Archives of physical medicine and rehabilitation · 2011
Efficacy of intra-articular injection of botulinum toxin type A in refractory hemiplegic shoulder pain.
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Castiglione Alberto, Bagnato Sergio, Boccagni Cristina, Romano Marcello C, Galardi Giuseppe
Аннотация
OBJECTIVE: To evaluate the efficacy of intra-articular injection of botulinum toxin type A (BTX-A) in relieving hemiplegic shoulder pain (HSP).
DESIGN: Pilot study with assessments before and after BTX-A intra-articular injection.
SETTING: Hospital rehabilitation department.
PARTICIPANTS: Patients (N=5) with HSP refractory to standard treatments and pain score at rest greater than 7 on a pain visual analog scale (VAS) of 0 to 10cm.
INTERVENTION: Intra-articular BTX-A injection.
MAIN OUTCOME MEASURE: Variation in VAS score at rest and during 90° passive arm abduction 2 and 8 weeks after BTX-A intra-articular injection.
RESULTS: Baseline VAS score was 8.7±1 at rest and 9.8±0.4 during passive arm abduction. It clearly decreased at 2 (1.5±1.1 at rest, P=.001; 3±1.2 during arm abduction, P<.001) and 8 weeks (1.5±1.2 at rest, P=.001; 2.3±1.1 during arm abduction, P<.001) after BTX-A intra-articular injection.
CONCLUSIONS: We found a strong correlation between intra-articular BTX-A injection and pain relief in patients with HSP. This result could provide the rationale for blind randomized controlled trials designed to better evaluate the safety and efficacy of intra-articular BTX-A injection in patients with refractory HSP.
DESIGN: Pilot study with assessments before and after BTX-A intra-articular injection.
SETTING: Hospital rehabilitation department.
PARTICIPANTS: Patients (N=5) with HSP refractory to standard treatments and pain score at rest greater than 7 on a pain visual analog scale (VAS) of 0 to 10cm.
INTERVENTION: Intra-articular BTX-A injection.
MAIN OUTCOME MEASURE: Variation in VAS score at rest and during 90° passive arm abduction 2 and 8 weeks after BTX-A intra-articular injection.
RESULTS: Baseline VAS score was 8.7±1 at rest and 9.8±0.4 during passive arm abduction. It clearly decreased at 2 (1.5±1.1 at rest, P=.001; 3±1.2 during arm abduction, P<.001) and 8 weeks (1.5±1.2 at rest, P=.001; 2.3±1.1 during arm abduction, P<.001) after BTX-A intra-articular injection.
CONCLUSIONS: We found a strong correlation between intra-articular BTX-A injection and pain relief in patients with HSP. This result could provide the rationale for blind randomized controlled trials designed to better evaluate the safety and efficacy of intra-articular BTX-A injection in patients with refractory HSP.