Contractures and involuntary muscle overactivity in severe brain injury
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Abstract
Primary objective: The aim of the present study was to evaluate the association of contractures with an increase or reduction of non-spastic muscle overactivity due to severe cerebral damage. Methods and procedures: Forty-five patients with tetraparesis after severe cerebral damage were investigated. Three groups were defined based on the presence of spasticity (revealed as resistance to passive stretch (= hypertonia)), and the presence of contracture of the relevant knee joint: Groups (17 patients with hypertonia without contracture), Groups+c (20 patients with hypertonia and contracture), and Groupc (eight patients without hypertonia and with contracture). In all groups spontaneous involuntary muscle activity was assessed continuously over a 12-hour period through isometric measurement of knee joint flexion torque. A mathematical algorithm differentiated an hourly muscle activity spectrum (PIh). The frequency of peaks (peaksh) from the activity spectrum was determined. Main outcomes and results: We revealed that Groups had higher PIh and more frequent peaksh compared with Groups+c and Groupc (p ≤ 0.05). Groupc had comparable PIh and peaksh compared with Groups+c (p ≥ 0.05). Conclusion: The presence of contractures was associated with lower involuntary muscle overactivity in terms of lower PIh and less frequent peaksh, indicating that contractures may be associated with reduced non-spastic positive features of the upper motor neurone syndrome in patients with severe brain damage.
Details
Originalsprache | Englisch |
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Seiten (von - bis) | 421-432 |
Seitenumfang | 12 |
Fachzeitschrift | Brain injury |
Jahrgang | 21 |
Ausgabenummer | 4 |
Publikationsstatus | Veröffentlicht - 2007 |
Peer-Review-Status | Ja |
Externe IDs
PubMed | 17487640 |
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Schlagworte
ASJC Scopus Sachgebiete
Schlagwörter
- Muscle contracture, Muscle overactivity, Spasticity, Upper motor neurone syndrome