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DR.ZIKRULLAH
 Introduction to ECT
 History
 Indications
 Practicalities
 Side Effects
 Anaesthesia for ECT
 Patient factors – Hx / Exam / Ix
 Venue / Equipment
 Conduct
 Induction / Muscle relaxation
 Recovery
 It is a treatment for severe mental illness in
which brief application of electrical stimulus
is used to produce genaralized seizure.
 ECT induces a generalized, tonic–clonic
epileptic seizure, yet despite being first
described in 1937 the exact mechanism of
action remains elusive.
 1934 Von Meduna – Insulin
induced seizures for
schizophrenia
 1937 Cerletti and bini–
Electric shock induced
seizures
 For almost 30 year it was
used without anaesthesia.
 Safer (Mortality 2-5 : 100
000)
 Life threatening illness
 Sever depression- if drug tt fail or is not tolerated.
 Bipolar disorder- manic or depressed phase.
 Acute or catatonic schizophrenia.
 Refusal of food / fluids
 Depressive delusions / hallucinations
 Prolonged / severe manic episode
 Treatment resistance
 Depression
 Mania
 Schizophrenia (4th line treatment)
 Patient choice
 In- or out-patients
 First / repeat visit
 Consent
 ECT suite
 Anaesthetic
Equipment
 ECT machine
 EEG monitor
 Electrode placement
 Dosing / duration
 Anaesthetic
 Recovery / Home
 ABSOLUTE-
CVS-
-Recent MI<3mths
-Sever angina, CHF
-Aneurysm
-Pheocromocytoma
CNS-
-Cerebral tumor or
aneurysm
-Recent CVA<1mth
RESPIRATORY-
Severe resp. failure
 RELATIVE-
- Pregnacy
- Thyrotoxicosis
- Cardiac
dysrythmias
- Glaucoma
- Retinal
detatchment
 An electrical current applied transcutaneous
to brain via two electrode positioned either
bilaterally or unilaterally.
BILATERAL ECT- used more commonly and
preferred when speed of clinical recovery
take priority.
UNILATERAL ECT- performed on nondominant
hemisphere.
-it performed twice weekly until lack of
further improvement( on average 3-4 week)
 Genaralized seizure for 30-60s in duration
are required for therapeutic effect.
- To short(<10s) or to long(>120s) may
reduce clinical efficacy.
- Amount of current deliverd is more
important than length of seizure.
- Almost 75-90% pt exhibit dramatic and
sustained improvement.
- Transient neurological deficit but permanent
neurological deficit is rare.
 Initial parasympathetic discharge(15 s )
- Coincident with tonic phase
- Bradicardia <30 bpm
- Transient asystole
- Sustained sympathetic discharge(1-3min)
-Coicident with clonic phase
-Tachycardia
- Hypertension
- dysarrythmias and T wave abnormalities.
CNS-
 Initial vasoconstriction.
 Sustained increase in cerebral blood flow.
 Increase cerebral metabolism.
 Increase intracranial HTN.
 TIA,intracranial haemorrhage,cortical
blindness.
 Cognitve adverse effects-disorientation,
impaired attention, Short term memory
loss.
- Intraocular and intragastric pressure rises.
 Unmodified ECT- Incidence of fracture and
dislocation( now rare).
- Headache ,myalgia.
- Drowsiness,weakness, nausea , anorexia.
- Increased salivation.
- Dental damage and oral cavity laceration.
 Procedure should be provided at remote site.
 Anaesthesia should be provided by
experienced anaesthetist.
 Appropriate resuscitation equipment drugs
must be immediately available.
- Trained assistance and recovery facilities
must be available.
 Routine Hx
 Previous Anaes Hx
 IHD / MI / HT /
Valvular pathology /
Dysrhythmias
 CVA / Raised ICP
 HH / GORD
 Diabetes
 Medications
 Drugs / Alcohol
 Behaviour
 Airway (incl
wobbly teeth)
 Vitals
 Routine
Examination
 Ix only as needed
 Uncontrolled CCF
 DVT (untreated)
 Acute respiratory tract infection
 Recent MI / CVA
 Unstable major fracture
 Untreated phaeochromocytoma
 Raised ICP / untreated cerebral aneurysm
 ECT Suite – Remote site !
 Resuscitation equipment
 Experienced Anaesthetist
 Minimum mandatory
monitoring +/- PNS
 Tilting trolley / padded cot
sides
 Flow controlled oxygen supply
+ suction
 Anaesthetic / Emergency
drugs
 Airway / Circuits / Disposables
 Mouth guards
 EEG machine / ECT machine
 Staffed recovery area
 Written records
 IV access
 Monitoring
 Pre-oxygenation
 IV induction
 Muscle relaxant
 Mouth block
 Seizure induction
 Recovery
 To provide ultra brief, light general
anaesthesia with moderate degree of
musle relaxation.
 Minimizing aforementioned physiological
and physical effect.
 Avoiding drug having anticonvulsant
properties.
 Balance b/w to provide adequte
anaesthesia without affecting efficacy of
ECT.
 Rapid unconciousness.
 Painless on injection.
 No hemodynamics effect.
 No anticonvulsant properties.
 Rapid recovery.
 Inexpensive.
CONT.
 Methohexitol- 0.5-1mg/kg
 Thiopental - 2-4mg/kg
 Ketamine - 0.5- 2mg/kg
 Propofol - 1.5-3mg/kg
 Etomidate - 0.15- 0.3mg/kg
 Gold standard.
 Methylbarbiturate.
 White powder with 6% anhydrous sodium
carbonate.
 Induction similar to STP.
 Less cvs and respiratory depression than STP.
 Recovery within 3-4 min after single dose.
S/E-
- Pain on injection.
- causes convulsion in epileptic pt.
- incidence of involuntary movement, hiccup
and laryngospasm.
 Phenol derivative.
 Widely used.
 Increase seizure threshold, reduces duration.
 Better cardiovascular stability.
 Imidazole derivatives.
 Greater hemodynamic response.
 Longer seizure duration.
 Useful in resistant cases.
 PONV/HP axis suppresion.
Objective-
 to prevent injuries to musculoskeletal system.
 to improve airways management.
 adequecy of muscle relaxation should be
ascertained before applying ECT stimulus.
Cont.
 Suxamethonium – 0.5-1mg/kg
 Atracurium - 0.3-0.5mg/kg
 Mivacurium - 0.15-0.2mg/kg
 Rocuronium - 0.45-0.6mg/kg
 Adequate no. of trained personnel.
 Should be Fully equipped
 O2 until awake and maintaining Saturation.
 Written instructions
 ECT is safe and effective if appropriately
administered.
- Anaesthetics must be aware of not only
physiological response to ECT and how to
modify this, but also understand the
anaesthetic factors that may influence the
efficacy of ECT.
THANKS

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Anaesthesia for ELECTROCONVULSIVE THERAPY/ECT

  • 2.  Introduction to ECT  History  Indications  Practicalities  Side Effects  Anaesthesia for ECT  Patient factors – Hx / Exam / Ix  Venue / Equipment  Conduct  Induction / Muscle relaxation  Recovery
  • 3.  It is a treatment for severe mental illness in which brief application of electrical stimulus is used to produce genaralized seizure.  ECT induces a generalized, tonic–clonic epileptic seizure, yet despite being first described in 1937 the exact mechanism of action remains elusive.
  • 4.  1934 Von Meduna – Insulin induced seizures for schizophrenia  1937 Cerletti and bini– Electric shock induced seizures  For almost 30 year it was used without anaesthesia.  Safer (Mortality 2-5 : 100 000)
  • 5.  Life threatening illness  Sever depression- if drug tt fail or is not tolerated.  Bipolar disorder- manic or depressed phase.  Acute or catatonic schizophrenia.  Refusal of food / fluids  Depressive delusions / hallucinations  Prolonged / severe manic episode  Treatment resistance  Depression  Mania  Schizophrenia (4th line treatment)  Patient choice
  • 6.
  • 7.  In- or out-patients  First / repeat visit  Consent  ECT suite  Anaesthetic Equipment  ECT machine  EEG monitor  Electrode placement  Dosing / duration  Anaesthetic  Recovery / Home
  • 8.  ABSOLUTE- CVS- -Recent MI<3mths -Sever angina, CHF -Aneurysm -Pheocromocytoma CNS- -Cerebral tumor or aneurysm -Recent CVA<1mth RESPIRATORY- Severe resp. failure
  • 9.  RELATIVE- - Pregnacy - Thyrotoxicosis - Cardiac dysrythmias - Glaucoma - Retinal detatchment
  • 10.  An electrical current applied transcutaneous to brain via two electrode positioned either bilaterally or unilaterally. BILATERAL ECT- used more commonly and preferred when speed of clinical recovery take priority. UNILATERAL ECT- performed on nondominant hemisphere. -it performed twice weekly until lack of further improvement( on average 3-4 week)
  • 11.
  • 12.  Genaralized seizure for 30-60s in duration are required for therapeutic effect. - To short(<10s) or to long(>120s) may reduce clinical efficacy. - Amount of current deliverd is more important than length of seizure. - Almost 75-90% pt exhibit dramatic and sustained improvement. - Transient neurological deficit but permanent neurological deficit is rare.
  • 13.  Initial parasympathetic discharge(15 s ) - Coincident with tonic phase - Bradicardia <30 bpm - Transient asystole - Sustained sympathetic discharge(1-3min) -Coicident with clonic phase -Tachycardia - Hypertension - dysarrythmias and T wave abnormalities.
  • 14. CNS-  Initial vasoconstriction.  Sustained increase in cerebral blood flow.  Increase cerebral metabolism.  Increase intracranial HTN.  TIA,intracranial haemorrhage,cortical blindness.  Cognitve adverse effects-disorientation, impaired attention, Short term memory loss. - Intraocular and intragastric pressure rises.
  • 15.  Unmodified ECT- Incidence of fracture and dislocation( now rare). - Headache ,myalgia. - Drowsiness,weakness, nausea , anorexia. - Increased salivation. - Dental damage and oral cavity laceration.
  • 16.  Procedure should be provided at remote site.  Anaesthesia should be provided by experienced anaesthetist.  Appropriate resuscitation equipment drugs must be immediately available. - Trained assistance and recovery facilities must be available.
  • 17.  Routine Hx  Previous Anaes Hx  IHD / MI / HT / Valvular pathology / Dysrhythmias  CVA / Raised ICP  HH / GORD  Diabetes  Medications  Drugs / Alcohol
  • 18.  Behaviour  Airway (incl wobbly teeth)  Vitals  Routine Examination  Ix only as needed
  • 19.  Uncontrolled CCF  DVT (untreated)  Acute respiratory tract infection  Recent MI / CVA  Unstable major fracture  Untreated phaeochromocytoma  Raised ICP / untreated cerebral aneurysm
  • 20.  ECT Suite – Remote site !  Resuscitation equipment  Experienced Anaesthetist  Minimum mandatory monitoring +/- PNS  Tilting trolley / padded cot sides  Flow controlled oxygen supply + suction  Anaesthetic / Emergency drugs  Airway / Circuits / Disposables  Mouth guards  EEG machine / ECT machine  Staffed recovery area  Written records
  • 21.  IV access  Monitoring  Pre-oxygenation  IV induction  Muscle relaxant  Mouth block  Seizure induction  Recovery
  • 22.  To provide ultra brief, light general anaesthesia with moderate degree of musle relaxation.  Minimizing aforementioned physiological and physical effect.  Avoiding drug having anticonvulsant properties.  Balance b/w to provide adequte anaesthesia without affecting efficacy of ECT.
  • 23.  Rapid unconciousness.  Painless on injection.  No hemodynamics effect.  No anticonvulsant properties.  Rapid recovery.  Inexpensive. CONT.
  • 24.  Methohexitol- 0.5-1mg/kg  Thiopental - 2-4mg/kg  Ketamine - 0.5- 2mg/kg  Propofol - 1.5-3mg/kg  Etomidate - 0.15- 0.3mg/kg
  • 25.  Gold standard.  Methylbarbiturate.  White powder with 6% anhydrous sodium carbonate.  Induction similar to STP.  Less cvs and respiratory depression than STP.  Recovery within 3-4 min after single dose. S/E- - Pain on injection. - causes convulsion in epileptic pt. - incidence of involuntary movement, hiccup and laryngospasm.
  • 26.  Phenol derivative.  Widely used.  Increase seizure threshold, reduces duration.  Better cardiovascular stability.
  • 27.  Imidazole derivatives.  Greater hemodynamic response.  Longer seizure duration.  Useful in resistant cases.  PONV/HP axis suppresion.
  • 28.
  • 29. Objective-  to prevent injuries to musculoskeletal system.  to improve airways management.  adequecy of muscle relaxation should be ascertained before applying ECT stimulus. Cont.
  • 30.  Suxamethonium – 0.5-1mg/kg  Atracurium - 0.3-0.5mg/kg  Mivacurium - 0.15-0.2mg/kg  Rocuronium - 0.45-0.6mg/kg
  • 31.  Adequate no. of trained personnel.  Should be Fully equipped  O2 until awake and maintaining Saturation.  Written instructions
  • 32.  ECT is safe and effective if appropriately administered. - Anaesthetics must be aware of not only physiological response to ECT and how to modify this, but also understand the anaesthetic factors that may influence the efficacy of ECT.