PMID- 30233861 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220409 IS - 2072-1439 (Print) IS - 2077-6624 (Electronic) IS - 2072-1439 (Linking) VI - 10 IP - 8 DP - 2018 Aug TI - Comparison of different methods of postoperative analgesia after thoracotomy-a randomized controlled trial. PG - 4874-4882 LID - 10.21037/jtd.2018.07.88 [doi] AB - BACKGROUND: Continuous thoracic epidural analgesia (TEA) is a preferred method of postoperative analgesia in thoracic surgery. Intravenous patient-controlled analgesia (IVPCA) may be an effective alternative. One of the most commonly used opioids in PCA is morphine. It has high antinociceptive efficacy but is associated with many adverse events. Oxycodone can be an alternative. A small number of scientific reports comparing morphine and oxycodone in PCA for the treatment of acute postoperative pain after thoracotomy was the reason to conduct this study. METHODS: Prospective, randomised, observational study. In total of 99 patients scheduled for elective thoracotomy were randomized into three study groups. TEA group received continuous TEA as a method of postoperative pain management, morphine (MF) group received morphine IVPCA, and morphine (OXY) group oxycodone IVPCA. For 48 hours' hemodynamic parameters, level of pain, sedation and the need for rescue analgesia were monitored. After 48 hours' patients were asked about their satisfaction with pain treatment using Likert scale and assessment of opioid related adverse events via overall benefit of analgesia score (OBAS). RESULTS: The level of pain in visual analogic score (VAS) and Prince Henry Hospital Pain Score (PHHPS) scales was significantly lower in TEA group with no significant difference between groups MF and OXY. Using morphine in PCA was associated with a significantly higher likelihood of need of rescue analgesia. The level of sedation in Ramsay scale was significantly higher in MF compared to OXY and TEA group. There were no significant differences between groups in OBAS scale. TEA group was characterized by the highest degree of patient satisfaction. CONCLUSIONS: TEA provided superior anaesthesia compared to PCA in our study group. Use of PCA oxycodone in postoperative pain management after open thoracotomy provides similar nociception control compared to morphine but is associated with less sedation and patients using oxycodone IVPCA require smaller doses of rescue analgesia compared to systemic morphine IVPCA. FAU - Bialka, Szymon AU - Bialka S AD - Department of Anaesthesiology and Critical Care, School of Medicine with Division of Dentistry in Zabrze, Medical University of Silesia, Zabrze, Poland. FAU - Copik, Maja AU - Copik M AD - Department of Anaesthesiology and Critical Care, School of Medicine with Division of Dentistry in Zabrze, Medical University of Silesia, Zabrze, Poland. FAU - Daszkiewicz, Andrzej AU - Daszkiewicz A AD - Department of Anaesthesiology and Critical Care, School of Medicine with Division of Dentistry in Zabrze, Medical University of Silesia, Zabrze, Poland. FAU - Rivas, Eva AU - Rivas E AD - Department of Outcomes Research, Cleveland Clinic, Cleveland, OH, USA. FAU - Ruetzler, Kurt AU - Ruetzler K AD - Department of Outcomes Research, Cleveland Clinic, Cleveland, OH, USA. FAU - Szarpak, Lukasz AU - Szarpak L AD - Faculty of Medicine, Lazarski University, Warsaw, Poland. AD - Department of Emergency Medicine, Warsaw Medical University, Warsaw, Poland. FAU - Misiolek, Hanna AU - Misiolek H AD - Department of Anaesthesiology and Critical Care, School of Medicine with Division of Dentistry in Zabrze, Medical University of Silesia, Zabrze, Poland. LA - eng PT - Journal Article PL - China TA - J Thorac Dis JT - Journal of thoracic disease JID - 101533916 PMC - PMC6129891 OTO - NOTNLM OT - Postoperative analgesia OT - morphine OT - oxycodone OT - patient-controlled analgesia (PCA) OT - thoracotomy COIS- Conflicts of Interest: The authors have no conflicts of interest to declare. EDAT- 2018/09/21 06:00 MHDA- 2018/09/21 06:01 PMCR- 2018/08/01 CRDT- 2018/09/21 06:00 PHST- 2018/09/21 06:00 [entrez] PHST- 2018/09/21 06:00 [pubmed] PHST- 2018/09/21 06:01 [medline] PHST- 2018/08/01 00:00 [pmc-release] AID - jtd-10-08-4874 [pii] AID - 10.21037/jtd.2018.07.88 [doi] PST - ppublish SO - J Thorac Dis. 2018 Aug;10(8):4874-4882. doi: 10.21037/jtd.2018.07.88.