Effect of Fentanyl-Based Intravenous Patient-Controlled Analgesia with and without Basal Infusion on Postoperative Opioid Consumption and Opioid-Related Side Effects: A Retrospective Cohort Study

Haesun Jung, Kook Hyun Lee, YoungHyun Jeong, Kang Hee Lee, Susie Yoon, Won Ho Kim, Ho-Jin Lee, Haesun Jung, Kook Hyun Lee, YoungHyun Jeong, Kang Hee Lee, Susie Yoon, Won Ho Kim, Ho-Jin Lee

Abstract

Purpose: We aimed to investigate the effect of a basal opioid infusion in fentanyl-based intravenous patient-controlled analgesia (IV-PCA) on postoperative opioid consumption, pain intensity, and occurrence of opioid-related side effects.

Patients and methods: We retrospectively reviewed 2097 consecutive patients who received IV-PCA after elective general, thoracic, urologic, and plastic surgery under general anesthesia between June 2019 and October 2019. The patients were divided into two groups: IV-PCA with basal infusion (basal group) and IV-PCA without basal infusion (no basal group). We performed a propensity score matching (PSM) analysis to adjust for baseline differences between both groups. We compared the fentanyl PCA consumption (mcg), pain intensity, rescue analgesic administration, and occurrence of opioid-related side effects (nausea, vomiting, somnolence or dizziness, and overall side effects) during the first 48 hours postoperatively between the two groups before and after PSM.

Results: We analyzed 1317 eligible patients. Of these, 757 (57.5%) patients received IV-PCA without basal infusion. The PSM of the total cohort yielded 539 pairs of cases. After PSM, the fentanyl PCA consumption was significantly lower in the no basal group at 48 hours postoperatively as compared to the basal group (at 24 hours, the median difference: -80 mcg, P<0.001, 95% CI=-112 - -45 mcg; at 48 hours, the median difference: -286 mcg, P<0.001, 95% CI=-380 - -190 mcg), without significantly increasing pain intensity and administration of rescue analgesia. The occurrence of overall opioid-related side effects was also significantly lower in the no basal group (at 24 hours: 31.0% vs 23.0%, OR=0.67, P=0.003, 95% CI=0.51 - 0.87; at 48 hours: 18.9% vs 11.0%, OR=0.48, P<0.001, 95% CI=0.31 - 0.75).

Conclusion: Basal infusion of fentanyl-based IV-PCA was significantly associated with an increase in fentanyl consumption and the occurrence of opioid-related side effects in postsurgical patients.

Keywords: acute pain; analgesia; opioids; pain; patient-controlled; perioperative medicine; postoperative.

Conflict of interest statement

The authors report no conflicts of interest in this work.

© 2020 Jung et al.

Figures

Figure 1
Figure 1
Flow diagram of the study.

References

    1. Chou R, Gordon DB, de Leon-casasola OA, et al. Management of postoperative pain: a clinical practice guideline from the American Pain Society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists’ Committee on Regio;nal Anesthesia, Executive Committee, and Administrative Council. J Pain. 2016;17(2):131–157. doi:10.1016/j.jpain.2015.12.008
    1. McNicol ED, Ferguson MC, Hudcova J. Patient controlled opioid analgesia versus non-patient controlled opioid analgesia for postoperative pain. Cochrane Database Syst Rev. 2015;6:Cd003348. doi:10.1002/14651858.CD003348.pub3
    1. Momeni M, Crucitti M, De Kock M. Patient-controlled analgesia in the management of postoperative pain. Drugs. 2006;66(18):2321–2337. doi:10.2165/00003495-200666180-00005
    1. Park KO, Lee YY. Orthostatic intolerance ambulation in patients using patient controlled analgesia. Korean J Pain. 2013;26(3):277–285. doi:10.3344/kjp.2013.26.3.277
    1. Oderda GM, Evans RS, Lloyd J, et al. Cost of opioid-related adverse drug events in surgical patients. J Pain Symptom Manage. 2003;25(3):276–283. doi:10.1016/s0885-3924(02)00691-7
    1. Eberhart LH, Morin AM, Wulf H, Geldner G. Patient preferences for immediate postoperative recovery. Br J Anaesth. 2002;89(5):760–761. doi:10.1093/bja/89.5.760
    1. Sinatra R, Chung KS, Silverman DG, et al. An evaluation of morphine and oxymorphone administered via patient-controlled analgesia (PCA) or PCA plus basal infusion in postcesarean-delivery patients. Anesthesiology. 1989;71(4):502–507. doi:10.1097/00000542-198910000-00005
    1. Parker RK, Holtmann B, White PF. Effects of a nighttime opioid infusion with PCA therapy on patient comfort and analgesic requirements after abdominal hysterectomy. Anesthesiology. 1992;76(3):362–367. doi:10.1097/00000542-199203000-00007
    1. Parker RK, Holtmann B, White PF. Patient-controlled analgesia. Does a concurrent opioid infusion improve pain management after surgery? JAMA. 1991;266:1947–1952. doi:10.1001/jama.1991.03470140059024
    1. Russell AW, Owen H, Ilsley AH, Kluger MT, Plummer JL. Background infusion with patient-controlled analgesia: effect on postoperative oxyhaemoglobin saturation and pain control. Anaesth Intensive Care. 1993;21(2):174–179. doi:10.1177/0310057X9302100207
    1. George JA, Lin EE, Hanna MN, et al. The effect of intravenous opioid patient-controlled analgesia with and without background infusion on respiratory depression: a meta-analysis. J Opioid Manag. 2010;6(1):47–54. doi:10.5055/jom.2010.0004
    1. Hwang J, Min SK, Chae YJ, Lim GM, Joe HB. Continuous fentanyl background infusion regimen optimised by patient-controlled analgesia for acute postoperative pain management: a randomised controlled trial. J Clin Med. 2020;9(1):211. doi:10.3390/jcm9010211
    1. Chae D, Kim SY, Song Y, et al. Dynamic predictive model for postoperative nausea and vomiting for intravenous fentanyl patient-controlled analgesia. Anaesthesia. 2020;75(2):218–226. doi:10.1111/anae.14849
    1. Lee CY, Narm KS, Lee JG, et al. A prospective randomized trial of continuous paravertebral infusion versus intravenous patient-controlled analgesia after thoracoscopic lobectomy for lung cancer. J Thorac Dis. 2018;10(6):3814–3823. doi:10.21037/jtd.2018.05.161
    1. Kim K-M. Analysis of the current state of postoperative patient-controlled analgesia in Korea. Anesth Pain Med. 2016;11(1):28–35. doi:10.17085/apm.2016.11.1.28
    1. von Elm E, Altman DG, Egger M, et al. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Int J Surg. 2014;12(12):1495–1499. doi:10.1016/j.ijsu.2014.07.013
    1. Protopapa KL, Simpson JC, Smith NC, Moonesinghe SR. Development and validation of the Surgical Outcome Risk Tool (SORT). Br J Surg. 2014;101(13):1774–1783. doi:10.1002/bjs.9638
    1. Grass JA. Patient-controlled analgesia. Anesth Analg. 2005;101(Supplement):S44–S61. doi:10.1213/01.ane.0000177102.11682.20
    1. Cepeda MS, Farrar JT, Baumgarten M, Boston R, Carr DB, Strom BL. Side effects of opioids during short-term administration: effect of age, gender, and race. Clin Pharmacol Ther. 2003;74(2):102–112. doi:10.1016/S0009-9236(03)00152-8
    1. Hutchison RW, Chon EH, Tucker WF, Gilder R, Moss J, Daniel P. A comparison of a fentanyl, morphine, and hydromorphone patient-controlled intravenous delivery for acute postoperative analgesia: a multicenter study of opioid-induced adverse reactions. Hosp Pharm. 2006;41(7):659–663. doi:10.1310/hpj4107-659
    1. Russo A, Grieco DL, Bevilacqua F, et al. Continuous intravenous analgesia with fentanyl or morphine after gynecological surgery: a cohort study. J Anesth. 2017;31(1):51–57. doi:10.1007/s00540-016-2268-0
    1. Shin S, Min KT, Shin YS, Joo HM, Yoo YC. Finding the ‘ideal’ regimen for fentanyl-based intravenous patient-controlled analgesia: how to give and what to mix? Yonsei Med J. 2014;55(3):800–806. doi:10.3349/ymj.2014.55.3.800
    1. Iwata Y, Mizota Y, Mizota T, Koyama T, Shichino T. Postoperative continuous intravenous infusion of fentanyl is associated with the development of orthostatic intolerance and delayed ambulation in patients after gynecologic laparoscopic surgery. J Anesth. 2012;26(4):503–508. doi:10.1007/s00540-012-1391-9
    1. Mota FA, Marcolan JF, Pereira MH, Milanez AM, Dallan LA, Diccini S. Comparison study of two different patient-controlled anesthesia regiments after cardiac surgery. Rev Bras Cir Cardiovasc. 2010;25(1):38–44. doi:10.1590/S0102-76382010000100011
    1. Hansen LA, Noyes MA, Lehman ME. Evaluation of patient-controlled analgesia (PCA) versus PCA plus continuous infusion in postoperative cancer patients. J Pain Symptom Manage. 1991;6(1):4–14. doi:10.1016/0885-3924(91)90066-D
    1. Guler T, Unlugenc H, Gundogan Z, Ozalevli M, Balcioglu O, Topcuoglu MS. A background infusion of morphine enhances patient-controlled analgesia after cardiac surgery. Can J Anaesth. 2004;51(7):718–722. doi:10.1007/BF03018432
    1. Alexander JC, Patel B, Joshi GP. Perioperative use of opioids: current controversies and concerns. Best Pract Res Clin Anaesthesiol. 2019;33(3):341–351. doi:10.1016/j.bpa.2019.07.009
    1. Colvin LA, Bull F, Hales TG. Perioperative opioid analgesia-when is enough too much? A review of opioid-induced tolerance and hyperalgesia. Lancet. 2019;393(10180):1558–1568. doi:10.1016/S0140-6736(19)30430-1
    1. Tripathy S, Rath S, Agrawal S, et al. Opioid-free anesthesia for breast cancer surgery: an observational study. J Anaesthesiol Clin Pharmacol. 2018;34(1):35–40. doi:10.4103/joacp.JOACP_143_1729
    1. Keller DS, Zhang J, Chand M. Opioid-free colorectal surgery: a method to improve patient & financial outcomes in surgery. Surg Endosc. 2019;33(6):1959–1966. doi:10.1007/s00464-018-6477-5

Source: PubMed

3
Se inscrever