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. 2021 Feb 5;13(2):120. doi: 10.3390/toxins13020120

Table 6.

Studies on the use of BoNT-A therapy in postherpetic neuralgia.

First Author [Ref.] Type of Study n BoNT-A Doses Follow-Up Retreatment Results
Ding [113], 2017 Prospective 58 50 to 100 2 weeks
1, 3, 6 months
No 75% of patients improved
(Variable VAS, NPS reduction)
Jain [112], 2017 Case report 2 500 units Dysport diluted with 5 mL of normal saline, making a concentration of 100 units/mL 1, 2, 4, 8, 12, 16 weeks No VAS for pain decreased from 9, 10 to 1
Moon [118], 2016 Case report 2 50 U BoNT-A and bupivacaine 0.1% injected under ultrasound guide in brachial plexus 5 months No VAS for pain decreased from 8 to 2, 3
Li [110], 2015 Case report (ophthalmic) 1 100 U of BoNT-A in the orbital region (subcutaneous) 6 months No VAS for pain decreased from 8–9 to 2–3
Apalla [115], 2013 Randomized, double-blind, placebo-controlled trial 29 (4 postherpetic) 20, 190 U of BoNT-A intradermally 16 weeks No VAS decreasing
Emad [114], 2011 interventional study 15U per 10 cm2
(The amount of toxin was different for every patient: not reported)
intradermally
2, 4 weeks No VAS decreasing
Xiao [109], 2010 Randomized, double-blind, placebo-controlled trial 60 5 U/mL of BoNT-A vs. 0.5% of lidocaine vs. 0.9% of saline 3 months No Decrease in VAS score and improving in sleep hours superior to control group
Sotiriou [108], 2009 Case reports 3 100 U of BoNT-A in 4 mL of saline; subcutaneous in chessboard pattern 12 weeks No Decrease in VAS score
Liu [116], 2006 Case report 1 100 U of BoNT-A injected in a fanning pattern 9 months No VAS pain reduction from 10 to 1