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Daily Vibrotactile Stimulation Exhibits Equal or Greater Spasticity Relief Than Botulinum Toxin in Stroke.
Seim, Caitlyn; Chen, Bingxian; Han, Chuzhang; Vacek, David; Lowber, Alexis; Lansberg, Maarten; Okamura, Allison M.
Afiliação
  • Seim C; Department of Mechanical Engineering, Stanford University, Stanford, CA. Electronic address: caitlyn.seim@gmail.com.
  • Chen B; Department of Bioengineering, Stanford University, Stanford, CA.
  • Han C; Department of Mechanical Engineering, Stanford University, Stanford, CA.
  • Vacek D; Department of Mechanical Engineering, Stanford University, Stanford, CA.
  • Lowber A; Department of Computer Science, Stanford University, Stanford, CA.
  • Lansberg M; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA.
  • Okamura AM; Department of Mechanical Engineering, Stanford University, Stanford, CA.
Arch Phys Med Rehabil ; 104(10): 1565-1572, 2023 10.
Article em En | MEDLINE | ID: mdl-37149017
ABSTRACT

OBJECTIVE:

To test the feasibility and efficacy of the VibroTactile Stimulation (VTS) Glove, a wearable device that provides VTS to the impaired limb to reduce spastic hypertonia.

DESIGN:

Prospective 2-arm intervention study-including 1 group of patients who use Botulinum toxin (BTX-A) for spasticity and 1 group of patients who do not use BTX-A.

SETTING:

Participants were recruited through rehabilitation and neurology clinics.

PARTICIPANTS:

Patients with chronic stroke (N=20; mean age=54 years, mean time since stroke=6.9 years). Patients who were previously receiving the standard of care (BTX-A injection) were eligible to participate and started the intervention 12 weeks after their last injection. INTERVENTION Participants were instructed to use the VTS Glove for 3 hours daily, at home or during everyday activities, for 8 weeks. MAIN OUTCOME

MEASURES:

Spasticity was assessed with the Modified Ashworth Scale and the Modified Tardieu Scale at baseline and then at 2-week intervals for 12 weeks. Primary outcomes were the difference from baseline and at week 8 (end of VTS Glove use) and week 12 (4 weeks after stopping VTS Glove use). Patients who were receiving BTX-A were also assessed during the 12 weeks preceding the start of VTS Glove use to monitor the effect of BTX-A on spastic hypertonia. Range of motion and participant feedback were also studied.

RESULTS:

A clinically meaningful difference in spastic hypertonia was found during and after daily VTS Glove use. Modified Ashworth and Modified Tardieu scores were reduced by an average of 0.9 (P=.0014) and 0.7 (P=.0003), respectively, at week 8 of daily VTS Glove use, and by 1.1 (P=.00025) and 0.9 (P=.0001), respectively, 1 month after stopping VTS Glove use. For participants who used BTX-A, 6 out of 11 showed greater change in Modified Ashworth ratings during VTS Glove use (mean=-1.8 vs mean=-1.6 with BTX-A) and 8 out of 11 showed their lowest level of symptoms during VTS Glove use (vs BTX-A).

CONCLUSIONS:

Daily stimulation from the VTS Glove provides relief of spasticity and hypertonia. For more than half of the participants who had regularly used BTX-A, the VTS Glove provided equal or greater symptom relief.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas Tipo A / Acidente Vascular Cerebral / Reabilitação do Acidente Vascular Cerebral / Fármacos Neuromusculares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas Tipo A / Acidente Vascular Cerebral / Reabilitação do Acidente Vascular Cerebral / Fármacos Neuromusculares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans / Middle aged Idioma: En Ano de publicação: 2023 Tipo de documento: Article