IBUPROFEN AFTER IMPACTED LOWER THIRD MOLAR EXTRACTION: A RANDOMIZED CONTROLLED CLINICAL TRIAL

dc.contributor.authorVallecillo, Cristina
dc.contributor.authorVallecillo-Rivas, Marta
dc.contributor.authorGalvez, Rafael
dc.contributor.authorVallecillo-Capilla, Manuel
dc.contributor.authorOlmedo-Gaya, Maria Victoria
dc.contributor.authoraffiliation[Vallecillo, Cristina] Univ Granada, Sch Dent, Dept Stomatol, Granada, Spain
dc.contributor.authoraffiliation[Vallecillo-Rivas, Marta] Univ Granada, Sch Dent, Dept Stomatol, Granada, Spain
dc.contributor.authoraffiliation[Olmedo-Gaya, Maria Victoria] Univ Granada, Sch Dent, Dept Stomatol, Granada, Spain
dc.contributor.authoraffiliation[Galvez, Rafael] Univ Granada, Dept Surg & Its Specialties, Granada, Spain
dc.contributor.authoraffiliation[Galvez, Rafael] Hosp Univ Virgen Las Nieves, Granada, Spain
dc.contributor.authoraffiliation[Vallecillo-Capilla, Manuel] Univ Granada, Dept Oral & Maxillofacial Surg, Granada, Spain
dc.date.accessioned2025-01-07T14:16:43Z
dc.date.available2025-01-07T14:16:43Z
dc.date.issued2021-11-21
dc.description.abstractObjectiveImpacted third molar extraction is associated with acute moderate-to-severe pain for up to 48 hours post-surgery. This trial was designed to compare the analgesic effectiveness, swelling, and adverse events after impacted third molar surgery following multimodal therapy with 75 mg tramadol hydrochloride plus 25 mg dexketoprofen or monotherapy with 400 mg ibuprofen.MethodsSeventy-two patients were randomly assigned to receiving ibuprofen (n = 36) or tramadol-dexketoprofen (n = 36). Postoperative pain intensity and swelling were measured using a visual analog scale (VAS); pain relief experienced was reported using a 4-point verbal rating scale; the rescue medication requirement, adverse effects, and global impression of the medication were recorded.ResultsNo statistically significant between-group difference in pain intensity was observed at any time point; however, pain relief was significantly higher in the tramadol-dexketoprofen treated-group at 6 and 36 hours. Self-reported verbal rating scale assessments showed significantly lower swelling in the tramadoldexketoprofen group at 24 hours post-surgery but not at 48 or 72 hours, and VAS swelling scores showed no significant between-group difference. The frequency of postoperative nausea and dizziness was significantly higher in the tramadoldexketoprofen group.ConclusionsMultimodal therapy proved more effective to manage moderate-severe pain after impacted third molar surgery in comparison to monotherapy. However, the improvement in relief must be balanced against the increased risk of adverse effects when considering this multimodal approach.
dc.identifier.doi10.1016/j.jebdp.2021.101618
dc.identifier.essn1532-3390
dc.identifier.issn1532-3382
dc.identifier.pmid34922724
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.jebdp.2021.101618
dc.identifier.urihttps://hdl.handle.net/10668/26261
dc.identifier.wosID721373800015
dc.issue.number4
dc.journal.titleJournal of evidence-based dental practice
dc.journal.titleabbreviationJ. evid.-based dent. pract.
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.publisherElsevier inc
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPain management
dc.subjectAnalgesia
dc.subjectAcute pain
dc.subjectMultimodal treatment
dc.subjectOral surgery
dc.subjectTo-severe pain
dc.subjectDexketoprofen trometamol
dc.subjectAnalgesic efficacy
dc.subjectSafety
dc.subjectTramadol
dc.subjectCombination
dc.subjectManagement
dc.subjectDifficulty
dc.subjectKetoprofen
dc.subjectPlacebo
dc.titleIBUPROFEN AFTER IMPACTED LOWER THIRD MOLAR EXTRACTION: A RANDOMIZED CONTROLLED CLINICAL TRIAL
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number21
dc.wostypeArticle

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