Effectiveness of Botulinum Toxin A for Persistent Upper Limb Pain After Breast Cancer Treatment: A Double-Blinded Randomized Controlled Trial
Adult
Shoulder
Antineoplastic Protocols
Breast Neoplasms
Middle Aged
Combined Modality Therapy
Exercise Therapy
3. Good health
Upper Extremity
03 medical and health sciences
Treatment Outcome
0302 clinical medicine
Double-Blind Method
Neuromuscular Agents
Musculoskeletal Pain
Quality of Life
Humans
Female
Botulinum Toxins, Type A
DOI:
10.1016/j.apmr.2017.12.032
Publication Date:
2018-02-01T15:07:38Z
AUTHORS (10)
ABSTRACT
To investigate the effect of a single botulinum toxin A (BTX-A) infiltration in the pectoralis major muscle in addition to a standard physical therapy program for treatment of persistent upper limb pain in breast cancer survivors.Double-blinded (patient and assessor) randomized controlled trial.A university hospital.Breast cancer patients (N=50) with pain.The intervention group received a single BTX-A infiltration. The control group received a placebo (saline) infiltration. Within 1 week after the infiltration, all patients attended an individual physical therapy program (12 sessions) during the first 3 months and a home exercise program up to 6 months after infiltration.The primary outcome was change in pain intensity at the upper limb (visual analog scale, 0-100) after 3 months. Secondary outcomes were prevalence rate of pain, pressure hypersensitivity, pain quality, shoulder function, and quality of life. Measures were taken before the intervention and at 1, 3, and 6 months' follow-up.No significant difference in change in pain intensity after 3 months was found (mean difference in change, 3/100; 95% confidence interval [CI], -13 to 19). From baseline up to 6 months, a significantly different change in upper limb pain intensity was found between groups in favor of the intervention group (mean difference in change, 16/100; 95% CI, 1-31).A single BTX-A infiltration in combination with an individual physical therapy program significantly decreased pain intensity at the upper limb in breast cancer survivors up to 6 months. However, the effect size was not clinically relevant, and no other beneficial effects were found.
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