Difference between revisions of "Electroconvulsive therapy"
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. | # <u>Background</u>:<ref name=":0">{{Cite book|last=Murray, Michael J, Steven H. Rose, Denise J. Wedel, C T. Wass, Barry A. Harrison, and Jeff T. Mueller.|first=|title=Faust's Anesthesiology Review|publisher=|year=2015|isbn=|location=Print|pages=Anesthesia for Electroconvulsive Therapy; 490-492}}</ref><ref name=":1">{{Cite book|last=Pardo, Manuel, Ronald D Miller|first=|title=Basics of Anesthesia 7th Edition|publisher=|year=2017|isbn=0323401155|location=Print|pages=669-671}}</ref> | ||
#* Seizures induced by ECT are generalized seizures that consist of a 2 to 3 second latent phase is followed by a tonic (prolonged muscular contraction) phase lasting 10 to 12 seconds, then a clonic (repeated contraction) phase of 30 to 50 seconds. | |||
#* Seizure duration monitored by EEG; goal seizure duration 30-60 seconds. If seizure > 120s consider termination with midazolam/propofol. | |||
#* Initial session may require a dose titration to determine the appropriate electrical stimulus to evoke a seizure, which requires an appropriate duration of anesthesia & neuromuscular blockade. | |||
#* Configuration of electrode placement: Left unilateral, Right unilateral, & Bifrontal | |||
#** Right unilateral most commonly used to minimize side effects of ECT (ex; short- term cognitive dysfunction) | |||
#* Both the duration of individual Seizure & cumulative seizure time between treatments correlated with clinical improvement of depression. The total # of treatments determined by Pt’s clinical response. | |||
#* Repeated rounds of ECT ↑ seizure threshold (try to decrease dose of methohexital or other induction agent if possible to limit size of electrical charge administered) | |||
# <u>Morbidity and Mortality Rates</u>:<ref name=":0" /> | |||
#* Mortality risk <1 in 75,000 treatments. | |||
#* Most common adverse outcomes:Transient arrhythmias (10%–40%), gastric aspiration (2.5%), & MSK disorders (0.4%), including fractures. | |||
#* Additional adverse events: Pulmonary edema, HA, memory disturbance, & agitation. Very rarely takotsubo cardiomyopathy, febrile reactions, or neurologic dysfunction may occur. | |||
# <u>Indications</u>:<ref name=":1" /><ref name=":2">{{Cite web|last=ACCRAC|date=2019-03-13|title=Episode 112: Anesthesia for ECT with Christina Miller|url=http://accrac.com/episode-112-anesthesia-for-ect-with-christina-miller/|access-date=2021-08-22|website=ACCRAC Podcast|language=en}}</ref> | |||
#* Refractory Depression (unipolar and bipolar types), Depression with Psychotic features, Catatonia, and schizophrenia | |||
# <u>ABSOLUTE Contraindications</u>:<ref name=":0" /><ref name=":2" /> | |||
#* Untreated Pheochromocytoma | |||
#* Intracranial mass/↑ ICP | |||
#* Recent MI or Stroke w/in last 30 days | |||
# <u>Relative Contraindications</u>:<ref name=":0" /> | |||
#* Angina pectoris, CHF | |||
#* COPD | |||
#* Glaucoma, Retinal detachment | |||
#* High-risk pregnancy | |||
#* Severe osteoporosis (fracture risk) | |||
#* Thrombophlebitis | |||
# <u>Physiologic Changes</u>:<ref name=":0" /><ref name=":2" /> | |||
#* ECT stimulus -> short initial parasympathetic response caused by vagal nerve stimulation followed by a large sympathetic discharge | |||
#* ''Cardiovascular'' | |||
#** 1st: Parasympathetic discharge may cause '''asystole''', bradycardia, PVCs, '''hypotension''', & ventricular escape rhythm. | |||
#*** ''If known profound parasympathetic response, can blunt with a small dose of glycopyrrolate pre-induciton'' | |||
#** 2<sup>nd</sup>: Sympathetic tone increases with seizure generation | |||
#*** Presents as increased HR, PVCs, bigeminy, trigeminy, sinus tachycardia, '''ST segment changes''' (↑ myocardial O2 consumption) & '''severe HTN'''. | |||
#*** Often resolves quickly, but if Pt requires intervention, consider esmolol or labetalol for tachycardia or HTN | |||
#* ''Respiratory'': | |||
#** During initial parasympathetic discharge at risk for laryngospasm, bronchoconstriction/wheezing | |||
#* ''Neuro'': | |||
#** Initial constriction of cerebral vessels is followed by ↑ cerebral blood flow (1.5–7 times baseline) secondary to ↑ cerebral O2 consumption & elevated BP -> ↑ ICP | |||
#** Preoxygenation prevent cerebral hypoxia. | |||
#* ''Neuroendocrine'': | |||
#** ↑ corticotropin, cortisol, & catecholamines. | |||
#** Effects on glucose levels vary; consider Pre/Post glucose in insulin dependent patients. | |||
#* ''GI'': ↑ intragastric pressure | |||
#* ''Eye'': ↑ intraocular pressure | |||
# <u>Pre-Induction Considerations: <ref name=":0" /><ref name=":1" /><ref name=":2" /></u> | |||
#* ''Medication Management'': | |||
#** Can continue MAO inhibitors, TCAs, SSRIs, & antipsychotics w/ ECT | |||
#** MAO Inhibitors: Avoid ephedrine (indirect-acting sympathomimetics cause exaggerated BP). Be aware they ↓ plasma cholinesterase activity → ↑ succinylcholine duration | |||
#** Lithium – Risk for delayed awakening, memory loss, and postictal confusion. Hold for 12hr before ECT | |||
#** ''Benzodiazepines'' – Hold for 12hr before ECT. May need to give flumazenil before ECT to have an adequate seizure duration. | |||
#* ''Pacemaker vs Implantable Cardioverter-Defibrillator (ICD)'': | |||
#** Pacemaker | |||
#*** If ''Not'' dependent on the device, a magnet should be available in event of device failure. | |||
#*** If Dependent on pacemaker, program device to asynchronous mode & a backup pacing mode should be available. | |||
#** ICD: | |||
#*** Risk that the device misinterprets muscle movements as an abnormal cardiac rhythm and a discharge is possible. | |||
#*** Device should be deactivated & an external defibrillator should be immediately available with placement of external defibrillator pads strongly considered. | |||
#** For a patient with an ICD & who is pacemaker dependent, the EP service should be consulted or in any other cases with pacing concerns. | |||
# <u>Position</u>: Supine or with HOB elevated | |||
# <u>Monitors</u>: Standard ASA monitors with 5 lead ECG. Single lead EEG | |||
# <u>Access</u>: PIV x 1 | |||
# <u>Management of Induction & Seizure Sequelae</u>: <ref name=":0" /><ref name=":1" /><ref name=":2" /> | |||
## '''Induction''': | |||
##* Methohexital (Brevital) 0.5 to 1 mg/kg; least effect on Sz threshold | |||
##* Etomidate: 0.2 to 0.3 mg/kg; maintains hemodynamic stability | |||
##* Propofol: ↑ seizure threshold & '''↓''' seizure duration. Need higher stimulus voltages to achieve adequate seizure. ''May be useful in patients with history of long seizures''. | |||
##* Ketamine: can cause post-ECT | |||
##* Remifentanil 200-400 mcg as an adjunct to lower dose of methohexital needed; net '''↓''' Sz threshold. Watch out for chest wall rigidity (difficult to mask) give succinylcholine asap if unable to ventilate. | |||
##* Sevoflurane can be used for inhalational induction when no IV access possible. | |||
## '''Paralytic''': | |||
### Succinylcholine 1- 1.5 mg/kg, titrate to adequate paralysis | |||
### Rocuronium - Low dose & only if patient has contraindication to succinylcholine (reverse with sugammadex) | |||
## '''Initial PARAsympathetic discharge''': | |||
### '''Glycopyrrolate''' 0.2mg to prevent bradycardia. Usually given prior to induction agents | |||
## '''Subsequent Sympathetic discharge''': | |||
### Nitroglycerin &/ot Beta blockers (esmolol, labetalol) can be used to attenuate sympathetic response. | |||
### ''Hyperglycemia'' often seen in insulin dependent Pt -> BG Pre/Post | |||
## '''Post-ECT delirium''' (or if flumazenil given Pre-Induction): | |||
### Midazolam | |||
# <u>General Procedural Steps</u>: <ref name=":1" /><ref name=":2" /> | |||
## Preoxygenate well prior to induction | |||
## Once induction medications given & patient unconscious start mask ventilating & give paralytic | |||
## Hyperventilate -> Hypocarbia (↓ seizure threshold) | |||
## Bite guard placed prior to ECT initiation | |||
## After ECT & seizure completed remove bite guard and provide supportive airway management until patient regains consciousness. | |||
# |
Revision as of 18:10, 21 August 2021
- Background:[1][2]
- Seizures induced by ECT are generalized seizures that consist of a 2 to 3 second latent phase is followed by a tonic (prolonged muscular contraction) phase lasting 10 to 12 seconds, then a clonic (repeated contraction) phase of 30 to 50 seconds.
- Seizure duration monitored by EEG; goal seizure duration 30-60 seconds. If seizure > 120s consider termination with midazolam/propofol.
- Initial session may require a dose titration to determine the appropriate electrical stimulus to evoke a seizure, which requires an appropriate duration of anesthesia & neuromuscular blockade.
- Configuration of electrode placement: Left unilateral, Right unilateral, & Bifrontal
- Right unilateral most commonly used to minimize side effects of ECT (ex; short- term cognitive dysfunction)
- Both the duration of individual Seizure & cumulative seizure time between treatments correlated with clinical improvement of depression. The total # of treatments determined by Pt’s clinical response.
- Repeated rounds of ECT ↑ seizure threshold (try to decrease dose of methohexital or other induction agent if possible to limit size of electrical charge administered)
- Morbidity and Mortality Rates:[1]
- Mortality risk <1 in 75,000 treatments.
- Most common adverse outcomes:Transient arrhythmias (10%–40%), gastric aspiration (2.5%), & MSK disorders (0.4%), including fractures.
- Additional adverse events: Pulmonary edema, HA, memory disturbance, & agitation. Very rarely takotsubo cardiomyopathy, febrile reactions, or neurologic dysfunction may occur.
- Indications:[2][3]
- Refractory Depression (unipolar and bipolar types), Depression with Psychotic features, Catatonia, and schizophrenia
- ABSOLUTE Contraindications:[1][3]
- Untreated Pheochromocytoma
- Intracranial mass/↑ ICP
- Recent MI or Stroke w/in last 30 days
- Relative Contraindications:[1]
- Angina pectoris, CHF
- COPD
- Glaucoma, Retinal detachment
- High-risk pregnancy
- Severe osteoporosis (fracture risk)
- Thrombophlebitis
- Physiologic Changes:[1][3]
- ECT stimulus -> short initial parasympathetic response caused by vagal nerve stimulation followed by a large sympathetic discharge
- Cardiovascular
- 1st: Parasympathetic discharge may cause asystole, bradycardia, PVCs, hypotension, & ventricular escape rhythm.
- If known profound parasympathetic response, can blunt with a small dose of glycopyrrolate pre-induciton
- 2nd: Sympathetic tone increases with seizure generation
- Presents as increased HR, PVCs, bigeminy, trigeminy, sinus tachycardia, ST segment changes (↑ myocardial O2 consumption) & severe HTN.
- Often resolves quickly, but if Pt requires intervention, consider esmolol or labetalol for tachycardia or HTN
- 1st: Parasympathetic discharge may cause asystole, bradycardia, PVCs, hypotension, & ventricular escape rhythm.
- Respiratory:
- During initial parasympathetic discharge at risk for laryngospasm, bronchoconstriction/wheezing
- Neuro:
- Initial constriction of cerebral vessels is followed by ↑ cerebral blood flow (1.5–7 times baseline) secondary to ↑ cerebral O2 consumption & elevated BP -> ↑ ICP
- Preoxygenation prevent cerebral hypoxia.
- Neuroendocrine:
- ↑ corticotropin, cortisol, & catecholamines.
- Effects on glucose levels vary; consider Pre/Post glucose in insulin dependent patients.
- GI: ↑ intragastric pressure
- Eye: ↑ intraocular pressure
- Pre-Induction Considerations: [1][2][3]
- Medication Management:
- Can continue MAO inhibitors, TCAs, SSRIs, & antipsychotics w/ ECT
- MAO Inhibitors: Avoid ephedrine (indirect-acting sympathomimetics cause exaggerated BP). Be aware they ↓ plasma cholinesterase activity → ↑ succinylcholine duration
- Lithium – Risk for delayed awakening, memory loss, and postictal confusion. Hold for 12hr before ECT
- Benzodiazepines – Hold for 12hr before ECT. May need to give flumazenil before ECT to have an adequate seizure duration.
- Pacemaker vs Implantable Cardioverter-Defibrillator (ICD):
- Pacemaker
- If Not dependent on the device, a magnet should be available in event of device failure.
- If Dependent on pacemaker, program device to asynchronous mode & a backup pacing mode should be available.
- ICD:
- Risk that the device misinterprets muscle movements as an abnormal cardiac rhythm and a discharge is possible.
- Device should be deactivated & an external defibrillator should be immediately available with placement of external defibrillator pads strongly considered.
- For a patient with an ICD & who is pacemaker dependent, the EP service should be consulted or in any other cases with pacing concerns.
- Pacemaker
- Medication Management:
- Position: Supine or with HOB elevated
- Monitors: Standard ASA monitors with 5 lead ECG. Single lead EEG
- Access: PIV x 1
- Management of Induction & Seizure Sequelae: [1][2][3]
- Induction:
- Methohexital (Brevital) 0.5 to 1 mg/kg; least effect on Sz threshold
- Etomidate: 0.2 to 0.3 mg/kg; maintains hemodynamic stability
- Propofol: ↑ seizure threshold & ↓ seizure duration. Need higher stimulus voltages to achieve adequate seizure. May be useful in patients with history of long seizures.
- Ketamine: can cause post-ECT
- Remifentanil 200-400 mcg as an adjunct to lower dose of methohexital needed; net ↓ Sz threshold. Watch out for chest wall rigidity (difficult to mask) give succinylcholine asap if unable to ventilate.
- Sevoflurane can be used for inhalational induction when no IV access possible.
- Paralytic:
- Succinylcholine 1- 1.5 mg/kg, titrate to adequate paralysis
- Rocuronium - Low dose & only if patient has contraindication to succinylcholine (reverse with sugammadex)
- Initial PARAsympathetic discharge:
- Glycopyrrolate 0.2mg to prevent bradycardia. Usually given prior to induction agents
- Subsequent Sympathetic discharge:
- Nitroglycerin &/ot Beta blockers (esmolol, labetalol) can be used to attenuate sympathetic response.
- Hyperglycemia often seen in insulin dependent Pt -> BG Pre/Post
- Post-ECT delirium (or if flumazenil given Pre-Induction):
- Midazolam
- Induction:
- General Procedural Steps: [2][3]
- Preoxygenate well prior to induction
- Once induction medications given & patient unconscious start mask ventilating & give paralytic
- Hyperventilate -> Hypocarbia (↓ seizure threshold)
- Bite guard placed prior to ECT initiation
- After ECT & seizure completed remove bite guard and provide supportive airway management until patient regains consciousness.
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 Murray, Michael J, Steven H. Rose, Denise J. Wedel, C T. Wass, Barry A. Harrison, and Jeff T. Mueller. (2015). Faust's Anesthesiology Review. Print. pp. Anesthesia for Electroconvulsive Therapy, 490–492.CS1 maint: multiple names: authors list (link)
- ↑ 2.0 2.1 2.2 2.3 2.4 Pardo, Manuel, Ronald D Miller (2017). Basics of Anesthesia 7th Edition. Print. pp. 669–671. ISBN 0323401155.CS1 maint: multiple names: authors list (link)
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 ACCRAC (2019-03-13). "Episode 112: Anesthesia for ECT with Christina Miller". ACCRAC Podcast. Retrieved 2021-08-22.
Top contributors: Alexander Jaksic, Tony Wang and Chris Rishel