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Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes?
Botulinum toxin serotype-A (BoNT-A) preparations are widely used to improve the appearance of wrinkles. While effective and well tolerated, patients require retreatment over time to re-establish the effects. There is growing interest from patients as to whether higher doses can prolong response with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310242/ https://www.ncbi.nlm.nih.gov/pubmed/34357966 http://dx.doi.org/10.3390/toxins13070494 |
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author | Kaufman-Janette, Joely Cox, Sue Ellen Dayan, Steven Joseph, John |
author_facet | Kaufman-Janette, Joely Cox, Sue Ellen Dayan, Steven Joseph, John |
author_sort | Kaufman-Janette, Joely |
collection | PubMed |
description | Botulinum toxin serotype-A (BoNT-A) preparations are widely used to improve the appearance of wrinkles. While effective and well tolerated, patients require retreatment over time to re-establish the effects. There is growing interest from patients as to whether higher doses can prolong response without significantly increasing side effects. We reviewed the efficacy and safety evidence for high-dose BoNT-A treatment of glabellar lines, by evaluating high-dose studies published since 2015. Toxins approved for glabellar line treatment in the US or Europe were considered. “High-dose” indicated doses above the licensed dose for each BoNT-A preparation. Five studies met the inclusion criteria and most were randomized, double-blind trials; designs and population sizes varied. Findings suggested that higher-dose BoNT-A treatment is feasible and may improve response duration without increased safety issues. Around 9 months’ median duration was achieved with a 2–2.5-fold increase of the abobotulinumtoxinA on-label dose, or with a 5-fold increase in incobotulinumtoxinA dose. A 2–4-fold increase of the onabotulinumtoxinA on-label dose yielded a median duration of around 6 months. Importantly, patient satisfaction and natural look remained with increasing abobotulinumtoxinA doses. While more data are needed, these findings may lead to more effective, individually tailored treatment plans to meet patient expectations. |
format | Online Article Text |
id | pubmed-8310242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83102422021-07-25 Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? Kaufman-Janette, Joely Cox, Sue Ellen Dayan, Steven Joseph, John Toxins (Basel) Review Botulinum toxin serotype-A (BoNT-A) preparations are widely used to improve the appearance of wrinkles. While effective and well tolerated, patients require retreatment over time to re-establish the effects. There is growing interest from patients as to whether higher doses can prolong response without significantly increasing side effects. We reviewed the efficacy and safety evidence for high-dose BoNT-A treatment of glabellar lines, by evaluating high-dose studies published since 2015. Toxins approved for glabellar line treatment in the US or Europe were considered. “High-dose” indicated doses above the licensed dose for each BoNT-A preparation. Five studies met the inclusion criteria and most were randomized, double-blind trials; designs and population sizes varied. Findings suggested that higher-dose BoNT-A treatment is feasible and may improve response duration without increased safety issues. Around 9 months’ median duration was achieved with a 2–2.5-fold increase of the abobotulinumtoxinA on-label dose, or with a 5-fold increase in incobotulinumtoxinA dose. A 2–4-fold increase of the onabotulinumtoxinA on-label dose yielded a median duration of around 6 months. Importantly, patient satisfaction and natural look remained with increasing abobotulinumtoxinA doses. While more data are needed, these findings may lead to more effective, individually tailored treatment plans to meet patient expectations. MDPI 2021-07-16 /pmc/articles/PMC8310242/ /pubmed/34357966 http://dx.doi.org/10.3390/toxins13070494 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kaufman-Janette, Joely Cox, Sue Ellen Dayan, Steven Joseph, John Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title | Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title_full | Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title_fullStr | Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title_full_unstemmed | Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title_short | Botulinum Toxin Type A for Glabellar Frown Lines: What Impact of Higher Doses on Outcomes? |
title_sort | botulinum toxin type a for glabellar frown lines: what impact of higher doses on outcomes? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310242/ https://www.ncbi.nlm.nih.gov/pubmed/34357966 http://dx.doi.org/10.3390/toxins13070494 |
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