Publication:
Does single, low-dose preoperative dexamethasone improve outcomes after colorectal surgery based on an enhanced recovery protocol? Double-blind, randomized clinical trial

dc.contributor.buuauthorKırdak, Türkay
dc.contributor.buuauthorYılmazlar, Aysun
dc.contributor.buuauthorKavun, Sinan
dc.contributor.buuauthorErcan, İlker
dc.contributor.buuauthorYılmazlar, Tuncay
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentFarmakoloji ve Klinik Farmakoloji Ana Bilim Dalı
dc.contributor.departmentBiyoistatistik Ana Bilim Dalı
dc.contributor.departmentAnesteziyoloji ve Reanimasyon Ana Bilim Dalı
dc.contributor.departmentCerrahi Ana Bilim Dalı
dc.contributor.orcid0000-0002-2382-290X
dc.contributor.researcheridAAC-9702-2019
dc.contributor.scopusid8704181100
dc.contributor.scopusid55899579900
dc.contributor.scopusid6507468595
dc.contributor.scopusid6603789069
dc.contributor.scopusid6701800362
dc.date.accessioned2022-03-14T11:32:53Z
dc.date.available2022-03-14T11:32:53Z
dc.date.issued2008-02
dc.description.abstractPreoperative single, high-dose methylprednisolone administration improves postoperative outcomes after colonic surgery. Several randomized studies, including major surgeries, assessed various high-dose steroid regimens; however, evidence about the effect of administration of lower doses on postoperative outcomes in colorectal surgery is not available. The aim of the present study is to determine whether the administration of a single, low dose of dexamethasone before surgery would confer an outcome advantage after colorectal surgery. Thirty patients undergoing colorectal surgery were included in this randomized, double-blind study. Patients received 8 mg dexamethasone or serum physiologic preoperatively. Levels of Interleukin-6 and C-reactive protein, pain scores, postoperative nausea and vomiting, mobilization, complications, hospital stay, and readmissions were compared. Age, sex, indications, and operations were similar in both groups (P > 0.05). C-reactive protein and Interleukin-6 levels increased significantly postoperatively in each group (P < 0.05), but there were no differences between groups when compared (P > 0.05). There were also no significant differences between pain scores, bowel functions, mobilization, hospital stay, complication rates, and readmission rates between the two groups (P > 0.05). Preoperative 8 mg dexamethasone administration has no significant effect on reducing postoperative inflammatory response and also does not improve outcomes of colorectal. surgery.
dc.identifier.citationKırdak, T. vd. (2008). ''Does single, low-dose preoperative dexamethasone improve outcomes after colorectal surgery based on an enhanced recovery protocol? Double-blind, randomized clinical trial''. American Surgeon, 74(2), 160-167
dc.identifier.endpage167
dc.identifier.issn0003-1348
dc.identifier.issue2
dc.identifier.pubmed18306871
dc.identifier.scopus2-s2.0-40949107237
dc.identifier.startpage160
dc.identifier.urihttp://hdl.handle.net/11452/24989
dc.identifier.volume74
dc.identifier.wos000253009300016
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSage Publications
dc.relation.journalAmerican Surgeon
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectLaparoscopic cholecystectomy
dc.subjectInflammatory response
dc.subjectCytokine response
dc.subjectSurgical stress
dc.subjectCancer
dc.subjectRehabilitation
dc.subjectMuscularis
dc.subjectMorbidity
dc.subjectNausea
dc.subjectSurgery
dc.subjectResection
dc.subject.emtreeC reactive protein
dc.subject.emtreeDexamethasone
dc.subject.emtreeInterleukin 6
dc.subject.emtreeAdult
dc.subject.emtreeAge distribution
dc.subject.emtreeAged
dc.subject.emtreeArticle
dc.subject.emtreeClinical article;
dc.subject.emtreeClinical protocol
dc.subject.emtreeClinical trial
dc.subject.emtreeColorectal cancer
dc.subject.emtreeColorectal surgery
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeControlled study
dc.subject.emtreeConvalescence
dc.subject.emtreeDose response
dc.subject.emtreeDouble blind procedure
dc.subject.emtreeDrug efficacy
dc.subject.emtreeFemale
dc.subject.emtreeHospital readmission
dc.subject.emtreeHospitalization
dc.subject.emtreeHuman
dc.subject.emtreeLow drug dose
dc.subject.emtreeMale
dc.subject.emtreeMobilization
dc.subject.emtreePain assessment
dc.subject.emtreePostoperative inflammation
dc.subject.emtreePostoperative nausea
dc.subject.emtreePostoperative pain
dc.subject.emtreePostoperative period
dc.subject.emtreePostoperative vomiting
dc.subject.emtreePreoperative care
dc.subject.emtreePrognosis
dc.subject.emtreeProtein blood level
dc.subject.emtreeRandomization
dc.subject.emtreeRandomized controlled trial
dc.subject.emtreeSex difference
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshAnti-inflammatory agents
dc.subject.meshClinical protocols
dc.subject.meshColon
dc.subject.meshDexamethasone
dc.subject.meshDouble-blind method
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshPreoperative care
dc.subject.meshRectum
dc.subject.meshTreatment outcome
dc.subject.scopusEnhanced Recovery; Colon Resection; Colorectal Surgery
dc.subject.wosSurgery
dc.titleDoes single, low-dose preoperative dexamethasone improve outcomes after colorectal surgery based on an enhanced recovery protocol? Double-blind, randomized clinical trial
dc.typeArticle
dc.wos.quartileQ3
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Cerrahi Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Anesteziyoloji ve Reanimasyon Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyoistatistik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Farmakoloji ve Klinik Farmakoloji Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

Files

License bundle

Now showing 1 - 1 of 1
Placeholder
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: