Luis Alberto Parra, Andreina Martinez Amado, Eugenia Cure, Ingrid Salas, Carolina Schneider, Andrea Marcela Parra
{"title":"Regional Variability in Botulinum Toxin Type A Practices: A Latin American Survey on Dosing, Preferences, and Clinical Outcomes","authors":"Luis Alberto Parra, Andreina Martinez Amado, Eugenia Cure, Ingrid Salas, Carolina Schneider, Andrea Marcela Parra","doi":"10.1002/der2.70054","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Regional practices for botulinum toxin type A (BoNT-A) in Latin America remain underexplored. This study characterizes dosing, brand preferences, and clinical outcomes across 12 countries.</p>\n </section>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>To characterize regional variations in BoNT-A dosing, brand preferences, and clinical outcomes for upper facial treatments.</p>\n </section>\n \n <section>\n \n <h3> Materials and Methods</h3>\n \n <p>A cross-sectional survey of 107 practitioners across 12 Latin American countries (March 2025) analyzed dosing (Speywood/International Units), duration, adverse events, and brand preferences using descriptive statistics.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Participants primarily practiced in Colombia (65.4%), Mexico (7.5%), and Central America (4.7%). AbobotulinumtoxinA required higher doses (total upper face: 114.98 ± 24.32 Speywood units) versus IncobotulinumtoxinA (66.36 ± 10.12 IU) and OnabotulinumtoxinA (62.94 ± 7.36 IU). Duration was comparable across brands (12.1–14.3 weeks). Regional preferences included AbobotulinumtoxinA in Brazil (55%) and IncobotulinumtoxinA in Mexico (48%), driven by cost or precision. Adverse events were transient (headache: 58.2%, ptosis: 12.2%).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Latin American practitioners balance cost-effectiveness and precision, with standardized dosing reflecting regional expertise. Long-term safety studies are warranted.</p>\n </section>\n </div>","PeriodicalId":100366,"journal":{"name":"Dermatological Reviews","volume":"6 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/der2.70054","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dermatological Reviews","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/ftr/10.1002/der2.70054","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Regional practices for botulinum toxin type A (BoNT-A) in Latin America remain underexplored. This study characterizes dosing, brand preferences, and clinical outcomes across 12 countries.
Objective
To characterize regional variations in BoNT-A dosing, brand preferences, and clinical outcomes for upper facial treatments.
Materials and Methods
A cross-sectional survey of 107 practitioners across 12 Latin American countries (March 2025) analyzed dosing (Speywood/International Units), duration, adverse events, and brand preferences using descriptive statistics.
Results
Participants primarily practiced in Colombia (65.4%), Mexico (7.5%), and Central America (4.7%). AbobotulinumtoxinA required higher doses (total upper face: 114.98 ± 24.32 Speywood units) versus IncobotulinumtoxinA (66.36 ± 10.12 IU) and OnabotulinumtoxinA (62.94 ± 7.36 IU). Duration was comparable across brands (12.1–14.3 weeks). Regional preferences included AbobotulinumtoxinA in Brazil (55%) and IncobotulinumtoxinA in Mexico (48%), driven by cost or precision. Adverse events were transient (headache: 58.2%, ptosis: 12.2%).
Conclusion
Latin American practitioners balance cost-effectiveness and precision, with standardized dosing reflecting regional expertise. Long-term safety studies are warranted.