FRCA Notes


Total Intravenous Anaesthesia

The curriculum is a bit vague on TIVA, asking for 'advantages and disadvantages' of the technique, correct set up of TCI for induction/maintenance and use in middle ear surgery.

The 2018 SAQ on TIVA (70% pass rate) saw examiners mostly critique candidates' handwriting, as well as lament a lack of knowledge of TCI systems.

Resources


  • Total IV anaesthesia (TIVA) is the provision of anaesthesia by IV infusions alone, typically sedative-hypnotic ± an analgesic
  • The IV agent is given either manually, as a 'simple' infusion or by an infusion device programmed with the pharmacokinetic models

Physical Pharmacokinetic Pharmacodynamic
Cheap Obeys a pharmacokinetic model Painless on injection
Stable/non-reactive Predictable relationship between plasma concentration and effec Analgesic | muscle relaxant | anti-emetic properties
Long shelf life No active metabolites No hypersensitivity reactions
Environmentally friendly Rapid onset & offset No toxic effects
  • Current drugs used include:
    • Propofol; either as a ml/hr infusion (e.g. ICU) or according to models such as Bristol, Schnider, Marsh or Eleveld
    • Remifentanil; Minto or Eleveld models
    • Alfentanil; Maitre model
    • Ketamine; Domino model

    • Other drugs are used on intensive care units to facilitate a form of TIVA in critically unwell patients e.g. fentanyl, midazolam, morphine but often as simple ml/hr infusions

Indications

Volatile contraindicated Volatile impractical Volatile or NMBA undesirable
Malignant hyperpyrexia Tubeless head & neck surgery Anticipated difficult airway (possibility of intermittent delivery)
Severe PONV Surgery requiring neurophysiological monitoring Neurosurgery where ↑ CBF is to be avoided
Some long-QT syndromes (QT >500ms) Non-theatre environment e.g. ICU, during transfer Associated with better survival after cancer surgery
Some neurological conditions Day surgery to reduce PONV risk

Disadvantages

  • No 'point of delivery' measure of the target concentration (e.g. no end-tidal inhalational agent equivalent)
  • Requires specialised pumps
  • Potential for propofol infusion syndrome
  • May cause greater haemodynamic instability or cardiac dysfunction, including bradycardias
  • AAGBI guidelines state must use depth of anaesthesia monitoring if using TIVA + NMBA, but some surgeries make using BIS impossible/invalid
  • Risk of awareness
  • Risk of delivery failure if poor or difficult venous access
  • Actual blood level of drug may be different to calculated plasma concentration; generally within 25% but still requires titration
  • Contraindicated in those with mitochondrial disease

  • Target controlled infusions (TCI) use micro-processor controlled infusion pumps pre-programmed according to a pharmacokinetic model for a given drug e.g. propofol's 3-compartment model
  • They allow selection of a target site concentration required for a certain effect (sedation, anaesthesia)
  • TCI pumps have other advantages such as providing a decrement time
  • Loss of consciousness typically occurs at a Ce of 1μg/ml although naturally this has inter-patient variability

Bristol

  • This is actually a manual TIVA model which targets a blood concentration of 3μg/ml within 2mins
  • It is based on patients who received temazepam pre-medication, 3μg/kg fentanyl and 1mg/kg propofol induction
  • One the provides a variable rate propofol infusion:
    • 10mg/kg/hr for 10mins
    • 8mg/kg/hr for 8mins
    • 6mg/kg/hr thereafter
  • Compared to the target controlled infusions below, it tends to use more propofol with consequent greater haemodynamic effects and a slower wake-up

Schnider TCI

  • 1998 model based on a study of 24 patients
  • Uses weight, age, height and gender
  • Allows plasma- and effect-site concentration targeting
  • Tends to underestimate plasma propofol level during the recovery phase

Marsh TCI

  • 1991 model based on data from the 1987 Gepts study (18 patients)
  • A 'linear' model based purely on weight (lean body mass), although not suitable for those <16yrs old so also asks for the patient's age.
  • Delivers a much large initial propofol bolus than Schnider due to a large central compartment size in the model
  • The standard Marsh model only allows plasma-site targeting although the modified Marsh model allows effect-site targeting

Eleveld TCI


  • The synergy between propofol and opioid TCI can provide both highly effective surgical anaesthesia and a propofol-sparing effect

Remifentanil

  • Remifentanil is an ultra-short acting synthetic opioid commonly used as a TCI alongside propofol
  • Available models: Minto, Eleveld
  • Its context-insensitive half-time make it a popular choice for TCI, as well as its synergy with propofol
  • Its short-acting nature necessitate the use of additional opioids towards the end of a case, while concerns remain over remifentanil-induced hyperalgesia

Alfentanil

  • Alfentanil is another short-acting synthetic opioid which became more popular as a choice for TCI during periods of remifentanil shortages
  • Available models:
    1. Maitre: weight, age, and sex covariates
    2. Scott: no covariates so the same dose is infused regardless of demographics

  • It benefits from having synergy with propofol, as well as a low lipid solubility reducing the rate of accumulation compared to fentanyl
  • Similar time to onset of effect as remifentanil, but longer offset when used as a TCI (BJA, 2022)
  • Although its context-sensitive half-time is predictable, it does rise to reach a CSHT of 1hr after 8hrs infusion
    • This is longer than propofol's CHST, therefore may require down-titrating towards the end of surgery

  • In some cases, 1-2mg of alfentanil are mixed with propofol in a single syringe, which is then used as a propofol TCI (a.k.a 'dirty TIVA')

Sufentanil

  • Sufentanil is a potent synthetic opioid which can be used as a TCI
  • Available models: Gepts

  • It benefits from a shorter CSHT than alfentanil, but still requires down-titration at the end of the case

Fentanyl

  • TCI models (McClain, Shafer) for fentanyl are not commercially available, so if an infusion is desired a manual regimen is required
  • An example manual regimen is:
    • 3μg/kg bolus
    • 2μg/kg/hr infusion for 30mins
    • 1.5μg/kg/hr infusion for the next 120mins
    • 1μg/kg/hr infusion thereafter
    • Infusion stopped 30mins before skin closure
  • The CSHT of fentanyl rises rapidly after 1hr, making it a poor choice for TCI unless rapid emergence is not required
  • Its longer duration may make it suitable if significant post-operative pain is anticipated

  • Other, non-opioid adjuncts may be used alongside propofol TIVA to provide both multi-modal analgesia and a propofol-sparing effect
Drug Regimen Reduction in propofol requirements
Dexmedetomidine 1μg/kg loading over 5-10mins
0.2 - 0.7μg/kg/hr infusion
20-50%
Ketamine 0.1 - 1mg/kg loading
0.1 - 0.2mg/kg/hr infusion
20-40%
Magnesium 20 - 50mg/kg loading over 20mins
6 - 20mg/kg/hr infusion
15-20%
Lidocaine 1 - 1.5mg/kg loading
1 - 2mg/kg/hr infusion
10-20%


  • If total body weight is used in the models then a greater induction dose will be delivered
  • Equally a higher-than-normal infusion rate will be delivered

  • Following NAP5, it was suggested using total body weight is probably better than ideal or lean body weight to reduce the risk of accidental awareness
  • SOBA say that one should use lean body weight for induction but then total body weight or ABW40 for maintenance

Model issues with high BMI

  • Marsh
    • A body weight of up to 150kg is allowed
    • However, entering actual body weight may lead to a significant overdose due to the linear nature of the model
    • Anecdotally, there is concern using lean body weight may conversely cause underdosing, and ABW40 is often used instead

  • Schnider
    • Calculates LBW as part of the model
    • Paradoxically smaller initial bolus dose when BMI exceeds 42kg/m2 (men) or 35kg/m2 (women)
    • Requires the use of 'fudge factors' e.g.
      • Increasing patient height until an allowable actual body weight can be put in
      • Use Servin's formula; input weight as IBW + 0.4(actual - ideal BW)

  • Minto
    • TBW probably better than LBW/IBW
    • However the pump won't allow extremely high BMI to be entered
    • Often the correct (total) weight is entered but a fudged height is used to bypass this

Alarms

  • High infusion pressure alarm
  • Low infusion pressure alarm
  • End-of-infusion warning (5mins)
  • End-of-infusion alarm
  • Disengagement of driver warning
  • Low battery or mains disconnection warning
  • Occlusion alarm

Syringe drivers

  • Displays drug and concentration on-screen to reduce risk of wrong-drug infusion
  • Confirms syringe driver and type to ensure correct rate of infusion
  • Syringe driver service record alerts to aid regular maintenance

  • Use a TCI system checklist
  • Regular TCI pump maintenance

  • Cannula-related factors:
    • Affixed firmly to patient's skin
    • Use anaesthetist-inserted cannula rather one from the ward
    • Visible so that disconnection, leakage or 'tissued' cannula are readily detected
    • Check infusion site if pump alarms
    • Routine checking of cannula during long cases

  • Syringe- and line-related
    • Only use Luer lock syringes
    • Standard order of syringes in the pumps (to prevent erroneous up- or down-titration of the incorrect agent)
    • Remifentanil syringe only labelled after drug added
    • Anti-siphon valve on drug lines
    • Non-return valve on IV fluid line
    • Minimal dead space distal to agent mixing