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LOW FLOW ANAESTHESIA
Dr Ravi Wadke
Dr Shreyas Kate
Introduction
• Reusing anaesthetic agents in exhaled gases.
• Environmental pollution.
• Breakthroughs:-
– Modern anaesthetic machines
– Gas analyser monitors
– Precision vapourisers
– Potent volatile agents
History
• Snow- exhaled gases re-inspired-prolong
narcotic effect.
• Waters-1924- To and fro absorption system-
avoid CO2 rebreathing.
• Brian Sword- 1930- Circle breathing system
with sodalime absorber-closed circuit
anaesthesia.
• Cyclopropane-1933- minimise excessive
overflow-risk of explosion.
Circle breathing system
History
• Halothane-1954- highly potent volatile
anesthetic agents with narrow therapeutic
indices.
• High fresh gas flows-negligible rebreathing-
semi closed use of rebreathing systems-
common practice.
• Virtue-1974- Minimal flow anaesthesia
techniques.
History
• Aldrete et al., Lowe , Ernst – 1980- Revive low
flow and closed system anaesthesia.
• Logan, Farmer 1989- Environmental hazards-
anaesthetic agents.
• Modern volatile anaesthetic - partially
substituted halogenated hydrocarbons &
nitrous oxide-
– Depletion of stratospheric ozone layer
– Greenhouse effect
History
• Kleeman 1990- improving heat and humidity
of rebreathed anaesthetic gases- preserving
functional and anatomical integrity of
epithelial cells in respiratory tract.
• Baum and Aitkenhead-1995- Economic and
environmental advantage.
Concept
• Administer FG mixture + composition of
anaesthetic gases.
• Uptake of agents in body-physical
characteristics of agent.
• Exhaled gas mixture- different composition-
uptake of agents & addition CO2.
• Low flow Anesthesia- replenish consumed
gases with as minimum FG as possible &
remove CO2 before recirculating.
Concept
• Challenge- control dynamic equilibrium of FG
composition
– Uptake & metabolism time sensitive
– Many factors influence consumption & production of
gaseous components
• Frequent adjustments gas flow controls
• Complex equations –estimate uptake
• Monitoring inspired and end tidal concentrations
using gas analyser –more accurate and
convenient.
Definition
• Any technique that employs FG flow less than the
alveolar ventilation –Low flow anaesthesia.
• Inhalation anesthetic technique –rebreathing
fraction at least amounts to 50% where at least
50% of exhaled gas mixture is returned to patient
after CO2 removal in next inspiration.
• Modern anaesthetic machine FGF reduced to
2L/min or less.
Advantages
Requirements for use of Low Flow
technique
• Flow meters calibrated to flows down to
50ml/min.
• Leak proof circle breathing system and airway
devices like cuffed ETT (Well fitting supraglottic
airway device can be used).
• Gas monitoring system –inspired and end tidal
concentrations of agents.
• Measurement of expiratory gas concentrations
closer to Y piece crucial (reflects pts alveolar gas
concentration).
Requirements for use of Low Flow
technique
• Vapourisers capable of delivering high
concentrations and calibrated accurate at low
FGF.
• Breathing system with minimal internal
volume to minimise reserve volume.
LFA not suitable
• Short term anaesthesia with FM.
• Procedures with imperfectly gas –tight airways
(i.e. bronchoscopies with rigid bronchoscope).
• Technically unsatisfactory equipment with a
high gas leakage, unsuitable for leak free
closed breathing systems.
• Inadequate monitoring (malfunction of gas
analyser).
LFA not suitable
• Situations –clinical issues like hemodynamic
instability.
• Anaesthesiologist not familiar with LFA.
Concerns
• Dilution of anaesthetic agents-
– Low FGF added to significant large reserve volume
– Rate of change of composition of gas in reserve
volume exponential
– time constant (RV/FGF)
– 3 time constants- to effect 95% change in gas
composition
– Steady state- LFA most economical use of
anaesthetic agents
Concerns
• Differential uptake of agents modifying
composition of gas mixture
– N2O carrier gas
– Uptake high initially followed by gross reduction in
uptake
– Change in trend in differential uptake –hypoxic
mixtures delivered
Concerns
• Ensuring enough oxygen for metabolism
– Wide range of variations in the gas composition is
possible while reducing the FG flow
– Pulse oximeter less sensitive surrogate monitor of
tissue oxygenation
– Oxygen analyser
– Lower limit FiO2 0.30
Concerns
• Delay in recovery from anaesthesia
– Long time constant –slow reduction in
concentration of volatile anaesthetic agents –
recovery phase
– Change over to high FGF – to reduce time constant
– Switch off vapourisers early
– Some machines- special charcoal filter
Disadvantages
• Low flow rate & long time constant- slower
induction and emergence
• Quick alteration of inspired concentrations not
possible
• Continuous vigilance and frequent flow
adjustments
– avoid hypoxic mixtures
– Under/over dosage anaesthetic agents
Disadvantages
• Higher consumption of CO2 absorbents
– frequent exhaustion of absorbers
– CO2 rebreathing
– Risk of hypercarbia
• Possible accumulation of undesirable trace
gases in system
– CO, Acetone, Methane, Hydrogen, Ethanol,
Compound A- haloalkene
– Flush high FGF once an hour
Disadvantages
• US FDA recommendations limit Sevoflurane
exposure to 2MAC hrs at flow rates 1 to <2
l/min of FGF rates
• FGF rates <1 l/min not recommended
Calculation of gas update
• Total gas uptake =sum of uptakes of O2+N2O
+Anaesthetic agents.
Use of N2O in LFA
LFA in paediatric population
• Concerns
– Leaks –use of uncuffed ETT
– Additional monitoring & breathing valves in circuit
adding to dead spaces & resistance to breathing
circuit
• Airway sealing uncuffed ETT or LMA sufficient to
perform LFA.
• Frink et al.-low concentrations compound A
measured in children during sevoflurane
anaesthesia -2l/min FGF.
• Younger the child, lower the concentrations of
Compound A.
• Practical & safe.
Conducting LFA
• Premedication, preoxygenation and induction
–as usual practice.
• Initiation-
– Objective-To achieve alveolar concentration of
anaesthetic agent adequate for producing surgical
anaesthesia.
Conducting LFA- Initiation
• Use of high flows during initial phase
– Time constant reduced, bringing the circuit
concentration to the desired concentration rapidly
– FGF 10L of desired gas concentration and 2 MAC
agent concentration
– 3min-3Time constant- circuit brought to desired
concentration
– Better denitrogenation
– Rapid achievement of desired concentration
– Counterbalancing large uptake encountered at the
start of anaesthesia
Conducting LFA- Initiation
• Use of prefilled circuit
– Use different circuit like magill’s for
preoxygenation
– Simultaneously circle system fitted with test lung
& circuit filled with gas mixture of desired
concentrations
– After tracheal intubation patient connected to
circle system
– Rapid achievement of the desired concentration in
circuit
Conducting LFA- Initiation
• Injection of volatile agent into the breathing
circuit
– Usual requirement of anaesthetic agent -400-500ml of
vapours in first 10 min( 40-50 ml/min)
– At 20degree C 1ml Isoflurane yields 196ml
– About 2 ml liquid agent injected in small increments
into expiratory limb of circuit
– Intermittent injections 0.2-0.5 ml aliquots manually
– Alternatively, continuous infusion –added advantage
doing away with peaks and troughs of intermittent
injections
Conducting LFA- Initiation
• Accurate dose requirement formulae
• Priming dose (ml vapour)=
Desired concentration*
([FRC+Circuit volume]+
[Cardiac output*blood gas coefficient])
Conducting LFA-Maintenance
• Maintain steady state concentration of
anaesthetic agents.
• Oxygen uptake constant- 200-250 ml/min
• Uptake of anaesthesia agents minimal
• Oxygen analyser- maintain O2 concentration at
least 30% at all times.
• Return sampling gas(200ml/min) back to circuit
to boost economy of FGF utilisation.
• Plenum vapourisers under delivers agent at low
flows-achievement of desired end tidal agent
concentration accurate- agent analyser or
haemodynamic stability.
Conducting LFA-Maintenance
Termination LFA
• Long time constants-recovery delayed
– Switch over to HFGF-wash out agent
– Use of activated charcoal to remove potent
vapours by absorption-rapid recovery
– N2O washed off- change over to 100% O2
Automated LFA
• Uses proprietary software algorithm to
determine agent and carrier gas administration to
attain targets with lowest surplus.
• ALFA machines-
– ZEUS-Drager Lubeck Germany- Closed circuit
– AISYS- GE Madison Wisconsin- minimal flow
(500ml/min FGF)
– FLOW-i –Maquet Solna Sweden
• Anaesthesiologist selects
– Target alveolar concentration(FAt) of inhaled
anesthetic
– Target O2%
• Either inspired –FiO2 ZEUS
• Or end expired –FaO2 AISYS
LFA for sustainable Anaesthesia
• Environmental stewardship as a prime priority.
• We decide FGF-directly responsible for
environmental impact of anaesthetic vapours
and gases.
• Average working day each anaesthesiologist
administering N2O or Desflurane contribute to
CO2 equivalent of more than 1000 km car
driving.
LFA for sustainable Anaesthesia
• Research underway to collect and resuse
anaesthetic gases.
• Zeolite filters –Deltasorb –Canada –
commercial use- scavenging system of
anaesthesia machine to adsorb anaesthetic.
• Later retrieving and purifying agents for reuse.
Summary
• Smooth and practical conduct of LFA
– Safety features of anaesthetic machines
– Accurate gas monitoring- gas analysers – FiO2, ETCO2,
agent monitoring
• Clinical application of LFA is simplified by
availability of reliable guidelines for safe
performance in routine clinical practice.
• Anaesthesiologist should take up LFA as
professional obligation to environment and
present and future generations.
Reference
•Thank You

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Low flow anesthesia

  • 1. LOW FLOW ANAESTHESIA Dr Ravi Wadke Dr Shreyas Kate
  • 2. Introduction • Reusing anaesthetic agents in exhaled gases. • Environmental pollution. • Breakthroughs:- – Modern anaesthetic machines – Gas analyser monitors – Precision vapourisers – Potent volatile agents
  • 3. History • Snow- exhaled gases re-inspired-prolong narcotic effect. • Waters-1924- To and fro absorption system- avoid CO2 rebreathing. • Brian Sword- 1930- Circle breathing system with sodalime absorber-closed circuit anaesthesia. • Cyclopropane-1933- minimise excessive overflow-risk of explosion.
  • 5. History • Halothane-1954- highly potent volatile anesthetic agents with narrow therapeutic indices. • High fresh gas flows-negligible rebreathing- semi closed use of rebreathing systems- common practice. • Virtue-1974- Minimal flow anaesthesia techniques.
  • 6. History • Aldrete et al., Lowe , Ernst – 1980- Revive low flow and closed system anaesthesia. • Logan, Farmer 1989- Environmental hazards- anaesthetic agents. • Modern volatile anaesthetic - partially substituted halogenated hydrocarbons & nitrous oxide- – Depletion of stratospheric ozone layer – Greenhouse effect
  • 7. History • Kleeman 1990- improving heat and humidity of rebreathed anaesthetic gases- preserving functional and anatomical integrity of epithelial cells in respiratory tract. • Baum and Aitkenhead-1995- Economic and environmental advantage.
  • 8. Concept • Administer FG mixture + composition of anaesthetic gases. • Uptake of agents in body-physical characteristics of agent. • Exhaled gas mixture- different composition- uptake of agents & addition CO2. • Low flow Anesthesia- replenish consumed gases with as minimum FG as possible & remove CO2 before recirculating.
  • 9. Concept • Challenge- control dynamic equilibrium of FG composition – Uptake & metabolism time sensitive – Many factors influence consumption & production of gaseous components • Frequent adjustments gas flow controls • Complex equations –estimate uptake • Monitoring inspired and end tidal concentrations using gas analyser –more accurate and convenient.
  • 10. Definition • Any technique that employs FG flow less than the alveolar ventilation –Low flow anaesthesia. • Inhalation anesthetic technique –rebreathing fraction at least amounts to 50% where at least 50% of exhaled gas mixture is returned to patient after CO2 removal in next inspiration. • Modern anaesthetic machine FGF reduced to 2L/min or less.
  • 11.
  • 13. Requirements for use of Low Flow technique • Flow meters calibrated to flows down to 50ml/min. • Leak proof circle breathing system and airway devices like cuffed ETT (Well fitting supraglottic airway device can be used). • Gas monitoring system –inspired and end tidal concentrations of agents. • Measurement of expiratory gas concentrations closer to Y piece crucial (reflects pts alveolar gas concentration).
  • 14. Requirements for use of Low Flow technique • Vapourisers capable of delivering high concentrations and calibrated accurate at low FGF. • Breathing system with minimal internal volume to minimise reserve volume.
  • 15. LFA not suitable • Short term anaesthesia with FM. • Procedures with imperfectly gas –tight airways (i.e. bronchoscopies with rigid bronchoscope). • Technically unsatisfactory equipment with a high gas leakage, unsuitable for leak free closed breathing systems. • Inadequate monitoring (malfunction of gas analyser).
  • 16. LFA not suitable • Situations –clinical issues like hemodynamic instability. • Anaesthesiologist not familiar with LFA.
  • 17. Concerns • Dilution of anaesthetic agents- – Low FGF added to significant large reserve volume – Rate of change of composition of gas in reserve volume exponential – time constant (RV/FGF) – 3 time constants- to effect 95% change in gas composition – Steady state- LFA most economical use of anaesthetic agents
  • 18. Concerns • Differential uptake of agents modifying composition of gas mixture – N2O carrier gas – Uptake high initially followed by gross reduction in uptake – Change in trend in differential uptake –hypoxic mixtures delivered
  • 19. Concerns • Ensuring enough oxygen for metabolism – Wide range of variations in the gas composition is possible while reducing the FG flow – Pulse oximeter less sensitive surrogate monitor of tissue oxygenation – Oxygen analyser – Lower limit FiO2 0.30
  • 20. Concerns • Delay in recovery from anaesthesia – Long time constant –slow reduction in concentration of volatile anaesthetic agents – recovery phase – Change over to high FGF – to reduce time constant – Switch off vapourisers early – Some machines- special charcoal filter
  • 21. Disadvantages • Low flow rate & long time constant- slower induction and emergence • Quick alteration of inspired concentrations not possible • Continuous vigilance and frequent flow adjustments – avoid hypoxic mixtures – Under/over dosage anaesthetic agents
  • 22. Disadvantages • Higher consumption of CO2 absorbents – frequent exhaustion of absorbers – CO2 rebreathing – Risk of hypercarbia • Possible accumulation of undesirable trace gases in system – CO, Acetone, Methane, Hydrogen, Ethanol, Compound A- haloalkene – Flush high FGF once an hour
  • 23. Disadvantages • US FDA recommendations limit Sevoflurane exposure to 2MAC hrs at flow rates 1 to <2 l/min of FGF rates • FGF rates <1 l/min not recommended
  • 24. Calculation of gas update • Total gas uptake =sum of uptakes of O2+N2O +Anaesthetic agents.
  • 25. Use of N2O in LFA
  • 26. LFA in paediatric population • Concerns – Leaks –use of uncuffed ETT – Additional monitoring & breathing valves in circuit adding to dead spaces & resistance to breathing circuit • Airway sealing uncuffed ETT or LMA sufficient to perform LFA. • Frink et al.-low concentrations compound A measured in children during sevoflurane anaesthesia -2l/min FGF. • Younger the child, lower the concentrations of Compound A. • Practical & safe.
  • 27. Conducting LFA • Premedication, preoxygenation and induction –as usual practice. • Initiation- – Objective-To achieve alveolar concentration of anaesthetic agent adequate for producing surgical anaesthesia.
  • 28. Conducting LFA- Initiation • Use of high flows during initial phase – Time constant reduced, bringing the circuit concentration to the desired concentration rapidly – FGF 10L of desired gas concentration and 2 MAC agent concentration – 3min-3Time constant- circuit brought to desired concentration – Better denitrogenation – Rapid achievement of desired concentration – Counterbalancing large uptake encountered at the start of anaesthesia
  • 29. Conducting LFA- Initiation • Use of prefilled circuit – Use different circuit like magill’s for preoxygenation – Simultaneously circle system fitted with test lung & circuit filled with gas mixture of desired concentrations – After tracheal intubation patient connected to circle system – Rapid achievement of the desired concentration in circuit
  • 30. Conducting LFA- Initiation • Injection of volatile agent into the breathing circuit – Usual requirement of anaesthetic agent -400-500ml of vapours in first 10 min( 40-50 ml/min) – At 20degree C 1ml Isoflurane yields 196ml – About 2 ml liquid agent injected in small increments into expiratory limb of circuit – Intermittent injections 0.2-0.5 ml aliquots manually – Alternatively, continuous infusion –added advantage doing away with peaks and troughs of intermittent injections
  • 31. Conducting LFA- Initiation • Accurate dose requirement formulae • Priming dose (ml vapour)= Desired concentration* ([FRC+Circuit volume]+ [Cardiac output*blood gas coefficient])
  • 32. Conducting LFA-Maintenance • Maintain steady state concentration of anaesthetic agents. • Oxygen uptake constant- 200-250 ml/min • Uptake of anaesthesia agents minimal • Oxygen analyser- maintain O2 concentration at least 30% at all times. • Return sampling gas(200ml/min) back to circuit to boost economy of FGF utilisation. • Plenum vapourisers under delivers agent at low flows-achievement of desired end tidal agent concentration accurate- agent analyser or haemodynamic stability.
  • 34. Termination LFA • Long time constants-recovery delayed – Switch over to HFGF-wash out agent – Use of activated charcoal to remove potent vapours by absorption-rapid recovery – N2O washed off- change over to 100% O2
  • 35. Automated LFA • Uses proprietary software algorithm to determine agent and carrier gas administration to attain targets with lowest surplus. • ALFA machines- – ZEUS-Drager Lubeck Germany- Closed circuit – AISYS- GE Madison Wisconsin- minimal flow (500ml/min FGF) – FLOW-i –Maquet Solna Sweden • Anaesthesiologist selects – Target alveolar concentration(FAt) of inhaled anesthetic – Target O2% • Either inspired –FiO2 ZEUS • Or end expired –FaO2 AISYS
  • 36. LFA for sustainable Anaesthesia • Environmental stewardship as a prime priority. • We decide FGF-directly responsible for environmental impact of anaesthetic vapours and gases. • Average working day each anaesthesiologist administering N2O or Desflurane contribute to CO2 equivalent of more than 1000 km car driving.
  • 37. LFA for sustainable Anaesthesia • Research underway to collect and resuse anaesthetic gases. • Zeolite filters –Deltasorb –Canada – commercial use- scavenging system of anaesthesia machine to adsorb anaesthetic. • Later retrieving and purifying agents for reuse.
  • 38. Summary • Smooth and practical conduct of LFA – Safety features of anaesthetic machines – Accurate gas monitoring- gas analysers – FiO2, ETCO2, agent monitoring • Clinical application of LFA is simplified by availability of reliable guidelines for safe performance in routine clinical practice. • Anaesthesiologist should take up LFA as professional obligation to environment and present and future generations.