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Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L
BACKGROUND: VYC-20L is a hyaluronic acid soft tissue filler with lidocaine designed to restore facial volume. OBJECTIVE: Evaluate the safety and effectiveness of VYC-20L in patients with chin retrusion. MATERIALS AND METHODS: Adults with chin retrusion were randomized (3:1) to receive VYC-20L in the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752233/ https://www.ncbi.nlm.nih.gov/pubmed/33347003 http://dx.doi.org/10.1097/DSS.0000000000002795 |
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author | Beer, Kenneth Kaufman-Janette, Joely Bank, David Biesman, Brian Dayan, Steven Kim, William Chawla, Smita Schumacher, Andrew |
author_facet | Beer, Kenneth Kaufman-Janette, Joely Bank, David Biesman, Brian Dayan, Steven Kim, William Chawla, Smita Schumacher, Andrew |
author_sort | Beer, Kenneth |
collection | PubMed |
description | BACKGROUND: VYC-20L is a hyaluronic acid soft tissue filler with lidocaine designed to restore facial volume. OBJECTIVE: Evaluate the safety and effectiveness of VYC-20L in patients with chin retrusion. MATERIALS AND METHODS: Adults with chin retrusion were randomized (3:1) to receive VYC-20L in the chin at study onset (treatment group) or 6 months later (control group). The primary effectiveness end point was ≥1-point improvement on the Allergan Chin Retrusion Scale (ACRS) from baseline at Month 6. Safety assessments included injection site responses (ISRs) and adverse events (AEs). RESULTS: VYC-20L was administered to 192 participants (treatment group, n = 144; control group, n = 48). At Month 6, significantly more participants had an ACRS response in the treatment versus control group (56.3% vs 27.5%; p = .0019). Effectiveness was also demonstrated by the proportion of participants with improved/much improved Global Aesthetic Improvement Scale scores and responses on the FACE-Q Satisfaction with Chin questionnaire and FACE-Q Psychological Wellbeing module. Treatment benefit remained evident at Month 12. Most common ISRs were tenderness (81.1%) and firmness (75.1%). One participant (0.5%) discontinued the study due to 2 treatment-related serious AEs of facial cellulitis and injection site inflammation, both resolved without sequelae. CONCLUSION: VYC-20L significantly improved an ACRS response and was generally safe and well tolerated. |
format | Online Article Text |
id | pubmed-7752233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-77522332020-12-22 Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L Beer, Kenneth Kaufman-Janette, Joely Bank, David Biesman, Brian Dayan, Steven Kim, William Chawla, Smita Schumacher, Andrew Dermatol Surg Original Article BACKGROUND: VYC-20L is a hyaluronic acid soft tissue filler with lidocaine designed to restore facial volume. OBJECTIVE: Evaluate the safety and effectiveness of VYC-20L in patients with chin retrusion. MATERIALS AND METHODS: Adults with chin retrusion were randomized (3:1) to receive VYC-20L in the chin at study onset (treatment group) or 6 months later (control group). The primary effectiveness end point was ≥1-point improvement on the Allergan Chin Retrusion Scale (ACRS) from baseline at Month 6. Safety assessments included injection site responses (ISRs) and adverse events (AEs). RESULTS: VYC-20L was administered to 192 participants (treatment group, n = 144; control group, n = 48). At Month 6, significantly more participants had an ACRS response in the treatment versus control group (56.3% vs 27.5%; p = .0019). Effectiveness was also demonstrated by the proportion of participants with improved/much improved Global Aesthetic Improvement Scale scores and responses on the FACE-Q Satisfaction with Chin questionnaire and FACE-Q Psychological Wellbeing module. Treatment benefit remained evident at Month 12. Most common ISRs were tenderness (81.1%) and firmness (75.1%). One participant (0.5%) discontinued the study due to 2 treatment-related serious AEs of facial cellulitis and injection site inflammation, both resolved without sequelae. CONCLUSION: VYC-20L significantly improved an ACRS response and was generally safe and well tolerated. Lippincott Williams & Wilkins 2021-01 2020-09-22 /pmc/articles/PMC7752233/ /pubmed/33347003 http://dx.doi.org/10.1097/DSS.0000000000002795 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society for Dermatologic Surgery, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Article Beer, Kenneth Kaufman-Janette, Joely Bank, David Biesman, Brian Dayan, Steven Kim, William Chawla, Smita Schumacher, Andrew Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title | Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title_full | Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title_fullStr | Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title_full_unstemmed | Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title_short | Safe and Effective Chin Augmentation With the Hyaluronic Acid Injectable Filler, VYC-20L |
title_sort | safe and effective chin augmentation with the hyaluronic acid injectable filler, vyc-20l |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752233/ https://www.ncbi.nlm.nih.gov/pubmed/33347003 http://dx.doi.org/10.1097/DSS.0000000000002795 |
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