranial mass lesion and clipping of aneurysm the objectives were achieved: * Reduction of cerebral energy metabolism with fentanyl (2-5 µg/kg/h) and thiopenthal (0.5-3 mg/kg/h); * Maintenance of colloid osmotic pressure with administration of red cell and albumin/plasma transfusions to maintain Hb/s 125-140 g/L and Alb/s ≈40 g/L; * Reduction of capillary hydrostatic pressure with α2-agonist clonidine (0.4-0.8 µg/kg, 1 x 4-6 iv.) and maintaining normovolaemia; * Reduction of mean arterial pressure and neuroprotection with Nimodipine infusion 5 ml per hour for 21 days and Urapidil 200 mg /200 ml, 7-10 ml/h. * Control of ICP, which can be in majority of patients, kept at values below 15 mmHg.
PROCEDURECerebral perfusion pressure-targeted therapy
* ICP monitoring using an external ventricular drain and CSF drainage as a first measure if ICP was increased (over 15-20 mmHg); * Maintenance of CPP over 70-80 mmHg (Triple 'H' therapy = 3L/24 hours including 1L of colloids - 5% albumin; drugs = dopamine, dobutamine); * No hyperventilation if ICP was under 20-25 mmHg and hyperventilation as a third measure if ICP was increased; * Osmotherapy (20% manitol, bolus 150-350 ml or 10% manitol, 50 ml/h for 10 hours and standard electrolytes \[Na, Cl and K\]);
Sponsors
University of Sarajevo
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
16 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* patients with subarachnoid haemorrhage who had anterior circulation aneurysm rupture only * multiple anterior aneurysm rupture * severe traumatic brain injury with isolated head injury and intradural focal lesions only
Exclusion criteria
* Glasgow Outcome Score of 3 with or without brainstem reflexes * Significant co-morbidities * posterior circulation aneurysm * multisystem injuries * diffuse axonal injuries
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mortality rate | 18 months | Measurement of outcome was done using the Glasgow Outcome Scale (GOS) after each specific intervention in all the patients. GOS 1 - dead, 2- vegetative, 3- severe disabled, 4- moderate disabled, 5- independent. |
Countries
Bosnia and Herzegovina
Outcome results
None listed