Electroconvulsive Therapy Pulse Amplitude and Clinical Outcomes.


Journal

The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
ISSN: 1545-7214
Titre abrégé: Am J Geriatr Psychiatry
Pays: England
ID NLM: 9309609

Informations de publication

Date de publication:
02 2021
Historique:
received: 08 12 2019
revised: 09 06 2020
accepted: 10 06 2020
pubmed: 12 7 2020
medline: 10 7 2021
entrez: 12 7 2020
Statut: ppublish

Résumé

Electroconvulsive therapy (ECT) pulse amplitude, which determines the induced electric field magnitude in the brain, is currently set at 800-900 milliamperes (mA) on modern ECT devices without any clinical or scientific rationale. The present study assessed differences in depression and cognitive outcomes for three different pulse amplitudes during an acute ECT series. We hypothesized that the lower amplitudes would maintain the antidepressant efficacy of the standard treatment and reduce the risk of neurocognitive impairment. This double-blind investigation randomized subjects to three treatment arms: 600, 700, and 800 mA (active comparator). Clinical, cognitive, and imaging assessments were conducted pre-, mid- and post-ECT. Subjects had a diagnosis of major depressive disorder, age range between 50 and 80 years, and met clinical indication for ECT. The 700 and 800 mA arms had improvement in depression outcomes relative to the 600 mA arm. The amplitude groups showed no differences in the primary cognitive outcome variable, the Hopkins Verbal Learning Test-Revised (HVLT-R) retention raw score. However, secondary cognitive outcomes such as the Delis Kaplan Executive Function System Letter and Category Fluency measures demonstrated cognitive impairment in the 800 mA arm. The results demonstrated a dissociation of depression (higher amplitudes better) and cognitive (lower amplitudes better) related outcomes. Future work is warranted to elucidate the relationship between amplitude, electric field, neuroplasticity, and clinical outcomes.

Identifiants

pubmed: 32651051
pii: S1064-7481(20)30377-8
doi: 10.1016/j.jagp.2020.06.008
pmc: PMC7744398
mid: NIHMS1610197
pii:
doi:

Substances chimiques

Antidepressive Agents 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

166-178

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH119285
Pays : United States
Organisme : NIMH NIH HHS
ID : U01 MH111826
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA MH002955
Pays : United States

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Christopher C Abbott (CC)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM. Electronic address: cabbott@salud.unm.edu.

Davin Quinn (D)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Jeremy Miller (J)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Enstin Ye (E)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Sulaiman Iqbal (S)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Megan Lloyd (M)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Thomas R Jones (TR)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Joel Upston (J)

Department of Psychiatry (CCA, DQ, JM, EY, SI, ML, TRJ, JU), University of New Mexico, Albuquerque, NM.

Zhi De Deng (Z)

Noninvasive Neuromodulation Unit (ZDD), Experimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD; Division of Brain Stimulation and Neurophysiology (SMM), Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC.

Erik Erhardt (E)

Department of Mathematics and Statistics (EE), University of New Mexico, Albuquerque, NM.

Shawn M McClintock (SM)

Division of Psychology, Department of Psychiatry (SMM), UT Southwestern Medical Center, Dallas, TX; Division of Brain Stimulation and Neurophysiology (SMM), Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC.

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