From: Intracranial emergencies in neurosurgical oncology: pathophysiology and clinical management
1) Positioning: • Elevate head of bed to 30o, adjust or remove jugular obstruction, and maintain head in neutral position • Facilitates venous blood drainage | |
2) Securing airway and hyperventilation: • Intubate for airway protection and hyperventilation • Establish a secure airway to allow the physician to identify and treat apnea quickly • Hyperventilation reduces pCO2, a potent cerebral vasodilator, and decreases cerebral blood volume. Over-aggressive hyperventilation should be avoided as it may critically decrease CBF and lead to ischemia/stroke • Hyperventilation has a fast onset and is effective for lowering high ICP, but its effect only lasts for a short duration and may be harmful if applied aggressively | |
3) Neuromuscular paralysis: • Facilitates intubation and prevents shivering | |
4) Fluid management: • Monitor fluid balance, body weight, serum electrolytes, and serum osmolality • Correct electrolyte disturbances and maintain euvolemia by giving isotonic (0.9%) saline • Avoid free water including D5W, half normal (0.45%) saline, and enteral free water • Serum osmolality should be kept > 280 mOsm/L (it is often kept in the 295 to 305 mOsm/L range) | |
5) BP control: • Maintain BP, minimize large shifts in BP, and avoid hypotension (may lead to ischemia) • BP should be sufficient to maintain CPP > 60 mmHg • Vasopressors and inotropes (e.g., dopamine or norepinephrine) can be used to increase MAP and achieve optimal CPP | |
6) Sedation: • Titrate propofol to a Ramsay score of 4. Do not exceed 5 mg/kg/h for more than 24 h. If maximum dose of propofol is reached while ICP > 20 mmHg, fentanyl drip can be started • Reduces metabolic demand, ventilator asynchrony, venous congestion, and the sympathetic responses of hypertension and tachycardia | |
7) Maintain normothermia and treat temperature > 37.5 oC by giving antipyretic agents (e.g., acetaminophen) | |
8) Hyperosmolar therapy (mannitol or hypertonic saline): • Give mannitol at dose of 1 g/kg IV for rapid reduction of ICP. Monitor fluids and electrolytes every 4 h (twice after each bolus) • Hypertonic saline can be alternatively used to maintain hyperosmolarity and rapidly reduce ICP. It may be effective when mannitol is not. It needs central line placement for administration. Adverse effects: congestive heart failure, hyperchloremic acidemia, hypernatremia, and seizures | |
9) Glucocorticoids: • Give dexamethasone (10–20 mg IV) followed by maintenance dose of 4–6 mg every 4–6 h • Reduces cerebral vasogenic edema • Adverse effects: hyperglycemia, insomnia, immunosuppression, mood fluctuations, myopathy, Cushing syndrome | |
10) Head CT as soon as possible. Moderate hyperventilation is advisable during transport and initial evaluation | |
11) Barbiturate coma therapy for refractory intracranial hypertension: • Pentobarbital is generally used with a loading dose of 5 to 20 mg/kg as bolus, followed by 1–4 mg/kg/h • Continuous EEG monitoring with EEG burst suppression as a guide to optimal dosage • Additional boluses can be given during infusion for acute spikes in ICP • Moderate doses cause sluggish pupils; large doses cause 3–5 mm nonreactive pupils • Watch for hypotension • Treatment should be assessed based on ICP and CPP response and development of unacceptable side effects | |
12) ICP monitoring: • Performed when GCS < 8 with signs of elevated ICP on CT scan • Ventriculostomy performed to drain CSF in case of hydrocephalus, and to monitor ICP | |
13) Surgical management: • Resection of space-occupying lesion • Decompressive craniectomy • Trephination |