Ann Rehabil Med.  2018 Jun;42(3):384-395. 10.5535/arm.2018.42.3.384.

Quantitative Evaluation of Post-stroke Spasticity Using Neurophysiological and Radiological Tools: A Pilot Study

Affiliations
  • 1Department of Rehabilitation Medicine, Konyang University College of Medicine, Daejeon, Korea. jbocean@hanmail.net
  • 2Department of Radiology, Konyang University College of Medicine, Daejeon, Korea.
  • 3Center for Medical Metrology, Korea Research Institute of Standards and Science (KRISS), Daejeon, Korea.
  • 4University of Science and Technology, Daejeon, Korea.

Abstract


OBJECTIVE
To determine the possibility of a new measurement tool using electromyography and ultrasonography for quantitative spasticity assessment in post-stroke patients.
METHODS
Eight hemiplegic stroke patients with ankle plantarflexor spasticity confirmed by a Modified Ashworth Scale (MAS) were enrolled. Spasticity was evaluated using the MAS and Modified Tardieu Scale (MTS). Each subject underwent surface electromyography (sEMG) using the Brain Motor Control Assessment (BMCA) protocol and was compared with a healthy control group. Using ultrasonography, muscle architecture and elasticity index were measured from the medial gastrocnemius muscle (GCM) on the affected and unaffected sides.
RESULTS
MAS and MTS revealed significant correlation with sEMG activity. The fascicle length and pennation angle were significantly decreased in the medial GCM on the hemiplegic side compared with the unaffected side. The elasticity index of the spastic medial GCM was significantly increased compared with the unaffected side. The MTS X and R2-R1 values were significantly correlated with the elasticity index in the hemiplegic GCM. The relationship between clinical evaluation tools and both BMCA and sonoelastography was linear, but not statistically significant in the multiple regression analysis.
CONCLUSION
The BMCA protocol and ultrasonographic evaluation provide objective assessment of post-stroke spasticity. Further studies are necessary to conduct accurate assessment and treatment of spasticity.

Keyword

Stroke; Muscle spasticity; Electromyography; Ultrasonography; Muscles

MeSH Terms

Ankle
Brain
Elasticity
Elasticity Imaging Techniques
Electromyography
Evaluation Studies as Topic*
Humans
Muscle Spasticity*
Muscle, Skeletal
Muscles
Pilot Projects*
Stroke
Ultrasonography

Figure

  • Fig. 1. Ultrasonographic images of medial gastrocnemius muscle of patient with hemiplegic stroke. (A) Muscle thickness in the transverse view. (B) The muscle fascicle length and fascicle pennation angle in the longitudinal view.

  • Fig. 2. Sonoelastographic images of unaffected (A) and affected (B) medial gastrocnemius (GCN) muscle in the transverse plane. Elastogram is red to green color in the unaffected muscles and green to blue color in the spastic muscles. Elasticity index (E2) is higher in spastic muscles and lower in unaffected muscles.

  • Fig. 3. Voluntary control of movement. Examples of right ankle dorsiflexion attempts: (A) healthy subject and stroke subjects—subject no#7 (B) and subject no#8 (C). In (B), generally increased muscle activity spread across many channels, with less movemet. In (C), even though the subject made considerable effort, there was relatively little activity in both right tibialis anterior and triceps surae muscles, and only trace movement. RQ, right quadriceps; RQ, right hip adductor; RHS, right hamstring; RTA, right tibialis anterior; RTS, right triceps surae; LQ left quadriceps; RQ, left hip adductor; LHS, left hamstring; LTA, left tibialis anterior; RLS, left triceps surae muscle.

  • Fig. 4. Voluntary response indices (VRIs) obtained from healthy control and stroke patients. (A) Ankle dorsiflexion of hemiplegic side. (B) Ankle plantarflexion of hemiplegic side. The VRI shows high similarity index (SI) values throughout all maneuvers for control group and a variable range of magnitude of response vector (RV). The SI values were significantly lower in the stroke group compared with the control group for hemiplegic ankle dorsiflexion and plantarflexion. The surface electromyography magnitudes were also lower in the stroke group, with no significant difference.

  • Fig. 5. The graph shows changes in magnitude of sEMG activity according the MAS category (A), MTS spasticity grade, X value (B) and MTS dynamic angle, R2–R1 (C). There was a significant relationship between the sEMG and clinical assessment tools (MAS, r=0.913 and p=0.001; X-value, r=0.869 and p=0.005; R2–R1 value, r=0.926 and p=0.002). The MAS scores were substituted by different grades: Grade 1 to 1, Grade 1+ to 2, Grade 2 to 3, Grade 3 to 4, and Grade 4 to 5. sEMG, surface electromyography; MAS, Modified Ashworth Scale; MTS, Modified Tardieu Scale.

  • Fig. 6. The graph shows changes in elasticity index according to the MAS category (A), MTS spasticity grade, X value (B), and MTS dynamic angle, R2–R1 (C). The MAS score was not significantly correlated with the elasticity index of the spastic GCM (r=0.371 and p=0.228). The X and R2-R1 values were significantly correlated with the elasticity index in the hemiplegic GCM (X value, r=0.913 and p=0.002; R2–R1 value, r=0.737 and p=0.037,). The MAS scores were substituted by grades: Grade 1 to 1, Grade 1+ to 2, Grade 2 to 3, Grade 3 to 4, and Grade 4 to 5. MAS, Modified Ashworth Scale; MTS, Modified Tardieu Scale; GCM, gastrocnemius muscle.


Reference

1. Lance JW. The control of muscle tone, reflexes, and movement: Robert Wartenberg Lecture. Neurology. 1980; 30:1303–13.
2. van Wijck FM, Pandyan AD, Johnson GR, Barnes MP. Assessing motor deficits in neurological rehabilitation: patterns of instrument usage. Neurorehabil Neural Repair. 2001; 15:23–30.
Article
3. Li F, Wu Y, Li X. Test-retest reliability and inter-rater reliability of the Modified Tardieu Scale and the Modified Ashworth Scale in hemiplegic patients with stroke. Eur J Phys Rehabil Med. 2014; 50:9–15.
4. Alibiglou L, Rymer WZ, Harvey RL, Mirbagheri MM. The relation between Ashworth scores and neuromechanical measurements of spasticity following stroke. J Neuroeng Rehabil. 2008; 5:18.
Article
5. Biering-Sorensen F, Nielsen JB, Klinge K. Spasticityassessment: a review. Spinal Cord. 2006; 44:708–22.
Article
6. Kreifeldt JG. Signal versus noise characteristics of filtered EMG used as a control source. IEEE Trans Biomed Eng. 1971; 18:16–22.
Article
7. Sherwood AM, McKay WB, Dimitrijevic MR. Motor control after spinal cord injury: assessment using surface EMG. Muscle Nerve. 1996; 19:966–79.
Article
8. Dimitrijevic MR, Hsu CY, McKay WB. Neurophysiological assessment of spinal cord and head injury. J Neurotrauma. 1992; 9 Suppl 1:S293–300.
9. Park GY, Kwon DR. Application of real-time sonoelastography in musculoskeletal diseases related to physical medicine and rehabilitation. Am J Phys Med Rehabil. 2011; 90:875–86.
Article
10. Drakonaki EE, Allen GM, Wilson DJ. Ultrasound elastography for musculoskeletal applications. Br J Radiol. 2012; 85:1435–45.
Article
11. Lee DC, Lim HK, McKay WB, Priebe MM, Holmes SA, Sherwood AM. Toward an objective interpretation of surface EMG patterns: a voluntary response index (VRI). J Electromyogr Kinesiol. 2004; 14:379–88.
Article
12. Sherwood AM, Priebe MM, Graves DE. Consistency of multi-channel surface EMG recordings: application in spinal cord injured subjects. J Electromyogr Kinesiol. 1997; 7:97–111.
Article
13. Sherwood AM, Graves DE, Priebe MM. Altered motor control and spasticity after spinal cord injury: subjective and objective assessment. J Rehabil Res Dev. 2000; 37:41–52.
14. Zoghi M, Galea M, Morgan D. A Brain Motor Control Assessment (BMCA) protocol for upper limb function. PLoS One. 2013; 8:e79483.
Article
15. Kwon DR, Park GY, Lee SU, Chung I. Spastic cerebral palsy in children: dynamic sonoelastographic findings of medial gastrocnemius. Radiology. 2012; 263:794–801.
Article
16. Maganaris CN, Baltzopoulos V, Sargeant AJ. In vivo measurements of the triceps surae complex architecture in man: implications for muscle function. J Physiol. 1998; 512(Pt 2):603–14.
17. Kesikburun S, Yasar E, Adıguzel E, Guzelkucuk U, Alaca R, Tan AK. Assessment of spasticity with sonoelastography following stroke: a feasibility study. PM R. 2015; 7:1254–60.
Article
18. Boyd RN, Graham HK. Objective measurement of clinical findings in the use of botulinum toxin type A for the management of children with cerebral palsy. Eur J Neurol. 1999; 6 Suppl 4:s23–35.
Article
19. Mayer NH, Esquenazi A. Muscle overactivity and movement dysfunction in the upper motoneuron syndrome. Phys Med Rehabil Clin N Am. 2003; 14:855–83.
Article
20. Wissel J, Schelosky LD, Scott J, Christe W, Faiss JH, Mueller J. Early development of spasticity following stroke: a prospective, observational trial. J Neurol. 2010; 257:1067–72.
Article
21. Vattanasilp W, Ada L, Crosbie J. Contribution of thixotropy, spasticity, and contracture to ankle stiffness after stroke. J Neurol Neurosurg Psychiatry. 2000; 69:34–9.
Article
22. Thibaut A, Chatelle C, Ziegler E, Bruno MA, Laureys S, Gosseries O. Spasticity after stroke: physiology, assessment and treatment. Brain Inj. 2013; 27:1093–105.
Article
23. Shortland AP, Harris CA, Gough M, Robinson RO. Architecture of the medial gastrocnemius in children with spastic diplegia. Dev Med Child Neurol. 2002; 44:158–63.
Article
24. Sherwood AM, Dimitrijevic MR, McKay WB. Evidence of subclinical brain influence in clinically complete spinal cord injury: discomplete SCI. J Neurol Sci. 1992; 110:90–8.
Article
25. McKay WB, Lim HK, Priebe MM, Stokic DS, Sherwood AM. Clinical neurophysiological assessment of residual motor control in post-spinal cord injury paralysis. Neurorehabil Neural Repair. 2004; 18:144–53.
Article
26. Legerlotz K, Smith HK, Hing WA. Variation and reliability of ultrasonographic quantification of the architecture of the medial gastrocnemius muscle in young children. Clin Physiol Funct Imaging. 2010; 30:198–205.
Article
27. Gao F, Grant TH, Roth EJ, Zhang LQ. Changes in passive mechanical properties of the gastrocnemius muscle at the muscle fascicle and joint levels in stroke survivors. Arch Phys Med Rehabil. 2009; 90:819–26.
Article
28. Friden J, Lieber RL. Spastic muscle cells are shorter and stiffer than normal cells. Muscle Nerve. 2003; 27:157–64.
Article
29. Yasar E, Adiguzel E, Kesikburun S, Yenihayat I, Yilmaz B, Alaca R, et al. Assessment of forearm muscle spasticity with sonoelastography in patients with stroke. Br J Radiol. 2016; 89:20160603.
30. Allison SC, Abraham LD, Petersen CL. Reliability of the Modified Ashworth Scale in the assessment of plantarflexor muscle spasticity in patients with traumatic brain injury. Int J Rehabil Res. 1996; 19:67–78.
Article
31. Vattanasilp W, Ada L. The relationship between clinical and laboratory measures of spasticity. Aust J Physiother. 1999; 45:135–9.
Article
32. Feldman RG, Young RR, Koella WP. Spasticity, disordered motor control. Chicago: Year Book Medical Publishers;1980. p. 485–500.
33. Dietz V, Sinkjaer T. Spastic movement disorder: impaired reflex function and altered muscle mechanics. Lancet Neurol. 2007; 6:725–33.
Article
34. Kawakami Y, Ichinose Y, Fukunaga T. Architectural and functional features of human triceps surae muscles during contraction. J Appl Physiol (1985). 1998; 85:398–404.
35. Dias CP, Freire B, Goulart NB, Onzi ES, Becker J, Gomes I, et al. Muscle architecture and torque production in stroke survivors: an observational study. Top Stroke Rehabil. 2017; 24:206–13.
Article
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