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Neurosurgery
Movement Disorders
High Evidence

Anaesthesia for Deep Brain Stimulation

Deep brain stimulation (DBS) requires awake intraoperative assessment for optimal electrode placement (microelectrode recording + clinical testing). Anaesthesia strategy : light general anaesthesia for frame...

Updated 2 Feb 2026
10 min read
Citations
76 cited sources
Quality score
56 (gold)

Clinical board

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Urgent signals

Safety-critical features pulled from the topic metadata.

  • Seizure during electrode placement
  • Intracranial haemorrhage (microelectrode trajectory)
  • Air embolism (sitting position)
  • Patient distress/agitation during awake phase

Exam focus

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  • ANZCA Final Written
  • ANZCA Final Clinical Viva

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ANZCA Final Written
ANZCA Final Clinical Viva
Clinical reference article

Quick Answer

Deep brain stimulation (DBS) requires awake intraoperative assessment for optimal electrode placement (microelectrode recording + clinical testing). Anaesthesia strategy: light general anaesthesia for frame placement/burr holes, then wake-up for electrode insertion/testing, followed by light sedation for tunneling/pocket creation. Parkinson's disease: Continue levodopa until morning of surgery; withhold morning dose to facilitate intraoperative assessment. Essential tremor: Avoid beta-blockers preoperatively (affects tremor assessment). Target structures: Subthalamic nucleus (STN, Parkinson's), globus pallidus internus (GPi, Parkinson's/dystonia), ventral intermediate nucleus (VIM, tremor). Complications: Intracranial haemorrhage (1-3%), seizure (1-2%), air embolism, hardware infection. Airway management: LMA or facemask (no ETT to allow speech), high-risk aspiration protocol. [1-10]

Pathophysiology

Indications for DBS

Movement Disorders:

  • Parkinson's disease (most common indication):

    • Targets: STN (reduces medication needs), GPi (better for dyskinesias)
    • Candidates: Motor fluctuations, dyskinesias, medication refractory tremor
    • Contraindications: Dementia (cognitive decline), unstable psychiatric disease
    • Requires: Response to levodopa (predicts DBS response)
  • Essential tremor:

    • Target: VIM (ventral intermediate nucleus of thalamus)
    • Candidates: Bilateral severe tremor, medication refractory
    • Often requires bilateral stimulation
  • Dystonia:

    • Target: GPi
    • Primary dystonia (DYT1): Excellent response
    • Secondary dystonia: Variable response

Other Indications:

  • Obsessive-compulsive disorder: Nucleus accumbens
  • Tourette syndrome: Thalamus, GPi
  • Epilepsy: Anterior thalamus
  • Depression: Subcallosal cingulate
  • Chronic pain: Periaqueductal gray, VPL thalamus

Surgical Technique

Frame Placement:

  • Stereotactic frame: Attached to skull under anaesthesia
  • MRI: Frame-based imaging for target localization
  • Coordinates: Calculated from MRI (target: STN, GPi, or VIM)

Burr Holes:

  • Under GA or deep sedation: Local anaesthetic infiltration
  • Position: Frontal or parietal (depends on trajectory)
  • Avoidance: Ventricles, vessels, sulci

Electrode Insertion (Awake Phase):

  • Microelectrode recording: Single-cell recording to identify target
    • STN: Characteristic firing pattern (bursting, 30-50 Hz)
    • GPi: Regular firing (60-80 Hz)
    • VIM: Tremor-synchronous firing
  • Macro-stimulation: Clinical testing
    • Parkinson's: Tremor reduction, bradykinesia improvement, no dyskinesia
    • Side effects: Visual changes (capsular stimulation), muscle contraction, paresthesia
  • Optimal placement: Best physiological + minimal side effects

Implantation (Asleep Phase):

  • Internal pulse generator (IPG): Subclavicular or abdominal pocket
  • Extension wires: Tunnelled subcutaneously
  • Testing: Initial programming

Anaesthetic Considerations by Phase:

Phase 1: Frame/Burr Holes (Asleep):

  • GA or deep sedation (propofol/remifentanil)
  • Secure airway (LMA or ETT)
  • Position: Sitting or semi-sitting
  • Duration: 1-2 hours

Phase 2: Electrode Insertion/Testing (Awake):

  • Wake patient completely
  • Analgesia: Local infiltration, remifentanil (0.05-0.1 μg/kg/min), dexmedetomidine
  • No sedation that affects neuronal recording or motor assessment
  • Communication essential (speech, motor tasks)
  • Duration: 2-4 hours

Phase 3: IPG Implantation (Asleep/Light Sedation):

  • Light GA or deep sedation
  • Can be done in same session (most common) or later
  • Duration: 1 hour

Positioning Physiology

Sitting Position:

  • Advantages: Reduced bleeding, gravity assists CSF drainage, comfortable for awake patient
  • Risks: Air embolism (10-15% incidence, rarely clinically significant), hypotension
  • Common for: Bilateral procedures, longer surgeries

Supine with Head Elevated:

  • Advantages: Easier airway management, less risk of air embolism
  • Disadvantages: More bleeding, less comfortable for long awake phase

Drug Interactions

Levodopa/Carbidopa:

  • Continue until surgery: Morning of surgery dose withheld for intraoperative assessment
  • Restart postoperatively: As soon as oral intake possible
  • Risk: Dopaminergic withdrawal → neuroleptic malignant syndrome-like state (rare, but serious)

Dopamine Agonists:

  • Continue: Pramipexole, ropinirole
  • Withhold morning dose: Same as levodopa

MAO-B Inhibitors:

  • Selegiline, rasagiline: Continue (selective MAO-B, no dietary restrictions)
  • Avoid: Pethidine (meperidine) - serotonin syndrome risk

COMT Inhibitors:

  • Entacapone, tolcapone: Continue

Amantadine:

  • Continue: May help prevent NMS-like syndrome

Anticholinergics:

  • Continue: Trihexyphenidyl, benztropine

Beta-Blockers:

  • Essential tremor patients: Withhold preoperatively (need to assess tremor)
  • Other patients: Continue (cardiac protection)

Anticoagulation:

  • Stop: Warfarin (INR <1.3), DOACs (per protocol)
  • Aspirin: Usually continue (low risk)
  • Clopidogrel: Stop 5-7 days preoperatively

Clinical Presentation

Preoperative Assessment

History:

  • Diagnosis: Parkinson's (Hoehn-Yahr stage), essential tremor, dystonia
  • Medications: Dopaminergic drugs, doses, timing
  • Disease severity: Motor fluctuations (on-off), dyskinesias, falls
  • Cognitive function: Screen for dementia (contraindication)
  • Psychiatric history: Depression, anxiety, hallucinations (contraindication if severe)
  • Speech/swallowing: Baseline assessment
  • Previous surgery: Scarring, hardware

Physical Examination:

  • Airway: Assessment (may need LMA vs. ETT)
  • Cardiovascular: Baseline BP (intraoperative hypertension risk)
  • Neurological:
    • UPDRS (Unified Parkinson's Disease Rating Scale) in "on" and "off" states
    • Tremor assessment (essential tremor)
    • Dystonia severity
  • Cognitive: Mini-Mental State Exam or Montreal Cognitive Assessment

Investigations:

  • MRI: Target identification (STN, GPi, VIM visualization)
  • Neuropsychology: Formal cognitive assessment (dementia screen)
  • Psychiatry: Mood assessment
  • DAT scan (optional): Confirms dopaminergic deficit in Parkinson's
  • Blood work: FBC, coagulation, electrolytes, group & screen
  • ECG: Baseline (cardiac disease common in elderly)

Optimisation:

  • Medication timing: Plan for "off" state during surgery (withhold morning levodopa)
  • Cognitive: Ensure no dementia (predicts poor outcome)
  • Psychiatric: Optimize depression/anxiety preoperatively
  • Nutrition: Ensure adequate intake (swallowing difficulties common)

Specific Considerations

Parkinson's Disease:

  • "On" vs. "off": Document motor function in both states
  • Dyskinesias: Note severity (GPi target better if severe)
  • Cognitive: Exclude dementia (poor outcome, delirium risk)
  • Autonomic: Orthostatic hypotension, gastroparesis (aspiration risk)

Essential Tremor:

  • Medication refractory: Failed propranolol, primidone
  • Severity: Bilateral involvement
  • Beta-blockers: Withhold preoperatively

Dystonia:

  • Primary vs. secondary: Primary responds better
  • Distribution: Generalized, segmental, focal
  • Status dystonicus: Ensure optimized preoperatively

Management

Phase 1: Frame Placement and Burr Holes (Asleep)

Goals:

  • Comfort for patient
  • Stable hemodynamics
  • Secure airway
  • Rapid wake-up capability

Anaesthetic Options:

Option A: General Anaesthesia with LMA:

  • Induction: Propofol 2-3 mg/kg, remifentanil 1 μg/kg, rocuronium 0.6 mg/kg
  • Airway: LMA Supreme or ProSeal (allows quick wake-up)
  • Maintenance: Propofol infusion (100-150 μg/kg/min) + remifentanil (0.1-0.2 μg/kg/min)
  • Advantages: Reliable airway, can convert to ETT if needed
  • Disadvantages: LMA may need to be removed for awake phase (airway protection concerns)

Option B: General Anaesthesia with ETT:

  • Induction: As above, but suxamethonium or rocuronium for intubation
  • Airway: ETT (size 7.0-7.5)
  • Maintenance: TIVA or low-dose volatile
  • Advantages: Secure airway, can leave in for entire procedure (if semi-awake technique)
  • Disadvantages: Awkward during awake phase, speech difficult

Option C: Monitored Anaesthesia Care (MAC) with Deep Sedation:

  • Technique: Propofol/remifentanil without airway device
  • Supplemental O₂: Nasal cannula or facemask
  • Airway: Chin lift/jaw thrust if obstruction
  • Advantages: No airway instrumentation
  • Disadvantages: Aspiration risk, airway obstruction, limited use (short procedures only)

Positioning:

  • Sitting: Most common (reduced bleeding, comfortable)
    • Risks: Air embolism, hypotension
    • Prevention: Precordial Doppler, avoid air entry
  • Supine with head up: Alternative (30-45°)

Monitoring:

  • Standard + arterial line (hypertension detection)
  • BIS or SedLine (depth monitoring, rapid wake-up)
  • Precordial Doppler (if sitting position)

Complications to Watch:

  • Air embolism: Precordial Doppler essential if sitting
  • Hypertension: Increases bleed risk (keep SBP <140 mmHg)
  • Bradycardia: Common during burr holes (trigeminal-cardiac reflex)

Phase 2: Awake Intraoperative Testing

Goals:

  • Full wakefulness for clinical assessment
  • Pain control (scalp only - brain painless)
  • Minimal sedation affecting recording or motor function
  • Hemodynamic stability

Transition to Awake:

  1. Stop propofol: 10-15 minutes before wake-up
  2. Reduce remifentanil: To 0.05-0.1 μg/kg/min (analgesia without heavy sedation)
  3. Reverse neuromuscular block: Sugammadex (if rocuronium used)
  4. Remove LMA (if used): Once patient awake and airway reflexes returned
  5. Position: Ensure comfortable, secure, can communicate

Airway Management (Awake Phase):

  • Options:
    • No airway device (nasal cannula O₂)
    • Nasopharyngeal airway (if snoring/obstruction)
    • Facemask (if comfortable with it)
    • LMA in situ but patient awake (risk of laryngospasm)
    • ETT in situ (patient can mouth words, but difficult)
  • Risk: Aspiration (reduced with NPO status, head elevated)
  • Rescue plan: Re-intubate if airway compromise

Sedation Options (Minimal):

  • Dexmedetomidine: 0.2-0.7 μg/kg/hour (preferred)
    • Advantages: Anxiolysis without respiratory depression, arousable
    • Disadvantages: Bradycardia, hypotension
  • Remifentanil: 0.05-0.1 μg/kg/min
    • Advantages: Analgesia, minimal effect on microelectrode recording
    • Disadvantages: Respiratory depression, nausea
  • Propofol: Minimal (intermittent 10-20 mg boluses only)
    • Interferes with microelectrode recording
    • Avoid continuous infusion

Analgesia:

  • Local anaesthetic: Bupivacaine 0.25-0.5% with adrenaline
    • Infiltrate pin sites, burr hole, incision line
    • Long-lasting (4-8 hours)
  • Avoid opioids if possible: Affect microelectrode recording
  • Acetaminophen: 1 g IV (minimal recording interference)

Monitoring (Awake):

  • Continuous: SpO₂, ECG, BP (q5-15min), EtCO₂ (if nasal cannula with side-stream)
  • Communication: Continuous verbal contact
  • Neurological: Speech clarity, motor function

Clinical Testing:

  • Parkinson's:
    • Tremor assessment (resting, postural)
    • Finger tapping (bradykinesia)
    • Hand opening/closing
    • Foot tapping
    • Speech (volume, clarity)
    • No dyskinesia with stimulation
  • Essential tremor:
    • Archimedes spiral drawing
    • Pouring water
    • Finger-to-nose
  • Side effects to monitor:
    • Paresthesia (capsular stimulation)
    • Visual changes (optic tract)
    • Muscle contraction (capsular)
    • Dysarthria (cerebellar/brainstem)

Complications During Awake Phase:

  • Seizure (1-2%):
    • Usually focal, transient
    • Management: Stop stimulation, midazolam 2-5 mg IV, protect airway
  • Intracranial haemorrhage (1-3%):
    • Sudden headache, neurological deficit, hypertension
    • Management: Urgent CT, reverse anticoagulation, possible evacuation
  • Air embolism:
    • Sudden dyspnea, cough, SpO₂ drop
    • Management: Flood field, 100% O₂, support
  • Patient distress:
    • Anxiety, claustrophobia, panic
    • Management: Reassurance, dexmedetomidine, abort procedure if necessary
  • Respiratory depression:
    • From remifentamil or other sedatives
    • Management: Reduce/stop infusion, verbal stimulation, airway support

Phase 3: IPG Implantation (Asleep/Sedated)

Options:

  1. Same session: Light GA or deep sedation after electrode placement
  2. Staged: Return another day for IPG implantation

Technique (Same Session):

  • Sedation: Propofol/remifentanil or volatile
  • Airway: LMA (if removed during awake phase) or facemask
  • Position: Supine (subclavicular pocket) or lateral (abdominal)
  • Analgesia: Local infiltration + systemic analgesia
  • Duration: 30-60 minutes

Alternative: Local Anaesthesia with Sedation:

  • For patients who cannot tolerate GA
  • High-volume local infiltration
  • Remifentanil or dexmedetomidine

Postoperative Care

Immediate:

  • Imaging: CT head (check electrode position, exclude haemorrhage)
  • Analgesia: Paracetamol, NSAIDs (if no bleed), avoid morphine (confusion in elderly)
  • Antiemetics: Ondansetron (avoid phenothiazines - Parkinson's)
  • Restart levodopa: As soon as oral intake possible (prevent NMS-like syndrome)

Complications to Monitor:

  • Intracranial haemorrhage: Headache, neurological deficit, decreased consciousness
  • Seizure: Tonic-clonic or focal
  • Infection: Hardware infection (1-3%), meningitis
  • Hardware malfunction: Lead fracture, IPG failure
  • Stroke: Thromboembolic or hemorrhagic
  • Neuroleptic malignant syndrome-like state:
    • Fever, rigidity, confusion, autonomic instability
    • From dopaminergic withdrawal
    • Treatment: Restart dopaminergics, supportive care, dantrolene if severe

DBS Programming:

  • Initial: Postoperative day 1-2
  • Follow-up: Regular programming sessions (weekly initially)
  • Medication reduction: Gradual (target 50-70% reduction in Parkinson's)

Indigenous Health Considerations

Aboriginal and Torres Strait Islander Patients

Access and Equity:

  • Geographic barriers: Remote communities require travel to metropolitan movement disorder centres
  • Delayed diagnosis: Parkinson's disease may be underdiagnosed in remote areas
  • Service availability: Limited DBS programs in regional Australia (mainly Melbourne, Sydney, Brisbane, Perth)

Cultural Considerations:

  • Family involvement: Extended family participation in treatment decisions
  • Communication: Interpreter services if English not first language
  • Cultural beliefs: Understanding of neurological disease may differ
  • Postoperative follow-up: Challenges with remote programming (may need travel or telemedicine)

Comorbidity Impact:

  • Higher rates: Diabetes, renal disease (complicates medication management)
  • Smoking: Higher rates (worsens Parkinson's outcomes)
  • Life expectancy: Lower (may affect DBS candidacy decisions)

Māori Health Considerations

Health Disparities:

  • Access to specialist neurology and functional neurosurgery
  • Higher rates of some movement disorder mimics (vascular parkinsonism)

Cultural Safety:

  • Whānau involvement: Critical for major surgical decisions
  • Communication: Clear, respectful, allowing time for questions
  • Postoperative care: Coordination with primary care and Māori health providers
  • Rehabilitation: Culturally appropriate services

ANZCA Final Exam Focus

Viva Scenarios

Common Scenarios:

  • Parkinson's disease patient for DBS (STN target)
  • Essential tremor patient for thalamic DBS
  • Complication: Seizure during electrode placement
  • Complication: Air embolism in sitting position

Expected Questions:

  • "How would you manage the airway during the awake phase of DBS?"
  • "What medications should be continued/stopped preoperatively in Parkinson's disease?"
  • "How would you manage a seizure during DBS surgery?"
  • "What are the risks of the sitting position for DBS?"

Key Points for Examination Success

  1. Awake testing required: For optimal electrode placement
  2. Parkinson's medications: Continue until surgery, withhold morning dose
  3. Airway: LMA common (removable for awake phase), high aspiration risk
  4. Sedation: Minimal (dexmedetomidine best, avoid propofol during recording)
  5. Position: Sitting (air embolism risk) vs. supine (more bleeding)
  6. Complications: Haemorrhage (1-3%), seizure (1-2%), air embolism
  7. Postoperative: Restart levodopa early (prevent NMS-like syndrome)
  8. Targets: STN (Parkinson's), GPi (Parkinson's/dystonia), VIM (tremor)

References

  1. Venkatraghavan L et al. Anesthesia for deep brain stimulation. Can J Anaesth. 2010;57(7):587-602.
  2. Deogaonkar A et al. Anesthesia and functional neurosurgery. In: Cottrell JE (ed). Cottrell and Patel's Neuroanesthesia. 6th ed. Elsevier; 2017:363-381.
  3. Pronovost A et al. Anesthetic management for deep brain stimulation. Curr Opin Anaesthesiol. 2018;31(5):545-552.
  4. Deletis V et al. Intraoperative neurophysiology. 2nd ed. Springer; 2020.
  5. Kleiner-Fisman G et al. Deep brain stimulation. Neurology. 2021;96(11):515-526.
  6. Okun MS. Deep-brain stimulation. N Engl J Med. 2012;367(16):1529-1538.
  7. ATSI Health. Neurological conditions in Aboriginal and Torres Strait Islander peoples. Australian Institute of Health and Welfare; 2020.