Awake craniotomy

Surgical approach

  • Indications: resection/biopsy near eloquent cortex (language, motor, sensory, visual pathways), epilepsy focus surgery, deep brain stimulation lead placement (variant)
    • Goal: maximise resection while preserving function using awake testing and/or electrocortical stimulation
  • Positioning: supine/lateral/park-bench; head fixed in Mayfield pins; limited access to airway once draped
    • Often pinned before incision; local infiltration at pin sites and incision line
  • Scalp incision → craniotomy flap → dural opening
    • Cortical mapping with stimulation; patient performs tasks (naming, counting, reading, limb movement)
    • Resection with repeated testing; haemostasis; dural closure; bone flap replacement; scalp closure
  • Key surgical stimuli: pinning, scalp incision, temporalis dissection, dural traction, cortical stimulation, irrigation, closure
    • Brain parenchyma is not pain sensitive; pain mainly from scalp, periosteum, muscle, dura

Anaesthetic management (overview)

  • Type of anaesthesia: awake with sedation + regional scalp block; or asleep–awake–asleep (AAA) with GA for opening/closure and awake mapping phase
    • Choice depends on patient factors, lesion location, expected mapping duration, surgeon preference, and airway risk
  • Airway: usually spontaneous ventilation; oxygen via nasal cannula/face mask; consider high-flow nasal oxygen; airway rescue equipment immediately available
    • ETT/SGA typically only if AAA (during asleep phases) or conversion to GA
  • Duration: commonly 3–6 hours (variable; mapping can be prolonged)
    • Plan for fatigue, hypothermia, pressure areas, and prolonged immobility
  • How painful: moderate without regional; can be well tolerated with scalp block + careful sedation; discomfort often from pins, incision, temporalis traction, neck/shoulder strain, anxiety
    • Dural manipulation may cause headache/nausea; cortical stimulation can provoke seizures
  • Key anaesthetic goals: cooperative patient for testing, immobility when required, stable haemodynamics/ICP, avoid respiratory depression/hypercapnia, rapid titratable sedation, seizure readiness, airway rescue plan
    • Maintain cerebral perfusion pressure (CPP) and avoid hypoxia/hypercapnia (↑CBF/ICP) and hypotension (↓CPP)

Indications and patient selection

  • Indications: lesions adjacent to eloquent cortex; need for real-time functional testing; epilepsy surgery requiring mapping; sometimes DBS (awake component differs)
  • Contraindications (relative): inability to cooperate (severe anxiety, confusion, dementia), severe OSA/obesity with high airway risk, uncontrolled reflux/aspiration risk, severe cough, inability to lie flat, severe dysphasia precluding testing, movement disorders, raised ICP with reduced compliance, severe cardiorespiratory instability
  • Pre-op counselling: explain phases, need to stay still, potential discomfort, seizure possibility, how communication will work, and conversion to GA possibility

Pre-operative assessment and optimisation

  • Neurological baseline: language, motor deficits, seizures frequency; document pre-op function for intra-op comparison
  • Seizure management: continue antiepileptics; check adherence; consider pre-op levels only if clinically indicated; avoid precipitants (sleep deprivation, hypoglycaemia)
  • Steroids: often on dexamethasone for oedema; consider glucose control and infection risk
  • Airway assessment: anticipate limited access once pinned/draped; plan rescue strategy (who will undrape/unpin; where equipment is)
  • PONV risk: high; plan multimodal prophylaxis

Technique options

  • Awake throughout (monitored anaesthesia care): scalp block + titrated sedation/analgesia; avoids airway instrumentation; continuous ability to test
    • Requires excellent regional technique and careful sedation to avoid hypoventilation/obstruction
  • Asleep–awake–asleep (AAA): GA for pinning/opening; wake for mapping/resection; GA again for closure
    • Airway: usually SGA or ETT during asleep phases; remove for awake phase (or lighten with SGA in situ in selected centres, but can interfere with speech testing)
    • Pros: comfort during most stimulating parts; cons: airway manipulation, emergence agitation, time, risk of coughing/straining/ICP surges
  • Choice of sedatives: propofol and remifentanil (titrated) or dexmedetomidine-based; avoid long-acting agents that delay testing
    • Dexmedetomidine: cooperative sedation with minimal respiratory depression; can cause bradycardia/hypotension
    • Propofol/remifentanil: very titratable but higher risk of apnoea/obstruction; stop/low dose during mapping

Regional anaesthesia: scalp block and infiltration

  • Scalp block targets: supraorbital, supratrochlear, zygomaticotemporal, auriculotemporal, greater occipital, lesser occipital nerves (bilateral as needed)
  • Local infiltration: pin sites, incision line, temporalis muscle, periosteum; surgeon often infiltrates dura (variable efficacy)
  • Local anaesthetic safety: calculate maximum dose (consider mixture and patient weight); use incremental aspiration; consider adrenaline-containing solutions for scalp (vascular) to reduce bleeding and prolong block
    • Be prepared for LAST: intralipid immediately available; team brief

Monitoring and access

  • Standard monitoring + invasive arterial line (beat-to-beat BP, blood gases if needed); capnography via nasal cannula; temperature; urinary catheter for long cases
  • IV access: at least 1–2 good cannulae; consider large-bore if expected blood loss; ensure lines are accessible after draping
  • Adjuncts: BIS/processed EEG may help titrate sedation; neurophysiology monitoring may be used (MEP/SSEP) depending on case

Intraoperative conduct (practical plan)

  • Team brief: phases of case; when patient must be interactive; seizure plan; airway rescue plan; who can rapidly remove drapes/unpin; acceptable BP/CO2 targets
  • Positioning: meticulous padding; avoid neck flexion/rotation causing venous obstruction/airway compromise; ensure patient comfort before pinning
  • Sedation strategy: aim for calm, cooperative (RASS around 0 to -2) during non-testing; lighten/stop sedatives during mapping; avoid oversedation
    • Analgesia: scalp block + small opioid boluses if needed; avoid large opioid doses before mapping
  • Ventilation: maintain spontaneous ventilation; avoid hypercapnia (↑CBF/ICP) and hypoventilation; provide supplemental O2; consider ABG if concerns
  • Haemodynamics: avoid hypertension (bleeding, oedema) and hypotension (↓CPP). Treat pain/anxiety first; then titrate vasoactive drugs as needed
    • Common agents: metaraminol/phenylephrine for hypotension; labetalol/esmolol for tachycardia/hypertension; avoid excessive sedation to treat BP
  • Fluids: aim euvolaemia; avoid hypotonic fluids; consider balanced crystalloids; manage glucose (steroids) and sodium (risk of SIADH/cerebral salt wasting is more post-op)
  • PONV: multimodal (e.g., dexamethasone if appropriate, ondansetron, droperidol); minimise opioids; treat early to avoid raised ICP and movement

Seizures during awake craniotomy

  • Triggers: cortical stimulation, local anaesthetic toxicity (rare), hypoglycaemia, sleep deprivation, withdrawal of antiepileptics
  • Immediate management: stop stimulation; call for cold saline irrigation to cortex; protect airway and patient from injury; ensure oxygenation and ventilation
  • Drug treatment (if prolonged/generalised): small IV boluses of propofol or midazolam; consider levetiracetam/phenytoin per local practice; be ready to convert to GA if airway/ventilation compromised
    • Balance seizure termination vs preserving ability to test; use minimal effective doses

Airway obstruction and conversion to GA

  • Risk factors: oversedation, OSA/obesity, head/neck position, secretions, opioid use
  • Early management: verbal/tactile stimulation, reduce sedatives, jaw thrust, airway adjuncts (nasopharyngeal/oropharyngeal), reposition head/neck if possible, HFNO/CPAP if feasible
  • Conversion to GA: pre-agreed plan; stop surgery; undrape as needed; consider SGA as quickest rescue; ETT if aspiration risk/need controlled ventilation; anticipate difficult access with pins and limited mouth opening
    • Have videolaryngoscope, bougie, suction, and emergency front-of-neck access kit immediately available

Complications

  • Intra-op: seizures, airway obstruction/apnoea, aspiration, agitation/panic, nausea/vomiting, pain, hypertension/hypotension, venous air embolism (rare but possible), bleeding, LAST
  • Neurosurgical: brain swelling, intracranial haemorrhage, new neurological deficit, CSF leak, infection
  • Post-op: PONV, headache, delirium, seizures, airway compromise (sedation/opioids), hyponatraemia, steroid hyperglycaemia

Post-operative care

  • Destination: PACU with neuro obs; consider HDU/ICU depending on comorbidity, intra-op events, and extent of surgery
  • Analgesia: paracetamol + NSAID if appropriate; minimise opioids; treat scalp pain; consider local infiltration top-ups by surgeon
  • Antiemetics: continue prophylaxis; low threshold to treat vomiting (risk of raised ICP and wound issues)
  • Seizure prophylaxis: continue antiepileptics; monitor; manage triggers (sleep, glucose, electrolytes)
You are asked to anaesthetise a patient for awake craniotomy for a left frontal tumour. What are your aims and how will you achieve them?

Structure: aims → technique choice → practical conduct → complication plans.

  • Aims: cooperative patient for language/motor testing, immobility during critical steps, stable physiology (avoid hypoxia/hypercapnia/hypotension), good analgesia, minimal PONV, readiness for seizures and airway rescue
  • Technique: awake with sedation + scalp block or AAA; choose based on patient cooperation, airway risk, and expected mapping
  • Analgesia: comprehensive scalp block + infiltration at pins/incision/temporalis; paracetamol ± NSAID
  • Sedation: dexmedetomidine or propofol/remifentanil titrated; lighten/stop during mapping; avoid long-acting drugs
  • Monitoring: A-line, nasal capnography, temperature; ensure IV access remains accessible
  • Plans: seizure management (stop stimulation, cold saline, small propofol/midazolam), airway rescue and conversion to GA, PONV treatment
Describe how you would perform a scalp block for awake craniotomy. Which nerves are blocked?

Expect to list nerves and demonstrate safe LA practice.

  • Nerves: supraorbital, supratrochlear (V1); zygomaticotemporal (V2); auriculotemporal (V3); greater occipital (C2 dorsal ramus); lesser occipital (C2 ventral ramus)
  • Technique principles: asepsis, incremental aspiration, avoid intravascular injection (scalp vascular), calculate max dose, consider adrenaline to reduce bleeding and prolong effect
  • Supplement: infiltration at Mayfield pin sites, incision line, temporalis muscle; consider surgeon infiltration of dura if needed
  • Safety: LAST recognition and immediate treatment readiness (lipid emulsion available, team aware)
Compare awake throughout vs asleep–awake–asleep (AAA) techniques. What are the advantages and disadvantages?
  • Awake throughout: avoids airway instrumentation; continuous testing possible; but requires excellent block and careful sedation; higher risk of discomfort/anxiety if analgesia inadequate
  • AAA: more comfort during pinning/opening/closure; controlled airway/ventilation during asleep phases; but risks with emergence, coughing/straining, time delays, airway manipulation and re-instrumentation, and potential interference with speech testing if airway device remains
  • Patient factors drive choice: cooperation, airway risk (OSA/obesity), reflux/aspiration risk, expected mapping duration, and team experience
What sedative/analgesic drugs are suitable for awake craniotomy and why? Include key side effects.
  • Dexmedetomidine: cooperative sedation, minimal respiratory depression, some analgesia; adverse effects bradycardia, hypotension, delayed arousal at higher doses
  • Propofol: rapid onset/offset, antiemetic; adverse effects respiratory depression/apnoea, hypotension; may need to stop for mapping
  • Remifentanil: ultra-short acting analgesia, titratable; adverse effects respiratory depression, chest wall rigidity (bolus), nausea; can impair cooperation if excessive
  • Avoid/limit: long-acting opioids and benzodiazepines (prolonged sedation, respiratory depression, impaired testing); ketamine may preserve respiration but can cause dysphoria and interfere with neuro testing in some patients
During cortical stimulation the patient has a seizure. Talk through your immediate management and how you balance seizure control with the need for awake testing.
  • Immediate: stop stimulation; call for cold saline irrigation to cortex; protect patient; ensure oxygenation and support ventilation
  • If ongoing/generalised: give small titrated IV propofol or midazolam; consider loading antiepileptic per local protocol; check glucose and correct
  • Balance: use minimal effective sedative dose to terminate seizure while preserving ability to wake quickly for testing; communicate with surgeon about pausing mapping and reattempting later
  • Escalation: if airway compromised or repeated seizures → convert to GA using pre-agreed plan
The patient becomes obstructed and hypoventilates after a propofol bolus. What do you do given the head is pinned and access is limited?
  • Call for help; stop/reduce sedatives/opioids; stimulate patient; apply jaw thrust and insert airway adjunct (OPA/NPA) if tolerated; increase oxygen and use nasal capnography to assess response
  • Check head/neck position (venous/airway obstruction) and adjust if possible; consider HFNO/CPAP if available
  • If not rapidly reversible: initiate conversion to GA per plan; coordinate undraping/unpinning if required; consider SGA as fastest rescue, then ETT if needed
  • Post-event: reassess sedation strategy (avoid boluses; use infusion with careful titration) and consider dexmedetomidine-based approach
What are the main causes of pain and discomfort during awake craniotomy, and how do you prevent/treat them?
  • Pain sources: scalp incision, periosteum, temporalis muscle traction, Mayfield pins; dura can cause headache; brain itself not pain sensitive
  • Prevention: meticulous scalp block + infiltration (pins/incision/temporalis); comfortable positioning and padding; avoid tight head/neck positions
  • Treatment: top-up local infiltration, small titrated opioid/remifentanil, treat anxiety with reassurance and careful sedation; treat PONV early
How do you manage haemodynamics and ventilation during an awake craniotomy? What targets are you aiming for?
  • Ventilation: maintain normoxia and normocapnia; avoid hypercapnia (↑CBF/ICP) and hypoventilation from sedation; use nasal capnography; consider ABG if concerns
  • Haemodynamics: maintain CPP; avoid hypotension (↓CPP) and hypertension (bleeding/oedema). Treat pain/anxiety first; then titrate vasoactive drugs
  • Practical: arterial line for beat-to-beat BP; avoid large sedative boluses; ensure adequate analgesia to blunt sympathetic responses
Discuss PONV in awake craniotomy: why it matters and how you prevent and treat it.
  • Why important: vomiting causes movement, aspiration risk, raised ICP, bleeding risk, and distress; can jeopardise mapping and surgical field
  • Prevention: multimodal antiemetics (e.g., ondansetron + droperidol + dexamethasone if appropriate), minimise opioids, maintain hydration, avoid hypotension
  • Treatment: early rescue antiemetic from different class; consider propofol small dose (antiemetic) if safe; stop causative stimuli; suction and protect airway
What are the key elements of your airway rescue plan for awake craniotomy?
  • Preparation: difficult airway assessment; agree triggers for conversion; ensure immediate availability of suction, OPA/NPA, SGA, videolaryngoscope, bougie, drugs, and FONA kit
  • Logistics: plan how drapes will be removed and whether pins can remain; assign roles (surgeon to pause and help access; runner for equipment)
  • Strategy: stepwise escalation from stimulation/jaw thrust → adjuncts/HFNO/CPAP → SGA → ETT; maintain oxygenation as priority
What complications are specific or particularly relevant to awake craniotomy and how do you reduce the risk?
  • Seizures: anticipate with cold saline ready; continue antiepileptics; avoid triggers; have propofol/midazolam drawn up
  • Airway obstruction: avoid oversedation; prefer agents with minimal respiratory depression; optimize positioning; continuous capnography
  • LAST: dose calculation, incremental injection/aspiration, intralipid available
  • PONV and agitation: prophylaxis, reassurance, avoid excessive opioids/benzodiazepines

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