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Botulinum toxin-A for the treatment of myogenous temporomandibular disorders : an umbrella review of systematic reviews

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorCanales, Giancarlo De la Torre
dc.contributor.authorCâmara-Souza, Mariana Barbosa
dc.contributor.authorErnberg, Malin
dc.contributor.authorAl-Moraissi, Essam Ahmed
dc.contributor.authorGrigoriadis, Anastasios
dc.contributor.authorPoluha, Rodrigo Lorenzi
dc.contributor.authorChristidis, Maria
dc.contributor.authorJasim, Hajer
dc.contributor.authorLövgren, Anna
dc.contributor.authorChristidis, Nikolaos
dc.date.accessioned2026-03-20T15:01:37Z
dc.date.available2026-03-20T15:01:37Z
dc.date.issued2024-06
dc.description.abstractObjective: Temporomandibular disorders (TMDs) encompass several conditions that cause pain and impair function of the masticatory muscles (M-TMDs) and temporomandibular joints. There is a large interest among clinicians and researchers in the use of botulinum toxin-A (BoNT-A) as a treatment for M-TMD. However, due to the lack of consistent evidence regarding the efficacy as well as adverse events of BoNT-A, clinical decision making is challenging. Therefore, this umbrella review aimed to systematically assess systematic reviews (SRs) evaluating BoNT-A treatment effects on pain intensity, mandibular movements, and adverse events in patients with M-TMDs. Method: An electronic search was undertaken in the databases MEDLINE, EMBASE, CINAHL, Cochrane Central Registry of Controlled Trials (CENTRAL), Web of Science, Epistemonikos, ClinicalTrials.gov, and ICTRP to identify SRs investigating BoNT-A effects on M-TMDs, published from the inception of each database until 6 December 2023. The quality of evidence was rated according to the critical appraisal checklist developed by the umbrella review methodology working group. Only high-quality SRs were included. Results: In total, 18 SRs were included. BoNT-A was shown to be more effective than placebo to reduce pain intensity, but not compared to standard treatments. Additionally, BoNT-A was not superior to placebo or standard treatments regarding improvement of mandibular movements. BoNT-A was considered to have a higher risk for adverse events on muscle and bony tissue compared with other treatments. Conclusion: The synthesis in this umbrella review provides the highest level of evidence present. Taken together, there are indications of effectiveness of BoNT-A for treatment of M-TMDs, supported by moderate evidence. However, considering the risk of causing serious adverse events, treatment with BoNT-A is recommended to be the last treatment alternative.eng
dc.identifier.citationDe la Torre Canales, G., Câmara-Souza, M.B., Ernberg, M. et al. Botulinum Toxin-A for the Treatment of Myogenous Temporomandibular Disorders: An Umbrella Review of Systematic Reviews. Drugs 84, 779–809 (2024). https://doi.org/10.1007/s40265-024-02048-x
dc.identifier.doi10.1007/s40265-024-02048-x
dc.identifier.issn1179-1950
dc.identifier.urihttp://hdl.handle.net/10400.26/62329
dc.language.isoeng
dc.peerreviewedyes
dc.publisherSpringer Nature
dc.relation.hasversionhttps://doi.org/10.1007/s40265-024-02048-x
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectTemporomandibular disorders
dc.subjectbotulinum toxin-A
dc.subjectBoNT-A
dc.subjectM-TMD
dc.titleBotulinum toxin-A for the treatment of myogenous temporomandibular disorders : an umbrella review of systematic reviewseng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.endPage809
oaire.citation.startPage779
oaire.citation.titleDrugs
oaire.citation.volume84
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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