Long-Term Efficacy of Extracorporeal Shock Wave Therapy on Lower Limb Post-Stroke Spasticity: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Emanuela Elena Mihai, Luminita Dumitru, Ilie Valentin Mihai, Mihai Berteanu, Emanuela Elena Mihai, Luminita Dumitru, Ilie Valentin Mihai, Mihai Berteanu

Abstract

The purpose of this systematic review and meta-analysis is to evaluate the long-term efficacy of Extracorporeal Shock Wave Therapy (ESWT) on reducing lower limb post-stroke spasticity in adults. A systematic electronic search of PubMed/ MEDLINE, Physiotherapy Evidence Database (PEDro), Scopus, Ovid MEDLINE(R), and search engine of Google Scholar was performed. Publications that ranged from January 2010 to August 2020, published in English, French, Spanish, Portuguese, and Italian language and available as full texts were eligible for inclusion and they were searched without any restrictions of country. The study was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines and followed the recommendations of the Cochrane Handbook for Systematic Reviews of Interventions. Two authors screened the references, extracted data, and assessed the risk of bias. The primary outcome was spasticity grade mainly assessed by the Modified Ashworth Scale (MAS). Secondary outcomes were passive range of motion (PROM), pain intensity, electrophysiological parameters, gait assessment, and adverse events. A total of seven recent randomized controlled trials (RCTs) were included in the systematic review and meta-analysis, and a beneficial effect on spasticity was found. The high level of evidence presented in this paper showed that ESWT ameliorates spasticity considering the parameters: MAS: standardized mean difference (SMD) = 0.53; 95% confidence interval (95% CI): (0.07-0.99); Modified Tardieu Scale (MTS): SMD = 0.56; 95% CI: (0.01-1.12); Visual Analogue Scale (VAS): SMD = 0.35; 95% CI: (-0.21-0.91); PROM: SMD = 0.69; 95% CI: (0.20-1.19). ESWT presented long-term efficacy on lower limb post-stroke spasticity, reduced pain intensity, and increased range of motion. The effect of this novel and non-invasive therapy was significant and the intervention did not present adverse events, proving a satisfactory safety profile.

Keywords: extracorporeal shock wave therapy; hemiplegia; neurological rehabilitation; spasticity; stroke.

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flow diagram of the selection process of studies for the systematic review and meta-analysis according to The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
Figure 2
Figure 2
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) for spasticity assessed by Modified Ashworth Scale (MAS) before and after extracorporeal shock wave therapy (ESWT) on the short-term. Wu et al. 2017a: radial ESWT (rESWT); Wu et al. 2017b: focused ESWT (fESWT); Tirbisch 2015a: soleus muscle assessment; Tirbisch 2015b: gastrocnemius muscle assessment; Lee et al. 2019a: follow-up at 30 min. after ESWT; Lee et al. 2019b: follow-up at one week after ESWT.
Figure 3
Figure 3
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) for spasticity assessed by Modified Ashworth Scale (MAS) before and after extracorporeal shock wave therapy (ESWT) on the long-term. Lee et al. 2019c: follow-up at four weeks after treatment; Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment; Tirbisch 2015a: soleus muscle assessment; Tirbisch 2015b: gastrocnemius muscle assessment; Wu et al. 2017a1: radial ESWT (rESWT) and follow-up at four weeks after treatment; Wu et al. 2017a2: radial ESWT (rESWT) and follow-up at eight weeks after treatment; Wu et al. 2017b1: focused ESWT (fESWT) and follow-up at four weeks after treatment; Wu et al. 2017b2: focused ESWT (fESWT) and follow-up at eight weeks after treatment; Yoon et al. 2017a: muscle belly application; Yoon et al. 2017b: myotendinous junction application.
Figure 4
Figure 4
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) for spasticity assessed by Modified Ashworth Scale (MAS) comparing the control group (CG) and the experimental group (EG) after extracorporeal shock wave therapy (ESWT) on the long-term. Lee et al. 2019c: follow-up at four weeks after treatment; Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment; Tirbisch 2015a: soleus muscle assessment; Tirbisch 2015b: gastrocnemius muscle assessment; Yoon et al. 2017a: muscle belly application; Yoon et al. 2017b: myotendinous junction application.
Figure 5
Figure 5
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) for spasticity assessed by Modified Ashworth Scale (MAS) comparing the control group (CG) and experimental group (EG) on the long-term. Sensitivity analysis. Lee et al. 2019c: follow-up at 4 weeks after treatment; Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment; Yoon et al. 2017a: muscle belly application; Yoon et al. 2017b: myotendinous junction application.
Figure 6
Figure 6
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) for spasticity assessed by Modified Tardieu Scale (MTS) before and after extracorporeal shock wave therapy (ESWT) on the long-term. Yoon et al. 2017a: muscle belly application; Yoon et al. 2017b: myotendinous junction application.
Figure 7
Figure 7
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating the short-term and long-term effects on pain intensity assessed by Visual Analogue Scale (VAS) before and after extracorporeal shock wave therapy (ESWT). Taheri et al. 2017: follow-up at one week after treatment; Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment.
Figure 8
Figure 8
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating the short-term and long-term effects on pain intensity assessed by Visual Analogue Scale (VAS) comparing the control group (CG) and experimental group (EG) after extracorporeal shock wave therapy (ESWT). Taheri et al. 2017: follow-up at one week after treatment; Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment.
Figure 9
Figure 9
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating long-term effects on pain intensity assessed by Visual Analogue Scale (VAS) comparing the control group (CG) and the experimental group (EG) after extracorporeal shock wave therapy (ESWT). Taheri et al. 2017a: follow-up at three weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment.
Figure 10
Figure 10
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating the short-term effects for Timed Up and Go Test (TUG) before and after extracorporeal shock wave therapy (ESWT). Radinmehr et al. 2017c1: follow-up immediately after treatment; Radinmehr et al. 2017c2: follow-up at 1 h after the end of treatment; Radinmehr et al. 2019c1: follow-up immediately after treatment; Radinmehr et al. 2019c2: follow-up at 1 h after the end of treatment.
Figure 11
Figure 11
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating the short-term effects on Hmax/Mmax ratio before and after extracorporeal shock wave therapy (ESWT). Radinmehr et al. 2017c1: follow-up immediately after treatment; Radinmehr et al. 2017c2: follow-up at 1 h after the end of treatment; Radinmehr et al. 2019c1: follow-up immediately after treatment; Radinmehr et al. 2019c2: follow-up at 1 h after the end of treatment.
Figure 12
Figure 12
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating the long-term effects on passive range of motion (PROM) before and after extracorporeal shock wave therapy (ESWT). Taheri et al. 2017a: follow-up at 3 weeks after treatment; Taheri et al. 2017b: follow-up at 12 weeks after treatment; Lee et al. 2019c: follow-up at four weeks after treatment.
Figure 13
Figure 13
Forest plot of the standardized mean difference (SMD) and 95% confidence interval (95% CI) evaluating short-term and long-term effects on passive range of motion (PROM) comparing focused extracorporeal shock wave therapy (fESWT) to radial extracorporeal shock wave therapy (rESWT). Wu et al. 2017c1: follow-up at 1 week after radial ESWT (rESWT) and focused ESWT (fESWT); Wu et al. 2017c2: follow-up at 4 weeks after radial ESWT (rESWT) and focused ESWT (fESWT); Wu et al. 2017c3: follow-up at 8 weeks after radial ESWT (rESWT) and focused ESWT (fESWT).

References

    1. Guzik A., Bushnell C. Stroke Epidemiology and Risk Factor Management. Contin. Lifelong Learn. Neurol. 2017;23:15–39. doi: 10.1212/CON.0000000000000416.
    1. Donkor E.S. Stroke in the 21st Century: A Snapshot of the Burden, Epidemiology, and Quality of Life. Stroke Res. Treat. 2018;2018 doi: 10.1155/2018/3238165.
    1. Johnson W., Onuma O., Owolabi M., Sachdev S. Stroke: A global response is needed. Bull. World Health Organ. 2016;94:634. doi: 10.2471/BLT.16.181636.
    1. Saleh M.A., Gaverth J., Yeung E., Marilyn M.L. Assessment of spasticity after stroke using clinical measures: A systematic review. Disabil. Rehabil. 2015;37:2313–2323. doi: 10.3109/09638288.2015.1014933.
    1. Mohr J.P., Choi D., Grotta J., Wolf P. Stroke: Pathophysiology, Diagnosis, and Management. 4th ed. Churchill Livingstone Hardcover; New York, NY, USA: 2004. pp. 62–101.
    1. Stein J., Harvey R.L., Macko R.F., Winstein C.J., Zorowitz R.D. Stroke Recovery and Rehabilitation. 1st ed. Demos Medical; New York, NY, USA: 2009. pp. 51–93.
    1. Feldmann R.G., Young R.R., Koella W.P. Spasticity, Disordered Motor Control. Symposia Specialists; Miami, FL, USA: 1980. pp. 485–495.
    1. Trompetto C., Marinelli L., Mori L., Pelosin E., Curra A., Molfetta L., Abbruzzese G. Pathophysiology of spasticity: Implications for neurorehabilitation. BioMed Res. Int. 2014;2014 doi: 10.1155/2014/354906.
    1. Zorowitz R.D., Gillard P.J., Brainin M. Poststroke spasticity: Sequelae and burden on stroke survivors and caregivers. Neurology. 2013;80(Suppl. S2):45–52. doi: 10.1212/WNL.0b013e3182764c86.
    1. Opheim A., Danielsson A., Murphy A.M., Persson H.C., Sunnerhagen K.S. Upper-limb spasticity during the first year after stroke: Stroke arm longitudinal study at the University of Gothenburg. Am. J. Phys. Med. Rehabil. 2014;93:884–896. doi: 10.1097/PHM.0000000000000157.
    1. Brainin M., Norrving B., Sunnerhagen K.S., Goldstein L.B., Cramer S.C., Donnan G.A., Duncan P.W., Francisco G., Good D., Graham G., et al. International PSS Disability Study Group. Poststroke chronic disease management: Towards improved identification and interventions for poststroke spasticity-related complications. Int. J. Stroke. 2011;6:42–46. doi: 10.1111/j.1747-4949.2010.00539.x.
    1. Gillard P.J., Sucharew H., Kleindorfer D., Belagaje S., Varon S., Alwell K., Moomaw C.J., Woo D., Khatri P., Flaherty M.L., et al. The negative impact of spasticity on the health-related quality of life of stroke survivors: A longitudinal cohort study. Health Qual. Life Outcomes. 2015;13 doi: 10.1186/s12955-015-0340-3.
    1. Cabanas V.R., Calvo S.J., Urrutia G., Serra L.P., Perez B.A., German R.A. The effectiveness of extracorporeal shock wave therapy to reduce lower limb spasticity in stroke patients: A systematic review and meta-analysis. Top. Stroke Rehabil. 2020;27:137–157. doi: 10.1080/10749357.2019.1654242.
    1. Jia G., Ma J., Wang S., Wu D., Tan B., Yin Y., Jia L., Cheng L. Long-term Effects of Extracorporeal Shock Wave Therapy on Poststroke Spasticity: A Meta-analysis of Randomized Controlled Trials. J. Stroke Cerebrovasc. Dis. 2020;29 doi: 10.1016/j.jstrokecerebrovasdis.2019.104591.
    1. Thibaut A., Chatelle C., Ziegler E., Bruno M.A., Laureys S., Gosseries O. Spasticity after stroke: Physiology, assessment and treatment. Brain Inj. 2013;27 doi: 10.3109/02699052.2013.804202.
    1. Salazar A.P., Pinto C., Ruschel M.J.V., Figueiro B., Lukrafka J.L., Pagnussat A.S. Effectiveness of static stretching positioning on post-stroke upper-limb spasticity and mobility: Systematic review with meta-analysis. Ann. Phys. Rehabil. Med. 2019;62:274–282. doi: 10.1016/j.rehab.2018.11.004.
    1. Costantino C., Galuppo L., Romiti D. Short-term effect of local muscle vibration treatment versus sham therapy on upper limb in chronic post-stroke patients: A randomized controlled trial. Eur. J. Phys. Rehabil. Med. 2017;53:32–40. doi: 10.23736/S1973-9087.16.04211-8.
    1. Kwong P.W., Ng G.Y., Chung R.C., Ng S.S. Transcutaneous electrical nerve stimulation improves walking capacity and reduces spasticity in stroke survivors: A systematic review and meta-analysis. Clin. Rehabil. 2018;32:1203–1219. doi: 10.1177/0269215517745349.
    1. McIntyre A., Lee T., Janzen S., Mays R., Mehta S., Teasell R. Systematic review of the effectiveness of pharmacological interventions in the treatment of spasticity of the hemiparetic lower extremity more than six months post stroke. Top. Stroke Rehabil. 2012;19:479–490. doi: 10.1310/tsr1906-479.
    1. Veerbeek J.M., van Wegen E., van Peppen R., van der Wees P.J., Hendriks E., Rietberg M., Kwakkel G. What is the evidence for physical therapy poststroke? A systematic review and meta-analysis. PLoS ONE. 2014;9 doi: 10.1371/journal.pone.0087987.
    1. Gracies J.M., Pradines M., Ghédira M. Guided Self-rehabilitation Contract vs conventional therapy in chronic stroke-induced hemiparesis: Neurorestore, a multicenter randomized controlled trial. BMC Neurol. 2019;39 doi: 10.1186/s12883-019-1257-y.
    1. Pound P., Bury M., Gompertz P., Ebrahim S. Views of survivors of stroke on benefits of physiotherapy. Qual. Health Care. 1994;3:69–74. doi: 10.1136/qshc.3.2.69.
    1. Poltawski L., Boddy K., Forster A., Goodwin V.A., Pavey A.C., Dean S. Motivators for uptake and maintenance of exercise: Perceptions of long-term stroke survivors and implications for design of exercise programmes. Disabil. Rehabil. 2015;37:795–801. doi: 10.3109/09638288.2014.946154.
    1. Khan F., Amatya B., Bensmail D., Yelnik A. Non-pharmacological interventions for spasticity in adults: An overview of systematic reviews. Ann. Phys. Rehabil. Med. 2019;62:265–273. doi: 10.1016/j.rehab.2017.10.001.
    1. Bakheit A.M. The pharmacological management of post-stroke muscle spasticity. Drugs Aging. 2012;29:941–947. doi: 10.1007/s40266-012-0034-z.
    1. Montane E., Vallano A., Laporte J.R. Oral antispastic drugs in nonprogressive neurologic diseases: A systematic review. Neurology. 2004;63:1357–1363. doi: 10.1212/01.WNL.0000141863.52691.44.
    1. Albrecht P., Jansen A., Lee J.I., Moll M., Ringelstein M., Rosenthal D., Bigalke H., Aktas O., Hartung H.P., Hefter H. High prevalence of neutralizing antibodies after long-term botulinum neurotoxin therapy. Neurology. 2019;92:48–54. doi: 10.1212/WNL.0000000000006688.
    1. Fabbri M., Leodori G., Fernandes R.M., Bhidayasiri R., Marti M.J., Colosimo M., Ferreira J.J. Neutralizing Antibody and Botulinum Toxin Therapy: A Systematic Review and Meta-analysis. Neurotox. Res. 2016;29:105–117. doi: 10.1007/s12640-015-9565-5.
    1. Brin M.F., Comella C.L., Jankovic J., Lai F., Naumann M. Long-term treatment with botulinum toxin type A in cervical dystonia has low immunogenicity by mouse protection assay. Mov. Disord. 2008;23:1353–1360. doi: 10.1002/mds.22157.
    1. Bethoux F. Spasticity Management After Stroke. Phys. Med. Rehabil. Clin. N. Am. 2015;26:625–639. doi: 10.1016/j.pmr.2015.07.003.
    1. Nair K.P., Marsden J. The management of spasticity in adults. BMJ. 2014 doi: 10.1136/bmj.g4737.
    1. Wu Y.T., Chang C.N., Chen Y.M., Hu G.C. Comparison of the effect of focused and radial extracorporeal shock waves on spastic equinus in patients with stroke: A randomized controlled trial. Eur. J. Phys. Rehabil. Med. 2018;54:518–525. doi: 10.23736/S1973-9087.17.04801-8.
    1. Radinmehr H., Ansari N.N., Naghdi S., Tabatabaei A., Moghimi E. Comparison of Therapeutic Ultrasound and Radial Shock Wave Therapy in the Treatment of Plantar Flexor Spasticity After Stroke: A Prospective, Single-blind, Randomized Clinical Trial. J. Stroke Cerebrovasc. Dis. 2019;28:1546–1554. doi: 10.1016/j.jstrokecerebrovasdis.2019.03.008.
    1. Manganotti P., Amelio E. Long-term effect of shock wave therapy on upper limb hypertonia in patients affected by stroke. Stroke. 2005;36:1967–1971. doi: 10.1161/01.STR.0000177880.06663.5c.
    1. Shrivastava S.K., Kailash Shock wave treatment in medicine. J. Biosci. 2005;30:269–275. doi: 10.1007/BF02703708.
    1. Dymarek R., Taradaj J., Rosinczuk J. The Effect of Radial Extracorporeal Shock Wave Stimulation on Upper Limb Spasticity in Chronic Stroke Patients: A Single-Blind, Randomized, Placebo-Controlled Study. Ultrasound Med. Biol. 2016;42:1862–1875. doi: 10.1016/j.ultrasmedbio.2016.03.006.
    1. Cleveland R.O., Chitnis P.V., McClure S.R. Acoustic field of a ballistic shock wave therapy device. Ultrasound Med. Biol. 2007;33:1327–1335. doi: 10.1016/j.ultrasmedbio.2007.02.014.
    1. Foldager C.B., Kearney C., Spector M. Clinical application of extracorpo- real shock wave therapy in orthopedics: Focused versus unfocused shock waves. Ultrasound Med. Biol. 2012;38:1673–1680. doi: 10.1016/j.ultrasmedbio.2012.06.004.
    1. Speed C. A systematic review of shockwave therapies in soft tissue con- ditions: Focusing on the evidence. Br. J. Sports Med. 2014;48:1538–1542. doi: 10.1136/bjsports-2012-091961.
    1. Chaussy C., Brendel W., Schmiedt E. Extracorporeally induced destruction of kidney stones by shock waves. Lancet. 1980;2:1265–1268. doi: 10.1016/S0140-6736(80)92335-1.
    1. Vrbanic S.L., Dobrović A.V., Sosa I., Cvijanovic O., Bobinac D. Effect of radial shock wave therapy on long bone fracture repair. J. Biol. Regul. Homeost. Agents. 2018;32:875–879.
    1. Frassanito P., Cavalieri C., Maestri R., Felicetti G. Effectiveness of Extracorporeal Shock Wave Therapy and kinesio taping in calcific tendinopathy of the shoulder: A randomized controlled trial. Eur. J. Phys. Rehabil. Med. 2018;54:333–340. doi: 10.23736/S1973-9087.17.04749-9.
    1. Stania M., Juras G., Chmielewska D., Polak A., Kucio C., Krol P. Extracorporeal Shock Wave Therapy for Achilles Tendinopathy. BioMed Res. Int. 2019;2019:3086910. doi: 10.1155/2019/3086910.
    1. Xiang J., Wang W., Jiang W., Qian Q. Effects of extracorporeal shock wave therapy on spasticity in post-stroke patients: A systematic review and meta-analysis of randomized controlled trials. J. Rehabil. Med. 2018;50:852–859. doi: 10.2340/16501977-2385.
    1. Guo P., Gao F., Zhao T., Sun W., Wang B., Li Z. Positive Effects of Extracorporeal Shock Wave Therapy on Spasticity in Poststroke Patients: A Meta-Analysis. J. Stroke Cerebrovasc. Dis. 2017;26:2470–2476. doi: 10.1016/j.jstrokecerebrovasdis.2017.08.019.
    1. Henarejos M.A.B., Meca J., Pina L.J.A., Hernandez C.R. Inter- and intra-rater reliability of the modified Ashworth scale: A systematic review and meta-analysis. Eur. J. Phys. Rehabil. Med. 2018;54:576–590. doi: 10.23736/S1973-9087.17.
    1. Dymarek R., Ptaszkowski K., Ptaszkowska L., Kowal M., Sopel M., Taradaj J., Rosinczuk J. Shock Waves as a Treatment Modality for Spasticity Reduction and Recovery Improvement in Post-Stroke Adults—Current Evidence and Qualitative Systematic Review. Clin. Interv. Aging. 2020;15:9–28. doi: 10.2147/CIA.S221032.
    1. Moher D., Liberati A., Tetzlaff J., Altman D.G. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. Int. J. Surg. 2010;8:336–341. doi: 10.1016/j.ijsu.2010.02.007.
    1. Higgins J., Thomas J., Chandler J., Cumpston M., Li T., Page M.J., Welch V.A. 2nd ed. John Wiley and Sons; Chichester, UK: 2019. Cochrane Handbook for Systematic Reviews of Interventions Version.
    1. Morton N.A. The PEDro scale is a valid measure of the methodological quality of clinical trials: A demographic study. Aust. J. Physiother. 2009;55:129–133. doi: 10.1016/S0004-9514(09)70043-1.
    1. Tirbisch L. Effets des ondes de choc radiales sur la spasticite du triceps sural de patients hemiplegiques en phase subaigue: Un essai controle randomise. Kinesither Rev. 2015;15 doi: 10.1016/j.kine.2015.05.008.
    1. Taheri P., Vahdatpour B., Mellat M., Ashtari F., Akbari M. Effect of Extracorporeal Shock Wave Therapy on Lower Limb Spasticity in Stroke Patients. Arch. Iran. Med. 2017;20:338–343.
    1. Yoon S.H., Shin M.K., Choi E.J., Kang H.J. Effective Site for the Application of Extracorporeal Shock-Wave Therapy on Spasticity in Chronic Stroke: Muscle Belly or Myotendinous Junction. Ann. Rehabil. Med. 2017;41:547–555. doi: 10.5535/arm.2017.41.4.547.
    1. Radinmehr H., Nakhostin A.N., Naghdi S., Olyaei G., Tabatabaei A. Effects of one session radial extracorporeal shockwave therapy on post-stroke plantarflexor spasticity: A single-blind clinical trial. Disabil. Rehabil. 2017;39:483–490. doi: 10.3109/09638288.2016.1148785.
    1. Lee C.H., Lee S.H., Yoo J.I., Lee S.U. Ultrasonographic Evaluation for the Effect of Extracorporeal Shock Wave Therapy on Gastrocnemius Muscle Spasticity in Patients With Chronic Stroke. PM&R. 2019;11:363–371. doi: 10.1016/j.pmrj.2018.08.379.
    1. Oh J.H., Park H.D., Han S.H., Shim G.Y., Choi K.Y. Duration of Treatment Effect of Extracorporeal Shock Wave on Spasticity and Subgroup-Analysis According to Number of Shocks and Application Site: A Meta-Analysis. Ann. Rehabil. Med. 2019;43:163–177. doi: 10.5535/arm.2019.43.2.163.
    1. Barton S. Which clinical studies provide the best evidence? The best RCT still trumps the best observational study. BMJ. 2000;321:255–256. doi: 10.1136/bmj.321.7256.255.
    1. Flansbjer U.B., Holmbback A.M., Downham D., Patten C., Lexell J. Reli- ability of gait performance tests in men and women with hemiparesis after stroke. J. Rehabil. Med. 2005;37:75–82. doi: 10.1080/16501970410017215.
    1. Yu S., Chen Y., Cai Q., Ma K., Zheng H., Xie L. A Novel Quantitative Spasticity Evaluation Method Based on Surface Electromyogram Signals and Adaptive Neuro Fuzzy Inference System. Front. Neurosci. 2020;14 doi: 10.3389/fnins.2020.00462.
    1. Pandyan A.D., Gregoric M., Barnes M.P., Wood D., Wijck V.F., Burridge J., Hermens H., Johnson G.R. Spasticity: Clinical perceptions, neurological realities and meaningful measurement. Disabil. Rehabil. 2005;27:2–6. doi: 10.1080/09638280400014576.
    1. Balci B.P. Spasticity Measurement. Arch. Neuropsychiatry. 2018;55(Suppl. S1):49–53. doi: 10.29399/npa.23339.
    1. Numanoglu A., Gunel M.K. Intraobserver reliability of modified Ashworth scale and modified Tardieu scale in the assessment of spasticity in children with cerebral palsy. Acta Orthop. Traumatol. Turc. 2012;46:196–200. doi: 10.3944/AOTT.2012.2697.
    1. Burridge J.H., Wood D.E., Hermens H.J., Voerman G.E., Johnson G.R., Wijck F., Platz T., Gregoric M., Hitchcock R., Pandyan A.D. Theoretical and methodological considerations in the measurement of spasticity. Disabil. Rehabil. 2005;27:69–80. doi: 10.1080/09638280400014592.
    1. Mariotto S., Prati A.C., Cavalieri E., Amelio E., Marlinghaus E., Suzuki H. Extracorporeal shock wave therapy in inflammatory diseases: Molecular mechanism that triggers anti-inflammatory action. Curr. Med. Chem. 2009;16:2366–2372. doi: 10.2174/092986709788682119.
    1. Mariotto S., Cavalieri E., Amelio E., Ciampa A.R., Prati A.C., Marlinghaus E., Russo S., Suzuki H. Extracorporeal shock waves: From lithotripsy to anti-inflammatory action by NO production. Nitric Oxide. 2005;12:89–96. doi: 10.1016/j.niox.2004.12.005.
    1. Leone J.A., Kukulka C.G. Effects of tendon pressure on alpha motoneuron excitability in patients with stroke. Phys. Ther. 1988;68:475–480. doi: 10.1093/ptj/68.4.475.
    1. Santamato A., Micello M.F., Panza F., Fortunato F., Logroscino G., Picelli A., Manganotti P., Smania N., Fiore P., Ranieri M. Extracorporeal shock wave therapy for the treatment of poststroke plantar-flexor muscles spasticity: A prospective open-label study. Top. Stroke Rehabil. 2014;21:17–24. doi: 10.1310/tsr21S1-S17.
    1. Bae H., Lee K.H., Lee J.M. The effects of extracorporeal shock wave therapy on spasticity in chronic stroke patients. Ann. Rehabil. Med. 2010;34:663–699. doi: 10.5535/arm.2013.37.4.461.
    1. Sohn M.K., Cho K.H., Kim Y.J., Hwang S.L. Spasticity and electrophysiologic changes after extracorporeal shock wave therapy on gastrocnemius. Ann. Rehabil. Med. 2011;35:599–604. doi: 10.5535/arm.2011.35.5.599.
    1. Moon S.W., Kim J.H., Jung M.J., Son S., Lee J.H., Shin H., Lee E.H., Yoon C.H., Oh M.K. The Effect of Extracorporeal Shock Wave Therapy on Lower Limb Spasticity in Subacute Stroke Patients. Ann. Rehabil. Med. 2013;37:461–470. doi: 10.5535/arm.2013.37.4.461.
    1. Daliri S.S., Forogh B., Razavi S., Ahadi T., Madjlesi F., Ansari N.N. A single blind, clinical trial to investigate the effects of a single session extracorporeal shock wave therapy on wrist flexor spasticity after stroke. NeuroRehabilitation. 2015;36:67–72. doi: 10.3233/NRE-141193.
    1. Wang T., Du L., Shan L., Dong H., Feng J., Kiessling M.C., Angstman B.A., Schmitz C., Jia F. A Prospective Case-Control Study of Radial Extracorporeal Shock Wave Therapy for Spastic Plantar Flexor Muscles in Very Young Children With Cerebral Palsy. Medicine. 2016;95:36–49. doi: 10.1097/MD.0000000000003649.
    1. Boot E., Ekker M.S., Putaala J., Kittner S., De Leeuw F.E., Tuladhar A.M. Ischaemic stroke in young adults: A global perspective. J. Neurol. Neurosurg. Psychiatry. 2020;91:411–417. doi: 10.1136/jnnp-2019-322424.

Source: PubMed

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