Possibilities of clinical application of articaine

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Abstract

Articaine is an intermediate-potency and short-acting amide local anesthetic with a fast metabolism due to an ester group in its structure. Articaine was widely used in dental practice, but now has an effective form for surgical and anesthetic use. Articaine is effective with local infiltration or peripheral nerve block in dentistry, when administered as a spinal, epidural, ocular, or regional nerve block, or when intravenously injected for regional anesthesia. Comparative trials have not revealed a generally significant difference in its clinical effects from those of other short-acting local anesthetics, such as lidocaine, prilocaine, and chloroprocaine, and no conclusive evidence has demonstrated above-average neurotoxicity. Thus, this review discusses the pharmacokinetics and pharmacodynamics, clinical efficacy, and possible side effects of articaine.

 

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About the authors

Aynagul Zh. Bayalieva

Kazan State Medical University

Author for correspondence.
Email: bayalieva1@yandex.ru
ORCID iD: 0000-0001-7577-3284
SPIN-code: 3098-0228

MD, Dr. Sci. (Med.), professor

Russian Federation, Kazan

Yulia N. Yankovich

Kazan State Medical University

Email: st.ketamine@yandex.ru
ORCID iD: 0000-0002-1399-9672
Russian Federation, Kazan

Munir Mohsin

Kazan State Medical University

Email: dr_mohsin2807@yahoo.com
ORCID iD: 0000-0001-7759-7528
Russian Federation, Kazan

Veronika R. Davydova

Kazan State Medical University

Email: vevojuyar@gmail.com
ORCID iD: 0000-0003-4718-5076
SPIN-code: 3881-2341
Scopus Author ID: 954645
Russian Federation, Kazan

References

  1. McLure HA, Rubin AP. Review of local anaesthetic agents. Minerva Anestesiol. 2005;71(3):59–74.
  2. Ferger P, Marxkors K. Ein neues Anästhetikum in der Zahnärztlichen Prosthetik. Dtsch Zahnarztl Z. 1973;(28):87–89.
  3. Hendolin H, Mattila M. Hoe-40045, ein neues Lokalanësthetikum verglichen mit Lidocain bei Epiduralanästhesie. Prakt Anaesth. 1974;(9):178–182.
  4. Brinklov MM. Clinical effects of carticaine, a new local anesthetic. A survey and a double-blind investigation comparing carticaine with lidocaine in epidural analgesia. Acta Anaesthesiol Scand. 1977;21(1):5–16. doi: 10.1111/j.1399-6576.1977.tb01186.x
  5. Wang GK, Calderon J, Jaw SJ, Wang SY. State-dependent block of Na+ channels by articaine via the local anesthetic receptor. J Membr Biol. 2009;229(1):1–9. doi: 10.1007/s00232-009-9170-8
  6. Sack U, Kleemann PP. Intraoral conduction anesthesia with epinephrine-containing local anesthetics and arterial epinephrine plasma concentration. Anesth Pain Control Dent. 1992;1(2):77–80.
  7. Mather LE, Tucker GT. Properties, absorption, and disposition of local anesthetic agents. In: Cousins MJ, Carr DB, Horlocker TT, Bridenbaugh PO, editors. Neural Blockade in Clinical Anesthesia and Pain Medicine, 4th ed. Philadelphia: Wolters Kluwer/Lippincott Williams and Wilkins; 2009. P:48–95.
  8. Vree TB, Gielen MJ. Clinical pharmacology and the use of articaine for local and regional anaesthesia. Best Pract Res Clin Anaesthesiol. 2005;19:293–308.
  9. Vree TB, Simon MA, Gielen MJ, Booij LH. Regional metabolism of articaine in 10 patients undergoing intravenous regional anaesthesia during day case surgery. Br J Clin Pharmacol. 1997;44(1):29–34. doi: 10.1046/j.1365-2125.1997.00621.x
  10. Grossmann M, Sattler G, Pistner H, et al. Pharmacokinetics of articaine hydrochloride in tumescent local anesthesia for liposuction. J Clin Pharmacol. 2004;44(11):1282–1289. doi: 10.1177/0091270004269014
  11. Malamed SF. Handbook of local anesthesia. 7th edition. St. Louis, MO: Elsevier Inc; 2020.
  12. Snoeck M. Articaine: a review of its use for local and regional anesthesia. Local Reg Anesth. 2012;5:23–33. doi: 10.2147/LRA.S16682
  13. Godzieba A, Smektała T, Jędrzejewski M, Sporniak-Tutak K. Clinical assessment of the safe use local anaesthesia with vasoconstrictor agents in cardiovascular compromised patients: a systematic review. Medical Science Monitor Journal. 2014;20:393–398.
  14. Bina B, Hersh EV, Hilario M, et al. True Allergy to Amide Local Anesthetics: A Review and Case Presentation. Anesth Prog. 2018;65(2):119–123. doi: 10.2344/anpr-65-03-06
  15. Yurtlu DA, Kaya K. Ropivacaine, articaine or combination of ropivacaine and articaine for epidural anesthesia in cesarean section: a randomized, prospective, double-blinded study. Braz J Anesthesiol. 2013;63(1):85–91. doi: 10.1016/j.bjane.2012.03.005
  16. Hagai A, Diav-Citrin O, Shechtman S, Ornoy A. Pregnancy outcome after in utero exposure to local anesthetics as part of dental treatment: A prospective comparative cohort study. J Am Dent Assoc. 2015;146(8):572–580. doi: 10.1016/j.adaj.2015.04.002
  17. Ouanounou A, Haas DA. Drug therapy during pregnancy: implications for dental practice. Br Dent J. 2016;220(8):413–417. doi: 10.1038/sj.bdj.2016.299
  18. Semenikhin AA, Kim En D. Prolonged epidural analgesia with ultracaine for labor pain relief. Anesteziol Reanimatol. 2001(2):28–30. (In Russ).
  19. Abenhaim HA, Fraser WD. Impact of pain level on second-stage delivery outcomes among women with epidural analgesia: results from the PEOPLE study. Am J Obstet Gynecol. 2008;199(5):500.e1–6. doi: 10.1016/j.ajog.2008.04.052
  20. Hamar O, Csomor S, Jr., Toth P, Marko J. [Comparative evaluation of carticaine and bupivacaine in epidural anesthesia in cesarean section]. Zentralbl Gynakol. 1986;108(12):739–743.
  21. Kaukinen L, Kaukinen S, Karkkainen S. [Epidural anesthesia with carticaine in cesarean section. A comparison with bupivacaine]. Reg Anaesth. 1986;9(3):79–83.
  22. Strasser K, Huch A, Huch R, Uihein M. Placental transfer of carticaine (ultracain) a new local anaesthetic agent. Z Geburtshilfe Perinatol. 1977;181:118–120.
  23. Zsigmond EK, Downs JR. Plasma cholinesterase activity in newborns and infants. Can Anaesth Soc J. 1971;18(3):278–285. doi: 10.1007/BF03025463
  24. Hoffman RS, Henry GC, Howland MA, et al. Association between life-threatening cocaine toxicity and plasma cholinesterase activity. Ann Emerg Med. 1992;21:247–253.
  25. Duysen EG, Lockridge O. Prolonged toxic effects after cocaine challenge in butyrylcholinesterase/plasma carboxylesterase double knockout mice: a model for butyrylcholinesterase-deficient humans. Drug Metab Dispos. 2011;39(8):1321–1323. doi: 10.1124/dmd.111.039917
  26. Ochoa J, Mair WG. The normal sural nerve in man. II. Changes in the axons and Schwann cells due to ageing. Acta Neuropathol. 1969;13(3):217-239. doi: 10.1007/BF00690643
  27. Dorfman LJ, Bosley TM. Age-related changes in peripheral and central nerve conduction in man. Neurology. 1979;29(1):38–44. doi: 10.1212/wnl.29.1.38
  28. Hanks RK, Pietrobon R, Nielsen KC, et al. The effect of age on sciatic nerve block duration. Anesth Analg. 2006;102(2):588–592. doi: 10.1213/01.ane.0000189552.85175.db
  29. Verdu E, Ceballos D, Vilches JJ, Navarro X. Influence of aging on peripheral nerve function and regeneration. J Peripher Nerv Syst. 2000;5(4):191–208. doi: 10.1046/j.1529-8027.2000.00026.x
  30. Werdehausen R, Fazeli S, Braun S, et al. Apoptosis induction by different local anaesthetics in a neuroblastoma cell line. Br J Anaesth. 2009;103(5):711–718. doi: 10.1093/bja/aep236
  31. Tsui BC, Wagner A, Finucane B. Regional anaesthesia in the elderly: a clinical guide. Drugs Aging. 2004;21(14):895–910. doi: 10.2165/00002512-200421140-00001
  32. Oertel R, Ebert U, Rahn R, Kirch W. The effect of age on pharmacokinetics of the local anesthetic drug articaine. Reg Anesth Pain Med. 1999;24(6):524–528. doi: 10.1016/s1098-7339(99)90043-3
  33. Calvo R, Carlos R, Erill S. Effects of disease and acetazolamide on procaine hydrolysis by red blood cell enzymes. Clin Pharmacol Ther. 1980;27(2):179–183. doi: 10.1038/clpt.1980.27
  34. De Martin S, Orlando R, Bertoli M, et al. Differential effect of chronic renal failure on the pharmacokinetics of lidocaine in patients receiving and not receiving hemodialysis. Clin Pharmacol Ther. 2006;80(6):597–606. doi: 10.1016/j.clpt.2006.08.020
  35. Simon MA, Gielen MJ, Alberink N, et al. Intravenous regional anesthesia (IVRA) with 0.5% articaine, 0.5% lidocaine, or 0.5% prilocaine. A double-blind randomized clinical study. Reg Anesth. 1997;22:29–34.
  36. Pitkanen MT, Xu M, Haasio J, Rosenberg PH. Comparison of 0.5% articaine and 0.5% prilocaine in intravenous regional anesthesia of the arm: a cross-over study in volunteers. Reg Anesth Pain Med. 1999;24(2):131–135.
  37. Kallio H, Snall EV, Luode T, Rosenberg PH. Hyperbaric articaine for day-case spinal anaesthesia. Br J Anaesth. 2006;97(5):704–709. doi: 10.1093/bja/ael222
  38. Ostgaard G, Hallaraker O, Ulveseth OK, Flaatten H. A randomised study of lidocaine and prilocaine for spinal anaesthesia. Acta Anaesthesiol Scand. 2000;44(4):436–440. doi: 10.1034/j.1399-6576.2000.440413.x
  39. Casati A, Danelli G, Berti M, et al. Intrathecal 2-chloroprocaine for lower limb outpatient surgery: a prospective, randomized, double-blind, clinical evaluation. Anesth Analg. 2006;103(1):234–238, table of contents. doi: 10.1213/01.ane.0000221441.44387.82
  40. Kaukinen S, Eerola R, Eerola M, Kaukinen L. A comparison of carticaine and lidocaine in spinal anaesthesia. Ann Clin Res. 1978;10(4):191–194.
  41. Timmerman L, van Dongen EP, Tromp E, et al. Articaine and lidocaine for spinal anaesthesia in day case surgery. Reg Anesth Pain Med. 2007;32 Suppl 1:9.
  42. Hendriks MP, de Weert CJ, Snoeck MM, et al. Plain articaine or prilocaine for spinal anaesthesia in day-case knee arthroscopy: a double-blind randomized trial. Br J Anaesth. 2009;102(2):259–263. doi: 10.1093/bja/aen357
  43. Förster JG, Kallio H, Rosenberg PH, et al. Chloroprocaine vs articaine as spinal anaesthetics for day-case knee arthroscopy. Acta Anaesthesiol Scand. 2011;55:273–281.
  44. Kozlov SP, Svetlov VA, Luk’ianov MV. Pharmacology of local anesthetics and clinical aspects of segmental blocking. II. Spinal anesthesia. Anesteziol Reanimatol. 1998(5):37–42. (In Russ).
  45. Dijkstra T, Reesink JA, Verdouw BC, et al. Spinal anaesthesia with articaine 5% vs bupivacaine 0.5% for day-case lower limb surgery: a double-blind randomized clinical trial. Br J Anaesth. 2008;100(1):104–108. doi: 10.1093/bja/aem332
  46. Bachmann M, Pere P, Kairaluoma P, et al. Randomized comparison of hyperbaric articaine and hyperbaric low-dose bupivacaine along with fentanyl in spinal anaesthesia for day-case inguinal herniorrhaphy. Eur J Anaesthesiol. 2012;29:22–27.
  47. de Weert K, Traksel M, Gielen M, et al. The incidence of transient neurological symptoms after spinal anaesthesia with lidocaine compared to prilocaine. Anaesthesia. 2000;55(10):1020–1024. doi: 10.1046/j.1365-2044.2000.01618-4.x
  48. van Oss GE, Vree TB, Baars AM, et al. Pharmacokinetics, metabolism, and renal excretion of articaine and its metabolite articainic acid in patients after epidural administration. Eur J Anaesthesiol. 1989;6(1):49–56.
  49. Vree TB, Van Oss GE, Gielen MJ, Booij LH. Epidural metabolism of articaine to its metabolite articainic acid in five patients after epidural administration of 600 mg articaine. J Pharm Pharmacol. 1997;49(2):158–163. doi: 10.1111/j.2042-7158.1997.tb06772.x
  50. Noyan A, Cepel S, Ural S, Ozel A. Continuous cervical epidural anesthesia in hand surgery. J Reconstr Microsurg. 2001;17(7):481–482; discussion 483–485. doi: 10.1055/s-2001-17750
  51. Veering BT, Cousins MJ. Epidural neural blockade. In: Cousins MJ, Carr DB, Horlocker TT, Bridenbaugh PO, editors. Neural Blockade in Clinical Anesthesia and Pain Medicine, 4th ed. Philadelphia: Wolters Kluwer/Lippincott Williams and Wilkins; 2009;241–295.
  52. Gerner P, Strichartz GR. Sensory and motor complications of local anesthetics. Muscle Nerve. 2008;37:421–425.
  53. Ovechkin AM. Intravenous lidocaine infusion: should we stop or continue? Regional Anesthesia and Acute Pain Management. 2021;15(1):5–8. (In Russ). doi: 10.17816/1993-6508-2021-15-1-5-8
  54. Zaric D, Christiansen C, Pace NL, Punjasawadwong Y. Transient neurologic symptoms (TNS) following spinal anaesthesia with lidocaine versus other local anaesthetics. Cochrane Database Syst Rev. 2005(4):CD003006. doi: 10.1002/14651858.CD003006.pub2
  55. Pogrel MA. Permanent nerve damage from inferior alveolar nerve blocks--an update to include articaine. J Calif Dent Assoc. 2007;35(4):271–273.
  56. Denson DD, Bridenbaugh PO, Turner PA, Phero JC. Comparison of neural blockade and pharmacokinetics after subarachnoid lidocaine in the rhesus monkey. II: Effects of volume, osmolality, and baricity. Anesth Analg. 1983;62(11):995–1001.
  57. Lakhin RE, Gemua IA, Averyanov DA. Double-blind randomized study of lidocaine, bupivacaine, levobupivacaine, and ropivacaine myotoxicity in rats. Regional Anesthesia and Acute Pain Management. 2020;14(2):93–108. (In Russ). doi: 10.17816/1993-6508-2020-14-2-93-108
  58. Nakamura T, Popitz-Bergez F, Birknes J, Strichartz GR. The critical role of concentration for lidocaine block of peripheral nerve in vivo: studies of function and drug uptake in the rat. Anesthesiology. 2003;99(5):1189–1197. doi: 10.1097/00000542-200311000-00028
  59. Mather LE, Copeland SE, Ladd LA. Acute toxicity of local anesthetics: underlying pharmacokinetic and pharmacodynamic concepts. Reg Anesth Pain Med. 2005;30(6):553–566. doi: 10.1016/j.rapm.2005.07.186
  60. Lachin RE, Bayalieva AZh, Ezhevsky AA, et al. Methodical recommendations of the ministry of health of the russian federation on systemic toxicity of local anesthetic. Regional Anesthesia and Acute Pain Management. 2019;13(1–4):31–41. (In Russ). doi: 10.17816/1993-6508-2019-13-1-4-31-41
  61. Rosenberg PH, Veering BT, Urmey WF. Maximum recommended doses of local anesthetics: a multifactorial concept. Reg Anesth Pain Med. 2004;29(6):564–575; discussion 524. doi: 10.1016/j.rapm.2004.08.003
  62. Wolfe JW, Butterworth JF. Local anesthetic systemic toxicity: update on mechanisms and treatment. Curr Opin Anaesthesiol. 2011;24(5):561–566. doi: 10.1097/ACO.0b013e32834a9394
  63. Drasner K. Local anesthetic toxicity: optimal management to avoid neurotoxic injury and treat cardiac arrest. ASA Refresher Courses in Anesthesiology. 2011;39:33–40.
  64. Szabo A, Szentandrassy N, Birinyi P, et al. Effects of articaine on action potential characteristics and the underlying ion currents in canine ventricular myocytes. Br J Anaesth. 2007;99(5):726–733. doi: 10.1093/bja/aem263
  65. Szentandrassy N., Szabo A., Almassy J., et al. Effects of articaine and ropivacaine on calcium handling and contractility in canine ventricular myocardium // Eur J Anaesthesiol. 2010;27(2):153-161. doi: 10.1097/EJA.0b013e328331a37b

Supplementary files

Supplementary Files
Action
1. JATS XML
2. Fig. The structure of the formula of three topical anesthetic drugs, lidocaine, articaine, and procaine.

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