2018A Question 06
Describe the washout (not offset) of sevoflurane from a patient following two hours of general anaesthesia. You may wish to use a graph to illustrate the description.
Examiner Report
54% of candidates achieved a pass in this question.
To achieve a pass in this question the following were required :
- A clear explanation of the elimination kinetics of Sevoflurane with due consideration to a time course appropriate to the termination of anaesthesia after two hours
- A washout graph including appropriate axis labelling, a multi exponential decay curve, time course and half times consistent with volatile washout
It was very difficult to pass the question without a washout graph. Wash-in graphs did not score points. - A description of the movement of Sevoflurane out of the alveolus, from plasma to alveolus, from the various compartments to plasma and their respective time courses and a description of factors which underpin those kinetics; including depth and duration of anaesthesia, alveolar ventilation and fresh gas flows, compartmental blood flows and solubilities
Common errors included:
- Confused graphs with no or inappropriate time courses indicated, nonsensical axis labelling or graphing of wash-in and wash-out on the same graph
- Detailed descriptions of Fick’s Law which wasted time and did not score points
- An overemphasis on the role of cardiac output in washout and incorrect assertions that increased cardiac output speeds washout
- Conflation of washout and awakening from anaesthetic as the same thing
- The incorrect assertion that following two hours the fat is completely saturated with Sevoflurane
- The confusion of partial pressures, concentrations and amounts
Model Answer
Structure:
- Emergence modeling
- Final end-tidal partial pressure
- Elimination from V1
Emergence Modeling
Washout time is a function of:
- Final partial pressure in effect site prior to washout
- Rate of elimination from V1
Compartment saturation at two hours:
Compartment | τ | Capacity | Saturation |
---|---|---|---|
V1 | 5.7 mins | Low | ~100% |
V2 | 2.3 hours | Moderate | ~50% |
V5 | 1.8 days | High | Minimal |
- Equilibration time constants:
- τ= 1/k
- τ= (V x λ) / Q
- Where: (V = volume of tissue, λ = tissue: Blood partition coefficient, Q = blood flow)
Final Effect-Site Partial Pressure
Effect site partial pressure:
- Correlates with that in V1
- May not be included in all kinetic models
- Rate of equilibration between effect site and V1 is:
- CBF (per unit mass, not percentage CO to brain)
Factor | Partial pressure decreased with: |
---|---|
Infusion | - ↓ Duration - ↓ Inspired % |
Drug | - ↑ Tissue:blood partition coefficients - ↑ Muscle:blood PC (sevo 3.1, des 2.0, iso 2.9) - ↑ Fat:blood PC (sevo 48, de+s 27, iso 45) - ↓ MAC (iso 1.2%, sevo 2%, des 6.6%) - Correlates with ↓ oil:gas PC (sevo 80, des 29, iso 98) - ↑ Metabolism |
Patient | - ↑ Cardiac output - ↑ Tissue volumes |
Elimination from V1
Factor | Elimination accelerated with: |
---|---|
Short case | Offset during distribution phase: - ↑ Cardiac output - ↑ Tissue:blood PC - ↑ Compartment volumes |
Long case | Offset during terminal elimination phase: (note bivalent factors!) - ↓ Cardiac output - ↓ Tissue:blood PC - ↓ Compartment volumes - ↑ Metabolism - ↑ Excretion: - ↑ Ratio VA:FRC (?Most important) - ↑ Ratio FGF rate : Circuit volume - ↓ Inspired % |