Volume 2, Issue 1 , Pages 22-35, January 2009
Repetitive transcranial magnetic stimulation-associated neurobehavioral gains during coma recovery
Background
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive method to induce changes in cortical neural excitability. This report presents findings from the first participant of a safety and efficacy study that examined a therapeutic rTMS protocol for persons with severe traumatic brain injury (TBI).
Objective
The primary hypothesis was that there will be no adverse events related to the provision of a 6-week rTMS protocol for persons with severe TBI who remain, at best, in a minimally conscious state for longer than 3 months. The secondary hypothesis was that the rTMS protocol would induce significant neurobehavioral gains during treatment and that these gains would persist at 6-week follow-up.
Methods
A 6-week rTMS protocol (30 sessions) was delivered to a 26-year-old man who remained in a vegetative state 287 days after severe TBI. Stimulation was directed over the right dorsolateral prefrontal cortex. Repeated safety measures, neurobehavioral assessments, clinical examinations, and evoked potentials (EP) were obtained at baseline, every fifth rTMS session (weekly), and at a 6-week follow-up.
Results
There were no adverse events related to the provision of rTMS treatment. A trend toward significant (P = .066) neurobehavioral gains was temporally related to provision of rTMS. Left-sided brain stem auditory EP wave V latencies and waves I to V interpeak latencies improved along with neurobehavioral gains during provision of rTMS, suggesting that improved neural conduction in the pathway mediated the neurobehavioral improvements.
Conclusions
Repetitive TMS merits further investigation as a safe therapeutic intervention to alter neural activity, to modulate neural activity, and/or to facilitate recovery in persons with disordered consciousness subsequent to severe TBI.
Keywords: neual stimulation, coma, treatment, intervention, traumatic brain injury
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Funding was provided by the Department of Veterans Affairs, Office of Research and Development, Rehabilitation Research and Development Service through an advanced research career development award (B3302K) and a career development transition award (B4949N). The research described in this article was also supported by the General Clinical Research Center (GCRC) of Northwestern University Feinberg School of Medicine. The GCRC is supported by Grant M01 RR-00048 from the National Center for Research Resources, National Institutes of Health. The Nick Kot Charity, a not-for-profit, also provided an unrestricted grant to support this project. Substantial in-kind contributions from the Departments of Neurosurgery and Physical Medicine and Rehabilitation, of Northwestern University Feinberg School of Medicine, and Marianjoy Rehabilitation Hospital also made this research possible. Additional in-kind contributions from Northwestern Memorial Hospital and the Rehabilitation Institute of Chicago are appreciated.
The views expressed in the article are those of the authors and do not necessarily reflect the views of the US federal government or the US Department of Veterans Affairs.
PII: S1935-861X(08)00335-5
doi:10.1016/j.brs.2008.09.004
© 2009 Elsevier Inc. All rights reserved.
Volume 2, Issue 1 , Pages 22-35, January 2009
