Anesthesia for Supratentorial Tumors Pekka O. Talke, MD Department of Anesthesia and Neurosurgery, Cottrell Chief of Neuroanesthesia University of California, San Francisco Title • • • • 35.000 brain tumors/yr 85% primary 60% primary and supratentorial 15% mets (1/6 of tumors) General Considerations • • • • • • Surgical exposure (retraction) Intracranial pressure (ICP) Secondary insult to brain Hemorrhage, seizures, air emboli Rapid emergence Stress response ICP • • • • Tissue, blood, CSF Intracranial-Volume relationship Effects of anesthetics on ICP Tumor mass and edema (steroids) Anesthetics • Intravenous anesthetics (not ketamine) are cerebral vasoconstrictors • Reduce CMR • CO2 reactivity intact Anesthetics cont. • Volatile anesthetics are cerebral vasodilators • Increase ICP • Reduce CMR • CO2 reactivity intact Anesthetics cont. • • • • • Nitrous oxide increases CMR and ICP Can be controlled by hypocapnia Opioids reduce CMR CO2 reactivity intact Nitroglycerine, nitroprusside, hydralazine are cerebral vasodilators Reduction of ICP • Intravenous anesthetics • Hyperventilation (30-35 mmHg) • Mannitol (0.5-1.0 gm/kg, 320 mOsm/kg), • • • • • (hypernatremia, hypokalemia, hypovolemia) hypertonic saline Lasix CSF drainage Hypoxia, hypovolemia Head position (venous drainage) Increase MAP Preop Plan • • • • • • Vascular access Fluid therapy Anesthetics Ventilation Monitoring Neuromonitoring Preop • Sedation=hypercapnia, hypoxia, obstruction • Stress: increased CMR, CBF • Analgesia/sedation midas 0.5.-2.0 mg/fentanyl (25- 100 ug) • Steroids • Anticonvulsants (relaxants, loading SLOW) Preop cont. • Two large Ivs • A-line (CPP, ABG, glucose, osm) • Asleep? To avoid stress Monitoring • • • • • • • BP, HR, CVP? Pulse ox ERTCo2 Temperature (hypothermia?) Urine Relaxometry (hemiplegia, dilantin, tegretol) Glucose, Hg, Hct Monitoring cont. • • • • EEG SSEP ICP? Motor mapping Induction • • • • • Avoid hypoxia, hypercarbia, stress response Propofol/pentothal/hyperventilate Opioids/relaxants Head position (venous obstruction) More drugs for intubation/pinning Maintenance • Control CMR, CBF • Good depth of anesthesia • Adequate CPP Maintenance cont. • Volatile (<1 MAC)/intravenous anesthetics/N2O • Mild hyperventilation • Aim for speedy emergence (CT scan) Increased ICP • • • • • • Hyperventilate Venous drainage Relaxation Change to IV anesthesia Delete N2O Diuretics Fluids • Not hypoosmolar • Colloids (bleeding) • Mannitol (320 mOsm/g) Emergence • Attenuate stress response (autoregulation • • • • impaired/labetalol) Avoid hypercarbia, hypoxia (opioids) Avoid coughing Slow awakening (CT) Seizure, edema, hematoma, pheumocephalus, vessel occlusion, ischemia, metabolic Title Title Title Intracranial • Increased intracranial pressure • Midline shift: tearing of the cerebral vessels • Herniation: falx, transtentorial, transforamen • Magnum, transcraniotomy • Epilepsy • Vasospasm Systemic • • • • • • • • Hypercapnia Hypoxemia Hypotension or hypertension Hypoosmolality or hyperosmolality Hypoglycemia Hyperglycemia Shivering or pyrexia Low cardiac output Prevention • No overhydration • Sedation, analgesia, anxiolysis • No noxious stimulus applied without sedation and Local Anesthesia • Head-up position, no compression of the jugular veins, head straight • Osmotic agents: mannitol, hypertonic saline Prevention cont. • • • • • • • Beta-blockers or clonidine or lidocaine Steroids, if a tumor is present Adequate hemodynamics: MAP, CVP, PCWP, HR Adequate ventilation: Paco2>100 mm Hg, Paco2 35 mm Hg Intrathoracic pressure as low as possible Hyperventilation on demand before induction Use of intravenous anesthetic agents for induction and maintenance in case of tensed brain Treatment • • • • CSF drainage if ventricular or lumbar catheter in situ Osmotic agents Hyperventilation Augmentation of anesthesia with intravenous anesthetic agents: propofol, thiopentone, etomidate • Muscle relaxant • Venous drainage: head up no PEEP, reduction of inspiratory time • Mild controlled hypertension if autoregulation present History • Seizure • Increased intracranial pressure (ICP): headache, nausea, vomiting, blurred vision • Decreased level of consciousness, somnolence • Focal neurologic signs: hemiparesis, sensory deficits, cranial nerve deficits, and so on • Paraneoplastic syndromes including presence of thrombosis Physical Evaluation • Mental status • Papilledema (increased ICP) • Signs of Cushing’s response: hypertensive • • • • bradycardia Pupil size, speech deficit, Glasgow coma score, focal signs Medication Steroids Antiepileptic drugs Technical Examination (CT or MRI Scan) • Size and location of the tumor: silent or eloquent area, near a major vessel, and so on • Intracranial mass effect: midline shift, decreased size of the ventricles, temporal lobe hernia • Intracranial mass effect: hydrocephalus, cerebrospinal fluid space around brainstem • Others: edema, brainstem involvement, pneumocephalus (recraniotomy) Evaluation of Hydration Status • • • • Duration of bed rest Fluid intake Diuretics Inappropriate secretion of antidiuretic hormone Induction • Adequate anxiolysis in the anesthetic room • Adequate fluid loading (5 to 7 ml/kg of NaCl 0.9%) • ECG leads in place; capnometer, pulse oximeter, and noninvasive blood pressure monitors • Insertion of intravenous and arterial lines under local anesthesia • Fentanyl 1 to 2 g/kg or alfentanil, sufentanil, or remifentanil Induction cont. • Preoxygenation and voluntary hyperventilation • Propofol 1.25 to 2.5 mg/kg or thiopentone 3 to 6 mg/kg for induction • Nondepolarizing muscle relaxant: vecuronium, rocuronium, or other controlled ventilation at Paco2 of 35 mm Hg • Propofol 50 to 150 g /kg/min or isoflurance 0.5% to 1.5% (or sevoflurane of desflurane) for maintenance and fentanyl (or alfentanil, sufentanil, or remifentanil) 1 to 2 g/kg or alfentanil, sufentanil, or remifentanil Induction cont. • Lignocaine 1.5 mg/kg • Intubation • Local anesthesia and intravenous fentanyl 2 g/kg for • • • • skull-pin head-holder placement and skin incision adequate head-up positioning; no compression of the jugular veins Mannitol 0.5 to 0.75 g/kg Insertion of a lumbar drain Possibly N2O when the dura is open and brain is slack Normovolemia with the use of NaCl 0.9% or starch 6%—no Ringer’s lactate ICP Control • Mild hyperosmolality (use NaCl 0.9% [304 mOsm/kg] as baseline infusion; give mannitol [1319 mOsm/kg] 0.5 to 0.75 g/kg or hypertonic saline [7.5% 2533 mOsm/kg] 3 to 5 ml/kg before bone flap removal) • Intravenous anesthetic agent (propofol), adequate depth of anesthesia • Mild hyperventilation, mild hyperoxygenation ICP Control cont. • Mild controlled hypertension: MAP maintained around 100 mm Hg in order to decrease CBV and ICP • Normovolemia; no vasodilators • Mild hyperoxia • Together with: – Adequate head-up positioning – Free venous drainage; no compression of the jugular veins – No PEEP, no ventilator fight (myorelaxants) – Lumbar drainage – Avoidance of brain retractors Awakening • Neurosurgical awakening should maintain: –Stable arterial blood pressure and thus cerebral blood flow and intracranial pressure –Stable oxygenation and carbon dioxide tension –Stable CMRO2 –Normothermia Awakening cont. • Neurosurgical awakening should avoid: –Coughing –Tracheal suctioning –Airway overpressure during extubation –Patient-ventilator dyssynchrony Awakening cont. • Neurosurgical awakening should provide: –Optimal conditions for neurologic examination
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