Amiodarone hepatotoxicity
- PMID: 18673162
- DOI: 10.2174/157016108784912019
Amiodarone hepatotoxicity
Abstract
Potential hepatotoxicity related to amiodarone therapy is often a concern when deciding whether to initiate or continue treatment with this medication. While mostly associated with long-term oral administration of the drug, toxicity has also been reported early during intravenous administration and months after discontinuation of therapy. In the majority of patients, it is discovered incidentally during routine testing of liver biochemistry and rarely do the hepatic effects develop into symptomatic liver injury or failure. Despite the widespread use of amiodarone, prospective clinical studies have been sparse and there has been little consensus among experts in the field regarding optimum monitoring for adverse effects in patients receiving this drug. In order to examine the current state of knowledge surrounding the incidence, pathogenesis and mechanism of liver effects associated with amiodarone, the existing literature was reviewed, with particular emphasis on clinical recommendations for monitoring.
Similar articles
-
[Amiodarone liver toxicity about two cases and review of literature].Rev Med Interne. 2004 May;25(5):386-9. doi: 10.1016/j.revmed.2004.02.005. Rev Med Interne. 2004. PMID: 15110957 Review. French.
-
Use of population modeling to define rational monitoring of amiodarone hepatic effects.Clin Pharmacol Ther. 2004 Apr;75(4):342-51. doi: 10.1016/j.clpt.2003.12.008. Clin Pharmacol Ther. 2004. PMID: 15060512
-
Clinical applications and acute hepatotoxicity of intravenous amiodarone.J Int Med Res. 2009 Nov-Dec;37(6):1928-36. doi: 10.1177/147323000903700631. J Int Med Res. 2009. PMID: 20146893
-
Three cases of severe acute hepatitis after parenteral administration of amiodarone: the active ingredient is not the only agent responsible for hepatotoxicity.Ann Ital Med Int. 2002 Jul-Sep;17(3):180-4. Ann Ital Med Int. 2002. PMID: 12402666
-
Acute Hepatotoxicity of Intravenous Amiodarone: Case Report and Review of the Literature.Am J Ther. 2016 Jan-Feb;23(1):e260-3. doi: 10.1097/MJT.0000000000000149. Am J Ther. 2016. PMID: 25259952 Review.
Cited by
-
Metformin as a protective agent against natural or chemical toxicities: a comprehensive review on drug repositioning.J Endocrinol Invest. 2020 Jan;43(1):1-19. doi: 10.1007/s40618-019-01060-3. Epub 2019 May 16. J Endocrinol Invest. 2020. PMID: 31098946 Review.
-
Falling between the cracks: a case of amiodarone toxicity.CMAJ. 2011 Sep 6;183(12):1393-7. doi: 10.1503/cmaj.100351. Epub 2011 Jul 11. CMAJ. 2011. PMID: 21746823 Free PMC article. No abstract available.
-
Mitochondria as the Target of Hepatotoxicity and Drug-Induced Liver Injury: Molecular Mechanisms and Detection Methods.Int J Mol Sci. 2022 Mar 18;23(6):3315. doi: 10.3390/ijms23063315. Int J Mol Sci. 2022. PMID: 35328737 Free PMC article. Review.
-
Development of HepG2-derived cells expressing cytochrome P450s for assessing metabolism-associated drug-induced liver toxicity.Chem Biol Interact. 2016 Aug 5;255:63-73. doi: 10.1016/j.cbi.2015.10.009. Epub 2015 Oct 22. Chem Biol Interact. 2016. PMID: 26477383 Free PMC article.
-
New Avenues for Treatment and Prevention of Drug-Induced Steatosis and Steatohepatitis: Much More Than Antioxidants.Adv Ther. 2021 May;38(5):2094-2113. doi: 10.1007/s12325-021-01669-y. Epub 2021 Mar 24. Adv Ther. 2021. PMID: 33761100 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical