Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29173
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dc.date.accessioned2022-10-21T07:00:08Z-
dc.date.available2022-10-21T07:00:08Z-
dc.date.issued2013-02-
dc.identifier.citationKasapoğlu, F. vd. (2013). "The effects of levobupivacaine infiltration on post-tonsillectomy pain relief in adults: a single-blinded, randomized, and controlled clinical study". European Archives of Oto-Rhino-Laryngology, 270(2), 761-766.en_US
dc.identifier.issn0937-4477-
dc.identifier.issn1434-4726-
dc.identifier.urihttps://doi.org/10.1007/s00405-012-2194-1-
dc.identifier.urihttps://link.springer.com/article/10.1007/s00405-012-2194-1-
dc.identifier.urihttp://hdl.handle.net/11452/29173-
dc.description.abstractThe aim of this prospective single-blinded and controlled study is to evaluate the efficacy of levobupivacaine infiltration on post-tonsillectomy pain relief in adults. The study was conducted with 40 adult patients who underwent tonsillectomy. These patients were randomized in either study group (SG) who received levobupivacaine infiltration to peritonsillary fossae prior to surgery or control group (CG) with no medication. After surgery, all the patients were queried for pain scores by visual analog scale. In addition, the volume of intraoperative bleeding, the duration of operation, the severity of postoperative complications, and the amount of analgesic requirement were the other outcome measures of this study. There were significant differences between groups regarding pain scores for the first 24 h in favor of SG. The analgesic requirement was also significantly lower in SG (p = 0.009). Although there was a sustained decrement at pain score during first 24 h for SG, however, the change from baseline score (immediate score) for each time interval revealed no significance compared to CG. In addition, the duration of operation and the volume of intraoperative bleeding were similar (p = 0.64 and p = 0.165). In conclusion, preincisional infiltration of levobupivacaine is a safe and reliable method for post-tonsillectomy pain reduction in adults. However, more in-depth, double-blinded and placebo controlled studies are required to elucidate its long term benefits.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOtorhinolaryngologyen_US
dc.subjectAdulten_US
dc.subjectTonsillectomyen_US
dc.subjectPostoperative painen_US
dc.subjectLevobupivacaineen_US
dc.subjectPediatric tonsillectomyen_US
dc.subjectTopical lidocaineen_US
dc.subjectControlled-trialen_US
dc.subjectBupivacaineen_US
dc.subjectMorbidityen_US
dc.subjectDexamethasoneen_US
dc.subjectMetaanalysisen_US
dc.subjectRopivacaineen_US
dc.subjectAnalgesiaen_US
dc.subjectTonsilsen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshAnesthesia, localen_US
dc.subject.meshAnesthetics, localen_US
dc.subject.meshBupivacaineen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshPain measurementen_US
dc.subject.meshPain, postoperativeen_US
dc.subject.meshSingle-blind methoden_US
dc.subject.meshTonsillectomyen_US
dc.subject.meshYoung adulten_US
dc.titleThe effects of levobupivacaine infiltration on post-tonsillectomy pain relief in adults: A single-blinded, randomized, and controlled clinical studyen_US
dc.typeArticleen_US
dc.identifier.wos000314295800050tr_TR
dc.identifier.scopus2-s2.0-84878376736tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Kulak Burun Boğaz Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Anesteziyoloji ve Reanimasyon Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-7684-4600tr_TR
dc.identifier.startpage761tr_TR
dc.identifier.endpage766tr_TR
dc.identifier.volume270tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalEuropean Archives of Oto-Rhino-Laryngologyen_US
dc.contributor.buuauthorKasapoǧlu, Fikret-
dc.contributor.buuauthorDemir, Uygar Levent-
dc.contributor.buuauthorKaya, Fatma Nur-
dc.contributor.buuauthorÇetin, Yaser Said-
dc.contributor.buuauthorYavaşçaoǧlu, Belgin-
dc.contributor.researcheridAAG-9356-2021tr_TR
dc.contributor.researcheridAAI-7914-2021tr_TR
dc.contributor.researcheridAAI-3877-2021tr_TR
dc.contributor.researcheridAAI-8213-2021tr_TR
dc.identifier.pubmed23053376tr_TR
dc.subject.wosOtorhinolaryngologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid56254721200tr_TR
dc.contributor.scopusid56868421800tr_TR
dc.contributor.scopusid7003619647tr_TR
dc.contributor.scopusid57202732676tr_TR
dc.contributor.scopusid6602742300tr_TR
dc.subject.scopusTonsillectomy; Hemorrhage; Postoperative Hemorrhageen_US
dc.subject.emtreeLevobupivacaineen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAnalgesiaen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDisease severityen_US
dc.subject.emtreeDrug administrationen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeOperation durationen_US
dc.subject.emtreeOutcome assessmenten_US
dc.subject.emtreePain assessmenten_US
dc.subject.emtreePostoperative complicationen_US
dc.subject.emtreePostoperative hemorrhageen_US
dc.subject.emtreePostoperative painen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProspective studyen_US
dc.subject.emtreeRandomized controlled trialen_US
dc.subject.emtreeSingle blind procedureen_US
dc.subject.emtreeTonsillectomyen_US
dc.subject.emtreeVisual analog scaleen_US
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