Abstract
Background: It is believed that preemptive IV lornoxicam treatment can reduce the consumption of other analgesics, improve analgesic efficacy, and ameliorate immune function during patient-controlled IV analgesia. However, the effects of preemptive IV lornoxicam treatment on the analgesic efficacy of patient-controlled epidural analgesia (PCEA) with morphine and on chemokine expression remain unknown.
Objective: The aim of this prospective, randomized, controlled study was to observe the effects of preemptive IV lornoxicam treatment on the analgesic efficacy of PCEA with morphine and on the expression of monocyte chemotactic protein-1 (MCP-1) and stromal cell-derived factor-1α (SDF-1α) in women undergoing hysterectomy.
Methods: Patients undergoing elective hysterectomy with combined spinal and epidural anesthesia were randomized to 1 of 3 groups to receive IV lornoxicam 8 mg before anesthesia (group 1), lornoxicam 16-mg injection before anesthesia (group 2), or isotonic saline (control) before anesthesia. PCEA was used to treat postoperative pain, and a visual analog scale (VAS) and the Bruggemann Comfort Scale (BCS) were used to evaluate analgesic efficacy. Morphine consumption was recorded. To measure plasma concentrations of MCP-1 and SDF-1α via enzyme-linked immunosorbent assay, venous blood samples were obtained from patients at 4 separate times: before anesthesia (baseline); 0 (immediately after anesthesia administration); and 24 and 48 hours after surgery.
Results: Forty-five patients (mean [SD] age, 41 [5] years; mean [SD] weight, 54 [6] kg) undergoing elective hysterectomy were included in the study. There were no significant differences in VAS scores, BCS scores, or morphine consumption between the 3 groups. Compared with baseline values, MCP-1 and SDF-1α concentrations were increased significantly immediately after surgery in all 3 groups (all, P < 0.01) and returned to near-baseline values at 24 hours postsurgery in groups 1 and 2, and by 48 hours postsurgery in the control group. MCP-1 and SDF-1α concentrations in groups 1 and 2 were significantly lower than those in the control group immediately (all, P < 0.01) and 24 hours postsurgery (all, P < 0.05).
Conclusion: Preemptive IV lornoxicam treatment was associated with attenuation of the plasma concentrations of MCP-1 and SDF-1α immediately after and 24 hours after hysterectomy and was associated with more rapid resolution to near-baseline concentrations of both cytokines in these patients compared with controls; however, it was not associated with significantly reducing epidural morphine consumption.
Key words: lornoxicam, morphine, analgesia, chemokine, hysterectomy
Full Text
The Full Text of this article is available as a PDF (662.0 KB).
References
- 1.Allendorf JD, Bessler M, Whelan RL. Postoperative immune function varies inversely with the degree of surgical trauma in a murine model. Surg Endosc. 1997;11:427–430. doi: 10.1007/s004649900383. [DOI] [PubMed] [Google Scholar]
- 2.Page GG. Surgery-induced immunosuppression and postoperative pain management. AACN Clin Issues. 2005;16:302–309. doi: 10.1097/00044067-200507000-00004. [DOI] [PubMed] [Google Scholar]
- 3.Kehlet H, Dahl JB. Anaesthesia, surgery, and challenges in postoperative recovery. Lancet. 2003;362:1921–1928. doi: 10.1016/S0140-6736(03)14966-5. [DOI] [PubMed] [Google Scholar]
- 4.Kelbel I, Weiss M. Anaesthetics and immune function. Curr Opin Anaesthesiol. 2001;14:685–691. doi: 10.1097/00001503-200112000-00015. [DOI] [PubMed] [Google Scholar]
- 5.Wang ZY, Wang CQ, Yang JJ. Which has the least immunity depression during postoperative analgesia—morphine, tramadol, or tramadol with lornoxicam? Clin Chim Acta. 2006;369:40–45. doi: 10.1016/j.cca.2006.01.008. [DOI] [PubMed] [Google Scholar]
- 6.Stephens JM, Pashos CL, Haider S, Wong JM. Making progress in the management of postoperative pain: a review of the cyclooxygenase 2-specific inhibitors. Pharmacotherapy. 2004;24:1714–1731. doi: 10.1592/phco.24.17.1714.52339. [DOI] [PubMed] [Google Scholar]
- 7.Feng Y, Ju H, Yang B, An H. Effects of a selective cyclooxygenase-2 inhibitor on postoperative inflammatory reaction and pain after total knee replacement. J Pain. 2008;9:45–52. doi: 10.1016/j.jpain.2007.08.003. [DOI] [PubMed] [Google Scholar]
- 8.Sapolya O, Karamanhoglu B, Memis D. Analgesic effects of lornoxicam after total abdominal hysterectomy. J Opioid Manag. 2007;3:155–159. doi: 10.5055/jom.2007.0053. [DOI] [PubMed] [Google Scholar]
- 9.Rollins BJ. Chemokines. Blood. 1997;90:909–928. [PubMed] [Google Scholar]
- 10.Risnes I, Ueland T, Lundblad R. Changes in the cytokine network and complement parameters during open heart surgery. Interact Cardiovasc Thorac Surg. 2003;2:19–24. doi: 10.1016/S1569-9293(02)00088-9. [DOI] [PubMed] [Google Scholar]
- 11.Kryczek I, Wei S, Keller E. Stroma-derived factor (SDF-1/CXCL12) and human tumor pathogenesis. Am J Physiol Cell Physiol. 2007;292:C987–C995. doi: 10.1152/ajpcell.00406.2006. [DOI] [PubMed] [Google Scholar]
- 12.Fischereder M. Chemokines and chemokine receptors in renal transplantation—from bench to bedside. Acta Physiol Hung. 2007;94:67–81. doi: 10.1556/APhysiol.94.2007.1-2.7. [DOI] [PubMed] [Google Scholar]
- 13.Kawahito K, Adachi H, Ino T. Influence of surgical procedures on interleukin-6 and monocyte chemotactic and activating factor responses: CABG vs valvular surgery. J Interferon Cytokine Res. 2000;20:1–6. doi: 10.1089/107999000312676. [DOI] [PubMed] [Google Scholar]
- 14.Tegeder I, Pfeilschifter J, Geisslinger G. Cyclooxygenase-independent actions of cyclooxygenase inhibitors. FASEB J. 2001;15:2057–2072. doi: 10.1096/fj.01-0390rev. [DOI] [PubMed] [Google Scholar]
- 15.Bonnet F, Marret E. Influence of anaesthetic and analgesic techniques on outcome after surgery. Br J Anaesth. 2005;95:52–58. doi: 10.1093/bja/aei038. [DOI] [PubMed] [Google Scholar]
