Comparison of oxycodone and fentanyl for postoperative patient-controlled analgesia after orthopedic surgery

Background: Oxycodone is widely used as bolus or patient-controlled analgesia (PCA) for control of postoperative pain. The aim of this study was to assess the efficacy and side effects of oxycodone for somatic pain by comparing oxycodone and fentanyl intravenous PCA after orthopedic surgery. Methods...

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Published inAnesthesia and pain medicine (Korean society of anesthesiologists) Vol. 13; no. 3; pp. 271 - 277
Main Authors Lee, Dong-won, An, Jihyun, Kim, Eunju, Lee, Ji-hyang, Kim, Hyun, Son, Jong-chul
Format Journal Article
LanguageEnglish
Published 대한마취통증의학회 31.07.2018
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Summary:Background: Oxycodone is widely used as bolus or patient-controlled analgesia (PCA) for control of postoperative pain. The aim of this study was to assess the efficacy and side effects of oxycodone for somatic pain by comparing oxycodone and fentanyl intravenous PCA after orthopedic surgery. Methods: Seventy-three patients undergoing orthopedic surgery were randomly assigned to receive fentanyl or oxycodone using intravenous PCA (potency ratio 1:60). Pain severity at rest and with movement and adverse effects were assessed at 1, 6, 24, and 48 hours after surgery. The PCA dose and patient satisfaction scores were measured at 48 hours after surgery. Results: The resting visual analogue scale (VAS) and moving VAS scores of the oxycodone group were significantly higher than those of the fentanyl group at 6 hours (P = 0.001, P = 0.021), but at 48 hours, the resting and moving VAS of the oxycodone group were significantly lower than those of the fentanyl group (P = 0.014, P = 0.037). There were no significant differences in adverse effects, satisfaction scores, dose of patientcontrolled mode, or total cumulative PCA dose. Conclusions: With a 1:60 ratio of oxycodone to fentanyl when using PCA for pain control after orthopedic surgery, the use of larger doses of oxycodone for 6 hours is effective in controlling early postoperative pain. KCI Citation Count: 0
Bibliography:https://doi.org/10.17085/apm.2018.13.3.271
ISSN:2383-7977
1975-5171
2383-7977
DOI:10.17085/apm.2018.13.3.271