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Physiologically based pharmacokinetic modelling of acute digoxin toxicity and the effect of digoxin-specific antibody fragments.

Lucy M BrackenBetty S H ChanNicholas Alan Buckley
Published in: Clinical toxicology (Philadelphia, Pa.) (2018)
Compared to conventional two-compartment modelling, PBPK modelling is superior in generating realistic simulations of acute digoxin toxicity and the response to digoxin-Fab. Simulation capacity provides realistic, continuous data which has the potential to substantiate alternative, less expensive, and safer digoxin-Fab dosing strategies for the treatment of acute digoxin toxicity.
Keyphrases
  • liver failure
  • respiratory failure
  • drug induced
  • oxidative stress
  • aortic dissection
  • risk assessment
  • climate change