Improved outcome of paracetamol-induced fulminant hepatic failure by late administration of acetylcysteine

Lancet. 1990 Jun 30;335(8705):1572-3. doi: 10.1016/0140-6736(90)91388-q.

Abstract

The influence of acetylcysteine, administered at presentation to hospital, on the subsequent clinical course of 100 patients who developed paracetamol-induced fulminant hepatic failure was analysed retrospectively. Mortality was 37% in patients who received acetylcysteine 10-36 h after the overdose, compared with 58% in patients not given the antidote. In patients given acetylcysteine, progression to grade III/IV coma was significantly less common than in those who did not receive the antidote (51% vs 75%), although the median peak prothrombin time was similar for both groups. Whether the beneficial effect is related to replenishment of glutathione stores or a consequence of another hepatic protective mechanism of acetylcysteine requires further study.

Publication types

  • Comparative Study

MeSH terms

  • Acetaminophen / poisoning*
  • Acetylcysteine / administration & dosage
  • Acetylcysteine / therapeutic use*
  • Acute Disease
  • Adult
  • Aspartate Aminotransferases / blood
  • Drug Evaluation
  • Female
  • Hepatic Encephalopathy / blood
  • Hepatic Encephalopathy / chemically induced*
  • Hepatic Encephalopathy / drug therapy
  • Hepatic Encephalopathy / mortality
  • Humans
  • Infusions, Intravenous
  • Liver / pathology
  • Male
  • Necrosis
  • Prognosis
  • Prothrombin Time
  • Retrospective Studies
  • Time Factors

Substances

  • Acetaminophen
  • Aspartate Aminotransferases
  • Acetylcysteine