Abstract | OBJECTIVE: DESIGN: Double-blind randomized clinical trial. PATIENTS: Of 31 patients enrolled from an acute-care hospital in Spain, 2 cases dropped out (drop-out rate 6.5%). Fourteen subjects were treated with infiltration of 500 units of botulinum toxin type A in the pectoralis major muscle of the paretic side, and 15 with a placebo. METHODS: After infiltration, both groups received transcutaneous electrical nerve stimulation for 6 weeks. Patients were assessed by the use of the Visual Analogue Scale for pain. A good result concerning pain was considered when the Visual Analogue Scale score was below 33.3 mm or less than half the initial score. The patients were followed-up for 6 months. RESULTS: The patients treated with botulinum toxin type A showed a significantly greater pain improvement from the first week post-infiltration. Persistent shoulder pain was observed more frequently in the placebo group, with relative risks in the range 0.32-0.41 during the follow-up period. CONCLUSION:
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Authors | Ester Marco, Esther Duarte, Joan Vila, Marta Tejero, Anna Guillen, Roser Boza, Ferran Escalada, Josep M Espadaler |
Journal | Journal of rehabilitation medicine
(J Rehabil Med)
Vol. 39
Issue 6
Pg. 440-7
(Jul 2007)
ISSN: 1650-1977 [Print] Sweden |
PMID | 17624477
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Neuromuscular Agents
- Botulinum Toxins, Type A
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Topics |
- Adult
- Aged
- Botulinum Toxins, Type A
(administration & dosage, therapeutic use)
- Double-Blind Method
- Female
- Follow-Up Studies
- Hemiplegia
(complications, etiology, rehabilitation)
- Humans
- Injections, Intramuscular
- Male
- Middle Aged
- Muscle Spasticity
(drug therapy, etiology)
- Neuromuscular Agents
(administration & dosage, therapeutic use)
- Pain Measurement
- Range of Motion, Articular
- Shoulder Pain
(drug therapy, etiology)
- Transcutaneous Electric Nerve Stimulation
- Treatment Outcome
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