Literature DB >> 7970010

Efficacy and safety of tizanidine in the treatment of spasticity in patients with spinal cord injury. North American Tizanidine Study Group.

P W Nance1, J Bugaresti, K Shellenberger, W Sheremata, A Martinez-Arizala.   

Abstract

Tizanidine, an imidazoline that acts as an agonist at alpha 2-adrenergic receptors, has been shown to be effective in reducing spasticity caused by MS. This multicenter study (14 sites) assessed the efficacy and safety of oral tizanidine in patients who had spinal cord injury of > 12 months' duration. Of the 124 patients admitted to the study, 78 completed it. Tizanidine was titrated to an optimized dosage in each patient to a maximum of 36 mg/d. Muscle tone, assessed by Ashworth score, was significantly reduced (p = 0.0001) by tizanidine treatment in comparison with placebo. Video motion analysis of the pendulum test showed improvement in the tizanidine-treated patients vs placebo (p = 0.04) and showed a significant correlation with the Ashworth score (p < 0.001). No significant alterations in muscle strength or vital signs were noted in either treatment group. The most common adverse events during tizanidine treatment were somnolence, xerostomia, and fatigue. It was concluded that, overall, tizanidine is effective in reducing spasticity in patients with spinal cord injury.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7970010

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  23 in total

1.  Interventions to Reduce Spasticity and Improve Function in People With Chronic Incomplete Spinal Cord Injury: Distinctions Revealed by Different Analytical Methods.

Authors:  Lynsey D Duffell; Geoffrey L Brown; Mehdi M Mirbagheri
Journal:  Neurorehabil Neural Repair       Date:  2014-11-14       Impact factor: 3.919

Review 2.  The challenge of recruitment for neurotherapeutic clinical trials in spinal cord injury.

Authors:  Andrew R Blight; Jane Hsieh; Armin Curt; James W Fawcett; James D Guest; Naomi Kleitman; Shekar N Kurpad; Brian K Kwon; Daniel P Lammertse; Norbert Weidner; John D Steeves
Journal:  Spinal Cord       Date:  2019-04-08       Impact factor: 2.772

3.  Comparison of Single-Session Dose Response Effects of Whole Body Vibration on Spasticity and Walking Speed in Persons with Spinal Cord Injury.

Authors:  Stephen Estes; Jennifer A Iddings; Somu Ray; Neva J Kirk-Sanchez; Edelle C Field-Fote
Journal:  Neurotherapeutics       Date:  2018-07       Impact factor: 7.620

Review 4.  Assessment and Measurement of Spasticity in MS: State of the Evidence.

Authors:  Cinda L Hugos; Michelle H Cameron
Journal:  Curr Neurol Neurosci Rep       Date:  2019-08-30       Impact factor: 5.081

5.  Antispastic effects of L-dopa.

Authors:  J Eriksson; B Olausson; E Jankowska
Journal:  Exp Brain Res       Date:  1996-09       Impact factor: 1.972

6.  Cost-effectiveness comparison of tizanidine and baclofen in the management of spasticity.

Authors:  David N Rushton; Adam C Lloyd; Pippa M Anderson
Journal:  Pharmacoeconomics       Date:  2002       Impact factor: 4.981

Review 7.  A review of the physiological effects of alpha2-agonists related to the clinical use of medetomidine in small animal practice.

Authors:  Melissa D Sinclair
Journal:  Can Vet J       Date:  2003-11       Impact factor: 1.008

8.  Quantification of the effects of an alpha-2 adrenergic agonist on reflex properties in spinal cord injury using a system identification technique.

Authors:  Mehdi M Mirbagheri; David Chen; W Zev Rymer
Journal:  J Neuroeng Rehabil       Date:  2010-06-23       Impact factor: 4.262

Review 9.  A benefit-risk assessment of baclofen in severe spinal spasticity.

Authors:  Alessandro Dario; Giustino Tomei
Journal:  Drug Saf       Date:  2004       Impact factor: 5.606

10.  Pediatric safety of tizanidine: clinical adverse event database and retrospective chart assessment.

Authors:  Herbert R Henney; Michael Chez
Journal:  Paediatr Drugs       Date:  2009       Impact factor: 3.022

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.