Transcript Management of Spasticity (Researchers)
THE MANAGEMENT OF SPASTICITY AFTER SCI
A SYSTEMATIC REVIEW
OF THE LITERATURE, 2000-2010
Systematic Review – Management of Spasticity
Compiled by the Shepherd Center Study Group in Atlanta, GA. Innovative Knowledge Dissemination & Utilization Project for Disability & Professional Stakeholder Organizations/ NIDRR Grant # (H133A050006) at Boston University Center for Psychiatric Rehabilitation.
Systematic Review – Management of Spasticity
A review was conducted using a system for rating the rigor and meaning of disability research (Farkas, Rogers and Anthony, 2008). The first instrument in this system is: “Standards for Rating Program Evaluation, Policy or Survey Research, Pre-Post and Correlational Human Subjects” (Rogers, Farkas, Anthony & Kash, 2008) and “Standards for Rating the Meaning of Disability Research” (Farkas & Anthony, 2008).
Shepherd Center Systematic Review Group
Leadership Team:
Lesley Hudson, MS David Apple, MD Deborah Backus, PhD, PT
Data Coordinator:
Rebecca Acevedo
Editor:
Leslie VanHiel, MSPT
Reviewers:
Jennith Bernstein, PT Amanda Gillot, OT Ashley Kim, PT Elizabeth Sasso, PT Kristen Casperson, PT Anna Berry, PT Liz Randall, SPT
Glossary of Abbreviations
General SCI - Spinal cord injury ASIA – American Spinal Injury Association AIS – ASIA Impairment Scale ISNCSCI – International Standards for the Neurological Classification of Spinal Cord Injury Assessment (formerly ASIA exam)
Glossary of Abbreviations
Research Studies and Interventions RCT – Randomized control trial LE – Lower extremity ROM – Range of motion TENS – Transcutaneous electrical nerve stimulation rTMS - Repeated transcranial magnetic stimulation eSCS - Spinal cord electrical stimulation FES – Functional electrical stimulation WBV – Whole body vibration
Glossary of Abbreviations
Outcome Measures for Research Studies AS – Ashworth Scale MAS – Modified Ashworth Scale CSS - Composite spasticity score (based on several AS scores) VAS – Visual Analog Scale MPSFS – Modified Penn Spasm Frequency Scale SCATS – Spinal Cord Assessment Tool for Spastic Reflexes SCI-SET – Spinal Cord Injury Spasticity Evaluation Tool Hmax/Mmax – Electrophysiological ratio measure of neural excitability EMG - Electromyography
Definitions of Spasticity
Involuntary muscle firing Velocity-dependent Increase resistance to stretch Abnormal processing of sensory input within networks of neurons in the spinal cord networks.
There are many definitions of spasticity, but the most referenced: Lance, 1980: “Spasticity is a motor disorder characterized by a velocity dependent increase in tonic stretch reflexes (muscle tone) with exaggerated tendon jerks, resulting from hyperexcitability of the stretch reflex, as one component of the upper motor neuron syndrome.”
Other Definitions
Decq’s definition, 2003 : “…a symptom of the upper motor neuron syndrome characterized by an exaggeration of the stretch reflex secondary to hyperexcitability of spinal reflexes.” It separates: Intrinsic tonic spasticity: exaggeration of the tonic component of the stretch reflex (hypertonia).
Intrinsic phasic spasticity: exaggeration of the phasic component of the stretch reflex (hyper-reflexia, clonus, velocity-dependent resistance).
Extrinsic spasticity: exaggeration of extrinsic flexion or extension spinal reflexes (spasms, withdrawal reflex).
Adams & Hicks, Spinal Cord, 2005
Positive Effects of Spasticity
Spasticity may: Be used to help with transfers, standing, walking, and ADLs.
Help prevent muscle atrophy. Muscles may appear to be healthier compared to those without spasticity.
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Negative Effects of Spasticity
However, spasticity may also lead to: Decreased range of motion (ROM) Inability to position the limbs safely Limited mobility Difficulty performing personal hygiene Discomfort and pain andgodlaughs.blogspot.com
Is Treatment Necessary?
If mild, wait and see?
Questions to ask: Does it cause pain?
Interfere with sleep?
Make function unsafe?
Cause secondary issues of Poor posture / asymmetric seating?
Pressure sores?
Make care difficult?
Affect hygiene?
Will treatment improve quality of life and safety?
Treatment Goals
Relieve signs & symptoms Decrease frequency and severity of spasticity Improve function Gait Posture Reach and grasp for ADLs Improve ease of care
Patient Evaluation and Treatment Planning Evaluate Patient:
Does spasticity/ overactivity interfere significantly with function?
Measures must include all aspects of spasticity Will it lead to musculoskeletal deformity?
Yes Patient and C aregiver Objectives
• Identify patient and caregiver goals
Functional Objectives
• Improve gait, hygiene, ADLs, pain relief, ease of care • Decrease spasm frequency & severity
No No treatment necessary Technical Objectives
• Promote tone reduction, improved range of motion, joint position • Decrease spasm frequency • Decrease hyper-reflexia
Spasticity Management Program
MODIFIED from Spasticity Treatment Planning. WEMOVE.org, 2005.
Spasticity is an ongoing problem, despite treatment options.
Traditional and surgical treatment options are routinely used to decrease spasticity… Yet, many persons with SCI continue to have problems related to spasticity: More than half of all persons surveyed with chronic SCI report symptoms and sequelae of spasticity (Sköld, et al. 1999; Maynard, et al. 1990).
Persons with cervical and motor incomplete injuries seem to have spasticity that is more frequent and more severe.
Conservative Treatment Options
Pharmacological Management Baclofen – oral or pump (intrathecal) Adjunct Dantrolene, Zanax, or Valium Physical and Occupational Therapy Range of motion (ROM) exercises & prolonged stretching Casting or splinting Electrical stimulation - transcutaneous nerve stimulation (TENS) Acupuncture Massage
If other options don’t work…
Surgery involves cutting pathways in the nervous system thought to be involved in spasticity.
However, forms of electrical stimulation to the spinal cord (epidural spinal cord stimulation) and electromagnetic stimulation to the brain (transcutaneous magnetic stimulation - TMS) may mimic the effects of surgical interventions.
Spasticity and its management in SCI is multi-faceted.
Spasticity is no longer just an extremity’s resistance to quick movement.
It includes spasms, overall hypertonia, hyper reflexia, and clonus.
The optimal treatment for each of these different aspects of spasticity is not yet clear.
The literature related to spasticity has not been evaluated in terms of what is meaningful to persons with SCI.
Purpose of Review
To evaluate all published research from the past 10 years related to the management of spasticity after spinal cord injury (SCI) to determine which evidence may be: Meaningful to persons with SCI who have spasticity (e.g. includes level and completeness of injury).
Related to any type of spasticity a person may experience (velocity-dependent resistance, spasms, hypertonia, clonus).
Definitions of types of spasticity used in this review
Velocity-dependent resistance = phasic (quick and short lasting) spasticity of resistance felt when an extremity is moved quickly Hypertonia = tonic (longer lasting, co-contraction) spasticity of increased resistance to movement throughout range Spasms = phasic spasticity of body movement into a flexor or extensor pattern Clonus = phasic spasticity of repeated movement of a body part when positioned with the muscle stretched Hyper-reflexia = increased reflex response (e.g. the knee reflex response)
The Review
Conducted by 7 clinicians.
Included all articles published between 2000 and 2010 related to the treatment of spasticity in persons with SCI. All articles rated on quality of the science & meaningfulness to persons with SCI, or their caregivers and clinicians, or payers.
Any article of high quality that was meaningful was considered for this summary.
Study Designs Accepted for Review
Experimental: Employed methods including a random assignment and a control group or a reasonably constructed comparison group.
Quasi-experimental: No random assignment, but either with a control group or a reasonably constructed comparison group.
Descriptive: Neither a control group, nor randomization, is used. These included case studies and reports, studies employing repeated measures, and pre-post designs .
Search Results
Of 49 papers reviewed: Seven papers met criteria of quality and meaningfulness.
Only 3 of the 7 papers defined spasticity, and these all differed.
Each of the 7 papers used different outcome measures of spasticity.
These are ongoing problems with research in this area.
Study Definition of Spasticity provided Aspect of spasticity measured
Bowden & Stokic 2009 Based on Lance, 1980: “…a motor disorder characterized by a velocity-dependent increase in tonic stretch reflex with exaggerated tendon jerks, resulting from hyperexcitability of the stretch reflex, as one component of upper motor neuron syndrome”; “…include clonus, involuntary muscle contractions or spasms, and muscle co-contraction.” Passive resistance to stretch Spasm frequency & severity Stretch reflex/hyper-reflexia Flexion withdrawal Kumru, et al. 2010 Based on Decq, 2003: “…a symptom of upper motor neuron syndrome, characterized by an exaggeration of the stretch reflex, spasms, and resistance to passive movement across a joint, secondary to hyperexcitability of spinal reflexes.” Velocity-dependent resistance to stretch Passive resistance to stretch Clonus Spasm frequency & severity Stretch reflex/hyper-reflexia Hypertonia Ness & Field-Foté 2009 Own definition: “…spastic hypertonia with increased reflex excitability and disordered motor output (i.e. spasticity, clonus, spastic gait patterns)…” Stretch reflex/quadriceps hyper-reflexia
Study
Chung & Cheng 2009
Definition of Spasticity provided
none provided
Aspect of spasticity measured
Velocity-dependent resistance to stretch Passive resistance Clonus Velocity-dependent resistance to stretch Kakebeeke TH, et al. 2005 none provided none provided Krause P et al. 2008 none provided Pinter MM, et al 2000 Passive resistance to stretch Stretch reflex/quadriceps hyper-reflexia Passive resistance to stretch Spasm frequency Stretch reflex/quadriceps hyper-reflexia
Experimental Study Design: Overview
2 of 7 studies used a randomized controlled trial (RCT).
Both of these studies used electrical stimulation for the treatment.
2 studies were longitudinal cohort designs.
1 study was a case study.
1 study used a pre-post design.
1 study used a cross-over design.
Experimental Study Design: RCT of TENS
Study
Chung BPH, Cheng BKK 2009
Intervention
60 mins active TENS or 60 mins placebo; over the common peroneal nerve
Study Design
RCT, n=18
Outcome Measures
Composite Spasticity Score Full range passive ankle dorsiflexion Ankle clonus
Participant Characteristics
14 male; 4 female 24-77 y.o.
C4-T12 AIS A, B, C, D 4 weeks to 364 weeks (approx. 5.5 years) post-SCI
Results: Reduction in Resistance and Clonus with TENS
TENS group showed significant decrease in: Composite Spasticity Score (29.5%, p=0.017) Resistance to full passive range at ankle dorsiflexion (31%, p=0.024) Ankle clonus (29.6%, p=0.023) Notes: Anti-spasticity medications were allowed.
No significant differences between groups at baseline.
Chung & Cheng 2009
Experimental Study Design: RCT of TMS
Study
Kumru H, Murillo N,
Intervention
Repetitive Transcranial Samso JV, et al. Magnetic 2010 Stimulation (TMS)
Study Design Outcome Measures Participant Characteristics
RCT with cross- over for sham group, n=15 MAS VAS for pain MPSFS SCAT SCI-SET Hmax/Mmax, Reflex (reflex responses on EMG as 12 male; 3 female 15-68 y.o.
C4-T12 AIS C, D 2-17 months post-SCI indicators of neural excitability) Withdrawal Reflex
RCT of TMS: Sample Notes
11 of 15 using Baclofen 4 of 15 on no anti-spasticity meds Not all traumatic SCIs: 4 of 15 etiology = tumor 4 of 15 etiology = myelitis Kumru et al., 2010
Results: Decrease in Some Spasticity, Motor Control Still Disordered
Neurophysiological function did not change.
TMS group, but not sham group, significantly decreased: MAS score (p<0.006) not significantly different between those with traumatic & non traumatic SCI MPSFS (p=0.01) SCATS (p<0.04) SCI-SET (p=0.003) MAS, SCATS, & SCI-SET results maintained one week after last session (p=0.049).
Kumru et al., 2010
Results (cont.):
14 of 15 reported significant improvement in pain on VAS (p<0.002).
Was maintained in 13 of 15 at end of the week after TMS (p=0.004) No significant change in measures when sham only.
Kumru et al., 2010
Experimental Study Design: Summary of RCTs
In persons with acute or chronic, motor complete or incomplete, paraplegia or tetraplegia, applying electrical stimulation peripherally (i.e. at the common peroneal nerve or the nerve innervating the muscle antagonistic to the spastic muscle, Chung & Cheng, 2009), or electromagnetic stimulation centrally (i.e. over the primary motor cortex, Kumru et al., 2010) for motor incomplete injuries led to a significant reduction in several different aspects of spasticity: – Velocity-dependent resistance to stretch – – – – Spasms Hypertonia Hyper-reflexia Clonus
Descriptive Study Design: Longitudinal Study, Epidural E-stim
Study
Pinter et al. 2000
Intervention
Epidural spinal cord electrical stimulation (eSCS)
Study Design
Longitudinal, n=8
Outcome Measures
EMG during passive stretch of LE & Pendulum Test Ashworth Scale Clinical rating scale
Participant Characteristics
4 male; 4 female 18-34 y.o.
C5-T6 AIS A, B, C 19-94 months post-SCI
Results: Epidural Stim Reduced Some Aspects of Spasticity
Significant reduction in: EMG activity in left and right legs (p=0.004, p=0.0035, respectively).
Except for quadriceps when analyzed independently Ashworth score (p=0.0117) 7 of 8 participants discontinued anti-spasticity medication.
Pinter et al., 2000
Descriptive Study Design: Case Study with Baclofen
Study
Bowden M, Stokic DS. 2009
Intervention
Pharma cologic, intrathecal baclofen
Study Design
Single subject case report
Outcome Measures
Ashworth Scale Lower extremity strength using ISNCSCI EMG H-Reflex & H/M ratio (reflex responses on EMG as indicators of neural excitability) Plantar Withdrawal Reflex Maximal Voluntary Dorsiflexion
Participant Characteristics
1 male 41 y.o.
T11, AIS D 8 years post-SCI
Strength Decreased, BUT Spasticity Decreased More
Dose-dependent decreases in: Ashworth score (p<0.01) Bilateral lower extremity strength (p<0.001) H/M ratio EMG amplitude and duration of the plantar withdrawal reflex Decrease in strength was less than decrease in spasticity.
After withdrawal of medication, the rebound in spasticity was less than increase in strength.
Descriptive Study Design: Pre-Post with Passive LE Cycling
Study
Kakebeeke et al. 2005
Intervention
30 mins passive lower extremity ergometry
Study Design
Pre-Post, n=10
Outcome Measures Participant Characteristics
Muscle strength testing using 9 male; isokinetic dynamometry (torque) in sitting & lying; movements of leg at 10 ° /sec & 120 ° /sec; taken before, after, & 1 week post passive cycling 1 female 23-60 y.o.
C6-T12 AIS A, B 1-25 years session post-SCI
Results: Strength Same, BUT Reports of Reduced Spasticity
No change in elicited peak torque before, immediately after, or one week after passive cycling. 6 of 10 participants reported reduced spasticity immediately after cycling.
Kakebeeke et al., 2005
Descriptive Study Design: Cross-over, FES & Passive Cycling
Study Intervention Study Design
Krause P, et al. 2008 Functional electrical stimulation cycling, Passive cycling Cross over, n=5
Outcome Measures Participant Characteristics
Modified AS of quads Pendulum Test of quads. Also during Pendulum Test: Peak Velocity (deg/s) during first swing Relaxation Index (A1/(1.6 x A0), where A1 & A0 = degrees of first swing in flexion, then extension, respectively) 3 male; 2 female 37-66 y.o.
T3-T7, AIS A 3-9 years post SCI
Results: Both Active & Passive Cycling Show Some Effects
Greater & significant increase in relaxation index (RI) after FES cycling (68%) than after passive cycling (12%) (p=0.01). Peak velocity (PV) significantly increased after FES cycling, unchanged after passive cycling (p=0.01).
MAS decreased significantly for both FES cycling (p<0.001) and passive cycling (p<0.05).
* Participants were not on anti-spasticity medications.
Descriptive Study Design: Longitudinal, Whole Body Vibration
Study
Ness LL, Field-Foté EC, 2009
Intervention Study Design
Whole body vibration on vibrating platform Longitudinal, n=16
Outcome Measures
Pendulum test
SCI Participant Characteristics
14 male; 3 female 28-65 y.o.
C4-T8 AIS C, D > 1 year post SCI
Results: Long Lasting Effects with WBV
Significant reduction in quadriceps spasticity (p=0.005).
Significant reduction within session (range p=0.005 to 0.006 for weeks 1, 2, 4).
No significant difference between those on anti spasticity meds and those not.
Effects lasted at least 6-8 weeks post-intervention.
Ness LL, Field-Foté EC, 2009
Medications Varied
7 of 16 on Baclofen 1 of 16 on Tizanidine 9 of 16 on no spasticity medication Ness LL, Field-Foté EC, 2009
Descriptive Study Design: Summary of Studies
These studies provide further support that: 1.
2.
stimulating the nervous system (e.g. electrical stimulation), OR altering the excitability in the nervous system (e.g. Baclofen) can lead to a reduction in spasticity in persons with complete or incomplete tetraplegia or paraplegia.
Methodological Considerations
Definitions of spasticity differ: A motor disorder characterized by a velocity-dependent increase in tonic stretch reflex, exaggerated tendon jerks; includes clonus, involuntary muscle contractions or spasms, and muscle co-contraction (Lance, 1980) Includes intrinsic tonic spasticity (i.e. the exaggeration of the tonic component of the stretch reflex, hypertonia), intrinsic phasic spasticity (i.e. the exaggeration of the phasic component of the stretch reflex or hyper-reflexia and clonus), and extrinsic spasticity, (i.e., the exaggeration of extrinsic flexion or extension spinal reflexes, spasms) (Adams & Hicks, 2005).
Study Limitations
Spasticity syndrome may be worse in people with cervical and incomplete injuries than those with thoracic and complete injuries.
(Kirshblum, 1999; Maynard et al, 1990; Sköld et al, 1999).
Even though studies included persons with complete and incomplete paraplegia and tetraplegia, as well as acute and chronic injuries, results were averaged and reported as a whole.
It remains unknown whether there is a differential response to the interventions.
Study Limitations
Studies included persons with chronic SCI, who may have musculoskeletal consequences to chronic spasticity.
Chronic spasticity has musculoskeletal effects, namely muscle shortening and contractures (Gracies et al., 1997).
Musculoskeletal parameters were not assessed in any of these studies. Improvements may have been neural or musculoskeletal or both.
Improving one and not the other may preclude maximal improvements.
Study Limitations
There were no functional assessments.
Whether reducing spasticity is necessary and sufficient for improving motor control and function remains unclear.
There were no studies addressing the cost effectiveness of treatments for spasticity.
Recommendations
Any stakeholder interested in the evidence related to the management of spasticity after SCI should consider: Outcome measures differed across all studies.
Different aspects of spasticity may be affected by a given intervention.
For instance, if spasms are the worse aspect of spasticity, rTMS, eSCS, or baclofen (all with evidence of reducing spasms in persons with SCI) may be pursued. Those with velocity-dependent resistance to stretch may choose TENS or rTMS, but rTMS may give the best results overall if there are multiple areas related to spasticity.
Recommended Future Research
Further study is warranted to determine: the differential responses to interventions in those with varying levels of injury, classifications of injury, and times since injury.
the differential effects of interventions on neural and musculoskeletal tissues.
the effects of interventions on function. the long-term effects of these interventions.
the cost-effectiveness of the various treatments for spasticity.
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