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dc.contributor.author이은경*
dc.date.accessioned2016-08-29T12:08:39Z-
dc.date.available2016-08-29T12:08:39Z-
dc.date.issued2016*
dc.identifier.issn1440-1681*
dc.identifier.otherOAK-19076*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/231762-
dc.description.abstractOxycodone is a -opioid receptor agonist and is generally indicated for the relief of moderate to severe pain. The aim of this study was to compare the analgesic efficacy of patient-controlled oxycodone and fentanyl for postoperative pain in patients undergoing colorectal surgery. Patients scheduled to undergo elective colorectal surgery (n=82) were allocated to receive oxycodone (n=41, concentration of 1mg/mL) or fentanyl (n=41, concentration of 15g/mL) for postoperative pain management. After the operation, pain using a numerical rating scale (NRS), delivery to demand ratio, infused dose of patient-controlled analgesia (PCA), side effects, and sedation levels were evaluated. Median (25%-75%) cumulative PCA dose of oxycodone group at 48hours (66.9, 58.4-83.7mL) was significantly less than that of fentanyl group (80.0, 63.4-103.3mL, P=.037). Six hours after surgery, the mean (SD) NRS scores of the oxycodone and fentanyl groups were 6.2 (2.4) and 6.8 (1.9), respectively (P=.216). The mean equianalgesic potency ratio of oxycodone to fentanyl was 55:1. The groups did not differ in postoperative nausea, vomiting, and level of sedation. Patient-controlled oxycodone provides similar effects for pain relief compared to patient-controlled fentanyl in spite of less cumulative PCA dose. Based on these results, oxycodone can be a useful alternative to fentanyl for PCA in patients after colorectal surgery.*
dc.languageEnglish*
dc.publisherWILEY-BLACKWELL*
dc.subjectfentanyl*
dc.subjectoxycodone*
dc.subjectpain relief*
dc.titleComparison of the analgesic effect of patient-controlled oxycodone and fentanyl for pain management in patients undergoing colorectal surgery*
dc.typeArticle*
dc.relation.issue8*
dc.relation.volume43*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage745*
dc.relation.lastpage752*
dc.relation.journaltitleCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY*
dc.identifier.doi10.1111/1440-1681.12586*
dc.identifier.wosidWOS:000379956200003*
dc.identifier.scopusid2-s2.0-84978834408*
dc.author.googleJung, Kyeo-Woon*
dc.author.googleKang, Hyeon-Wook*
dc.author.googlePark, Chan-Hye*
dc.author.googleChoi, Byung-Hyun*
dc.author.googleBang, Ji-Yeon*
dc.author.googleLee, Soo-Han*
dc.author.googleLee, Eun-Kyung*
dc.author.googleChoi, Byung-Moon*
dc.author.googleNoh, Gyu-Jeong*
dc.contributor.scopusid이은경(57188770360;57217075385)*
dc.date.modifydate20240123125059*
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