It is postulated that botulinum toxin type A (BTA) is effective in the treatment of the myofascial pain syndrome (MPS). However, previous studies have shown contradictory results. Our objective has been to evaluate the efficacy and safety of a single dose of BTA (Dysport庐) in primary MPS of cervical-dorsal localization.
A multicenter, randomized, double blind, parallel and placebo-controlled pilot study was performed. The participants (n = 24, 1:1 regime) were randomized to receive an intramuscular dose of Dysport庐 (maximum dose: 500 U) or placebo, with follow-up for 12 weeks. Pain intensity using the visual analogue scale (VAS) and pressure pain threshold with the algometry were measured. All of the participants were told to perform muscle stretchings.
The patients treated with placebo showed an initial decrease in pain intensity followed by a gradual increase of it while those who received Dysport庐 show a slower, but more continued improvement. After 12 weeks, the mean reductions on the VAS were 26%and 44.6%, respectively. The reduction in the patients who were treated with Dysport庐 was clinically relevant, although the difference between groups was not statistically significant. At 12 weeks, the pressure pain threshold had increased in both groups (36%placebo and 58%Dysport庐; P=.748 between treatments). Similar tendencies were seen in all the trigger points. Treatment with Dysport庐 was well tolerated.
These results suggest that Dysport庐 is beneficial in the treatment of cervical-dorsal MPS.