Table 4.
Study (Year) | Intervention | Results |
---|---|---|
Porta,103 2000 | BoNT-A (dose not reported), 0.5% bupivacaine, methylprednisolone | BoNT-A and steroid group had no significant differences in pain reduction at 1 mo; however, at 2 mo postinjection, there was a significant reduction in the BoNT-A group compared with the steroid group |
Lang,106 2004 | 5000 u BoNT-B | Significant reduction in hip and buttock pain at 4, 12, and 16 wk |
Fishman et al,107 2004 | 12,500 u BoNT-B | Combined with PT, 88.9% of patients injected had 50% improvement on the VAS |
Yoon et al,108 2007 | 150 u BoNT-A vs 5 mg dexamethasone/1% lidocaine | Pain significantly lower in Dysport group at 4, 8, and 12 wk vs baseline P < .0001 |
Childers et al,109 2002 | 100 u BoNT-A | Significant improvement in pain, spasm, distress, and interference with activities |
Fishman et al,110 2002 | 200 u BoNT-A vs 1.5 mL 2% lidocaine/20 mg triamcinolone, vs placebo | 50% improvement at last 2 visits following 20 mg TL vs placebo injection: P = .001; BoNT-A vs TL: P = .044; BoNT-A vs placebo: P = .001 |
Fishman et al,111 2017 | 300 u BoNT-A vs saline | VAS score decreased significantly at 2,4,6,8,10, and 12 wk compared with placebo |
Rodriguez-Pinero et al,112 2018 | 100 U BoNT-A | VAS scores and quality of life scores statistically significantly reduced at 1 and 6 mo after injection |
Yan,113 2021 | 100 u BoNT-A/1% lidocaine/0.5% bupivacaine vs 1% lidocaine/0.5% bupivacaine/4 mg dexamethasone | Median pain-free days were 30 d for the BoNT-A group and 1 d for the non–BoNT-A group |
Dr Chadwick has served as a consultant for Swing Therapeutics and receives research funding from the National Institutes of Health, National Institute of General Medical Sciences, Grant # K23GM123320.