Safety and Efficacy of PrabotulinumtoxinA (Nabota ® ) Injection for Cervical and Shoulder Girdle Myofascial Pain Syndrome: A Pilot Study

• Published in: Toxins 2018-09, Vol.10 (9), p.355
• Main Authors: Kim, Da-Ye, Kim, Jae Min
• Format: Article
• Language: English
• Subjects: Botulinum toxin; cervical; Chronic pain; Clinical trials; Conflicts of interest; Effectiveness; Injection; Laboratories; Muscles; myofascial pain syndrome; Neck; Pain; Patients; Pharmaceuticals; Population studies; Quality of life; Safety; Shoulder; Systematic review; Toxins
• ISSN: 2072-6651; 2072-6651
• DOI: 10.3390/toxins10090355

Myofascial pain syndrome is a common painful condition encountered in the general population. Previous studies evaluating the efficacy of botulinum toxin for the treatment of myofascial pain syndrome are limited, with variable results. This prospective study investigated the efficacy and safety of direct injection of Prabotulinumtoxin A (Nabota ) into painful muscle groups for cervical and shoulder girdle myofascial pain. Twelve patients with chronic myofascial pain syndrome of the neck and shoulder underwent an injection of Prabotulinumtoxin A. Painful muscles containing trigger points were injected in the mid-belly. Pain scores and quality of life measurements were assessed at baseline, as well as 6 weeks and 12 weeks post-injection. Safety and tolerability were also assessed. This trial is registered under clinical research information service (CRIS) number KCT0001634. Patients injected with Prabotulinumtoxin A showed a significant improvement in pain at 12 weeks ( < 0.001). At 6 weeks, the pain had not significantly improved compared with baseline ( = 0.063). However, at that time, 41.7% of patients were characterized as Prabotulinumtoxin A responders, with a 30% reduction in pain rating score compared to baseline. In the Neck Disability Index scores, the patients demonstrated significant improvement at both 6 weeks and 12 weeks. No serious adverse effects occurred during the study. Prabotulinumtoxin A injection into chronically painful muscles associated with cervical and shoulder girdle myofascial pain syndrome resulted in an improvement in pain scores and quality of life lasting at least 12 weeks. Additionally, the injections were well tolerated. As these are preliminary findings in a pilot study, future studies should carefully consider using randomized, controlled, prospective trials.