Interventions/Procedures Flashcards
AAA (EVAR)
Pre-operative
* careful pre-operative assessment for elective repair - multiple co-morbidities
* ?refused for open repair due to increased risk
* ECG, U+Es, dynamic assessment of heart
Intra-operative
* in radiology/angio suite
* GA/RA/LA
* invasive monitoring
* simple analgesia + local infiltration to insertion site
Post-operative
* ICU not usually needed
* ?HDU or vascular ward
* long term monitoring needed for Endoleak
AAA (Open Repair)
Pre-operative
* careful pre-operative assessment for elective repair - often multiple co-morbidities
* ECG, U+Es, dynamic cardiac assessment
* continue cardiac medications (MI risk)
Intra-operative
* thoracic epidural
* art line (awake) + 2x big drips + CVC +/- vascath +/- CO monitor
* full invasive monitoring +/- CO monitor
* warm upper body only
* opiate heavy induction
* may need vasoconstrictors pre-clamp/post unclamp
* may need vasodilatation post-clamp - wean prior to release (aim BP >110)
* aim for warm, pain free, non acidotic, non coagulopathic, well oxygenated + well filled patient
* cell salvage, TXA, calcium etc
Post-operative
* early extubation
* ICU/HDU
* continue epidural + multimodal analgesia
* monitor fluid balance, U+Es, may need RRT
Anaesthesia after Chemotherapy
Pre-operative assessment
* focused history of cancer management - detailed drug history including precise chemo regimen, and toxic effects suffered by the patient
* systems review
– respiratory - infection, metastatic disease, PE, drug induced pulmonary toxicity (e.g. pneumonitis, progressive pulmonary fibrosis)
– cardiovascular - hypotension, hypertension, arrhythmias (Torsades), MI, CCF, cardiomyopathy, myocarditis, pericarditis, pericardial effusion, tamponade, radiotherapy may cause damage to cardiac valves, vessels and pericardium
– renal - acute or chronic renal failure
– nervous system - peripheral neuropathy, muscle pain, cranial neuropathy, orthostatic hypotension (ANS), vocal cord palsy, seizures
– GI - common after most chemotherapy drugs - nausea, vomiting, mucositis, diarrhoea +/- dehydration
– hepatic - abnormal LFTs (metastases, infections, liver disease, hepatotoxic medications), chemotherapy related liver damage (parenchymal damage with fatty change, cholestasis, hepatocellular necrosis), many chemotherapy drugs are metabolised by the liver
– haematopoietic - myelosuppression with risk for lifethreatening sepsis in absence of typical signs/symptoms
* thorough examination including full neurological examination
* routine investigations - FBC, U+Es, coagulation, ECG
* additional investigations e.g. CXR, ABG, PFTs, echo may be required depending on the treatment regimen used
* minimise fasting/dehydration time
* fluid resuscitate + corrent U+Es prior to surgery if possible
* consider RSI if N+V
Pulmonary toxicity - cytotoxic antibiotics, nitrosureas, alkylating agents, anti-metabolites, plant alkaloids, biological response modifiers, taxol
Cardiotoxicity - cytotoxic antibiotics, plant alkaloids, alkylating agents, 5FU, cisplatin, interferon, IL2, taxol
Hepatotoxicity - nitrosureas, anti-metabolites, cytotoxic antibiotics, 5FU, vincristine, cisplatin
Nephrotoxicity - nitrosureas, bleomycin, cisplatin, cyclophosphamide, MTX, mitomycin C, vincristine
Neurotoxicity - vincristine, high dose MTX, cisplatin, paclitaxel, osaliplatin, ifosfamie
Intra-operative
* caution with laryngoscopy causing severe bleeding in presence of mucositis
* aim for SpO2 of 88-92% for bleomycin due to lifelong risk of lung injury, high O2 only with extreme caution for immediate life-saving indications
* caution with myocardial depressants - consider invasive arterial pressure and CO monitoring
* careful fluid optimisation
* multimodal analgesia (avoid NSAIDs if renal issues)
* maintain normothermia
* regional relatively contraindicated if patients has neurological side effects after chemotherapy - careful documentation of deficit if it is to be used
* drug dosing in renal/hepatic impairment
Post-operative
* respiratory - chest physio, good analgesic regimes, early mobilisation
* consider HDU
Emergency Ocular Surgery
Goals
* Provide a stationary globe
* Provide profound analgesia
* Monitoring and attenuation of the oculocardiac reflex
* Prevent harmful increases in IOP - limit coughing, retching, vomiting, forceful blinking, crying etc during emergence (risk of extrusion of globe contents with elevated IOP
Pre-operative
* may have full stomach even hours post injury
* common injury in paeds - need to avoid eye rubbing, crying, breath holding, screaming due to raised IOP
* analgesia pre-op (antiemetics if opioids)
Intra-operative
* LA technique can be used in some cases
* GA with armoured LMA/ETT (may need RSI)
* can use sux (raised IOP balanced by decreased with induction agent) or use roc + sugammadex
* avoid hypertensive response to laryngoscopy
* avoid coughing on emergence
Post-operative
* simple analgesics usually adequate + codeine/diclofenac
* consider regular anti-emetic
Anaesthetic Gas Monitoring
- IR absorption spectrophotometry
– light source passed through filter (of specific wavelength e.g. Co2 4.28micrometers) and then sample of gas, amount of light measured using a photo detector and converted to voltage and then to a visual display
– change wavelength of filter to detect different agents - separate filters/detectors or rotating
– sample analyser lined in sapphire, as this does not absorb IR
– absorption of light is proportional to the amount of molecules present in the sample
– blockage of sample lines, water vapour absorbs infrared across a wide spectrum, N2O cdan cause problems with CO2 measurement (collision broadening effect) - Photoacoustic spectrophotometry
– sample gas irradiated with pulsatile IR, of a suitable wavelength
– periodic expansion and contraction of the gas produces a pressure fluctuation of audible frequency that can be detected by a microphone
– extremely stable
– fast rise and fall times give a much truer representation of any change in CO2 - Raman scattering
– light passed through a gas sample causing reflective process
– incident light loses energy to the molecules of gas and is reflected at lower frequency
– magnitude of light frequency shift is specific to the gas and analysis of the reflected light allows identification of the gas
– rapid, with breath to breath analysis but bulky and heavy - Refractometry
– shining monochromatic light source through gaseous medium and focussing them on a screen
– pattern of light and dark bands appear, dependent on the medium’s refractive index and concentration
– difficult to use for breath-by-breath analysis
– used to calibrate vaporizer output and theatre and environmental exposure - Mass spectrometry
– sample gas drawn or injected into a low-pressure sample chamber that is attached to another chamber, at a pressure nearing that of a vacuum
– molecular leak pathway constructed between the chambers
– molecules ionised in second chamber and accelerated by a cathode plate
– fixed magnets or electro,agnets influence the ions and allow separation by the ion’s mass and charge
– ions are narrow-band filtered and detected by photo-voltatic receptors
– signal amplified and processes
– require powerful vacuum pumps and cannot return sample to patient
– response and delay times
– very accurate
Awake Craniotomy
Pre-operative
* appropriate patient selection
* anticonvulsant prophylaxis +/- dex (tumour surgery)
* well prepared patient + experienced staff
* as far craniotomy
Intra-operative
* LA + sedation or asleep-awake-asleep (LMA)
* routine monitoring as for craniotomy (BIS)
* ensure adequate sedation, analgesia, cardio-respiratory stability
* avoid hypercarbia, nausea and vomiting
* ensure awake, co-operative patient when required (TCI)
Post-operative
* as for craniotomy
* morphine at the end
Awake Tracheal Intubation
Indications
* suspected or known difficulty airway - reduced mouth opening, limited neck extension, OSA, morbid obesity, progressive airway compromise
* aspiration risk
* C-spine instability
Options
* FOI
* VL
* DL
* Blind nasal
Contraindications
* absolute - refusal despite careful discussion, lack of compliance
* relative - airway bleeding (+/- severe coagulopathy for nasal), operator inexperience, true LA intolerance, high risk for aspiration
Procedure
* Consent
* Preparation
– consider antisialogogue
– monitoring
– checklist
– ideally second anaesthetist for sedation
* Oxygenation
– apply HFNO early
– titrate HFNO from 30-70l/min
– continue HFNO throughout the procedure
* Topicalisation
– lidocaine 10% spray to oropharynx, tonsillar pillars, base of tongue (20-30 sprays during inspiration, over 5 minutes)
– co-phenelcaine to nose if nasal route
– test topicalisation atraumatically
– 2% lidocaine 2ml above, at and below vocal cords via MAD or epidural catheter
– max 9mg/kg lidocaine (lean body weight) for topicalisation
* Sedation
– remifentanil TCI Ce 1-3ng/ml
– midazolam 0.5-1mg
* Performance
– appropriate tracheal tube
– patient sitting up
– ensure operator can readily see patient monitor, infusion pumps and video screen
– clear secretions
– face patient for fibreoptic, behind patient for VL
– maximum 3+1 attempts
– two point check to confirm position of tracheal tube - visualisation of the tracheal lumen or tube through vocal cords + capnography
– timing of cuff inflation guided by relative risks of aspiration, patient movement, coughing and tracheal tube displacement
– induce anaesthesia
* Post intubation plan
– DAS guidelines for extubation
– NBM for at least 2hrs following airway topicalisation
– documentation
Blood Gas Analysis
- pH - pH electrode
– Ag/AgCl measuring electrode in KCl with H+ sensitive glass
– Ag/AgCl reference electrode
– blood sample passed by both electrodes
– difference in H+ concentration between blood sample and buffer solution generates an electromotive potential across the glass which is amplified and displayed - pCO2 - Severinghaus electrode
– CO2 diffuses across a CO2 permeable membrane in a bicarbonate solution
– dissociates to form H+ ions
– Ag/AgCl measuring electrode in buffer solution with H+ sensitive glass
– Ag/AgCl reference electrode in KCl
– difference in H+ concentration between the samples generates an electromotive potential across the glass which is amplified and displayed - pO2 - Clarke polarographic electrode
– Ag/AgCl anode
– platinum cathode
– KCl electrolyte solution
– oxygen diffuses into KCl through a semi-permeable membrane
– oxygen reacts with electrons in solution, generating voltage bewteen anode and cathode - HCO3 is calculated from the Henderson-Hasselbalch equation
- BE and O2 saturation derived
- Hb - absorption spectroscopy
Blood Pressure Measurement
Non Invasive + Intermittent
* Palpation
* Auscultation
* Oscillotonometric - von Recklinghausen
* Oscillometric - DINAMAP
– computer controlled inflation and deflation of cuff, looking for pulsations from the artery
– first oscillations = systolic BP
– cessation of oscillations = diastolic BP
– maximum oscillation amplitude = MAP
* Manual sphygmomanometer
– cuff (bladder ~80% of the circumference of the arm)
– compression of bronchial artery
– auscultation over brachial artery - Korotkoff sounds caused by turbulent flow
– sharp tapping (phase 1) = systolic pressure
– change from softer thump to softer, blowing, muffled sound (phase 3–>4) = diastolic pressure
Non Invasive + Continuous
* Finapres - Penaz technique
– small cuff partially occluding arterial supply to a finger with a LED and photodiode
– cuff changes in pressure to the keep the volume in the artery the same - this pressure change is proportional to the blood pressure
* Radial accelerometry
* Doppler USS
Invasive
* Arterial line
– cannula (short, wide) in artery connected to a transducer with a tube of fluid between them (short, wide, stiff tubing)
– saline keeps the cannula patent and flushes the line at ~3ml/hr
– transducer at the level of the patients heart creates an electrical signal from arterial pulsations
– monitor displays arterial trace
Overdamped signal - take a long time to respond to a step change –> squashed arterial trace
Underdamped signal - hyper resonant and overreads any changes in pressure
Optimal damping - rapid return to zero with a minimal (but present) overshoot
Brainstem Dead Organ Donor
- I+V, critical care area, confirmed dead by neurological criteria
Process
* Early recognition and referral
* Assessment of suitability
* Collaborative approach to family (explain 24-48hrs likely minimum time frame)
* Formal consent process + medical, social, travel history, discuss special requests
* Further patient assessment
* Blood testing - blood group, HLA typing, birology
* Liaise with coroner/ME if needed
* Register donor with ODT hub - matching process (ABO compatibility, HLA compatibility, waiting time, locations, matchability)
* Activate NORS team
* Organ retrieval and thorough documentation
* Post donation family support
Physiological Optimisation
* Assess fluid status and correct hypovolaemia with fluid boluses
* Introduce vasopressin infusion where required, wean noradrenaline/adrenaline
* Perform lung recruitment maneouvres to correct atelectasis
* Identify, arrest and reverse effects of DI
* Administer methylprednisolone
Use donor optimisation care bundle
* Airway - ensure cuff of ETT is appropriately inflated
* Breathing - lung protective ventilatory strategy, chest physio + suctioning, 30-45 degrees elevation, patient positioning, bronch +/- BAL?
* Circulation - monitor CO, vasopressin +/- dopamine rather than noradrenaline/adrenaline, correct hypovolaemia
* Fluids and metabolic - methylpred 15mg/kg, maintain Na <150mmol/L (IV crystalloid/NG water)
* Maintain UO 0.2-5ml/kg/hr (may need DDAVP)
* Insulin to maintain BM 4-10
* Continue NG feeding
* VTE prophylaxis - TEDS/Flowtrons/LMWH
* Lines and monitoring - left arterial, RIJ CVC, hrly obs, normothermia, 12-lead ECG, CVR +/- echo
* Review and stop all unnecessary meds
Capnography
IR absorption spectrophotometry
– light source passed through filter (of specific wavelength e.g. Co2 4.28micrometers) and then sample of gas, amount of light measured using a photo detector and converted to voltage and then to a visual display
– sample analyser lined in sapphire, as this does not absorb IR
– absorption of light is proportional to the amount of molecules present in the sample
– blockage of sample lines, water vapour absorbs infrared across a wide spectrum, N2O cdan cause problems with CO2 measurement (collision broadening effect)
Sidestream vs Mainstream
* Sidestream - 150-250ml/min of gas from patient end of circuit, added back in after analysis
– monitoring equipemnt on machine rather than patient
– larger analysers, able to measure more agents
– length of tube proportional to the delay between breath and capnograph response
* Mainstream - attached directly to the breathing circuit
– clips around a clear plastic window in the breathing circuit
– minimal delay in response
– typically only measure CO2 due to size and battery dependence
– usually small and portable
– can get hot
– can be unreliable due to water vapour problems
What can capnography tell us?
* presence of venous return (CO2 from tissues to heart)
* presence of pulmonary blood flow (CO2 from heart to lungs)
* presence of ventilation (effective movement of gas in and out of the lungs)
* confirmation of tracheal tube placement
* rate of ventilation
* quality of chest compressions (ETCO2 >2kPa with consistent waveform)
* ROSC during CPR
* guide to prognostication
* shape of trace
Normal Capnogram
* Phase 1 (inspiratory baseline) - inspired gas, normally devoid of CO2
* Phase 2 (expiratory upstroke) - transition between dead space and alveolar gas from respiratory bronchioles and alveoli
* Phase III (alveolar plateau) - end tidal at point just prior to inspiration
* Phase O (inspiratory downstroke) - the beginning of the next inspiration
* ETCO2 only represents alveolar CO2 when a relatively horizontal plateau phase is seen
CO2 Traces
* Low ETCO2
– decreased CO2 production - hypothermia
– pulmonary perfusion - reduced CO, hypotension, hypovolaemia, cardiac arrest, PE
– alveolar ventilation - hyperventilation, apnoea, total airway obstruction, extubation
– apparatus malfunctioning - circuit disconnection, leak sampling tube, ventilator malfunction, gas monitor zero
* High ETCO2
– increased CO2 production - sepsis, MH, endocrine causes, exogenous CO2, tourniquet release, sodium bicarbonate
– pulmonary perfusion - increased CO, increased BP
– alveolar ventilation - hypoventilation, bronchial intubation, partial airway obstruction, rebreathing
– apparatus malfunction - exhausted CO2 absorber, inadequate fresh gas flows, ventilator malfunction, leaks in ventilator tubing
* Sudden drop in ETCO2 to zero - kinked ET tube, defective analyser, total disconnection, ventilator defective
* Flat ETCO2 trace - ventilator disconnection, airway misplaced, capnograph not connected, respiratory/cardiac arrest, apnoea test, capnography obstruction
* Sudden change in baseline (not to zero) - calibration error, water drops/condensation, saturated CO2 absorber
* Sudden increase in ETCO2 - ROSC, correction of ETT obstruction
* Elevated inspiratory baseline - CO2 rebreathing, contamination, inspiratory valve malfunction
* Slanting and prolonged phase 2, increased slope of phase 3 - obstruction/COPD/bronchospasm
Cardiac Surgery (Off Pump)
Management is as for CABG but without bypass and using a “stabiliser” to keep the heart as still as possible e.g. Octopus
- keep well filled with crystalloid
- keep warm
- may need vasoconstrictor
- consider TOE/oesophageal Doppler
- may still required full/half dose heparin - aim ACT 250-300
- 1-10% may need bypass
- use depth of anaesthesia monitoring to avoid over-anaesthetising
- pace if bradycardic but void tachycardia
- maintain contractility
- correct U+E disturbance
Cardiac Surgery (On Pump)
Pre-operative
* careful pre-op assessment
* bloods, ECG, radiology
* cardiac investigations - TTE/TOE, catheter studies, cardiac MRI, digital subtraction angiography, angio
* euroscore risk calculation
* pre-med —> aim for relaxed, non tachy patient - benzo/morphine/hyoscine/O2
Intra-operative
* large bore IV and arterial access
* consider haemodynamic goals
* ensure lack of awareness
* benzo/opiate heavy induction + long acting NMBA
* CVC +/- PA sheath +/- TOE +/- NIRS +/- BIS
* phenylephrine
* TIVA/fent + isoflurane
* TXA 30mg/kg
* heparinisation + CPB —> propofol maintenance (ACT aim 4x baseline >480s)
* support CVS/RS, reverse coagulation post CPB
Post-operative
* cardiac ITU management
* extubate once warm, awake, weaned and not bleeding
Cardioplegia
Used for myocardial protection and facilitation of surgery requiring a still heart.
Features:
- Potassium 20mmol/L
inactivates fast inward Na channels
prevents upstroke of the myocyte action potential
diastolic arrest with an unexcitable myocardium - Mannitol - to make solution slightly hyperosmolar to limit tissue oedema
- Bicarbonate or histidine to offset acidosis from tissue ischaemia
- Calcium (at a lower than normal plasma level) to maintain cell membrane integrity while avoiding myocardial activity
- Magnesium to prevent loss of magnesium from cells and stabilise the myocardial membrane
- Procaine to decrease excitability at reperfusion
- Glutamate/aspartate to promote oxidative metabolism in energy-depleted hearts
Carotid Endarterectomy
Pre-operative
* usually high risk patients
* check normal blood pressure (to target intra-op)
* assess and document neurology
* continue anti-hypertensives (not ACEI/ARB), beta blockers + statins, anti-platelets can continue
Intra-operative
* GA vs regional (superficial/intermediate/deep cervical plexus blocks)
* consider invasive haemodynamic monitoring
* augment arterial pressure as required within 20% of baseline
* consider pre-med if GA
* 2x IV access + ETT
* consider cerebral monitoring techniques
Post-operative
* monitor neurology
* airway oedema is common
* control BP (risk of hyperperfusion)
Cataract Surgery
Pre-operative
* often elderly
* co-morbidities and anti-coagulants
Intra-operative
* positioning - head horizontal
* monitoring
* cannula?
* topical, blocks, GA (LD, kids, dementia)
Post-operative
* typically day case
Categorising Mechanical Ventilation
Primary ventilator target during inspiration
* pressure (pressure generator)
* flow/volume (flow generator) - constant flow, decelerating profile
* dual mode - tidal volume guarantee with advantages of pressure control
What starts inspiration?
* time cycled - RR, I:E ratio, insp/exp time
* patient triggered - pressure trigger or flow trigger
* mixture
What ends inspiration?
* time
* drop in flow (pressure control)
Cerebral Monitoring
- Monitoring ICP
— intraventricular - catheter inserted into lateral ventricle via a burr hole (also allows drainage), risk of haemorrhage and infection, insertion may be challenging
— intraparenchymal - most commonly used - micro-miniature silicone strain gauge monitor inserted into the brain parenchyma, accurate and relatively easy to insert
— subdural/subarachnoid - Monitoring cerebral oxygenation
— jugular venous oxygen saturation
— NIRS
— direct brain tissue oxygenation - Monitoring CBF
— transcranial Doppler/colour coded duplex
— radiological imaging e.g. CT perfusion, xenon enhanced CT, perfusion weighted MRI, nuclear medicine methods (PET/SPECT) - Monitoring cerebral metabolism
— microdialysis
ICP waveforms - 4 kinds
* Normal - systolic upstroke, diastolic downstroke with a dichrotic notch
* A waves - plateau waves - steep increases in ICP lasting 5-10 minutes, always pathological, indicative of early brain herniation
* B waves - oscillations of ICP 0.5-2 waves per minute - associated with unstable ICP, possible due to cerebral vasospasm
* C waves - oscillations that occur 4-8 waves per minute - likely reflection of cardiac and respiratory cycles
Circle system
Benefits
* preserves anaesthetic gases making volatile anaesthesia cost-effective
* preserves medical gases (oxygen) which is useful in reousrce-limited settings
* preserves heat and moisture
* reduces fire risk
Closed-circuit system
* requires re-breathing of expired gases
* CO2 is actively removed
* only gases which must be replaced are those consumed by the patient or lost via leak
Components
* Y piece connecting the circuit to the patient
* Expiratory and inspiratory valves - ensuring unidirectional flow
* A means of generating pressure - ventilator and reservoir bag with APL valve (typically placed on expiratory limb)
* Soda lime to absorb CO2 (NaOH + Ca(OH)2 + H2O)
* Fresh gas flow
* Separate high pressure high flow oxygen flush which bypasses the vapouriser
Complications of Epidurals
- 1:8 inadequate
- 1:20 GA required for section
- 1:50 hypotension
- 1:100 PDPH (1:500 for spinal)
- 1:1000 nerve damage
- 1:13000 nerve damage lasting more than 12 months
- 1:50000 epidural abscess
- 1:100000 epidural haematoma
- 1:100000 meningitis
- 1:250000 severe injury including paralysis
Consent for Regional Anaesthesia
Contraindications:
Absolute
* patient refusal
* sepsis at injection site
* allergy to LA agents
Relative
* coagulopathy
* pre-existing neuropathy
* systemic infection
* altered anatomy
Specific blocks
* SCB - severe respiratory disease
* ICB - contralateral phrenic/recurrent laryngeal nerve palsy, pneumothorax or pneumonectomy, severe respiratory disease, bilateral blocks
Benefits:
* Reduction in acute pain, PONV, delirium, CPSP, stress response, cost, post-operative morbidity
* Possible reduction in cancer recurrence
* Avoidance of GA and it’s associated risks
* Improved sleep, surgical function (e.g. AV fistula), patient satisfaction
Risks/Complications:
* Failure of block
* LA toxicity
* Infection
* Haematoma
* Temporary nerve damage <1:10
* Permanent nerve damage 1:2-5000
* Effects of block
* - risk of injury while anaesthetised
* - block specific effects
* – arterial puncture
* – pneumothorax
* – Horner’s Syndrome
* – Phrenic nerve palsy
* – Recurrent laryngeal nerve palsy
* – Autonomic blockade
Depth of Anaesthesia Monitoring
Non specific
- clinical signs
- CVS parameters
- agent monitoring (end tidal volatile)
Specific
- HR/ECG variability
- lower oesophageal sphincter contractility
- isolated forearm technique
- BIS/entropy/processed EEG
- Auditory evoked potentials
- Skin conductance
Detecting Venous Air Embolism
- ETCO2 - causes sudden drop
- Precordial Doppler - most sensitive non invasive monitor but limited by positioning, interference from diathermy and not quantitative
- TOE - more sensitive but invasive, placement and interpretation difficult
- PA catheter - invasive but sensitive, not specific for air, not routinely used
- Precordial/oesophageal stethoscope - least sensitive - “Mill Wheel Murmur” only apparent after massive venous air embolism
ECT
Induction of a generalised, tonic-clonic seizure
Indications
* severe medication-resistant depression
* mania
* catatonia
Contraindications
* raised ICP
* recent CVA
* untreated cerebral aneurysm
* MI or uncontrolled cardiac failure
* unstable major fracture
* severe osteoporosis
* DVT until anticoagulated
* phaeochromocytoma
* retinal detachment or glaucoma
* cochlear impants
Challenges
* remote site - must have appropraite resuscitation equipment and drugs, and meet standards for monitoring, trained assestance and recovery facilities
* elderly patients
* significant co-morbidities - discussion about whether anaesthesia should take place somewhere else
* patients can be poor historians
* consent
* seizure threshold with anaesthetic agents
Involves:
* Electrical current applied transcutaneously to the brain, via two electrodes positioned bilasterally or unilaterally.
* Bilateral ECT more common
* Unilateral ECT over the non-dominant hemisphere minimises cognitive adverse effects
* Overall aim is to induce a generalised seizure with characteristic EEG changes (>10s, <120s)
* Typically performed twice weekly until there is a lack of further improvement
Pre-operative
* Full pre-op assessment
* Check for reflux or and contraindication
* Clarify current medications
* Physical examination for evidence of cardiac failure, severe valvular disease, dysrhythmia, uncontrolled hypertension, poor dentition or dehydration requiring fluid therapy
* Blood tests, ECG + other investigations as indicated
* Time to optimize balanced against urgency of ECT
Intra-operative
* Consent
* Fasting
* Continue regular medications
* Avoid pre-medication
* Empty bladder prior to anaesthesia
* Pre-oxygenation
* Induction - methohexital 0.5-1.5mg/kg (gold standard - minimal anticonvulsant properties), propofol, etomidate
* NMBA - decrease the risk of severe injury - sux most commonly used
* Airway management - FM, bite block
* Gentle hand ventilation until breathing resumes
Post-operative
* Standard monitoring and oxygen supplementation
* Risk of emergence agitation - secluded, calm recovery environment, small doses of midazolam