How to Modulate Peripheral and Central Nervous System to Treat Acute Postoperative Pain and Prevent Pain Persistence


Cite item

Full Text

Abstract

Chronic postoperative pain (CPSP) is a major issue after surgery, which may impact on patient’s quality of life. Traditionally, CPSP is believed to rely on maladaptive hyperalgesia and risk factors have been identified that predispose to CPSP, including acute postoperative pain. Despite new models of prediction are emerging, acute pain is still a modifiable factor that can be challenged with perioperative analgesic strategies. In this review we present the issue of CPSP, focusing on molecular mechanism underlying the development of acute and chronic hyperalgesia. Also, we focus on how perioperative strategies can impact directly or indirectly (by reducing postoperative pain intensity) on the development of CPSP.

About the authors

Sara Cazzaniga

Emergency and Intensive Care Department, ASST Papa Giovanni XXIII

Email: info@benthamscience.net

Giovanni Real

Department of Health Sciences, University of Milan

Email: info@benthamscience.net

Simone Finazzi

Department of Health Sciences, University of Milan

Email: info@benthamscience.net

Luca Lorini

Emergency and Intensive Care Department, ASST Papa Giovanni XXIII

Email: info@benthamscience.net

Patrice Forget

School of Medicine, Medical Sciences and Nutrition, Epidemiology Group, Institute of Applied Health Sciences, University of Aberdeen

Email: info@benthamscience.net

Dario Bugada

Emergency and Intensive Care Department, ASST Papa Giovanni XXIII

Author for correspondence.
Email: info@benthamscience.net

References

  1. Schug, S.A.; Lavand’homme, P.; Barke, A.; Korwisi, B.; Rief, W.; Treede, R.D. The IASP classification of chronic pain for ICD-11: Chronic postsurgical or posttraumatic pain. Pain, 2019, 160(1), 45-52. doi: 10.1097/j.pain.0000000000001413 PMID: 30586070
  2. Grosu, I.; de Kock, M. New concepts in acute pain management: Strategies to prevent chronic postsurgical pain, opioid-induced hyperalgesia, and outcome measures. Anesthesiol. Clin., 2011, 29(2), 311-327. doi: 10.1016/j.anclin.2011.04.001 PMID: 21620345
  3. Perkins, F.M.; Kehlet, H. Chronic pain as an outcome of surgery. A review of predictive factors. Anesthesiology, 2000, 93(4), 1123-1133. doi: 10.1097/00000542-200010000-00038 PMID: 11020770
  4. Wall, P.D.; Jones, M. Defeating Pain: The war against a silent epidemic; Springer: New York, 1991. doi: 10.1007/978-1-4899-6551-6
  5. Fletcher, D.; Stamer, U.M.; Pogatzki-Zahn, E.; Zaslansky, R.; Tanase, N.V.; Perruchoud, C.; Kranke, P.; Komann, M.; Lehman, T.; Meissner, W. Chronic postsurgical pain in Europe. Eur. J. Anaesthesiol., 2015, 32(10), 725-734. doi: 10.1097/EJA.0000000000000319 PMID: 26241763
  6. Schug, S.A.; Bruce, J. Risk stratification for the development of chronic postsurgical pain. Schmerz, 2018, 32(6), 471-476. doi: 10.1007/s00482-018-0332-4 PMID: 30324317
  7. Voon, P.; Karamouzian, M.; Kerr, T. Chronic pain and opioid misuse: A review of reviews. Subst. Abuse Treat. Prev. Policy, 2017, 12(1), 36. doi: 10.1186/s13011-017-0120-7 PMID: 28810899
  8. Correll, D. Chronic postoperative pain: recent findings in understanding and management. F1000 Res., 2017, 6, 1054. doi: 10.12688/f1000research.11101.1 PMID: 28713565
  9. Edgley, C.; Hogg, M.; De Silva, A.; Braat, S.; Bucknill, A.; Leslie, K. Severe acute pain and persistent post-surgical pain in orthopaedic trauma patients: A cohort study. Br. J. Anaesth., 2019, 123(3), 350-359. doi: 10.1016/j.bja.2019.05.030 PMID: 31248645
  10. Guimarães-Pereira, L.; Reis, P.; Abelha, F.; Azevedo, L.F.; Castro-Lopes, J.M. Persistent postoperative pain after cardiac surgery: A systematic review with meta-analysis regarding incidence and pain intensity. Pain, 2017, 158(10), 1869-1885. doi: 10.1097/j.pain.0000000000000997 PMID: 28767509
  11. Sadosky, A.; Parsons, B.; Schaefer, C.; Mann, R.; Daniel, S.; Nalamachu, S.; Stacey, B.R.; Nieshoff, E.; Tuchman, M.; Anschel, A. Economic and humanistic burden of post-trauma and post-surgical neuropathic pain among adults in the United States. J. Pain Res., 2013, 6, 459-469. doi: 10.2147/JPR.S44939 PMID: 23825931
  12. Gilron, I.; Vandenkerkhof, E.; Katz, J.; Kehlet, H.; Carley, M. Evaluating the association between acute and chronic pain after surgery. Clin. J. Pain, 2017, 33(7), 588-594. doi: 10.1097/AJP.0000000000000443 PMID: 28145910
  13. Zhang, Y.; Zhou, R.; Hou, B.; Tang, S.; Hao, J.; Gu, X.; Ma, Z.; Zhang, J. Incidence and risk factors for chronic postsurgical pain following video-assisted thoracoscopic surgery: A retrospective study. BMC Surg., 2022, 22(1), 76. doi: 10.1186/s12893-022-01522-1 PMID: 35236334
  14. Jin, J.; Du, X.; Min, S.; Liu, L. Comparison of chronic postsurgical pain between single-port and multi-port video-assisted thoracoscopic pulmonary resection: A prospective study. Thorac. Cardiovasc. Surg., 2022, 70(5), 430-438. doi: 10.1055/s-0042-1744546 PMID: 35439833
  15. Bugada, D.; Lavand’homme, P.; Ambrosoli, A.L.; Klersy, C.; Braschi, A.; Fanelli, G.; Saccani Jotti, G.M.R.; Allegri, M.; Baciarello, M.; Bettinelli, S.; Cobianchi, L.; De Gregori, M.; Di Matteo, M.; Guarisco, S.; Krizova, P.; Marangoni, F.; Minella, C.E.; Niebel, T.; Peloso, A.; Repetti, F. Effect of postoperative analgesia on acute and persistent postherniotomy pain: A randomized study. J. Clin. Anesth., 2015, 27(8), 658-664. doi: 10.1016/j.jclinane.2015.06.008 PMID: 26329661
  16. Spivey, T.L.; Gutowski, E.D.; Zinboonyahgoon, N.; King, T.A.; Dominici, L.; Edwards, R.R.; Golshan, M.; Schreiber, K.L. Chronic Pain After Breast Surgery: A Prospective, Observational Study. Ann. Surg. Oncol., 2018, 25(10), 2917-2924. doi: 10.1245/s10434-018-6644-x PMID: 30014456
  17. Katz, J.; Weinrib, A.; Fashler, S.; Katznelson, R.; Shah, B.; Ladak, S.; Jiang, J.; Li, Q.; McMillan, K.; Santa Mina, D.; Wendtlandt, K.; McRae, K.; Tamir, D.; Lyn, S.; de Perrot, M.; Rao, V.; Grant, D.; Roche-Nagle, G.; Cleary, S.; Hofer, S.; Gilbert, R.; Wijeysundera, D.; Ritvo, P.; Janmohamed, T.; O’Leary, G.; Clarke, H. The Toronto General Hospital Transitional Pain Service: Development and implementation of a multidisciplinary program to prevent chronic postsurgical pain. J. Pain Res., 2015, 8, 695-702. doi: 10.2147/JPR.S91924 PMID: 26508886
  18. Theunissen, M.; Peters, M.L.; Bruce, J.; Gramke, H.F.; Marcus, M.A. Preoperative anxiety and catastrophizing: A systematic review and meta-analysis of the association with chronic postsurgical pain. Clin. J. Pain, 2012, 28(9), 819-841. doi: 10.1097/AJP.0b013e31824549d6 PMID: 22760489
  19. Haroutiunian, S.; Nikolajsen, L.; Finnerup, N.B.; Jensen, T.S. The neuropathic component in persistent postsurgical pain: A systematic literature review. Pain, 2013, 154(1), 95-102. doi: 10.1016/j.pain.2012.09.010 PMID: 23273105
  20. Beloeil, H.; Sion, B.; Rousseau, C.; Albaladejo, P.; Raux, M.; Aubrun, F.; Martinez, V. Early postoperative neuropathic pain assessed by the DN4 score predicts an increased risk of persistent postsurgical neuropathic pain. Eur. J. Anaesthesiol., 2017, 34(10), 652-657. doi: 10.1097/EJA.0000000000000634 PMID: 28437260
  21. Forstenpointner, J.; Ruscheweyh, R.; Attal, N.; Baron, R.; Bouhassira, D.; Enax-Krumova, E.K.; Finnerup, N.B.; Freynhagen, R.; Gierthmühlen, J.; Hansson, P.; Jensen, T.S.; Maier, C.; Rice, A.S.C.; Segerdahl, M.; Tölle, T.; Treede, R.D.; Vollert, J. No pain, still gain (of function): The relation between sensory profiles and the presence or absence of self-reported pain in a large multicenter cohort of patients with neuropathy. Pain, 2021, 162(3), 718-727. doi: 10.1097/j.pain.0000000000002058 PMID: 32868752
  22. Edwards, R.R. Optimizing and accelerating the development of precision pain treatments for chronic pain: IMMPACT review and recommendations. J. Pain, 2023, 24(2), 204-225. doi: 10.1016/j.jpain.2022.08.010 PMID: 36198371
  23. Sangesland, A.; Støren, C.; Vaegter, H.B. Are preoperative experimental pain assessments correlated with clinical pain outcomes after surgery? A systematic review. Scand. J. Pain, 2017, 15(1), 44-52. doi: 10.1016/j.sjpain.2016.12.002 PMID: 28850344
  24. van Helmond, N.; Aarts, H.M.; Timmerman, H.; Olesen, S.S.; Drewes, A.M.; Wilder-Smith, O.H.; Steegers, M.A.; Vissers, K.C. Is preoperative quantitative sensory testing related to persistent postsurgical pain? A systematic literature review. Anesth. Analg., 2020, 131(4), 1146-1155. doi: 10.1213/ANE.0000000000004871 PMID: 32925335
  25. Petersen, K.K.; Vaegter, H.B.; Stubhaug, A.; Wolff, A.; Scammell, B.E.; Arendt-Nielsen, L.; Larsen, D.B. The predictive value of quantitative sensory testing: A systematic review on chronic postoperative pain and the analgesic effect of pharmacological therapies in patients with chronic pain. Pain, 2021, 162(1), 31-44. doi: 10.1097/j.pain.0000000000002019 PMID: 32701654
  26. Koulouris, A.E.; Edwards, R.R.; Dorado, K.; Schreiber, K.L.; Lazaridou, A.; Rajan, S.; White, J.; Garcia, J.; Gibbons, C.; Freeman, R. Reliability and validity of the boston bedside quantitative sensory testing battery for neuropathic pain. Pain Med., 2020, 21(10), 2336-2347. doi: 10.1093/pm/pnaa192 PMID: 32895703
  27. Lavand’homme, P. The progression from acute to chronic pain. Curr. Opin. Anaesthesiol., 2011, 24(5), 545-550. doi: 10.1097/ACO.0b013e32834a4f74 PMID: 21772141
  28. Arendt-Nielsen, L.; Nie, H.; Laursen, M.B.; Laursen, B.S.; Madeleine, P.; Simonsen, O.H.; Graven-Nielsen, T. Sensitization in patients with painful knee osteoarthritis. Pain, 2010, 149(3), 573-581. doi: 10.1016/j.pain.2010.04.003 PMID: 20418016
  29. Coluzzi, F.; Bifulco, F.; Cuomo, A.; Dauri, M.; Leonardi, C.; Melotti, R.M.; Natoli, S.; Romualdi, P.; Savoia, G.; Corcione, A. The challenge of perioperative pain management in opioid-tolerant patients. Ther. Clin. Risk Manag., 2017, 13, 1163-1173. doi: 10.2147/TCRM.S141332 PMID: 28919771
  30. Gandhi, R.; Santone, D.; Takahashi, M.; Dessouki, O.; Mahomed, N.N. Inflammatory predictors of ongoing pain 2 years following knee replacement surgery. Knee, 2013, 20(5), 316-318. doi: 10.1016/j.knee.2012.10.015 PMID: 23157967
  31. Bugada, D.; Allegri, M.; Gemma, M.; Ambrosoli, A.L.; Gazzerro, G.; Chiumiento, F.; Dongu, D.; Nobili, F.; Fanelli, A.; Ferrua, P.; Berruto, M.; Cappelleri, G. Effects of anaesthesia and analgesia on long-term outcome after total knee replacement. Eur. J. Anaesthesiol., 2017, 34(10), 665-672. doi: 10.1097/EJA.0000000000000656 PMID: 28767456
  32. Belluzzi, E.; El Hadi, H.; Granzotto, M.; Rossato, M.; Ramonda, R.; Macchi, V.; De Caro, R.; Vettor, R.; Favero, M. Systemic and local adipose tissue in knee osteoarthritis. J. Cell. Physiol., 2017, 232(8), 1971-1978. doi: 10.1002/jcp.25716 PMID: 27925193
  33. Daoudia, M.; Decruynaere, C.; Le Polain de Waroux, B.; Thonnard, J.L.; Plaghki, L.; Forget, P. Biological inflammatory markers mediate the effect of preoperative pain-related behaviours on postoperative analgesics requirements. BMC Anesthesiol., 2015, 15(1), 183. doi: 10.1186/s12871-015-0167-9 PMID: 26674471
  34. Parisien, M.; Lima, L.V.; Dagostino, C.; El-Hachem, N.; Drury, G.L.; Grant, A.V.; Huising, J.; Verma, V.; Meloto, C.B.; Silva, J.R.; Dutra, G.G.S.; Markova, T.; Dang, H.; Tessier, P.A.; Slade, G.D.; Nackley, A.G.; Ghasemlou, N.; Mogil, J.S.; Allegri, M.; Diatchenko, L. Acute inflammatory response via neutrophil activation protects against the development of chronic pain. Sci. Transl. Med., 2022, 14(644), eabj9954. doi: 10.1126/scitranslmed.abj9954 PMID: 35544595
  35. Bartley, E.J.; Fillingim, R.B. Sex differences in pain: A brief review of clinical and experimental findings. Br. J. Anaesth., 2013, 111(1), 52-58. doi: 10.1093/bja/aet127 PMID: 23794645
  36. Vollert, J.; Trewartha, N.; Kemkowski, D.; Cremer, A.F.; Zahn, P.K.; Segelcke, D.; Pogatzki-Zahn, E.M. Conditioned pain modulation and offset analgesia: Influence of sex, sex hormone levels and menstrual cycle on the magnitude and retest reliability in healthy participants. Eur. J. Pain, 2022, 26(9), 1938-1949. doi: 10.1002/ejp.2014 PMID: 35856832
  37. Horn-Hofmann, C.; Scheel, J.; Dimova, V.; Parthum, A.; Carbon, R.; Griessinger, N.; Sittl, R.; Lautenbacher, S. Prediction of persistent post-operative pain: Pain-specific psychological variables compared with acute post-operative pain and general psychological variables. Eur. J. Pain, 2018, 22(1), 191-202. doi: 10.1002/ejp.1115 PMID: 28940665
  38. Hollins, M.; Harper, D.; Gallagher, S.; Owings, E.W.; Lim, P.F.; Miller, V.; Siddiqi, M.Q.; Maixner, W. Perceived intensity and unpleasantness of cutaneous and auditory stimuli: An evaluation of the generalized hypervigilance hypothesis. Pain, 2009, 141(3), 215-221. doi: 10.1016/j.pain.2008.10.003 PMID: 19121558
  39. White, K.P.; Carette, S.; Harth, M.; Teasell, R.W. Trauma and fibromyalgia: Is there an association and what does it mean? Semin. Arthritis Rheum., 2000, 29(4), 200-216. doi: 10.1016/S0049-0172(00)80009-8 PMID: 10707989
  40. Kalkman, J.C.; Visser, K.; Moen, J.; Bonsel, J.G.; Grobbee, E.D.; Moons, M.K.G. Preoperative prediction of severe postoperative pain. Pain, 2003, 105(3), 415-423. doi: 10.1016/S0304-3959(03)00252-5 PMID: 14527702
  41. Janssen, K.J.M.; Kalkman, C.J.; Grobbee, D.E.; Bonsel, G.J.; Moons, K.G.M.; Vergouwe, Y. The risk of severe postoperative pain: modification and validation of a clinical prediction rule. Anesth. Analg., 2008, 107(4), 1330-1339. doi: 10.1213/ane.0b013e31818227da PMID: 18806049
  42. van Reij, R.R.I. The association between genome-wide polymorphisms and chronic postoperative pain: A prospective observational study. Anaesthesia, 2020, 75(Suppl. 1), e111-e120. doi: 10.1111/anae.14832
  43. Deumens, R.; Steyaert, A.; Forget, P.; Schubert, M.; Lavand’homme, P.; Hermans, E.; De Kock, M. Prevention of chronic postoperative pain: Cellular, molecular, and clinical insights for mechanism-based treatment approaches. Prog. Neurobiol., 2013, 104, 1-37. doi: 10.1016/j.pneurobio.2013.01.002 PMID: 23410739
  44. James, S.K. Chronic postsurgical pain: Is there a possible genetic link? Br. J. Pain, 2017, 11(4), 178-185. doi: 10.1177/2049463717723222 PMID: 29123662
  45. Bugada, D.; Lorini, L.F.; Fumagalli, R.; Allegri, M. Genetics and opioids: Towards more appropriate prescription in cancer pain. Cancers, 2020, 12(7), 1951. doi: 10.3390/cancers12071951 PMID: 32708424
  46. Kehlet, H.; Jensen, T.S.; Woolf, C.J. Persistent postsurgical pain: Risk factors and prevention. Lancet, 2006, 367(9522), 1618-1625. doi: 10.1016/S0140-6736(06)68700-X PMID: 16698416
  47. Jacobs, A.; Lemoine, A.; Joshi, G.P.; Van de Velde, M.; Bonnet, F.; Pogatzki-Zahn, E.; Schug, S.; Kehlet, H.; Rawal, N.; Delbos, A.; Lavand’homme, P.; Beloeil, H.; Raeder, J.; Sauter, A.; Albrecht, E.; Lirk, P.; Freys, S.; Lobo, D. PROSPECT guideline for oncological breast surgery: A systematic review and procedure‐specific postoperative pain management recommendations. Anaesthesia, 2020, 75(5), 664-673. doi: 10.1111/anae.14964 PMID: 31984479
  48. Bugada, D.; Lorini, L.F. Lavand’Homme, P. Opioid free anesthesia: Evidence for short and long-term outcome. Minerva Anestesiol., 2021, 87(2), 230-237. doi: 10.23736/S0375-9393.20.14515-2 PMID: 32755088
  49. Fletcher, D.; Lavand’homme, P. Towards better predictive models of chronic post-surgical pain: Fitting to the dynamic nature of the pain itself. Br. J. Anaesth., 2022, 129(3), 281-284. doi: 10.1016/j.bja.2022.06.010 PMID: 35835605
  50. van Helmond, N.; Olesen, S.S.; Wilder-Smith, O.H.; Drewes, A.M.; Steegers, M.A.; Vissers, K.C. Predicting Persistent Pain After Surgery. Anesth. Analg., 2018, 127(5), 1264-1267. doi: 10.1213/ANE.0000000000003318 PMID: 29505448
  51. Chen, J.H.; Asch, S.M. Machine learning and prediction in medicine — Beyond the peak of inflated expectations. N. Engl. J. Med., 2017, 376(26), 2507-2509. doi: 10.1056/NEJMp1702071 PMID: 28657867
  52. Bugada, D.; Mariano, E.R. Predictors of chronic postsurgical pain: A step forward towards personalized medicine. Minerva Anestesiol., 2022, 88(10), 764-767. doi: 10.23736/S0375-9393.22.16861-6 PMID: 36254696
  53. Tighe, P.J.; Harle, C.A.; Hurley, R.W.; Aytug, H.; Boezaart, A.P.; Fillingim, R.B. Teaching a machine to feel postoperative pain: combining high-dimensional clinical data with machine learning algorithms to forecast acute postoperative pain. Pain Med., 2015, 16(7), 1386-1401. doi: 10.1111/pme.12713 PMID: 26031220
  54. van Driel, M.E.C.; van Dijk, J.F.M.; Baart, S.J.; Meissner, W.; Huygen, F.J.P.M.; Rijsdijk, M. Development and validation of a multivariable prediction model for early prediction of chronic postsurgical pain in adults: A prospective cohort study. Br. J. Anaesth., 2022, 129(3), 407-415. doi: 10.1016/j.bja.2022.04.030 PMID: 35732539
  55. Primary and Secondary Hyperalgesia; Encycl. Pain, 2013, p. 3174-3174. doi: 10.1007/978-3-642-28753-4_201764
  56. Armstrong, S.A.; Herr, M. J. Physiology, Nociception; StatPearls: Treasure Island, FL, 2022.
  57. Devor, M. Ectopic discharge in Aβ afferents as a source of neuropathic pain. Exp. Brain Res., 2009, 196(1), 115-128. doi: 10.1007/s00221-009-1724-6 PMID: 19242687
  58. Weinbroum, A.A. Postoperative hyperalgesia-A clinically applicable narrative review. Pharmacol. Res., 2017, 120, 188-205. doi: 10.1016/j.phrs.2017.02.012 PMID: 28365208
  59. Pacharinsak, C.; Khasabov, S.G.; Beitz, A.J.; Simone, D.A. NK-1 receptors in the rostral ventromedial medulla contribute to hyperalgesia produced by intraplantar injection of capsaicin. Pain, 2008, 139(1), 34-46. doi: 10.1016/j.pain.2008.02.032 PMID: 18407414
  60. Pertovaara, A. A neuronal correlate of secondary hyperalgesia in the rat spinal dorsal horn is submodality selective and facilitated by supraspinal influence. Exp. Neurol., 1998, 149(1), 193-202. doi: 10.1006/exnr.1997.6688 PMID: 9454628
  61. Kovelowski, C.J.; Ossipov, M.H.; Sun, H.; Lai, J.; Malan, T.P., Jr; Porreca, F. Supraspinal cholecystokinin may drive tonic descending facilitation mechanisms to maintain neuropathic pain in the rat. Pain, 2000, 87(3), 265-273. doi: 10.1016/S0304-3959(00)00290-6 PMID: 10963906
  62. Burgess, S.E.; Gardell, L.R.; Ossipov, M.H.; Malan, T.P., Jr; Vanderah, T.W.; Lai, J.; Porreca, F. Time-dependent descending facilitation from the rostral ventromedial medulla maintains, but does not initiate, neuropathic pain. J. Neurosci., 2002, 22(12), 5129-5136. doi: 10.1523/JNEUROSCI.22-12-05129.2002 PMID: 12077208
  63. Porreca, F.; Burgess, S.E.; Gardell, L.R.; Vanderah, T.W.; Malan, T.P., Jr; Ossipov, M.H.; Lappi, D.A.; Lai, J. Inhibition of neuropathic pain by selective ablation of brainstem medullary cells expressing the mu-opioid receptor. J. Neurosci., 2001, 21(14), 5281-5288. doi: 10.1523/JNEUROSCI.21-14-05281.2001 PMID: 11438603
  64. Zhang, W. Neuropathic pain is maintained by brainstem neurons co-expressing opioid and cholecystokinin receptors. Brain, 2009, 132(Pt 3), 778-787. doi: 10.1093/brain/awn330
  65. Géranton, S.M.; Tochiki, K.K.; Chiu, W.W.Y.; Stuart, S.A.; Hunt, S.P. Injury induced activation of extracellular signal-regulated kinase (ERK) in the rat rostral ventromedial medulla (RVM) is age dependant and requires the lamina I projection pathway. Mol. Pain, 2010, 6, 1744-8069-6-54. doi: 10.1186/1744-8069-6-54 PMID: 20840753
  66. Suzuki, R.; Rahman, W.; Rygh, L.J.; Webber, M.; Hunt, S.P.; Dickenson, A.H. Spinal-supraspinal serotonergic circuits regulating neuropathic pain and its treatment with gabapentin. Pain, 2005, 117(3), 292-303. doi: 10.1016/j.pain.2005.06.015 PMID: 16150546
  67. Costa-Pereira, J.T.; Serrão, P.; Martins, I.; Tavares, I. Serotoninergic pain modulation from the rostral ventromedial medulla (RVM) in chemotherapy‐induced neuropathy: The role of spinal 5‐HT3 receptors. Eur. J. Neurosci., 2020, 51(8), 1756-1769. doi: 10.1111/ejn.14614 PMID: 31691396
  68. Wang, W.; Zhong, X.; Li, Y.; Guo, R.; Du, S.; Wen, L.; Ying, Y.; Yang, T.; Wei, X.H. Rostral ventromedial medulla‐mediated descending facilitation following P2X7 receptor activation is involved in the development of chronic post‐operative pain. J. Neurochem., 2019, 149(6), 760-780. doi: 10.1111/jnc.14650 PMID: 30570747
  69. Li, J.; Wei, Y.; Zhou, J.; Zou, H.; Ma, L.; Liu, C.; Xiao, Z.; Liu, X.; Tan, X.; Yu, T.; Cao, S. Activation of locus coeruleus-spinal cord noradrenergic neurons alleviates neuropathic pain in mice via reducing neuroinflammation from astrocytes and microglia in spinal dorsal horn. J. Neuroinflammation, 2022, 19(1), 123. doi: 10.1186/s12974-022-02489-9 PMID: 35624514
  70. Cao, S.; Fisher, D.W.; Rodriguez, G.; Yu, T.; Dong, H. Comparisons of neuroinflammation, microglial activation, and degeneration of the locus coeruleus-norepinephrine system in APP/PS1 and aging mice. J. Neuroinflammation, 2021, 18(1), 10. doi: 10.1186/s12974-020-02054-2 PMID: 33407625
  71. Suárez-Pereira, I.; Llorca-Torralba, M.; Bravo, L.; Camarena-Delgado, C.; Soriano-Mas, C.; Berrocoso, E. The role of the locus coeruleus in pain and associated stress-related disorders. Biol. Psychiatry, 2022, 91(9), 786-797. doi: 10.1016/j.biopsych.2021.11.023 PMID: 35164940
  72. Araque, A.; Parpura, V.; Sanzgiri, R.P.; Haydon, P.G. Tripartite synapses: Glia, the unacknowledged partner. Trends Neurosci., 1999, 22(5), 208-215. doi: 10.1016/S0166-2236(98)01349-6 PMID: 10322493
  73. Wang, H.; Guo, W.; Yang, K.; Wei, F.; Dubner, R.; Ren, K. Contribution of primary afferent input to trigeminal astroglial hyperactivity, cytokine induction and NMDA receptor phosphorylation. Open Pain J., 2010, 3(1), 144-152. doi: 10.2174/1876386301003010144 PMID: 21170295
  74. Chen, Y.; Ju, P.; Xia, Q.; Cheng, P.; Gao, J.; Zhang, L.; Gao, H.; Cheng, X.; Yu, T.; Yan, J.; Wang, Q.; Zhu, C.; Zhang, X. Potential role of pain catastrophic thinking in comorbidity patients of depression and chronic pain. Front. Psychiatry, 2022, 13, 839173. doi: 10.3389/fpsyt.2022.839173 PMID: 35898637
  75. Dublin, P.; Hanani, M. Satellite glial cells in sensory ganglia: Their possible contribution to inflammatory pain. Brain Behav. Immun., 2007, 21(5), 592-598. doi: 10.1016/j.bbi.2006.11.011 PMID: 17222529
  76. Hanani, M.; Huang, T.Y.; Cherkas, P.S.; Ledda, M.; Pannese, E. Glial cell plasticity in sensory ganglia induced by nerve damage. Neuroscience, 2002, 114(2), 279-283. doi: 10.1016/S0306-4522(02)00279-8 PMID: 12204197
  77. Jasmin, L.; Vit, J.P.; Bhargava, A.; Ohara, P.T. Can satellite glial cells be therapeutic targets for pain control? Neuron Glia Biol., 2010, 6(1), 63-71. doi: 10.1017/S1740925X10000098 PMID: 20566001
  78. Liu, F.Y.; Sun, Y.N.; Wang, F.T.; Li, Q.; Su, L.; Zhao, Z.F.; Meng, X.L.; Zhao, H.; Wu, X.; Sun, Q.; Xing, G.G.; Wan, Y. Activation of satellite glial cells in lumbar dorsal root ganglia contributes to neuropathic pain after spinal nerve ligation. Brain Res., 2012, 1427, 65-77. doi: 10.1016/j.brainres.2011.10.016 PMID: 22050959
  79. Zhang, H.; Mei, X.; Zhang, P.; Ma, C.; White, F.A.; Donnelly, D.F.; Lamotte, R.H. Altered functional properties of satellite glial cells in compressed spinal ganglia. Glia, 2009, 57(15), 1588-1599. doi: 10.1002/glia.20872 PMID: 19330845
  80. Ji, R.R.; Berta, T.; Nedergaard, M. Glia and pain: Is chronic pain a gliopathy? Pain, 2013, 154(1), S10. doi: 10.1016/j.pain.2013.06.022
  81. Kehlet, H.; Wilmore, D.W. Multimodal strategies to improve surgical outcome. Am. J. Surg., 2002, 183(6), 630-641. doi: 10.1016/S0002-9610(02)00866-8 PMID: 12095591
  82. Gritsenko, K.; Khelemsky, Y.; Kaye, A.D.; Vadivelu, N.; Urman, R.D. Multimodal therapy in perioperative analgesia. Baillieres. Best Pract. Res. Clin. Anaesthesiol., 2014, 28(1), 59-79. doi: 10.1016/j.bpa.2014.03.001 PMID: 24815967
  83. Stasiowska, M.K.; Ng, S.C.; Gubbay, A.N.; Cregg, R. Postoperative pain management. Br. J. Hosp. Med., 2015, 76(10), 570-575. doi: 10.12968/hmed.2015.76.10.570 PMID: 26457937
  84. Gupta, A.; Bah, M. NSAIDs in the treatment of postoperative pain. Curr. Pain Headache Rep., 2016, 20(11), 62. doi: 10.1007/s11916-016-0591-7 PMID: 27841015
  85. Cashman, J.N. The mechanisms of action of NSAIDs in analgesia. Drugs, 1996, 52(Suppl. 5), 13-23. doi: 10.2165/00003495-199600525-00004
  86. Burian, M.; Geisslinger, G. COX-dependent mechanisms involved in the antinociceptive action of NSAIDs at central and peripheral sites. Pharmacol. Ther., 2005, 107(2), 139-154. doi: 10.1016/j.pharmthera.2005.02.004 PMID: 15993252
  87. Malmberg, A.B.; Yaksh, T.L. Antinociceptive actions of spinal nonsteroidal anti-inflammatory agents on the formalin test in the rat. J. Pharmacol. Exp. Ther., 1992, 263(1), 136-146. https://pubmed.ncbi.nlm.nih.gov/1403779/
  88. Seybold, V.S.; Jia, Y.P.; Abrahams, L.G. Cyclo-oxygenase-2 contributes to central sensitization in rats with peripheral inflammation. Pain, 2003, 105(1), 47-55. doi: 10.1016/S0304-3959(03)00254-9 PMID: 14499419
  89. Chou, R.; Gordon, D.B.; de Leon-Casasola, O.A.; Rosenberg, J.M.; Bickler, S.; Brennan, T.; Carter, T.; Cassidy, C.L.; Chittenden, E.H.; Degenhardt, E.; Griffith, S.; Manworren, R.; McCarberg, B.; Montgomery, R.; Murphy, J.; Perkal, M.F.; Suresh, S.; Sluka, K.; Strassels, S.; Thirlby, R.; Viscusi, E.; Walco, G.A.; Warner, L.; Weisman, S.J.; Wu, C.L. 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 regional anesthesia, executive committee, and administrative council. J. Pain, 2016, 17(2), 131-157. doi: 10.1016/j.jpain.2015.12.008 PMID: 26827847
  90. Doleman, B.; Leonardi-Bee, J.; Heinink, T.P.; Boyd-Carson, H.; Carrick, L.; Mandalia, R.; Lund, J.N.; Williams, J.P. Pre-emptive and preventive NSAIDs for postoperative pain in adults undergoing all types of surgery. Cochrane Libr., 2021, 2021(6), CD012978. doi: 10.1002/14651858.CD012978.pub2 PMID: 34125958
  91. Chang, R.W.; Tompkins, D.M.; Cohn, S.M. Are NSAIDs Safe? assessing the risk-benefit profile of nonsteroidal anti-inflammatory drug use in postoperative pain management. Am. Surg., 2021, 87(6), 872-879. doi: 10.1177/0003134820952834 PMID: 33238721
  92. Sugita, R.; Kuwabara, H.; Kubota, K.; Sugimoto, K.; Kiho, T.; Tengeiji, A.; Kawakami, K.; Shimada, K. Simultaneous inhibition of PGE2 and PGI2 signals is necessary to suppress hyperalgesia in rat inflammatory pain models. Mediators Inflamm., 2016, 2016, 1-10. doi: 10.1155/2016/9847840 PMID: 27478311
  93. van Helmond, N.; Steegers, M.A.; Filippini-de Moor, G.P.; Vissers, K.C.; Wilder-Smith, O.H. Hyperalgesia and persistent pain after breast cancer surgery: a prospective randomized controlled trial with perioperative cox-2 inhibition. PLoS One, 2016, 11(12), e0166601. doi: 10.1371/journal.pone.0166601 PMID: 27935990
  94. Pak, D.J.; Yong, R.J.; Kaye, A.D.; Urman, R.D. Chronification of pain: mechanisms, current understanding, and clinical implications. Curr. Pain Headache Rep., 2018, 22(2), 9. doi: 10.1007/s11916-018-0666-8 PMID: 29404791
  95. Schmid, R.L.; Sandler, A.N.; Katz, J. Use and efficacy of low-dose ketamine in the management of acute postoperative pain: A review of current techniques and outcomes. Pain, 1999, 82(2), 111-125. doi: 10.1016/S0304-3959(99)00044-5 PMID: 10467917
  96. Orser, B.A.; Pennefather, P.S.; MacDonald, J.F. Multiple mechanisms of ketamine blockade of N-methyl-D-aspartate receptors. Anesthesiology, 1997, 86(4), 903-917. doi: 10.1097/00000542-199704000-00021 PMID: 9105235
  97. Mion, G.; Villevieille, T. Ketamine pharmacology: An update (pharmacodynamics and molecular aspects, recent findings). CNS Neurosci. Ther., 2013, 19(6), 370-380. doi: 10.1111/cns.12099 PMID: 23575437
  98. Mikkelsen, S.; Ilkjaer, S.; Brennum, J.; Borgbjerg, F.M.; Dahl, J.B. The effect of naloxone on ketamine-induced effects on hyperalgesia and ketamine-induced side effects in humans. Anesthesiology, 1999, 90(6), 1539-1545. doi: 10.1097/00000542-199906000-00007 PMID: 10360849
  99. Kreutzwiser, D.; Tawfic, Q.A. Expanding role of NMDA receptor antagonists in the management of pain. CNS Drugs, 2019, 33(4), 347-374. doi: 10.1007/s40263-019-00618-2 PMID: 30826987
  100. Sinner, B.; Graf, B.M. Ketamine. Handb. Exp. Pharmacol., 2008, 182(182), 313-333. doi: 10.1007/978-3-540-74806-9_15 PMID: 18175098
  101. Taniguchi, T.; Shibata, K.; Yamamoto, K. Ketamine inhibits endotoxin-induced shock in rats. Anesthesiology, 2001, 95(4), 928-932. doi: 10.1097/00000542-200110000-00022 PMID: 11605934
  102. Dale, O.; Somogyi, A.A.; Li, Y.; Sullivan, T.; Shavit, Y. Does intraoperative ketamine attenuate inflammatory reactivity following surgery? A systematic review and meta-analysis. Anesth. Analg., 2012, 115(4), 934-943. doi: 10.1213/ANE.0b013e3182662e30 PMID: 22826531
  103. Inaba, H.; Kochi, A.; Yorozu, S. Suppression by methylprednisolone of augmented plasma endotoxin-like activity and interleukin-6 during cardiopulmonary bypass. Br. J. Anaesth., 1994, 72(3), 348-350. doi: 10.1093/bja/72.3.348 PMID: 8130057
  104. Gao, M.; Jin, W.; Qian, Y.; Ji, L.; Feng, G.; Sun, J. Effect of N-methyl-D-aspartate receptor antagonist on T helper cell differentiation induced by phorbol-myristate-acetate and ionomycin. Cytokine, 2011, 56(2), 458-465. doi: 10.1016/j.cyto.2011.06.022 PMID: 21795061
  105. Gao, M.; Sun, J.; Jin, W.; Qian, Y. Morphine, but not ketamine, decreases the ratio of Th1/Th2 in CD4-positive cells through T-bet and GATA3. Inflammation, 2012, 35(3), 1069-1077. doi: 10.1007/s10753-011-9413-6 PMID: 22160839
  106. De Kock, M.; Loix, S.; Lavand’homme, P. Ketamine and peripheral inflammation. CNS Neurosci. Ther., 2013, 19(6), 403-410. doi: 10.1111/cns.12104 PMID: 23574634
  107. Consensus Guidelines on the Use of Intravenous Ketamine Infusions for Acute Pain Management From the American Society of Regional Anesthesia and Pain Medicine. the American Academy of Pain Medicine, and the American Society of Anesthesiologists. Reg. Anesth. Pain Med., 2018, 43(5), 455-466. https://pubmed.ncbi.nlm.nih.gov/29870457/
  108. Urman, R.D.; Vadivelu, N.; Schermer, E.; Kodumudi, V.; Belani, K.; Kaye, A. Role of ketamine for analgesia in adults and children. J. Anaesthesiol. Clin. Pharmacol., 2016, 32(3), 298-306. doi: 10.4103/0970-9185.168149 PMID: 27625475
  109. Nielsen, R.V.; Fomsgaard, J.S.; Nikolajsen, L.; Dahl, J.B.; Mathiesen, O. Intraoperative S-ketamine for the reduction of opioid consumption and pain one year after spine surgery: A randomized clinical trial of opioid-dependent patients. Eur. J. Pain, 2019, 23(3), 455-460. doi: 10.1002/ejp.1317 PMID: 30246357
  110. Nguyen, L.; Thomas, K.L.; Lucke-Wold, B.P.; Cavendish, J.Z.; Crowe, M.S.; Matsumoto, R.R. Dextromethorphan: An update on its utility for neurological and neuropsychiatric disorders. Pharmacol. Ther., 2016, 159, 1-22. doi: 10.1016/j.pharmthera.2016.01.016 PMID: 26826604
  111. Taylor, C.P.; Traynelis, S.F.; Siffert, J.; Pope, L.E.; Matsumoto, R.R. Pharmacology of dextromethorphan: Relevance to dextromethorphan/quinidine (Nuedexta®) clinical use. Pharmacol. Ther., 2016, 164, 170-182. doi: 10.1016/j.pharmthera.2016.04.010 PMID: 27139517
  112. King, M.R.; Ladha, K.S.; Gelineau, A.M.; Anderson, T.A. Perioperative dextromethorphan as an adjunct for postoperative pain. Anesthesiology, 2016, 124(3), 696-705. doi: 10.1097/ALN.0000000000000950 PMID: 26587683
  113. Prostran, M.; Vujovic, K.; Kosutic, J.; Milovanovic, A.; Vuckovic, S.; Srebro, D. Magnesium in pain research: State of the Art. Curr. Med. Chem., 2017, 24(4), 424-434. doi: 10.2174/0929867323666161213101744 PMID: 27978803
  114. Morel, V.; Pickering, M.E.; Goubayon, J.; Djobo, M.; Macian, N.; Pickering, G. Magnesium for pain treatment in 2021? State of the art. Nutrients, 2021, 13(5), 1397. doi: 10.3390/nu13051397 PMID: 33919346
  115. Helander, E.M.; Menard, B.L.; Harmon, C.M.; Homra, B.K.; Allain, A.V.; Bordelon, G.J.; Wyche, M.Q.; Padnos, I.W.; Lavrova, A.; Kaye, A.D. Multimodal analgesia, current concepts, and acute pain considerations. Curr. Pain Headache Rep., 2017, 21(1), 3. doi: 10.1007/s11916-017-0607-y PMID: 28132136
  116. Sanchez, M.M.C.; De Kock, M.; Forget, P. What is the place of clonidine in anesthesia? Systematic review and meta-analyses of randomized controlled trials. J. Clin. Anesth., 2017, 38, 140-153. doi: 10.1016/j.jclinane.2017.02.003 PMID: 28372656
  117. Wang, X.; Liu, N.; Chen, J.; Xu, Z.; Wang, F.; Ding, C. Effect of intravenous dexmedetomidine during general anesthesia on acute postoperative pain in adults. Clin. J. Pain, 2018, 34(12), 1180-1191. doi: 10.1097/AJP.0000000000000630 PMID: 29771731
  118. Blaudszun, G.; Lysakowski, C.; Elia, N.; Tramèr, M.R. Effect of perioperative systemic α2 agonists on postoperative morphine consumption and pain intensity: Systematic review and meta-analysis of randomized controlled trials. Anesthesiology, 2012, 116(6), 1312-1322. doi: 10.1097/ALN.0b013e31825681cb PMID: 22546966
  119. Peng, K.; Zhang, J.; Meng, X.; Liu, H.Y.; Ji, F.H. Optimization of postoperative intravenous patient-controlled analgesia with opioid-dexmedetomidine combinations: An updated meta-analysis with trial sequential analysis of randomized controlled trials. Pain Physician, 2017, 20(7), 569-595. doi: 10.36076/ppj/2017.7.569
  120. Feng, M.; Chen, X.; Liu, T.; Zhang, C.; Wan, L.; Yao, W. Dexmedetomidine and sufentanil combination versus sufentanil alone for postoperative intravenous patient-controlled analgesia: A systematic review and meta-analysis of randomized controlled trials. BMC Anesthesiol., 2019, 19(1), 81. doi: 10.1186/s12871-019-0756-0 PMID: 31103031
  121. Lavand’homme, P.M.; Roelants, F.; Waterloos, H.; Collet, V.; De Kock, M.F. An evaluation of the postoperative antihyperalgesic and analgesic effects of intrathecal clonidine administered during elective cesarean delivery. Anesth. Analg., 2008, 107(3), 948-955. doi: 10.1213/ane.0b013e31817f1595 PMID: 18713912
  122. Wu, C.T.; Jao, S.W.; Borel, C.O.; Yeh, C.C.; Li, C.Y.; Lu, C.H.; Wong, C.S. The effect of epidural clonidine on perioperative cytokine response, postoperative pain, and bowel function in patients undergoing colorectal surgery. Anesth. Analg., 2004, 99(2), 502-509. doi: 10.1213/01.ANE.0000117146.46373.51 PMID: 15271731
  123. Nafziger, A.N.; Barkin, R.L. Opioid therapy in acute and chronic pain. J. Clin. Pharmacol., 2018, 58(9), 1111-1122. doi: 10.1002/jcph.1276 PMID: 29985526
  124. Frauenknecht, J.; Kirkham, K.R.; Jacot-Guillarmod, A.; Albrecht, E. Analgesic impact of intra‐operative opioids vs. opioid‐free anaesthesia: A systematic review and meta‐analysis. Anaesthesia, 2019, 74(5), 651-662. doi: 10.1111/anae.14582 PMID: 30802933
  125. Toleska, M.; Dimitrovski, A. Is opioid-free general anesthesia more superior for postoperative pain versus opioid general anesthesia in laparoscopic cholecystectomy? Prilozi (Makedon. Akad. Nauk. Umet. Odd. Med. Nauki), 2019, 40(2), 81-87. doi: 10.2478/prilozi-2019-0018 PMID: 31605587
  126. Simpson, J.; Bao, X.; Agarwala, A. Pain Management in Enhanced Recovery after Surgery (ERAS) Protocols. Clin. Colon Rectal Surg., 2019, 32(2), 121-128. doi: 10.1055/s-0038-1676477 PMID: 30833861
  127. Van de Velde, F.P.; Pogatzki-Zahn, E. Opioid-Free Anaesthesia: Should we all adopt it? An overview of current evidence. Eur. J. Anaesthesiol., 2022, 40(8), 539-541.
  128. Mathieson, S.; Lin, C.W.C.; Underwood, M.; Eldabe, S. Pregabalin and gabapentin for pain. BMJ, 2020, 369, m1315. doi: 10.1136/bmj.m1315 PMID: 32345589
  129. Rai, A.S.; Khan, J.S.; Dhaliwal, J.; Busse, J.W.; Choi, S.; Devereaux, P.J.; Clarke, H. Preoperative pregabalin or gabapentin for acute and chronic postoperative pain among patients undergoing breast cancer surgery: A systematic review and meta-analysis of randomized controlled trials. J. Plast. Reconstr. Aesthet. Surg., 2017, 70(10), 1317-1328. doi: 10.1016/j.bjps.2017.05.054 PMID: 28751024
  130. Seib, R.K.; Paul, J.E. Preoperative gabapentin for postoperative analgesia: A meta-analysis. Can. J. Anaesth., 2006, 53(5), 461-469. doi: 10.1007/BF03022618 PMID: 16636030
  131. Rai, A.S.; Khan, J.S.; Dhaliwal, J.; Busse, J.W.; Choi, S.; Devereaux, P.J.; Clarke, H. Preoperative pregabalin or gabapentin for acute and chronic postoperative pain among patients undergoing breast cancer surgery: A systematic review and meta-analysis of randomized controlled trials. J. Plast. Reconstr. Aesthet. Surg., 2017, 70(10), 1317-1328. doi: 10.1016/j.bjps.2017.05.054 PMID: 28751024
  132. Becker, D.E.; Reed, K.L. Local anesthetics: review of pharmacological considerations. Anesth. Prog., 2012, 59(2), 90-102. doi: 10.2344/0003-3006-59.2.90 PMID: 22822998
  133. Cassuto, J.; Sinclair, R.; Bonderovic, M. Anti-inflammatory properties of local anesthetics and their present and potential clinical implications. Acta Anaesthesiol. Scand., 2006, 50(3), 265-282. doi: 10.1111/j.1399-6576.2006.00936.x PMID: 16480459
  134. MacGregor, R.R.; Thorner, R.E.; Wright, D.M. Lidocaine inhibits granulocyte adherence and prevents granulocyte delivery to inflammatory sites. Blood, 1980, 56(2), 203-209. doi: 10.1182/blood.V56.2.203.203 PMID: 7397378
  135. Cullen, B.F.; Haschke, R.H. Local anesthetic inhibition of phagocytosis and metabolism of human leukocytes. Anesthesiology, 1974, 40(2), 142-145. doi: 10.1097/00000542-197402000-00009 PMID: 4812712
  136. Mikawa, K.; Akamatsu, H.; Nishina, K.; Shiga, M.; Obara, H.; Niwa, Y. Effects of ropivacaine on human neutrophil function: Comparison with bupivacaine and lidocaine. Eur. J. Anaesthesiol., 2003, 20(2), 104-110. doi: 10.1097/00003643-200302000-00004 PMID: 12622492
  137. Sasagawa, S. Inhibitory effects of local anesthetics on migration, extracellular release of lysosomal enzyme, and superoxide anion production in human polymorphonuclear leukocytes. Immunopharmacol. Immunotoxicol., 1991, 13(4), 607-622. doi: 10.3109/08923979109019726 PMID: 1663527
  138. Hammer, R.; Dahlgren, C.; Stendahl, O. Inhibition of human leukocyte metabolism and random mobility by local anaesthesia. Acta Anaesthesiol. Scand., 1985, 29(5), 520-523. doi: 10.1111/j.1399-6576.1985.tb02246.x PMID: 2994345
  139. Takao, Y.; Mikawa, K.; Nishina, K.; Maekawa, N.; Obara, H. Lidocaine attenuates hyperoxic lung injury in rabbits. Acta Anaesthesiol. Scand., 1996, 40(3), 318-325. doi: 10.1111/j.1399-6576.1996.tb04439.x PMID: 8721462
  140. Allegri, M.; Bugada, D.; De Gregori, M.; Avanzini, M.A.; De Silvestri, A.; Petroni, A.; Sala, A.; Filisetti, C.; Icaro, C.A.; Cobianchi, L. Continuous wound infusion with chloroprocaine in a pig model of surgical lesion: Drug absorption and effects on inflammatory response. J. Pain Res., 2017, 10, 2515-2524. doi: 10.2147/JPR.S139856 PMID: 29184436
  141. Niraj, G.; Kelkar, A.; Kaushik, V.; Tang, Y.; Fleet, D.; Tait, F.; Mcmillan, T.; Rathinam, S. Audit of postoperative pain management after open thoracotomy and the incidence of chronic postthoracotomy pain in more than 500 patients at a tertiary center. J. Clin. Anesth., 2017, 36, 174-177. doi: 10.1016/j.jclinane.2016.10.011 PMID: 28183561
  142. Lavand’homme, P. From preemptive to preventive analgesia: Time to reconsider the role of perioperative peripheral nerve blocks? Reg. Anesth. Pain Med., 2011, 36(1), 4-6. doi: 10.1097/AAP.0b013e31820305b8 PMID: 21455081
  143. Andreae, M.H.; Andreae, D.A. Local anaesthetics and regional anaesthesia for preventing chronic pain after surgery. Cochrane Libr., 2012, 10(10), CD007105. doi: 10.1002/14651858.CD007105.pub2 PMID: 23076930
  144. Lim, J.; Chen, D.; McNicol, E.; Sharma, L.; Varaday, G.; Sharma, A.; Wilson, E.; Wright-Yatsko, T.; Yaeger, L.; Gilron, I.; Finnerup, N.B.; Haroutounian, S. Risk factors for persistent pain after breast and thoracic surgeries: A systematic literature review and meta-analysis. Pain, 2022, 163(1), 3-20. doi: 10.1097/j.pain.0000000000002301 PMID: 34001769
  145. Zinboonyahgoon, N.; Patton, M.E.; Chen, Y.Y.K.; Edwards, R.R.; Schreiber, K.L. Persistent post-mastectomy pain: The impact of regional anesthesia among patients with high vs. low baseline catastrophizing. Pain Med., 2021, 22(8), 1767-1775. doi: 10.1093/pm/pnab039 PMID: 33560352
  146. Harkouk, H.; Fletcher, D.; Martinez, V. Paravertebral block for the prevention of chronic postsurgical pain after breast cancer surgery. Reg. Anesth. Pain Med., 2021, 46(3), 251-257. doi: 10.1136/rapm-2020-102040 PMID: 33414157
  147. Beswick, A.D.; Dennis, J.; Gooberman-Hill, R.; Blom, A.W.; Wylde, V. Are perioperative interventions effective in preventing chronic pain after primary total knee replacement? A systematic review. BMJ Open, 2019, 9(9), e028093. doi: 10.1136/bmjopen-2018-028093 PMID: 31494601
  148. Geradon, P.; Lavand’homme, P. Use of regional analgesia to prevent the conversion from acute to chronic pain. Curr. Opin. Anaesthesiol., 2022, 35(5), 641-646. doi: 10.1097/ACO.0000000000001175 PMID: 35942702
  149. WHO. ICD-11: International classification of diseases. 11th revision, 2019. Available From: https://icd.who.int/en (accessed Oct. 24, 2022).
  150. Levy, N.; Mills, P.; Mythen, M. Is the pursuit of DREAMing (drinking, eating and mobilising) the ultimate goal of anaesthesia? Anaesthesia, 2016, 71(9), 1008-1012. doi: 10.1111/anae.13495 PMID: 27079158

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2024 Bentham Science Publishers