AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (1 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

The clinical effect of vagus nerve stimulation in the treatment of patients with a minimally conscious state

Neurosurgery Department, Guangxi Jiangbin Hospital, Nanning 530021, Guangxi, China
Show Author Information

Abstract

Objective:

Vagus nerve stimulation (VNS) has recently been used in neurorehabilitation and the recovery of consciousness based on its effects on cortical plasticity. The aim of this study was to examine the therapeutic effects of VNS on patients with a minimally conscious state (MCS).

Methods:

All patients included in the study were assessed more than 5 months after injury and were receiving regular rehabilitation at our hospital from August 2018 to October 2019. Ten patients diagnosed with MCS by Coma Recovery Scale-Revised (CRS-R) test who underwent VNS surgery were enrolled. The scores on CRS-R evaluation at baseline (before VNS implantation) and 1, 3, and 6 months after VNS treatment were recorded. The stimulation parameters were chosen according to a previous study. All clinical rehabilitation protocols remained unchanged during the study. Furthermore, safety was assessed by analyzing treatment-emergent adverse events (TEAEs).

Results:

No significant improvement in the total CRS-R scores at the end of the 1-month follow-up was observed (p > 0.05). After 3 months of stimulation, a significant difference (p = 0.0078) was observed in the total CRS-R scores compared with the baseline. After 6 months of VNS treatment, CRS-R assessments showed a continuous significant improvement (p = 0.0039); one patient emerged from the MCS and recovered functional communication and object use. Interestingly, one item of CRS-R scores on visual domain was sensitive to VNS treatment (p = 0.0039). Furthermore, no serious adverse event occurred throughout the study.

Conclusion:

This exploratory study provides preliminary evidence suggesting that VNS is a safe and effective tool for consciousness recovery in patients with MCS.

References

[1]
JT Giacino, JJ Fins, S Laureys, et al. Disorders of consciousness after acquired brain injury: the state of the science. Nat Rev Neurol. 2014, 10(2): 99-114.
[2]
JT Giacino, DI Katz, ND Schiff, et al. Comprehensive systematic review update summary: disorders of consciousness: report of the guideline development, dissemination, and implementation subcommittee of the American academy of neurology; the American congress of rehabilitation medicine; and the national institute on disability, independent living, and rehabilitation research. Neurology. 2018, 91(10): 461-470.
[3]
R Hodelín-Tablada. Minimally conscious state: evolution of concept, diagnosis and treatment. MEDICC Rev. 2016, 18(4): 43-46.
[4]
A Thibaut, N Schiff, J Giacino, et al. Therapeutic interventions in patients with prolonged disorders of consciousness. Lancet Neurol. 2019, 18(6): 600-614.
[5]
C Schnakers, A Vanhaudenhuyse, J Giacino, et al. Diagnostic accuracy of the vegetative and minimally conscious state: Clinical consensus versus standardized neurobehavioral assessment. BMC Neurol. 2009, 9(1): 1-5.
[6]
D Rodriguez Moreno, ND Schiff, J Giacino, et al. A network approach to assessing cognition in disorders of consciousness. Neurology. 2010, 75(21): 1871-1878.
[7]
D Fernández-Espejo, A Soddu, D Cruse, et al. A role for the default mode network in the bases of disorders of consciousness. Ann Neurol. 2012, 72(3): 335-343.
[8]
SS Chen, XH Wu, LB Wang, et al. Disrupted interactions between arousal and cortical awareness networks in MCS and VS/UWS patients: evidence from resting-state functional imaging connectivity. Neuroscience. 2018, 382: 115-124.
[9]
Y Cui, M Song, DM Lipnicki, et al. Subdivisions of the posteromedial cortex in disorders of consciousness. Neuroimage Clin. 2018, 20: 260-266.
[10]
L Naccache. Minimally conscious state or cortically mediated state? Brain. 2018, 141(4): 949-960.
[11]
O Gosseries, V Charland-Verville, M Thonnard, et al. Amantadine, apomorphine and zolpidem in the treatment of disorders of consciousness. Curr Pharm Des. 2014, 20(26): 4167-4184.
[12]
JT Giacino, J Whyte, E Bagiella, et al. Placebo-controlled trial of amantadine for severe traumatic brain injury. N Engl J Med. 2012, 366(9): 819-826.
[13]
J Whyte, R Rajan, A Rosenbaum, et al. Zolpidem and restoration of consciousness. Am J Phys Med Rehabil. 2014, 93(2): 101-113.
[14]
TL Pape, JM Rosenow, M Steiner, et al. Placebo-controlled trial of familiar auditory sensory training for acute severe traumatic brain injury: a preliminary report. Neurorehabil Neural Repair. 2015, 29(6): 537-547.
[15]
C Abbate, PD Trimarchi, I Basile, et al. Sensory stimulation for patients with disorders of consciousness: from stimulation to rehabilitation. Front Hum Neurosci. 2014, 8: 616.
[16]
L Padua, C Cuccagna, C Pazzaglia. Novel sensory paradigms for neuromodulation in disorders of consciousness in traumatic brain injury. Curr Opin Neurol. 2019, 32(6): 844-849.
[17]
L Wojtecki, D Petri, S Elben, et al. Modulation of central thalamic oscillations during emotional-cognitive processing in chronic disorder of consciousness. Cortex. 2014, 60: 94-102.
[18]
GT Saleem, JB Ewen, JE Crasta, et al. Single-arm, open-label, dose escalation phase I study to evaluate the safety and feasibility of transcranial direct current stimulation with electroencephalography biomarkers in paediatric disorders of consciousness: a study protocol. BMJ Open. 2019, 9(8): e029967.
[19]
ZH Liang, JN Li, XY Xia, et al. Long-range temporal correlations of patients in minimally conscious state modulated by spinal cord stimulation. Front Physiol. 2018, 9: 1511.
[20]
Y Bai, XY Xia, JN Kang, et al. Evaluating the effect of repetitive transcranial magnetic stimulation on disorders of consciousness by using TMS-EEG. Front Neurosci. 2016, 10: 473.
[21]
M Corazzol, G Lio, A Lefevre, et al. Restoring consciousness with vagus nerve stimulation. Curr Biol. 2017, 27(18): R994-R996.
[22]
A Rezaei Haddad, V Lythe, AL Green. Deep brain stimulation for recovery of consciousness in minimally conscious patients after traumatic brain injury: a systematic review. Neuromodulation. 2019, 22(4): 373-379.
[23]
Y Wang, Y Bai, XY Xia, et al. Spinal cord stimulation modulates complexity of neural activities in patients with disorders of consciousness. Int J Neurosci. 2020, 130(7): 662-670.
[24]
P Bourdillon, B Hermann, JD Sitt, et al. Electromagnetic brain stimulation in patients with disorders of consciousness. Front Neurosci. 2019, 13: 223.
[25]
J Hakon, M Moghiseh, I Poulsen, et al. Transcutaneous vagus nerve stimulation in patients with severe traumatic brain injury: a feasibility trial. Neuromodulation. 2020, in press, .
[26]
H Xie, TY Ji, JY Ma, et al. Remote programming: a convenient and cost-effective measure of vagus nerve stimulation for children with epilepsy. Epilepsy Res. 2020, 159: 106246.
[27]
ST Aaronson, P Sears, F Ruvuna, et al. A 5-year observational study of patients with treatment-resistant depression treated with vagus nerve stimulation or treatment as usual: comparison of response, remission, and suicidality. Am J Psychiatry. 2017, 174(7): 640-648.
[28]
MP Kilgard. Harnessing plasticity to understand learning and treat disease. Trends Neurosci. 2012, 35(12): 715-722.
[29]
SA Hays. Enhancing rehabilitative therapies with vagus nerve stimulation. Neurotherapeutics. 2016, 13(2): 382-394.
[30]
LD Hachem, SM Wong, GM Ibrahim. The vagus afferent network: emerging role in translational connectomics. Neurosurg Focus. 2018, 45(3): E2.
[31]
ND Engineer, TJ Kimberley, CN Prudente, et al. Targeted vagus nerve stimulation for rehabilitation after stroke. Front Neurosci. 2019, 13: 280.
[32]
EC Meyers, N Kasliwal, BR Solorzano, et al. Enhancing plasticity in central networks improves motor and sensory recovery after nerve damage. Nat Commun. 2019, 10(1): 5782.
[33]
EC Meyers, BR Solorzano, J James, et al. Vagus nerve stimulation enhances stable plasticity and generalization of stroke recovery. Stroke. 2018, 49(3): 710-717.
[34]
JE Childs, AC Alvarez-Dieppa, CK McIntyre, et al. Vagus nerve stimulation as a tool to induce plasticity in pathways relevant for extinction learning. J Vis Exp. 2015(102): e53032.
[35]
C Rodenkirch, Q Wang. Rapid and transient enhancement of thalamic information transmission induced by vagus nerve stimulation. J Neural Eng. 2020, 17(2): 026027.
[36]
JY Cao, KH Lu, TL Powley, et al. Vagal nerve stimulation triggers widespread responses and alters large-scale functional connectivity in the rat brain. PLoS One. 2017, 12(12): e0189518.
[37]
JT Giacino, S Ashwal, N Childs, et al. The minimally conscious state: definition and diagnostic criteria. Neurology. 2002, 58(3): 349-353.
[38]
AM Lozano. Harnessing plasticity to reset dysfunctional neurons. N Engl J Med. 2011, 364(14): 1367-1368.
[39]
SA Hays, RL Rennaker, MP Kilgard. Targeting plasticity with vagus nerve stimulation to treat neurological disease. Prog Brain Res. 2013, 207: 275-299.
[40]
M Bagary. Epilepsy, consciousness and neurostimulation. Behav Neurol. 2011, 24(1): 75-81.
[41]
BA Malow, J Edwards, M Marzec, et al. Vagus nerve stimulation reduces daytime sleepiness in epilepsy patients. Neurology. 2001, 57(5): 879-884.
[42]
P Rizzo, M Beelke, F de Carli, et al. Chronic vagus nerve stimulation improves alertness and reduces rapid eye movement sleep in patients affected by refractory epilepsy. Sleep. 2003, 26(5): 607-611.
[43]
YT Yu, Y Yang, LB Wang, et al. Transcutaneous auricular vagus nerve stimulation in disorders of consciousness monitored by fMRI: The first case report. Brain Stimul. 2017, 10(2): 328-330.
[44]
E Noé, J Ferri, C Colomer, et al. Feasibility, safety and efficacy of transauricular vagus nerve stimulation in a cohort of patients with disorders of consciousness. Brain Stimul. 2020, 13(2): 427-429.
[45]
XY Dong, Z Feng. Wake-promoting effects of vagus nerve stimulation after traumatic brain injury: upregulation of orexin-A and orexin receptor type 1 expression in the prefrontal cortex. Neural Regen Res. 2018, 13(2): 244-251.
[46]
D Martínez-Vargas, A Valdés-Cruz, VM Magdaleno-Madrigal, et al. Effects of electrical stimulation of the vagus nerve on the development of visual habituation in the cat. Behav Brain Res. 2009, 205(1): 45-49.
[47]
ND Engineer, JR Riley, JD Seale, et al. Reversing pathological neural activity using targeted plasticity. Nature. 2011, 470(7332): 101-104.
[48]
S Laureys. The neural correlate of (un)awareness: lessons from the vegetative state. Trends Cogn Sci. 2005, 9(12): 556-559.
Journal of Neurorestoratology
Pages 160-171
Cite this article:
Xiang X-J, Sun L-Z, Xu C-B, et al. The clinical effect of vagus nerve stimulation in the treatment of patients with a minimally conscious state. Journal of Neurorestoratology, 2020, 8(3): 160-171. https://doi.org/10.26599/JNR.2020.9040016

946

Views

62

Downloads

10

Crossref

8

Web of Science

0

Scopus

Altmetrics

Received: 24 May 2020
Revised: 03 July 2020
Accepted: 08 July 2020
Published: 14 September 2020
© The authors 2020

This article is published with open access at http://jnr.tsinghuajournals.com

Return