Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27480
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dc.contributor.authorAmer, Halima-
dc.contributor.authorArcher, John R H-
dc.contributor.authorLayne, Kerry-
dc.contributor.authorDines, Alison M-
dc.contributor.authorWood, David M-
dc.contributor.authorGreene, Shaun L-
dc.contributor.authorDargan, Paul I-
dc.date2021-09-05-
dc.date.accessioned2021-09-13T05:58:06Z-
dc.date.available2021-09-13T05:58:06Z-
dc.date.issued2022-
dc.identifier.citationBritish journal of clinical pharmacology 2022; 88(3): 1258-1267en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27480-
dc.description.abstractToxicity 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 4h nomogram-adjusted level (APAPpl /APAPt ). We conducted a retrospective observational study of all patients (N = 1159) presenting to two 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. Median ingested dose of paracetamol was low in both groups (10g). 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 = 0.0329). Although there was a trend towards a lower risk of pre-defined 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: ALT > 2x ULN, 7.7% vs 5.7% (p = 0.6480); ALT > 1000 IU/L, 2.4% vs 0 (p = 0.2145); INR > 1.3, 8.6% vs 4.4% (p = 0.2774); and transfer to tertiary liver unit, 0.2% vs 0 (p NS). Our study does not support a change in current clinical practise beyond standard testing at four hours or longer post ingestion for mixed low dose paracetamol-opioid overdose.en
dc.language.isoeng-
dc.subjectclinical toxicologyen
dc.subjectopioidsen
dc.subjectoverdose and poisoningen
dc.subjecttoxicityen
dc.titleParacetamol toxicity in mild overdose in combination with opioids: a retrospective observational study.en
dc.typeJournal Articleen
dc.identifier.journaltitleBritish Journal of Clinical Pharmacologyen
dc.identifier.affiliationFaculty of Life Sciences and Medicine, King's College London, London, UKen
dc.identifier.affiliationToxicologyen
dc.identifier.affiliationDepartment of Clinical Toxicology, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UKen
dc.identifier.affiliationDepartment of Clinical Pharmacology, University College London, London, UKen
dc.identifier.affiliationVictorian Poisons Information Centreen
dc.identifier.doi10.1111/bcp.15070en
dc.type.contentTexten
dc.identifier.orcid0000-0003-3956-7787en
dc.identifier.orcid0000-0002-2880-9333en
dc.identifier.orcid0000-0002-4740-0664en
dc.identifier.pubmedid34486149-
local.name.researcherGreene, Shaun L
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptEmergency-
crisitem.author.deptToxicology-
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