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)

Test yourself…

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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