Cortical and spinal excitability changes after repetitive transcranial magnetic stimulation combined to physiotherapy in stroke spastic patients

Objective Repetitive Transcranial Magnetic Stimulation (rTMS) has been used to treat post-stroke upper limb spasticity (ULS) in addition to physiotherapy (PT). To determine whether rTMS associated with PT modulates cortical and spinal cord excitability as well as decreases ULS of post-stroke patient...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurological sciences 2019-06, Vol.40 (6), p.1199-1207
Hauptverfasser: dos Santos, Rebeka Borba Costa, Galvão, Silvana Carla Barros, Frederico, Labibe Mara Pinel, Amaral, Nathália Serrano Lucena, Carneiro, Maíra Izzadora Souza, de Moura Filho, Alberto Galvão, Piscitelli, Daniele, Monte-Silva, Kátia
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective Repetitive Transcranial Magnetic Stimulation (rTMS) has been used to treat post-stroke upper limb spasticity (ULS) in addition to physiotherapy (PT). To determine whether rTMS associated with PT modulates cortical and spinal cord excitability as well as decreases ULS of post-stroke patients. Methods Twenty chronic patients were randomly assigned to either the intervention group-1 Hz rTMS on the unaffected hemisphere and PT, or control group- sham stimulation and PT, for ten sessions. Before and after sessions, ULS was measured using the modified Ashworth scale and cortical excitability using the output intensity of the magnetic stimulator (MSO). The spinal excitability was measured by the Hmax/Mmax ratio of the median nerve at baseline, at the end of treatment, and at the 4-week follow-up. Results The experimental group showed at the end of treatment an enhancement of cortical excitability, i.e., lower values of MSO, compared to control group ( p  = 0.044) and to baseline ( p  = 0.028). The experimental group showed a decreased spinal cord excitability at the 4-week follow-up compared to control group ( p  = 0.021). ULS decreased by the sixth session in the experimental group ( p  
ISSN:1590-1874
1590-3478
DOI:10.1007/s10072-019-03765-y