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 |
Paediatric TIVA
Paediatric TIVA
The curriculum asks for knowledge of the 'maintenance of anaesthesia for children aged 1 year and above', which I suppose includes TIVA.
Resources
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