Presentation on theme: "1. FES FOR THE PAINFUL HEMIPLEGIC SHOULDER Overview Summary of research evidence Implications for PT practice Arlene Mendoza, Janet Sanabria, Telan Nelson,"— Presentation transcript:
FES FOR THE PAINFUL HEMIPLEGIC SHOULDER Overview Summary of research evidence Implications for PT practice Arlene Mendoza, Janet Sanabria, Telan Nelson, Amanda Lonsdale, Allison Pieracci, & Heather Nordberg
By the end of the presentation the learner will be able to: Describe the incidence and etiology of hemiplegic shoulder pain (HSP). Explain the methods for preventing and treating HSP. Define Functional Electrical Stimulation (FES). Explain how FES possibly decreases HSP & increases function. Conclude whether the use of FES post-stroke to treat HSP is effective and recommended. Explain how time post stroke relates to effectiveness of FES treatment. Learning Objectives
Review of the Hemiplegic Shoulder Muscle tone change in the UE from the early to late phase of recovery: Continuum from flacidity-> hypotonicity-> normal tone-> hypertonicity-> rigidity Problems that can result from flaccidity: GH subluxation and stretching of the capsule, ligaments, muscles, and nerves Problems that can result from hypertonicity: Flexion synergy pattern in which shoulder is add and IR. Teasell, R. et al. (2008)
Incidence of HSP o In a sample of 10 studies, the incidence of HSP varied from 9-73% of hemiplegic stroke patients. o The onset of HSP ranged from 2 weeks to 6 months post-stroke. o There is no standardized method for determining/measuring the epidemiology of HSP. o The incidence of HSP seems to increase over time following stroke. Teasell, R. et al. (2008)
Etiology of HSP Multi-factorial GH subluxation Impingement Decreased ROM/Frozen Shoulder CRPS (Complex Regional Pain Syndrome) Spasticity Ada, L., & Foongchomcheay, A (2002), Chantraine, A. et al. (1999) Teasell, R. et al. (2008), Walsh, K. (2001), Vaugnat, H. et al. (2003).
Prevention and Treatment of HSP Acute: Prevention and Treatment: Positioning/PROM/Handling/Family education/E-stim Chronic: Treatment: Positioning Injections (steroid, Botox) Aromatherapy and acupressure Electrical stimulation TENS FES Teasell, R. et al. (2008), Walsh, K. (2001), Vaugnat, H. et al. (2003)
Definition of FES FES utilizes electrical currents to activate nerves in areas of a patients body affected by paralysis, stroke, traumatic brain injuries, and other neurological disorders to restore some movement & function. - Cleveland FES Center, OH
How Does FES Reduce HSP? Shoulder subluxation and ER One proposed mechanism of reducing HSP, however it is uncertain that shoulder subluxation is the cause of HSP. Chantraine, A. et al. (1999), Ada, L., & Foongchomcheay (2002), Wang, RY et al. (2000), Price, C & Pandyan, A (2009), Teasell, R. et al. (2008)
How Does FES Reduce HSP? (continued) Other proposed mechanisms include: Stimulation of somatosensory cortex by augmented sensory feedback Increased proprioceptive stimulation Repetitive movements important for motor re-learning Increased muscle strength sNMES of cutaneous sensory nerves may modulate pain via gating pathways and central neuromodulation. Church, C. et al. (2006)
Shoulder Pain and Dysfunction in Hemiplegia: Effects of Functional Electrical Stimulation. Chantraine, A. et al. (1999) Controlled study of 24 months beginning in the first month after onset of stroke. Included CVA and Brain Injury subjects. 120 patients with a subluxed and painful hemiplegic shoulder (HSP). Patients were assigned to a control group or treatment group for a total of 5 weeks Control Group: conventional therapy (60 subjects) Treatment Group: FES and conventional therapy (60 subjects)
Treatment group: FES with Conventional Therapy Chantraine, A. et al. (1999) Sequence of FES Program 1 st Sequence 90 min, rectangular biphasic, 8 Hz, 350 usec, 1:5, 4 channel 2 nd Sequence 30 min, 40 Hz 3 rd Sequence 10 min, 1 Hz
Reduction in PAIN Treatment group vs. Control group Chantraine, A. et al. (1999) FESControlp value Time% pain reduction 3 mo p< mo p< mo p< mo p<.03
Improvement in Subluxation Grades Treatment group vs. Control group Chantraine, A. et al. (1999) de Bats Subluxation Scale Grade 1: Widening of the GH joint line or outward gliding of humeral head. No rupture of the scapulohumeral girdle. Grade 2: Evidence of the beginning of scapulohumeral girdle rupture. Grade 3: The scapulohumeral girdle rupture is complete. The joint is somewhat impaired. FESControlp value Time % Improvement of subluxation grade 6 mo p< mo p< mo p<.05
Improvement in Recovery of Motor Function Treatment group vs. Control group Chantraine, A. et al. (1999) FESControlp value Time % Recovery of Motor Function 6 mo p< mo p< mo p<.01
At all measurement stages the FES group had statistically significant improvements in subluxation, pain, and ROM as compared to the control group. Maintained for at least 24 mos. Treatment group: Maximum improvement in pain, subluxation, and motor recovery was observed at 6 months. Control group: Slow & progressive improvement reaching a max improvement after 1 yr. Overall: Two thirds of the cases improved in pain, subluxation, and remained constant up to 24 months. Results Chantraine, A. et al. (1999)
Conclusion Chantraine, A. et al. (1999) FES appears to decrease pain, subluxation, improve ROM, and increase motor function and therefore directly influences the degree and rate of recovery.
Intramuscular Electrical Stimulation for Hemiplegic Shoulder Pain Yu DT, Chae, J. et al (2004) oSubjects: 61 Treatment Group: 32 (intramuscular NMES) Control Group: 29 (Cuff-type sling) oInclusion criteria: >12 weeks post-stroke Pain rating >2 on the 11 pt. NRS 1/2 fingerbreadth of inferior glenohumeral subluxation
oTreatment Group: Intramuscular stimulation 6 hours/day for 6 weeks 20 sec on time/10 sec off time 20 mA and Intramuscular electrodes placed in the supraspinatus, posterior deltoid, middle deltoid, and upper trapezius. The electrodes were placed in the clinic and left in for the duration of the study. oControl Group: Cuff-type hemisling for 6 weeks Study Parameters Yu DT, Chae, J. et al (2004)
oPrimary Outcome Measures: BPI 12--A pain questionnaire that assesses pain intensity (0-10) scale as well as interference of pain in daily activites. oSecondary Outcome Measures: BPI question 23 Subluxation (assessed radiographically) Pain- free passive ER ROM Hemiparetic upper limb strength and coordination measured through the Fugl-Meyer motor assessment Spasticity assessed with Ashworth scale Upper limb-related activity limitation assessed by FIM instrument and Arm Motor Ability Test Outcome Measures Yu DT, Chae, J. et al (2004)
Results: Pain improvement Early group vs. Late group Chae, J. et al (2007) Percent of treatment successes based on the 2- point success criterion. ES = electrical stimulation. *P =.001. **P <.001. Percent of treatment successes based on the 30% success criterion. ES = electrical stimulation. *P =.001. **P <.001.
Results: Early Group vs. Late Group Mean change in BPI 12 scores Chae, J. et al (2007) ES (n=16)Control (n=14) EOT months months months ES (n=16)Control (n=15) EOT months months months Early group (<77 weeks post stroke) Late group (>77 weeks post stroke)
Results: Treatment Group vs. Control Group Chae, J. et al (2007) At end of treatment (EOT), 84% of the ES group experienced a 2 pain scale reduction compared to 31% of the control group. At 12 months, 78% of the ES group experienced a 2 pain scale reduction compared to 52% of the control group. A significantly higher success rate was seen for the ES group compared to the control group at EOT but not at 3, 6, and 12 months. There was no significant difference in any of the secondary outcomes measured.
FES can be beneficial for HSP if treated early (<77 weeks), and effects can be seen up to 12 months after treatment. Late treatment (>77 weeks) showed no significant improvements and any effects are only seen short- term. The treatment group had a higher success rate at EOT, but there was no significant difference between the treatment group and the control group at all of the follow-up measurements. Conclusion Chae, J. et al (2007)
RCT to Evaluate the Effect of sNMES to the Shoulder After Acute Stroke Church, C. et al. (2006) 176 Stroke patients, within 10 days post stroke Treatment Group: (90 patients) surface neuromuscular electric stimulation (sNMES) and stroke unit rehab One electrode over supraspinatus and one over posterior deltoid 30 Hz; 15sec on/ 15sec off (3 sec ramp) Increase intensity until visible contraction Treated 1hr, 3x/day for 1 month Control Group: (86 patients) sham sNMES and stroke unit rehab
Outcome Measures Church et al. (2006) Primary (at 3 months): Action Research Arm Test (ARAT) Secondary (at 4 weeks and at 3 months): Motricity Index Frenchay Arm Test 0-10 Numerical Pain Rating Scale (UE) 5-point adjectival scale (UE pain) Star Cancellation (for cortical function) Participants views regarding the sNMES Global health status at 3 months (Nottingham Health Profile and Oxford Handicap Scale)
Results Church et al. (2006) Results at 4 weeks: o There were no significant differences in any of the outcome measures between the control group and the treatment group. Results at 3 months: o There were no statistically significant differences in: Arm function (ARAT total) Upper limb pain Star Cancellation Global health status
Is sNMES hazardous for stroke patients with severe upper limb impairment? Church et al. (2006) There was a statistically significant difference in the grasp and gross subsections of the ARAT and Frenchay Arm Test and the arm portion of the Motricity Index in favor of the control group. Some upper limb function at baseline ARAT>0 No upper limb function at baseline ARAT=0 Treatment vs. Control Treatment vs. Control 4 weeks No Significant Difference 3 months No Significant DifferenceSignificant Difference in Favor of Control Group
Many hypotheses why poor outcome with severely impaired UE Church et al. (2006) Abnormal afferent stimulation causes maladaptive plasticity. Early over-use of the affected arm Unable to report adverse events or wrong delivery Overstimulation leading to shoulder subluxation May have promoted learned non-use of this arm.
Conclusion Church et al. (2006) For typical stroke patients treated in stroke rehab units: sNMES does NOT improve upper limb function, nor decrease pain after acute stroke. Routine use of sNMES CANNOT be recommended as it can pose potential negative consequences in those with initial severe impairment. Further research is needed to determine if there is a benefit to using sNMES for specific patient populations.
The Evidence-Based Review of Stroke Rehabilitation Teasell, R. et al., 2008 Canadian Systematic Review Over 15 Studies included There is conflicting evidence that FES reduces pain, improves function and reduces subluxation after stroke. FES may not help with recovery of hemiplegic shoulder.
Implications for PT Standardization is needed in reporting HSP Inconclusive if FES reduces HSP Inconclusive if FES improves function FES may be beneficial for treating GH subluxation Earlier initiation of FES treatment may result in a better outcome
Describe the incidence and etiology of hemiplegic shoulder pain (HSP). Explain the methods for preventing and treating HSP. Define Functional Electrical Stimulation (FES). Explain how FES possibly decreases HSP & increases function. Conclude whether the use of FES post-stroke to treat HSP is effective and recommended. Explain how time post stroke relates to effectiveness of FES treatment. Review Learning Objectives
REFERENCES Ada, L., & Foongchomcheay, A. (2002). Efficacy of electrical stimulation in preventing or reducing subluxation of the shoulder after stroke: A meta-analysis. Australian Journal of Physiotherapy, 48: Chantraine, A., Baribault, A., Uebelhart, D., & Gremion, G. (1999). Shoulder pain and dysfunction in hemiplegia: Effects of functional electrical stimulation. Archives of Physical Medicine and Rehabilitation, 80: Chae J et al. Intramuscular Electrical Stimulation for Hemiplegic Shoulder Pain: a 12 month follow up of a multiple center, randomized clinical trial. Am J Phys Med Rehabil. 2005;84: Church, C., Price, C., Pandyan, AD., Huntley, S., Curless, R., Rodgers, H. (2006). Randomized controlled trial to evaluate the effect of surface neuromuscular electrical stimulation to the shoulder after acute stroke. Stroke, 37: 2995–3001.
REFERENCES Price, CIM., & Pandyan, AD. (2009). Electrical stimulation for preventing and treating post-stroke shoulder pain. Cochrane Database of Systematic Reviews 2009 (1). Scott, Tom. "Functional Electrical Stimulation: The Future of Rehabilitation." Cleveland FES Center. United Spinals Action Online Magazine, 17 Nov Web. 24 Apr Teasell, R., Foley, N., Bhogal, S. (2008). Version 11: Painful hemiplegic shoulder. Obtained from the WWW April 7, 2009 at Vaugnat, H. & Chantraine, A. (2003). Shoulder pain in hemiplegia revisited:Contribution of functional electrical stimulation and other therapies. Journal of Rehabilitative Medicine, 35:
REFERENCES o Wang, RY., Chan, RC., & Tsai, MW. (2000). Functional electrical stimulation on chronic and acute hemiplegic shoulder subluxation. American Journal of Physical Medicine and Rehabilitation, 79 (4): o Walsh, K. (2001). Management of shoulder pain in patients with stroke. Postgraduate Medical Journal, 77: o Yu DT, Chae J, Walker ME, et al. Intramuscular neuromuscular electrical stimulation for post-stroke shoulder pain: a multi- center randomized clinical trial. Arch Phys Med Rehabil. 2004;85: