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J Venom Anim Toxins Incl Trop Dis. 2018 Feb 28;24:7. doi: 10.1186/s40409-018-0144-0. eCollection 2018.

Antivenom therapy: efficacy of premedication for the prevention of adverse reactions.

The journal of venomous animals and toxins including tropical diseases

Victor Morais

Affiliations

  1. Department of Biotechnology, Institute of Hygiene, Faculty of Medicine, University of the Republic, Uruguay, Av. Alfredo Navarro, 3051 Montevideo, Uruguay.

PMID: 29507580 PMCID: PMC5831611 DOI: 10.1186/s40409-018-0144-0

Abstract

Antivenoms or antitoxins have been effectively used for more than a century. During this time, these products have always proven to be highly effective in the treatment of infections and envenomations. However, antivenoms did not exhibit good safety results in their initial applications. After many improvements, antivenoms have substantially better safety profiles but still have some side effects. Due to the occurrence of adverse reactions, the practice of using premedication with the intent to decrease side effects has become accepted or mandatory in many countries. The drugs used for premedication belong to the histamine H1 antagonist, glucocorticoid and catecholamine groups. Currently, this practice is being questioned due to low or controversial efficacies in clinical assays. In this article, we discuss the causes of adverse reactions, the mechanisms of drugs that block the undesired effects and the results obtained in clinical trials. Although these three families of drugs could have positive effects on reducing adverse reactions, only adrenaline has demonstrated positive results in clinical assays.

Keywords: Adrenaline; Adverse reactions; Antihistaminic; Hydrocortisone; Premedication; Snakebite accident

Conflict of interest statement

Not applicable.Not applicable.The author declares that he has no competing interests.Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliatio

References

  1. Am J Trop Med Hyg. 1998 Feb;58(2):183-9 - PubMed
  2. Toxicon. 2009 Nov;54(6):779-83 - PubMed
  3. PLoS One. 2012;7(6):e38739 - PubMed
  4. Cochrane Database Syst Rev. 2000;(2):CD002153 - PubMed
  5. PLoS Med. 2011 May;8(5):e1000435 - PubMed
  6. Front Public Health. 2016 Aug 26;4:178 - PubMed
  7. BMJ. 1999 Apr 17;318(7190):1041-3 - PubMed
  8. PLoS Negl Trop Dis. 2017 Mar 17;11(3):e0005458 - PubMed
  9. Microbes Infect. 2002 Jul;4(8):837-51 - PubMed
  10. Nat Immunol. 2000 Dec;1(6):453-5 - PubMed
  11. Rev Inst Med Trop Sao Paulo. 1994 Sep-Oct;36(5):451-7 - PubMed
  12. Med J Aust. 2008 Apr 21;188(8):473-6 - PubMed
  13. Toxicon. 1998 Jun;36(6):823-46 - PubMed
  14. J Venom Anim Toxins Incl Trop Dis. 2015 Jun 17;21:21 - PubMed
  15. Toxicon. 2007 May;49(6):780-92 - PubMed
  16. Trans R Soc Trop Med Hyg. 2006 Dec;100(12 ):1173-82 - PubMed
  17. J Venom Anim Toxins Incl Trop Dis. 2016 Mar 16;22:11 - PubMed
  18. Br J Clin Pharmacol. 2016 Mar;81(3):446-52 - PubMed
  19. Toxicon. 2003 Apr;41(5):541-57 - PubMed
  20. Clin Sci (Lond). 1998 Jun;94(6):557-72 - PubMed
  21. J Venom Anim Toxins Incl Trop Dis. 2017 Mar 16;23 :14 - PubMed
  22. Br Med J (Clin Res Ed). 1986 Jan 4;292(6512):17-20 - PubMed
  23. Am J Trop Med Hyg. 2014 Mar;90(3):574-84 - PubMed
  24. Drug Saf. 2011 Oct 1;34(10):869-80 - PubMed
  25. Toxicon. 2012 Feb;59(2):315-9 - PubMed
  26. Med J Aust. 2004 Jan 5;180(1):20-3 - PubMed
  27. PLoS Negl Trop Dis. 2013 Jul 25;7(7):e2326 - PubMed
  28. Toxicon. 2010 Jun 15;55(7):1195-212 - PubMed
  29. J Venom Anim Toxins Incl Trop Dis. 2016 Jun 08;22:20 - PubMed
  30. Toxicon. 2013 Dec 15;76:63-76 - PubMed
  31. Toxins (Basel). 2017 May 13;9(5):null - PubMed
  32. Toxicon. 2016 Sep 15;120:159-65 - PubMed
  33. BMJ. 1999 May 29;318(7196):1451-2 - PubMed

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