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OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients
BACKGROUND: Atypical odontalgia (AO) manifests as continuous pain in the region of one or several teeth, in the absence of signs of dental pathology. Currently, there is insufficient evidence to establish treatment guidelines for AO. The aim of this study was to describe the effectiveness and safety...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112804/ https://www.ncbi.nlm.nih.gov/pubmed/30197533 http://dx.doi.org/10.2147/JPR.S169701 |
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author | García-Sáez, Rafael Gutiérrez-Viedma, Álvaro González-García, Nuria Gómez-Mayordomo, Víctor Porta-Etessam, Jesús Cuadrado, María-Luz |
author_facet | García-Sáez, Rafael Gutiérrez-Viedma, Álvaro González-García, Nuria Gómez-Mayordomo, Víctor Porta-Etessam, Jesús Cuadrado, María-Luz |
author_sort | García-Sáez, Rafael |
collection | PubMed |
description | BACKGROUND: Atypical odontalgia (AO) manifests as continuous pain in the region of one or several teeth, in the absence of signs of dental pathology. Currently, there is insufficient evidence to establish treatment guidelines for AO. The aim of this study was to describe the effectiveness and safety of treatment with OnabotulinumtoxinA (OnabotA) on a series of patients with AO. METHODS: Nine patients with AO (four males and five females, aged between 31 and 77 years) received injections of OnabotA in the region of pain. The dosage used in each procedure ranged between 10 and 30 U, spread between 4 and 12 injection sites along the gums (n=9), the lips (n=3), and the hard palate (n=1). The median follow-up time was 27 months (interquartile range, IQR 20–40) and the median number of injection sessions per patient was seven (IQR 4.5–9). The assessment variables included the change in the maximal intensity of pain on a 0–10 numerical rating scale (NRS), the response latency, and the duration of the effect. RESULTS: All patients experienced a significant improvement, with ≥50% of reduction in the intensity of the maximal pain. The median of reduction of maximal pain after treatment was six points on the NRS (IQR 5–8.5). The response latency was 2–15 days and the duration of the effect was 2–6 months. No significant adverse reactions were registered. CONCLUSION: OnabotA may be a safe and effective option for the treatment of AO. |
format | Online Article Text |
id | pubmed-6112804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61128042018-09-07 OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients García-Sáez, Rafael Gutiérrez-Viedma, Álvaro González-García, Nuria Gómez-Mayordomo, Víctor Porta-Etessam, Jesús Cuadrado, María-Luz J Pain Res Original Research BACKGROUND: Atypical odontalgia (AO) manifests as continuous pain in the region of one or several teeth, in the absence of signs of dental pathology. Currently, there is insufficient evidence to establish treatment guidelines for AO. The aim of this study was to describe the effectiveness and safety of treatment with OnabotulinumtoxinA (OnabotA) on a series of patients with AO. METHODS: Nine patients with AO (four males and five females, aged between 31 and 77 years) received injections of OnabotA in the region of pain. The dosage used in each procedure ranged between 10 and 30 U, spread between 4 and 12 injection sites along the gums (n=9), the lips (n=3), and the hard palate (n=1). The median follow-up time was 27 months (interquartile range, IQR 20–40) and the median number of injection sessions per patient was seven (IQR 4.5–9). The assessment variables included the change in the maximal intensity of pain on a 0–10 numerical rating scale (NRS), the response latency, and the duration of the effect. RESULTS: All patients experienced a significant improvement, with ≥50% of reduction in the intensity of the maximal pain. The median of reduction of maximal pain after treatment was six points on the NRS (IQR 5–8.5). The response latency was 2–15 days and the duration of the effect was 2–6 months. No significant adverse reactions were registered. CONCLUSION: OnabotA may be a safe and effective option for the treatment of AO. Dove Medical Press 2018-08-23 /pmc/articles/PMC6112804/ /pubmed/30197533 http://dx.doi.org/10.2147/JPR.S169701 Text en © 2018 García-Sáez et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research García-Sáez, Rafael Gutiérrez-Viedma, Álvaro González-García, Nuria Gómez-Mayordomo, Víctor Porta-Etessam, Jesús Cuadrado, María-Luz OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title | OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title_full | OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title_fullStr | OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title_full_unstemmed | OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title_short | OnabotulinumtoxinA injections for atypical odontalgia: an open-label study on nine patients |
title_sort | onabotulinumtoxina injections for atypical odontalgia: an open-label study on nine patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112804/ https://www.ncbi.nlm.nih.gov/pubmed/30197533 http://dx.doi.org/10.2147/JPR.S169701 |
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