Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/68597
Full metadata record
DC FieldValueLanguage
dc.creatorGustavo Henrique Mattos Pereirapt_BR
dc.creatorRafael Paschoal Esteves Limapt_BR
dc.creatorLuis Otávio de Miranda Cotapt_BR
dc.creatorFernando de Oliveira Costapt_BR
dc.date.accessioned2024-05-24T19:04:46Z-
dc.date.available2024-05-24T19:04:46Z-
dc.date.issued2020-01-01-
dc.citation.volume12pt_BR
dc.citation.issue1pt_BR
dc.citation.spagee71pt_BR
dc.citation.epagee78pt_BR
dc.identifier.doihttps://doi.org/10.4317%2Fmedoral.56171pt_BR
dc.identifier.issn19895488pt_BR
dc.identifier.urihttp://hdl.handle.net/1843/68597-
dc.description.resumoPreemptive analgesia has as its basic principle the administration of analgesics before the onset of painful stimuli, in order to reduce or prevent postoperative pain, but this question is little explored in implantology. Thus, this study was conducted in order to evaluate the clinical efficacy of ibuprofen in pain prevention after unit implant surgery. Material and Methods For this triple-blind, parallel, placebo-controlled and randomized clinical trial, 54 insertion surgeries of unitary implants were performed. Two groups have received two different protocols 1 hour before surgery: Ibuprofen group (IBU) 600 mg of ibuprofen; and (2) placebo group (maize starch). The intensity of the pain was evaluated through the visual analogue scale (VAS) in 6 times (1, 6, 12, 24, 48 and 72 hours after the surgery). Patients were instructed to take 750 mg of paracetamol as rescue medication, if necessary. The occurrence and the intensity of pain were analyzed by means of an analysis of variance ANOVA with repeated measurements using the general linear model procedure. Results The IBU group had significantly lower VAS scores overall (IBU = 0.30, ± 0.57; placebo = 1.14, ± 1.07; p<0.001) and at all times in the intra, intergroup comparisons and time/group interaction than the placebo group (p<0.001). The use of rescue medication was significantly lower and the postoperative time was longer in the IBU group compared to placebo (p = 0.002). Conclusions The single use of ibuprofen was found to be significantly superior in reducing pain after unit implant surgery compared to placebo.pt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Minas Geraispt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICApt_BR
dc.publisher.initialsUFMGpt_BR
dc.relation.ispartofJournal of Clinical and Experimental Dentistrypt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectpreemptive analgesiapt_BR
dc.subjectibuprofen acesso open busca dia 23/05/2024Effect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trialpt_BR
dc.subjectimplat surgery Journal of clinical and experimental dentistrypt_BR
dc.subjectpain fao clínica busca dia 23/05/2024Effect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trialpt_BR
dc.subject.otherAnalgesiapt_BR
dc.subject.otherDental implantspt_BR
dc.subject.otherIbuprofenpt_BR
dc.subject.otherPain measurementpt_BR
dc.subject.otherPlacebospt_BR
dc.titleEffect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trialpt_BR
dc.typeArtigo de Periódicopt_BR
dc.url.externahttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969969/pt_BR
Appears in Collections:Artigo de Periódico



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.