Intracranial Hypertension Clinical Trial
Official title:
Pilot Trial on the Effect of Mild Hypothermia on Intracranial Pressure in Patients With Hyperacute Liver Failure
Treatment options in patients with high intracranial pressure due to acute liver failure are limited. This study intends to evaluate the effect of prophylactic hypothermia on preventing high intracranial pressure and compromised cerebral oxidative metabolism.
Acute liver failure (ALF) is associated with a high mortality. With severe hepatic
encephalopathy and elevated arterial ammonia concentration (< 200 micromol/L) more than 50%
of the patients will develop high intracranial pressure (ICP) and risk cerebral
incarceration and death. The therapeutic options are limited in treating and preventing this
condition and new interventions are much sought after. As in hypothermia used for patients
after cardiac resuscitation it could be speculated that hypothermia and the reduced cerebral
metabolic rate would contribute to neuroprotection and reduce the risk of cerebral
hypertension in patients with ALF. We have designed this open, randomized and unblinded
study in order to evaluate the effect of prophylactic hypothermia on ICP, cerebral
hemodynamics and oxidative metabolism. Patients are randomized to standard medical treatment
(SMT) or SMT and hypothermia 33° C for 72 hours using a cooling mattress (Blanketrol II,
Cincinnati Sub-Zero). All patients will receive mechanical ventilation, antibiotics,
inotropic support and monitored with invasive and non-invasive equipment in accordance to
local guidelines. In Copenhagen monitoring cerebral hemodynamics includes:
Placement of a intracranial pressure measuring catheter (Camino (R), Integra) for monitoring
ICP. Furthermore, a microdialysis catheter (CMA-70) placed in brain cortex is used for
monitoring brain metabolism. Finally, cerebral perfusion can be monitored by measuring mean
flow velocity using transcranial doppler and/or oxygen saturation in blood from the jugular
vein.
Ethical considerations:
The Helsinki II declaration will be followed and informed consent is mandatory for
enrollment. In any patient where hypothermia is believed or suspected to be harmful the
study should be stopped and the primary investigator should be notified immediately. All
adverse effects will be recorded and published together with the full paper.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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