Perioperative C-reactive protein is associated with pain outcomes after major laparoscopic abdominal surgery: a retrospective analysis

Hey-Ran Choi, In-Ae Song, Tak Kyu Oh, Young-Tae Jeon, Hey-Ran Choi, In-Ae Song, Tak Kyu Oh, Young-Tae Jeon

Abstract

Purpose: This study is aimed to investigate an association between perioperative C-reactive protein (CRP) levels and both opioid consumption and postoperative pain scores in postoperative days (PODs) in patients who underwent laparoscopic major abdominal surgery. We hypothesized that postoperative opioid requirements and numeric rating scale (NRS) pain scores would be positively associated with perioperative CRP levels. Patients and method: Medical records from 4,653 patients who underwent a laparoscopic major abdominal surgery from January 2010 to December 2016 were retrospectively reviewed. Generalized linear regression analysis was used to identify the association of preoperative and postoperative CRP levels, and increase in CRP level (postoperative CRP level - preoperative CRP level) with postoperative pain outcomes during POD 0-3. Results: An increase of 1 mg dL-1 of postoperative CRP level was significantly associated with 1.4% increase morphine equivalent consumption [exponentiated regression (Exp) coefficient: 0.014, 95% CI (0.011, 0.016), P<0.001], whereas preoperative CRP levels were not significantly associated with morphine equivalent consumption on POD 0-3 (P=0.450). A 1 mg dL-1 of increase in CRP level was significantly associated with 1% increase of morphine equivalent consumption [Exp coefficient: 0.010, 95% CI (0.008, 0.012), P<0.001]. Postoperative CRP levels were positively associated with NRS pain scores on POD 1, POD 2, and POD 3 (P<0.001). Increases of CRP levels were also positively associated with NRS pain scores on POD 0, POD 1, POD2, and POD3 (P<0.05). Conclusion: These results suggest postoperative CRP levels and increases in CRP levels are positively associated with opioid consumption and higher pain scores after major laparoscopic abdominal surgery.

Keywords: C-reactive protein; analgesia; anesthesia; numeric rating scale; opioid analgesics; pain; postoperative.

Conflict of interest statement

The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Flowchart for patient selection; 16,147 patients were excluded in the final analysis due to 10 causes. Abbreviation: POD, postoperative day.
Figure 2
Figure 2
Relationship between morphine equivalent consumption on POD 0–3, and preoperative CRP (A), postoperative CRP (B), and increase of CRP (C) levels. Increase of CRP (mg dL−1): postoperative CRP – preoperative CRP. Abbreviations: POD, postoperative day; CRP, C-reactive protein.

References

    1. Brownstein MJ. A brief history of opiates, opioid peptides, and opioid receptors. Proc Natl Acad Sci U S A. 1993;90(12):5391–5393.
    1. Wu CL, Raja SN. Treatment of acute postoperative pain. Lancet. 2011;377(9784):2215–2225. doi:10.1016/S0140-6736(11)60245-6
    1. Stein C. Targeting pain and inflammation by peripherally acting opioids. Front Pharmacol. 2013;4:123. doi:10.3389/fphar.2013.00123
    1. Endres-Becker J, Heppenstall PA, Mousa SA, et al. Mu-opioid receptor activation modulates transient receptor potential vanilloid 1 (TRPV1) currents in sensory neurons in a model of inflammatory pain. Mol Pharmacol. 2007;71(1):12–18. doi:10.1124/mol.106.026740
    1. Stein C, Lang LJ. Peripheral mechanisms of opioid analgesia. Curr Opin Pharmacol. 2009;9(1):3–8. doi:10.1016/j.coph.2008.12.009
    1. Rogers TJ, Peterson PK. Opioid G protein-coupled receptors: signals at the crossroads of inflammation. Trends Immunol. 2003;24(3):116–121.
    1. Reece AS. High-sensitivity CRP in opiate addiction: relative and age-dependent elevations. Cardiovasc Toxicol. 2012;12(2):149–157. doi:10.1007/s12012-012-9154-2
    1. Pepys MB, Hirschfield GM. C-reactive protein: a critical update. J Clin Invest. 2003;111(12):1805–1812. doi:10.1172/JCI18921
    1. Ghazavi A, Solhi H, Moazzeni SM, Rafiei M, Mosayebi G. Cytokine profiles in long-term smokers of opium (Taryak). J Addict Med. 2013;7(3):200–203. doi:10.1097/ADM.0b013e31828baede
    1. Nabati S, Asadikaram G, Arababadi MK, et al. The plasma levels of the cytokines in opium-addicts and the effects of opium on the cytokines secretion by their lymphocytes. Immunol Lett. 2013;152(1):42–46. doi:10.1016/j.imlet.2013.04.003
    1. Chopan M, Littenberg B. C-reactive protein and prescription opioid use. J Nat Sci. 2015;1(6):122.
    1. Cabellos Olivares M, Labalde Martinez M, Torralba M, Rodriguez Fraile JR, Atance Martinez JC. C-reactive protein as a marker of the surgical stress reduction within an ERAS protocol (Enhanced Recovery After Surgery) in colorectal surgery: A prospective cohort study. J Surg Oncol. 2018;117(4):717–724. doi:10.1002/jso.24909
    1. Park JS, Han HS, Hwang DW, et al. Current status of laparoscopic liver resection in Korea. J Korean Med Sci. 2012;27(7):767–771. doi:10.3346/jkms.2012.27.7.767
    1. Hwang SH, Park DJ, Jee YS, et al. Risk factors for operative complications in elderly patients during laparoscopy-assisted gastrectomy. J Am Coll Surg. 2009;208(2):186–192. doi:10.1016/j.jamcollsurg.2008.10.023
    1. Kang SB, Park JW, Jeong SY, et al. Open versus laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): short-term outcomes of an open-label randomised controlled trial. Lancet Oncol. 2010;11(7):637–645. doi:10.1016/S1470-2045(10)70131-5
    1. Eom BW, Jang JY, Lee SE, Han HS, Yoon YS, Kim SW. Clinical outcomes compared between laparoscopic and open distal pancreatectomy. Surg Endosc. 2008;22(5):1334–1338. doi:10.1007/s00464-007-9660-7
    1. Mercadante S, Caraceni A. Conversion ratios for opioid switching in the treatment of cancer pain: a systematic review. Palliat Med. 2011;25(5):504–515. doi:10.1177/0269216311406577
    1. Armstrong RA. When to use the Bonferroni correction. Ophthalmic Physiol Opt. 2014;34(5):502–508. doi:10.1111/opo.12131
    1. Facy O, Paquette B, Orry D, et al. Diagnostic accuracy of inflammatory markers as early predictors of infection after elective colorectal surgery: results from the IMACORS study. Ann Surg. 2016;263(5):961–966.
    1. Houten JK, Tandon A. Comparison of postoperative values for C-reactive protein in minimally invasive and open lumbar spinal fusion surgery. Surg Neurol Int. 2011;2:94. doi:10.4103/2152-7806.82575
    1. Kehlet H. Surgical stress: the role of pain and analgesia. Br J Anaesth. 1989;63(2):189–195.
    1. Ortega-Deballon P, Lagoutte N, Facy O. Inflammatory markers as predictors of surgical site infection after elective colorectal cancer surgery. Langenbecks Arch Surg. 2014;399(6):795–796. doi:10.1007/s00423-014-1209-3
    1. Straatman J, Cuesta MA, Tuynman JB, Veenhof A, Bemelman WA, van der Peet DL. C-reactive protein in predicting major postoperative complications are there differences in open and minimally invasive colorectal surgery? Substudy from a randomized clinical trial. Surg Endosc. 2017;32:2877–2885.
    1. Liu SS, Wu CL. Effect of postoperative analgesia on major postoperative complications: a systematic update of the evidence. Anesth Analg. 2007;104(3):689–702. doi:10.1213/01.ane.0000255040.71600.41
    1. McSorley ST, Ramanathan ML, Horgan PG, McMillan DC. Postoperative C-reactive protein measurement predicts the severity of complications following surgery for colorectal cancer. Int J Colorectal Dis. 2015;30(7):913–917. doi:10.1007/s00384-015-2229-3
    1. Grimm MC, Ben-Baruch A, Taub DD, et al. Opiates transdeactivate chemokine receptors: delta and mu opiate receptor-mediated heterologous desensitization. J Exp Med. 1998;188(2):317–325.
    1. Merighi S, Gessi S, Varani K, Fazzi D, Stefanelli A, Borea PA. Morphine mediates a proinflammatory phenotype via mu-opioid receptor-PKCvarepsilon-Akt-ERK1/2 signaling pathway in activated microglial cells. Biochem Pharmacol. 2013;86(4):487–496. doi:10.1016/j.bcp.2013.05.027
    1. Peng X, Mosser DM, Adler MW, Rogers TJ, Meissler JJ Jr., Eisenstein TK. Morphine enhances interleukin-12 and the production of other pro-inflammatory cytokines in mouse peritoneal macrophages. J Leukoc Biol. 2000;68(5):723–728.
    1. Ke JJ, Zhan J, Feng XB, Wu Y, Rao Y, Wang YL. A comparison of the effect of total intravenous anaesthesia with propofol and remifentanil and inhalational anaesthesia with isoflurane on the release of pro- and anti-inflammatory cytokines in patients undergoing open cholecystectomy. Anaesth Intensive Care. 2008;36(1):74–78.
    1. Zheng X, Huang H, Liu J, Li M, Liu M, Luo T. Propofol attenuates inflammatory response in LPS-activated microglia by regulating the miR-155/SOCS1 pathway. Inflammation. 2018;41(1):11–19. doi:10.1007/s10753-017-0658-6

Source: PubMed

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