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Paracetamol toxicity in mild overdose in combination with opioids: A retrospective observational study.
Amer, Halima; Archer, John R H; Layne, Kerry; Dines, Alison M; Wood, David M; Greene, Shaun L; Dargan, Paul I.
Afiliação
  • Amer H; Department of Clinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
  • Archer JRH; Department of Clinical Pharmacology, University College London, London, UK.
  • Layne K; Department of Clinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
  • Dines AM; Faculty of Life Sciences and Medicine, King's College London, London, UK.
  • Wood DM; Department of Clinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
  • Greene SL; Department of Clinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
  • Dargan PI; Faculty of Life Sciences and Medicine, King's College London, London, UK.
Br J Clin Pharmacol ; 88(3): 1258-1267, 2022 03.
Article em En | MEDLINE | ID: mdl-34486149
ABSTRACT

AIMS:

Toxicity in paracetamol overdose with opioid co-ingestion is poorly understood. We compared outcomes in both paracetamol-only and paracetamol-opioid overdoses to determine whether toxicity differed significantly between the groups, and to assess the utility of the ratio of measured plasma paracetamol concentration relative to the 4-hour nomogram-adjusted level (APAPpl /APAPt ).

METHODS:

We conducted a retrospective observational study of all patients (n = 1159) presenting to 2 large UK hospitals between 2005 and 2013 with acute single-dose ingestion paracetamol overdose, with (n = 221) or without (n = 938) opioid co-ingestion. Adverse outcomes included biomarkers of hepatotoxicity and the need for extended treatment. Several outcomes were assessed in relation to the APAPpl /APAPt ratio.

RESULTS:

Median ingested dose of paracetamol was low in both groups (10 g). Statistical comparison of the median APAPpl /APAPt ratios showed a significant difference (0.65 vs. 0.56 for the paracetamol-only and paracetamol-opioid groups respectively, P = .0329). Although there was a trend towards a lower risk of predefined toxic outcomes with opioid co-ingestion, statistical analysis did not show a significant difference, with outcomes for the paracetamol-only and paracetamol-opioid groups including the following alanine transaminase >2× upper limit of normal, 7.7 vs. 5.7% (P = .6480); alanine transaminase >1000 IU/L, 2.4 vs. 0% (P = .2145); international normalised ratio > 1.3, 8.6 vs. 4.4% (P = .2774); and transfer to tertiary liver unit, 0.2 vs. 0% (P nonsignificant).

CONCLUSION:

Our study does not support a change in current clinical practise beyond standard testing at 4 hours or longer post ingestion for mixed low dose paracetamol-opioid overdose.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Analgésicos não Narcóticos / Doença Hepática Induzida por Substâncias e Drogas / Overdose de Drogas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Analgésicos não Narcóticos / Doença Hepática Induzida por Substâncias e Drogas / Overdose de Drogas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article