Sedation in the operating room, the Post Anesthesia Care Unit and the Intensive Care Unit is common and often necessary for patients with intracranial brain tumor. Repeated neurological function assessments is needed in those locations, especially in patients with tumors in or near eloquent regions, this is to monitor their neurologic performance to determine if there are alterations that require treatment. Some slowly infiltrative low-grade gliomas near eloquent regions do not show any detectable neurologic deficits, perhaps from reorganization, but with sedation by some sedatives such as benzodiazepine midazolam and anesthetic hypnotic propofol, the disease may seem much worse resulting in inappropriately aggressive treatment. This may be especially problematic in patients undergoing awake craniotomy for tumors in eloquent regions. This is a single-center perspective study. Patients will be mildly sedated to keep them responsive and cooperative. Motor and sensory function will be evaluated before and after mild sedation. Specific benzodiazepine antagonist will be used if sedated by midazolam. The purpose of this study is to observe if commonly used benzodiazepine midazolam exacerbates or unmasks motor and sensory function in patients with intracranial eloquent area gliomas. Hypothesis: mild sedation can unmasks or exacerbate motor and sensory deficits in patients with eloquent area glioma but not in non-neurosurgical patients/healthy volunteers. If the neurologic deficits induced by benzodiazepine agonist, then can be reversed by flumazenil.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
36
specific benzodiazepine agonist midazolam will be used titrate to desired sedation level, its specific antagonist flumazenil will also be used
Beijing Tiantan Hospital, Capital Medical University
Beijing, Beijing Municipality, China
Task Completing Time Change Between Sedation and Baseline Measured by 9-hole Peg Test
this is a focal neurologic deficits induced by sedatives, the outcome is the performing time changes after sedation as : sedation-baseline.
Time frame: after sedation
Number of Participants With OAA/S=4 After Sedation
OAA/S is Observer Assessment of Sedation with 5 levels (5 = alert, 4 = lethargic, 3 = aroused by voice, 2 = aroused by shaking, 1 = deep sleep), all participants have to achieve OAA/S=4 after sedation.
Time frame: withing 1 hour
Mean Arterial Blood Pressure (MAP) as a Measure of Physiological Change
The MAP was measured at three time points: baseline, sedation and sedation reversal.
Time frame: 1 hour
Heart Rate as a Measure of Physiological Change
The HR was measured at three time points: baseline, sedation and sedation reversal.
Time frame: 1 hour
Brain Glioma Pathological Diagnose as a Measure of Tumor Type
the WHO grade and the type of glioma (WHO glioma grade I\~II is regarded as low grade glioma, WHO glioma grade III\~IV is regarded as high grade glioma)
Time frame: 2 weeks
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