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AAGBI Safety Guideline
Management of Severe Local Anaesthetic Toxicity


    1
                                        Signs of severe toxicity:
                                        • Sudden alteration in mental status, severe agitation or loss of consciousness,
                                          with or without tonic-clonic convulsions
                                        • Cardiovascular collapse: sinus bradycardia, conduction blocks, asystole and
    Recognition                           ventricular tachyarrhythmias may all occur
                                        • Local anaesthetic (LA) toxicity may occur some time after an initial injection



    2
                                        • Stop injecting the LA
                                        • Call for help
                                        • Maintain the airway and, if necessary, secure it with a tracheal tube
    Immediate                           • Give 100% oxygen and ensure adequate lung ventilation (hyperventilation may
                                          help by increasing plasma pH in the presence of metabolic acidosis)
    management                          • Confirm or establish intravenous access
                                        • Control seizures: give a benzodiazepine, thiopental or propofol in small
                                          incremental doses
                                        • Assess cardiovascular status throughout
                                        • Consider drawing blood for analysis, but do not delay definitive treatment to do
                                          this



    3
                                        In cIrculatory arreSt                                      WIthout cIrculatory arreSt
                                        • Start cardiopulmonary resuscitation                      Use conventional therapies to treat:
                                          (CPR) using standard protocols                           • hypotension,
                                                                                                   • bradycardia,
    Treatment                           • Manage arrhythmias using the
                                          same protocols, recognising that                         • tachyarrhythmia
                                          arrhythmias may be very refractory to
                                          treatment
                                        • Consider the use of cardiopulmonary
                                          bypass if available

                                        GIve IntravenouS                                           conSIder IntravenouS
                                        lIpId emulSIon                                             lIpId emulSIon
                                        (following the regimen overleaf)                           (following the regimen overleaf)
                                        • Continue CPR throughout treatment                        • Propofol is not a suitable substitute
                                          with lipid emulsion                                        for lipid emulsion
                                        • Recovery from LA-induced cardiac                         • Lidocaine should not be used as an
                                          arrest may take >1 h                                       anti-arrhythmic therapy
                                        • Propofol is not a suitable substitute
                                          for lipid emulsion
                                        • Lidocaine should not be used as an
                                          anti-arrhythmic therapy



    4
                                        • Arrange safe transfer to a clinical area with appropriate equipment and suitable
                                          staff until sustained recovery is achieved
                                        • Exclude pancreatitis by regular clinical review, including daily amylase or lipase
                                          assays for two days
    Follow-up                           • Report cases as follows:
                                              in the United Kingdom to the National Patient Safety Agency
                                              (via www.npsa.nhs.uk)
                                              in the Republic of Ireland to the Irish Medicines Board (via www.imb.ie)
                                        If Lipid has been given, please also report its use to the international registry at
                                        www.lipidregistry.org. Details may also be posted at www.lipidrescue.org

your nearest bag of lipid emulsion is kept
This guideline is not a standard of medical care. The ultimate judgement with regard to a particular clinical procedure or treatment plan
must be made by the clinician in the light of the clinical data presented and the diagnostic and treatment options available.
© The Association of Anaesthetists of Great Britain & Ireland 2010
ImmedIately


               Give an initial intravenous bolus
                                                                                  Start an intravenous infusion of 20%
               injection of 20% lipid emulsion                       and
                                                                                     lipid emulsion at 15 ml.kg –1.h –1
                      1.5 ml.kg –1 over 1 min




   after 5 mIn


           Give a maximum of two repeat                                          Continue infusion at same rate, but:
           boluses (same dose) if:                                               Double the rate to 30 ml.kg –1.h –1 at
           • cardiovascular stability has not                                    any time after 5 min, if:
             been restored or                                                    • cardiovascular stability has not been
           • an adequate circulation                                 and           restored or
             deteriorates                                                        • an adequate circulation deteriorates
           Leave 5 min between boluses                                           Continue infusion until stable and
           A maximum of three boluses can be                                     adequate circulation restored or
           given (including the initial bolus)                                   maximum dose of lipid emulsion given



                               Do not exceed a maximum cumulative dose of 12 ml.kg–1




An approximate dose regimen for a 70-kg patient would be as follows:


   ImmedIately


               Give an initial intravenous bolus
                                                                                  Start an intravenous infusion of 20%
               injection of 20% lipid emulsion                       and
                                                                                      lipid emulsion at 1000 ml.h –1
                      100 ml over 1 min




   after 5 mIn


                                                                                     Continue infusion at same rate
               Give a maximum of two repeat                          and            but double rate to 2000 ml.h –1 if
                      boluses of 100 ml
                                                                                         indicated at any time


                                  Do not exceed a maximum cumulative dose of 840 ml




                    This AAGBI Safety Guideline was produced by a Working Party that comprised:
                    Grant Cave, Will Harrop-Griffiths (Chair), Martyn Harvey, Tim Meek, John Picard, Tim Short and Guy Weinberg.

                    this Safety Guideline is endorsed by the australian and new Zealand college of anaesthetists (anZca).



© The Association of Anaesthetists of Great Britain & Ireland 2010

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La toxicity 2010_0

  • 1. AAGBI Safety Guideline Management of Severe Local Anaesthetic Toxicity 1 Signs of severe toxicity: • Sudden alteration in mental status, severe agitation or loss of consciousness, with or without tonic-clonic convulsions • Cardiovascular collapse: sinus bradycardia, conduction blocks, asystole and Recognition ventricular tachyarrhythmias may all occur • Local anaesthetic (LA) toxicity may occur some time after an initial injection 2 • Stop injecting the LA • Call for help • Maintain the airway and, if necessary, secure it with a tracheal tube Immediate • Give 100% oxygen and ensure adequate lung ventilation (hyperventilation may help by increasing plasma pH in the presence of metabolic acidosis) management • Confirm or establish intravenous access • Control seizures: give a benzodiazepine, thiopental or propofol in small incremental doses • Assess cardiovascular status throughout • Consider drawing blood for analysis, but do not delay definitive treatment to do this 3 In cIrculatory arreSt WIthout cIrculatory arreSt • Start cardiopulmonary resuscitation Use conventional therapies to treat: (CPR) using standard protocols • hypotension, • bradycardia, Treatment • Manage arrhythmias using the same protocols, recognising that • tachyarrhythmia arrhythmias may be very refractory to treatment • Consider the use of cardiopulmonary bypass if available GIve IntravenouS conSIder IntravenouS lIpId emulSIon lIpId emulSIon (following the regimen overleaf) (following the regimen overleaf) • Continue CPR throughout treatment • Propofol is not a suitable substitute with lipid emulsion for lipid emulsion • Recovery from LA-induced cardiac • Lidocaine should not be used as an arrest may take >1 h anti-arrhythmic therapy • Propofol is not a suitable substitute for lipid emulsion • Lidocaine should not be used as an anti-arrhythmic therapy 4 • Arrange safe transfer to a clinical area with appropriate equipment and suitable staff until sustained recovery is achieved • Exclude pancreatitis by regular clinical review, including daily amylase or lipase assays for two days Follow-up • Report cases as follows: in the United Kingdom to the National Patient Safety Agency (via www.npsa.nhs.uk) in the Republic of Ireland to the Irish Medicines Board (via www.imb.ie) If Lipid has been given, please also report its use to the international registry at www.lipidregistry.org. Details may also be posted at www.lipidrescue.org your nearest bag of lipid emulsion is kept This guideline is not a standard of medical care. The ultimate judgement with regard to a particular clinical procedure or treatment plan must be made by the clinician in the light of the clinical data presented and the diagnostic and treatment options available. © The Association of Anaesthetists of Great Britain & Ireland 2010
  • 2. ImmedIately Give an initial intravenous bolus Start an intravenous infusion of 20% injection of 20% lipid emulsion and lipid emulsion at 15 ml.kg –1.h –1 1.5 ml.kg –1 over 1 min after 5 mIn Give a maximum of two repeat Continue infusion at same rate, but: boluses (same dose) if: Double the rate to 30 ml.kg –1.h –1 at • cardiovascular stability has not any time after 5 min, if: been restored or • cardiovascular stability has not been • an adequate circulation and restored or deteriorates • an adequate circulation deteriorates Leave 5 min between boluses Continue infusion until stable and A maximum of three boluses can be adequate circulation restored or given (including the initial bolus) maximum dose of lipid emulsion given Do not exceed a maximum cumulative dose of 12 ml.kg–1 An approximate dose regimen for a 70-kg patient would be as follows: ImmedIately Give an initial intravenous bolus Start an intravenous infusion of 20% injection of 20% lipid emulsion and lipid emulsion at 1000 ml.h –1 100 ml over 1 min after 5 mIn Continue infusion at same rate Give a maximum of two repeat and but double rate to 2000 ml.h –1 if boluses of 100 ml indicated at any time Do not exceed a maximum cumulative dose of 840 ml This AAGBI Safety Guideline was produced by a Working Party that comprised: Grant Cave, Will Harrop-Griffiths (Chair), Martyn Harvey, Tim Meek, John Picard, Tim Short and Guy Weinberg. this Safety Guideline is endorsed by the australian and new Zealand college of anaesthetists (anZca). © The Association of Anaesthetists of Great Britain & Ireland 2010