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Intravenous and Subcutaneous Tramadol for Inguinal Herniorrhaphy: Comparative Study

dc.contributor.authorDias dos Santos, Talita Oliveira
dc.contributor.authorEstrela, Tomaz Gonzalez
dc.contributor.authorFernandes de Azevedo, Vera Lucia [UNESP]
dc.contributor.authorCarvalho de Oliveira, Onofre Eduardo
dc.contributor.authorOliveira Junior, Gildasio
dc.contributor.authorFigueiredo, Gilvan da Silva
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionNorthwestern Univ
dc.date.accessioned2020-12-10T16:30:43Z
dc.date.available2020-12-10T16:30:43Z
dc.date.issued2010-09-01
dc.description.abstractBackground and objectives: Inguinal herniorrhaphy is one of the most common surgeries in men. Neuroaxis block is the anesthetic technique used more often and in the majority of the cases the patient is ready to be discharged from the hospital a few hours after the procedure, as long as satisfactory analgesia is present and nausea and vomiting are absent. Tramadol is an analgesic drug that can be used in postoperative analgesia, but it has important side effects, such as nausea and vomiting whose incidence can range from 0% to 50%. The objective of the present study was to compare the incidence of nausea and vomiting and the quality of postoperative analgesia of subcutaneous and intravenous tramadol in patients undergoing inguinal herniorrhaphy. Methods: This is a prospective study with 30 patients undergoing inguinal herniorrhaphy. Patients were divided into two groups: Group C (n = 15) received 1.5 mg.kg(-1) of subcutaneous Tramadol, and Group V (n = 15) received 1.5 mg.kg-1 of intravenous Tramadol. All patients underwent continuous epidural anesthesia with 0.5% levobupivacaine. Anthropometric data, quality of analgesia, and the development of postoperative nausea and vomiting in the first eight hours were recorded. Results: Statistically significant differences were not observed between both groups for anthropometric data, quality of analgesia, and the development of nausea and vomiting. Conclusions: The present study demonstrates the absence of statistically significant differences regarding the incidence of nausea and vomiting and quality of analgesia when using intravenous and subcutaneous Tramadol.en
dc.description.affiliationFMB Unesp, Sao Paulo, Brazil
dc.description.affiliationNorthwestern Univ, Chicago, IL 60611 USA
dc.description.affiliationUnespFMB Unesp, Sao Paulo, Brazil
dc.format.extent522-527
dc.identifierhttp://dx.doi.org/10.1590/S0034-70942010000500008
dc.identifier.citationRevista Brasileira De Anestesiologia. New York: Elsevier Science Inc, v. 60, n. 5, p. 522-527, 2010.
dc.identifier.doi10.1590/S0034-70942010000500008
dc.identifier.fileS0034-70942010000500008.pdf
dc.identifier.issn0034-7094
dc.identifier.scieloS0034-70942010000500008
dc.identifier.urihttp://hdl.handle.net/11449/194582
dc.identifier.wosWOS:000208748900008
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofRevista Brasileira De Anestesiologia
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectANALGESIA: Postoperative
dc.subjectDRUGS: tramadol
dc.subjectSURGERY, Abdominal: inguinal hemiorrhaphy
dc.subjectCOMPLICATIONS: nausea and vomit
dc.titleIntravenous and Subcutaneous Tramadol for Inguinal Herniorrhaphy: Comparative Studyen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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