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Clin Toxicol (Phila) ; 49(7): 643-7, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21854081

ABSTRACT

CONTEXT: Current treatment of paracetamol (acetaminophen) poisoning involves initiating a 3-phase N-acetylcysteine (NAC) infusion after comparing a plasma concentration, taken ≥ 4 h post-overdose, to a nomogram. This may result in dosing errors, a delay in treatment, or possibly more adverse effects - due to the use of a high dose rate for the first infusion when treatment is initiated. OBJECTIVE: Our aim was to investigate a novel dosing regimen for the immediate administration of NAC on admission at a lower infusion rate. METHODS: We used a published population pharmacokinetic model of NAC to simulate a scenario where a patient presents to the hospital 2 h post-overdose. The conventional regimen is commenced 6 h post-overdose when the 4-h plasma paracetamol concentration is available. We investigated an NAC infusion using a lower dosing rate initiated immediately on presentation. We determined a dosing rate that gave an area under the curve (AUC) of the concentration-time curve that was the same or greater than that from the conventional regimen on 90% of occasions. RESULTS: Lower dosing rates of NAC initiated immediately resulted in a similar exposure to NAC. An infusion of 110 mg/kg over the first 5 h (22 mg/kg/h) followed by the last two phases of the conventional regimen, or 200 mg/kg over 9 h (22.6 mg/kg/h) followed by the last phase of the conventional regimen could be used. CONCLUSION: The novel dosing regimen allowed immediate treatment of a patient using a lower dosing rate. This greatly simplifies the current dosing regimen and may reduce NAC adverse effects while ensuring the same amount of NAC is delivered.


Subject(s)
Acetaminophen/poisoning , Acetylcysteine/administration & dosage , Analgesics, Non-Narcotic/poisoning , Antidotes/administration & dosage , Antioxidants/administration & dosage , Acetaminophen/pharmacokinetics , Acetylcysteine/adverse effects , Acetylcysteine/pharmacokinetics , Adult , Analgesics, Non-Narcotic/pharmacokinetics , Antidotes/adverse effects , Antidotes/pharmacokinetics , Antioxidants/adverse effects , Antioxidants/pharmacokinetics , Area Under Curve , Computer Simulation , Drug Administration Schedule , Drug Overdose/drug therapy , Humans , Infusions, Intravenous , Models, Biological
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