TY - JOUR
T1 - OnabotulinumtoxinA and AbobotulinumtoxinA Dose Conversion
T2 - A Systematic Literature Review
AU - Dashtipour, Khashayar
AU - Chen, Jack J.
AU - Espay, Alberto J.
AU - Mari, Zoltan
AU - Ondo, William
N1 - Publisher Copyright:
© 2016 International Parkinson and Movement Disorder Society.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Objective: This systematic review was performed to elucidate dosing practices, dosing conversions, and related outcomes from randomized, controlled trials that directly compared onabotulinumtoxinA (ONA) and abobotulinumtoxinA (ABO) at various dose conversion ratios for therapeutic use in movement disorders. Methods: A systematic review of three medical literature databases (PubMed, the Cochrane Library, and EMBASE) was performed to identify relevant comparative clinical studies, systematic reviews, and meta-analyses published in the English language between January 1991 and January 2015. Studies that met predefined inclusion criteria were selected for formal data extraction and quality assessment. Results: A total of 182 manuscripts were identified, of which four were included for analysis. Targeted clinical applications included neurological disorders. The studies compared ONA to ABO dose conversion ratios of 1:2.5 (n = 1), 1:3 (n = 2), and 1:4 (n = 2). One study compared both 1:3 and 1:4 ratios. An ONA:ABO conversion factor of 1:2.5 was associated with similar efficacy and side effects. An ONA:ABO ratio of 1:3 provided similar or higher efficacy, but an increased rate of adverse effects, and an ONA:ABO ratio of 1:4 was associated with higher efficacy, but with an excessive rate of intolerable side effects. Conclusion: A dose conversion ratio of ONA to ABO between 1:2.5 and 1:3.0 provides comparable safety and efficacy for therapeutic movement disorders chemodenervation procedures.
AB - Objective: This systematic review was performed to elucidate dosing practices, dosing conversions, and related outcomes from randomized, controlled trials that directly compared onabotulinumtoxinA (ONA) and abobotulinumtoxinA (ABO) at various dose conversion ratios for therapeutic use in movement disorders. Methods: A systematic review of three medical literature databases (PubMed, the Cochrane Library, and EMBASE) was performed to identify relevant comparative clinical studies, systematic reviews, and meta-analyses published in the English language between January 1991 and January 2015. Studies that met predefined inclusion criteria were selected for formal data extraction and quality assessment. Results: A total of 182 manuscripts were identified, of which four were included for analysis. Targeted clinical applications included neurological disorders. The studies compared ONA to ABO dose conversion ratios of 1:2.5 (n = 1), 1:3 (n = 2), and 1:4 (n = 2). One study compared both 1:3 and 1:4 ratios. An ONA:ABO conversion factor of 1:2.5 was associated with similar efficacy and side effects. An ONA:ABO ratio of 1:3 provided similar or higher efficacy, but an increased rate of adverse effects, and an ONA:ABO ratio of 1:4 was associated with higher efficacy, but with an excessive rate of intolerable side effects. Conclusion: A dose conversion ratio of ONA to ABO between 1:2.5 and 1:3.0 provides comparable safety and efficacy for therapeutic movement disorders chemodenervation procedures.
KW - AbobotulinumtoxinA
KW - Blepharospasm
KW - Botulinum toxin
KW - Cervical dystonia
KW - Dose conversion ratio
KW - OnabotulinumtoxinA
UR - http://www.scopus.com/inward/record.url?scp=85031722824&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85031722824&partnerID=8YFLogxK
U2 - 10.1002/mdc3.12235
DO - 10.1002/mdc3.12235
M3 - Article
AN - SCOPUS:85031722824
SN - 2330-1619
VL - 3
SP - 109
EP - 115
JO - Movement Disorders Clinical Practice
JF - Movement Disorders Clinical Practice
IS - 2
ER -