Aneurysm Clinical Trial
Official title:
Real Time Continuous Neurophysiological Monitoring for Early Detection of Cerebral Vasospasm in Aneurysmal Subarachnoid Hemorrhage Subjects
Aneurysmal subarachnoid hemorrhage (bleeding on the brain due to a ruptured aneurysm) is a
serious condition with a high morbidity (incidence of having ill health) and mortality
(death). There are approximately 11 cases per 100,000 in the population per year, and
approximately 40% of these cases are fatal. (Ingall) Among the fortunate subjects who
survive the initial bleed, vasospasm and subsequent stroke are a major cause of morbidity.
Vasospasm is defined as a prolonged severe, although reversible cause of arterial narrowing
that occurs after bleeding into the subarachnoid space, most commonly after aneurysmal
rupture. (Youman) The reduced arterial diameter inhibits blood flow and deprives the brain
of oxygen, which often results in a stroke.
Vasospasm is a major problem when treating subjects with aneurysmal subarachnoid hemorrhage.
For these reasons, it is essential to diagnose cerebral vasospasm early, before permanent
deficits develop.
There may be another option to solve this dilemma. The field of neuro-monitoring
(neurological monitoring) has the technology available to continuously monitor brain
activity of these sedated ICU subjects. This may allow for early diagnosis and possibly
identify changes in neurologic function before they become symptomatic. In the past,
neuro-monitoring was primarily used in the operating room to monitor neurologic function
during surgery in and around the spinal cord. Surgery to the spine or spinal cord also
carries its own form of risk, either from mechanical trauma to the spinal cord or its nerve
roots, or from interruption of the blood supply to these structures. Should damage to nerve
fibers occur, the end result could be paralysis, loss of sensation, and onset of severe
burning (i.e. neuropathic) pain. The field of intraoperative neuro-monitoring (IOM) was
developed to address these risks during spine surgery, whereby nerves rostral (toward the
head) or caudal (toward the feet) to the site of surgery are stimulated (usually via
electrical pulses) and signals are recorded from the side opposite to the site of
stimulation. Thus, the signals carried by nerve fibers are forced to pass through the region
at risk from the surgery. In the event that changes in nerve responses are seen, the
surgical team is notified, and they can change what they're doing to try and restore
signals, thereby preserving function in the nerve fibers.
This same technology has been used in the neurosurgical ICU to monitor subjects with severe
brain injury from trauma, stroke, intracranial hemorrhage and subarachnoid hemorrhage. Using
continuous electroencephalogram (EEG) monitoring combined with somatosensory evoked
potentials (SSEPs) (a type of neuro monitoring) has been used to determine prognosis,
identify subjects in subclinical status epilepticus (state of brain being in a constant
seizure), predict elevations in the intracranial pressure Increased pressure within the
skull), and diagnose cerebral hypoxia (not enough oxygen in the brain) (Amantini)
Aneurysmal subarachnoid hemorrhage is a serious condition with a high morbidity and
mortality. There are approximately 11 cases per 100,000 population per year, and
approximately 40% of these cases are fatal. (Ingall) Among the fortunate subjects who
survive the initial bleed, vasospasm and subsequent stroke are a major cause of morbidity.
Vasospasm is defined as a prolonged severe, although reversible cause of arterial narrowing
that occurs after bleeding into the subarachnoid space, most commonly after aneurismal
rupture. (Youman) The reduced arterial diameter inhibits blood flow and deprives the brain
of oxygen, which often results in a stroke.
Vasospasm is a major problem when treating subjects with aneurismal subarachnoid hemorrhage.
Up to 75% of subjects with aneurismal subarachnoid hemorrhage will develop vasospasm, and
30% of subarachnoid hemorrhage subjects will become clinically symptomatic, with muscle
weakness as the primary symptom. (Dorsch) Even with intervention, 12% of patents with
symptomatic vasospasm will develop permanent clinical deficits (after a ruptured aneurysm)
including hemiplegia, aphasias, and visual loss. Less severe strokes may lead to modest loss
of strength and sensation on one side of the body, and/or deterioration in higher brain
functions, such as memory, speech comprehension, and planning.
Continuous Neuro-monitoring has previously been used in the trauma ICU setting as a means to
detect deterioration in brain function after closed head injury (Amantini, Daubin), ischemic
encephalopathy (Hakimi) and in subjects with MCA stroke to determine function (Tzvetanov).
It was also observed that monitoring changes occur prior to ICP elevations in critically ill
subjects (Amantini). These studies have demonstrated the feasibility as well as the safety
of monitoring in an ICU.
No studies to date have attempted monitoring for vasospasm in subjects who suffered an
aneurysmal subarachnoid hemorrhage. Motor evoked potential have also not been trialed in the
ICU, although MEP may be more useful to determine both cerebral ischemia, as well as
functional outcome.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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