Publication:
Propofol-Ketamine Versus Propofol-Tramadol Sedation in Children Undergoing Gastrointestinal Endoscopy

dc.authorscopusid55554062700
dc.authorscopusid36707874100
dc.authorscopusid57795877300
dc.authorscopusid7003928585
dc.authorscopusid55440112000
dc.authorscopusid54956571900
dc.contributor.authorÜstün, Y.B.
dc.contributor.authorKöksal, E.
dc.contributor.authorKaya, Cumali
dc.contributor.authorBilgin, S.
dc.contributor.authorDost, B.
dc.contributor.authorÇaltepe, Gönül
dc.date.accessioned2025-12-11T00:28:45Z
dc.date.issued2021
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Üstün] Yasemin Burcu, Department of Anesthesiology, Ondokuz Mayis University, Medical School, Samsun, Turkey; [Köksal] Ersin, Department of Anesthesiology, Ondokuz Mayis University, Medical School, Samsun, Turkey; [Kaya] Cengiz, Department of Anesthesiology, Ondokuz Mayis University, Medical School, Samsun, Turkey; [Bilgin] Sezgin, Department of Anesthesiology, Ondokuz Mayis University, Medical School, Samsun, Turkey; [Dost] Burhan, Department of Anesthesiology, Ondokuz Mayis University, Medical School, Samsun, Turkey; [Çaltepe] Gönül Dinler, Department of Gastroenterology, Ondokuz Mayis University, Medical School, Samsun, Turkeyen_US
dc.description.abstractNumerous combinations of drugs are used for sedation in upper gastrointestinal endoscopies. The aim of this study was to compare the quality of two sedation regimens in upper gastrointestinal endoscopy performed on pediatric patients. After the study approval by the local ethics committee of Ondokuz Mayıs University Hospital, written informed consent was obtained from parents. Eighty patients between the ages of 1 and 18 were randomized into two groups. Group K (n=40) received propofol 1 mg/kg + 1 mg/kg ketamine intravenously. Group T (n=40) received propofol 1 mg/kg + 1 mg/kg tramadol intravenously. In both groups, additional propofol (0.5 mg/kg) was administrated when a patient showed signs of discomfort, in order to maintain a Ramsey Sedation Scale of 4 to 5. In Group K, additional propofol requirements were significantly lower compared to Group T (p=0.003). Group K had significantly higher sedation scores than Group T at 3rd min. (p=0.028) and 20th min. (p=0.015). Recovery time increased significantly in Group K (p=0.002). Although there was no difference between two groups concerning the propofol consumption, both groups required additional propofol and tramadol resulted in a shorter recovery time compared to ketamine. © 2021 Ondokuz Mayis Universitesi. All rights reserved.en_US
dc.identifier.doi10.5835/jecm.omu.38.01.001
dc.identifier.endpage4en_US
dc.identifier.issn1309-4483
dc.identifier.issn1309-5129
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85105474295
dc.identifier.scopusqualityQ4
dc.identifier.startpage1en_US
dc.identifier.urihttps://doi.org/10.5835/jecm.omu.38.01.001
dc.identifier.urihttps://hdl.handle.net/20.500.12712/36595
dc.identifier.volume38en_US
dc.language.isoenen_US
dc.publisherOndokuz Mayis Universityen_US
dc.relation.ispartofJournal of Experimental and Clinical Medicine (Turkey)en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnesthesia Recovery Perioden_US
dc.subjectDeep Sedationen_US
dc.subjectDigestive System Endoscopyen_US
dc.subjectPediatric Nursingen_US
dc.titlePropofol-Ketamine Versus Propofol-Tramadol Sedation in Children Undergoing Gastrointestinal Endoscopyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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