Literature DB >> 2785079

Amiodarone hepatotoxicity: prevalence and clinicopathologic correlations among 104 patients.

J H Lewis1, R C Ranard, A Caruso, L K Jackson, F Mullick, K G Ishak, L B Seeff, H J Zimmerman.   

Abstract

The prevalence of apparent amiodarone-related hepatic injury in 104 patients followed prospectively is compared to that reported in the literature. Asymptomatic elevation of serum aminotransferase levels was detected in approximately one-fourth of the patients, a figure similar to the average of reported cases. The frequency of extrahepatic organ toxicity was increased in patients with elevated levels. Symptomatic "hepatitis" developed in 3% of this series and in less than 1% of cases in the literature. Evidence of hepatic phospholipidosis and the development of pseudoalcoholic liver injury is most likely due to the biochemical effects of the drug and to possible metabolic idiosyncrasy, respectively. Serial blood enzyme measurements, as recommended by the manufacturer, may offer some protection against the development of more serious liver injury. However, levels of amiodarone may persist in various tissues for weeks to months following withdrawal, and stopping the drug does not guarantee the prompt reversal of any organ toxicity. Accordingly, the risks posed and benefits offered by amiodarone should be carefully weighed prior to discontinuing the drug, as the risk of sudden cardiac death may outweigh the hazards of ongoing hepatic, pulmonary or other toxicity.

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Year:  1989        PMID: 2785079     DOI: 10.1002/hep.1840090504

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  51 in total

1.  Amiodarone-induced acute hepatotoxicity.

Authors:  Usha Rao; Ajit Agarwal
Journal:  Eur J Clin Pharmacol       Date:  2011-10-12       Impact factor: 2.953

2.  [Anti-arrhythmic drug therapy in impaired liver function].

Authors:  C Perings
Journal:  Internist (Berl)       Date:  2002-08       Impact factor: 0.743

3.  Glucosylceramide and lysophosphatidylcholines as potential blood biomarkers for drug-induced hepatic phospholipidosis.

Authors:  Kosuke Saito; Keiko Maekawa; Masaki Ishikawa; Yuya Senoo; Masayo Urata; Mayumi Murayama; Noriyuki Nakatsu; Hiroshi Yamada; Yoshiro Saito
Journal:  Toxicol Sci       Date:  2014-06-30       Impact factor: 4.849

4.  Acute hepatic failure following intravenous amiodarone.

Authors:  Robert Grecian; Mark Ainslie
Journal:  BMJ Case Rep       Date:  2012-12-18

5.  Development of HepG2-derived cells expressing cytochrome P450s for assessing metabolism-associated drug-induced liver toxicity.

Authors:  Jiekun Xuan; Si Chen; Baitang Ning; William H Tolleson; Lei Guo
Journal:  Chem Biol Interact       Date:  2015-10-22       Impact factor: 5.192

6.  Acute hepatitis after amiodarone infusion.

Authors:  Paulo Fonseca; Adelaide Dias; Helena Gonçalves; Aníbal Albuquerque; Vasco Gama
Journal:  World J Clin Cases       Date:  2015-10-16       Impact factor: 1.337

7.  Ventricular tachycardia in acute fulminant myocarditis: medical management and follow-up.

Authors:  J R Sharma; S Sathanandam; S P Rao; S Acharya; V Flood
Journal:  Pediatr Cardiol       Date:  2008-03       Impact factor: 1.655

Review 8.  Drug-induced steatohepatitis.

Authors:  Vaishali Patel; Arun J Sanyal
Journal:  Clin Liver Dis       Date:  2013-09-04       Impact factor: 6.126

9.  A Physiologically Based Pharmacokinetic Model of Amiodarone and its Metabolite Desethylamiodarone in Rats: Pooled Analysis of Published Data.

Authors:  Jing-Tao Lu; Ying Cai; Feng Chen; Wei-Wei Jia; Zhe-Yi Hu; Yuan-Sheng Zhao
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2016-12       Impact factor: 2.441

10.  Tumor necrosis factor-alpha potentiates the cytotoxicity of amiodarone in Hepa1c1c7 cells: roles of caspase activation and oxidative stress.

Authors:  Jingtao Lu; Kazuhisa Miyakawa; Robert A Roth; Patricia E Ganey
Journal:  Toxicol Sci       Date:  2012-10-05       Impact factor: 4.849

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