Magnetic Seizure Therapy in Treatment-Resistant Schizophrenia: A Pilot Study.

Published online

Journal Article

Objective: Electroconvulsive therapy is effective in treatment-resistant schizophrenia (TRS) but use is limited due to stigma and concerns around cognitive adverse effects. Magnetic seizure therapy (MST) is a promising new neuromodulation technique that uses transcranial magnetic stimulation to induce therapeutic seizures. Studies of MST in depression have shown clinical improvement with a favorable adverse effect profile. No studies have examined the clinical utility of MST in schizophrenia. Methods: We conducted an open-label pilot clinical trial of MST in eight TRS patients. Up to 24 MST treatments were delivered depending on treatment response. We assessed clinical outcome through the Brief Psychiatric Rating Scale (BPRS) and the Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q). Cognitive testing included a neuropsychological test battery, the Autobiographical Memory Inventory (AMI), Montreal Cognitive Assessment (MoCA), and reorientation time. Results: Four patients completed the trial as per protocol. For all patients and for trial completers alone, there was a significant clinical and quality of life improvement. Three met pre-determined criteria for remission (total score ≤25 on the BPRS) and one met criteria for response (i.e., ≥25% BPRS improvement from baseline for two consecutive assessments). Pre and post neurocognitive data showed no significant cognitive adverse effects apart from a decrease in AMI scores. Conclusion: In this pilot study, MST demonstrated evidence for feasibility in patients with TRS, with promise for clinical efficacy and negligible cognitive side effects. Further study in larger clinical populations is needed. Clinical Trial Registration: www.ClinicalTrials.gov, Identifier NCT01596608.

Full Text

Duke Authors

Cited Authors

  • Tang, VM; Blumberger, DM; McClintock, SM; Kaster, TS; Rajji, TK; Downar, J; Fitzgerald, PB; Daskalakis, ZJ

Published Date

  • 2017

Published In

Volume / Issue

  • 8 /

Start / End Page

  • 310 -

PubMed ID

  • 29387022

Pubmed Central ID

  • 29387022

International Standard Serial Number (ISSN)

  • 1664-0640

Digital Object Identifier (DOI)

  • 10.3389/fpsyt.2017.00310

Language

  • eng

Conference Location

  • Switzerland