FRCA Notes


Paediatric TIVA



Patient Surgical Procedural
Malignant hyperpyrexia risk Airway surgery Remote-site anaesthesia e.g. MRI
History of PONV Shared airway procedures Muscle biopsy for neuromuscular diagnosis
Prior emergence delirium Neurosurgery Patient transfer
History or suspicion of reactive airway e.g. URTI Middle ear surgery
Fear of facemask/gas induction not possible High-risk PONV
Muscular dystrophy Neurophysiological monitoring



Advantages Disadvantages
↓ airway reactivity & risk of laryngospasm/stridor Pain on injection
Does not rely on the airway for anaesthetic delivery Risk of PRIS
↓ risk of ambient pollution Need for IV access
Improved ciliary function Need for specialised infusion pumps
Preserved hypoxic pulmonary vasoconstriction Risk of bacterial contamination
↓ PONV Environmental waste (plastic, propofol)
↓ emergence delirium No point-of-care propofol measurement system/reliance on pEEG
No interference with neurophysiological monitoring Caution in obese due to accumulation
Overall ↓ costs Disposables may be costly


  • There is pharmacokinetic and pharmacodynamic variability between different ages of paediatric patient owing to the effect of maturation on propofol metabolism
  • In neonates, ex-prem infants and the critically ill propofol TIVA should be used with caution owing to extremely variable propofol pharmacokinetics and non-linear changes in both VD and propofol clearance

Pharmacokinetic changes with age

  • Larger central compartment and volume of distribution in infants, which decrease to adult levels over time
  • There is greater clearance (peak at 1yr of age), which also decreases over time
  • This necessitates a higher bolus dose and maintenance rates in younger populations
  • In the obese, propofol induction doses are proportional to lean body mass but maintenance doses are linked to total body weight
  • The context-sensitive half-life in children is longer than in adults:
    • 10.4min after 1hr of infusion (6.7min in adults)
    • 19.6min after 4hrs of infusion (9.5min in adults)

Propofol manual models

  • Steur regimen, for those <3yrs old
  • McFarlane regimen for 3-11yr olds

  • Both regimens target a plasma propofol concentration (Cp) of 3mcg/ml, which may be inadequate to provide suitable depth of anaesthesia in a paediatric population without adjuncts or additional 1mg/kg boluses of propofol

Propofol pharmacokinetic models

  • Paedfusor
    • Age range 1 - 16yrs
    • Weight range 5 - 61kg

  • Kataria
    • Age range 3 - 16yrs
    • Weight range 15 - 61kg
  • Paedfusor and Kataria models use plasma concentration targeting (Cpt), therefore should allow adequate equilibration between Cp and Ce before up/down-titrating

  • Eleveld
    • Modelling excluded obese children
    • Effect-site targeting (Cet) possible

Remifentanil models

  • Minto
    • Minimum age 12yrs
    • Minimum weight 30kg
    • Also uses height as a covariate
    • Largely impractical in the bulk of paediatric cases

  • Eleveld

Safety

  • Ensure safety precautions are in place as in adult TIVA
    • 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

Performance

  • Use lidocaine to avoid pain on induction
  • In general, a propofol concentration of approximately 4.5μg/ml gives a BIS of roughly 50
  • May need higher (e.g. 5 or 6μg/ml) if propofol is the sole agent used, or lower (~3μg/ml) if adjuncts are used

  • Remifentanil is usually titrated to an equivalent 0.05 - 0.3μg/kg/min dose
    • 0.1 - 0.2μg/kg/min might suffice for mild pain
    • 0.3 - 0.4μg/kg/min for moderate or severe pain