Evidence map›Paper›PMID 39068527›Full record

ArticleThe Journal of international medical research2024

Patterns of acetaminophen toxicity among patients with low-risk serum concentrations.

Abdullah M Alhammad, Ghada Alajmi, Aljawharah Alkhodair, Wael H Mansy, Mohammad H Aljawadi, Rania Aljadeed, Reem Alshammari, Raghad Alshehri, Mohammed N Alarifi, Badr Alyahya

Abstract read
In one paragraph

Article in The Journal of international medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Observational
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Abdullah M AlhammadDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-9806-2503
Ghada AlajmiCorporate Department of Pharmacy Services, King Saud University Medical City, Riyadh, Saudi Arabia.
Aljawharah AlkhodairCorporate Department of Pharmacy Services, King Saud University Medical City, Riyadh, Saudi Arabia.
Wael H MansyDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-7988-2717
Mohammad H AljawadiDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Rania AljadeedDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Reem AlshammariCollege of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Raghad AlshehriCollege of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Mohammed N AlarifiDepartment of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Badr AlyahyaDepartment of Emergency Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn 2012, the Commission on Human Medicines mandated lowering the acetaminophen toxicity nomogram treatment threshold in the UK to 100 µg/ml at 4 h post-ingestion. The present study aim was to evaluate biochemical and liver toxicity patterns in patients who presented with acetaminophen overdose and had low serum acetaminophen concentrations (<150 µg/ml).

methodsPatients admitted to the emergency department with a clear history of acute acetaminophen overdose with or without other medication or ethanol were consecutively enrolled into this retrospective cohort study. Patients with serum acetaminophen concentration >150 µg/ml or an unknown ingestion time were excluded. Data were extracted from electronic medical records and are presented as mean ± SD or median (interquartile range).

resultsA total of 103 patients were included (median age, 17 [4-21] years) and 80 (78%) were female. The median ingested acetaminophen dose was 5000 (2850-7650) mg. At baseline, the median serum acetaminophen concentration was 42 (4.5-64.8) µg/ml, and median alanine aminotransferase and aspartate aminotransferase levels were 22 (17-28) and 27 (16-45) IU/L, respectively. Twenty patients were treated with acetylcysteine, with none developing adverse reactions. No patient developed hepatotoxicity, including patients with initial multiple product ingestion or other risk factors.

conclusionsPatients presenting with an acute acetaminophen overdose with acetaminophen level <150 µg/ml, including patients with other risk factors, are at low risk of hepatotoxicity.

Indexed as

AcetaminophenChemical and Drug Induced Liver InjuryDrug OverdoseAcetylcysteineAdolescentAdultAlanine TransaminaseAnalgesics, Non-NarcoticAspartate AminotransferasesChildChild, PreschoolFemaleHumansMaleRetrospective StudiesRisk FactorsAcetaminophenAcetylcysteineAlanine TransaminaseAnalgesics, Non-NarcoticAspartate AminotransferasesAcetylcysteineantidotehepatotoxicitynomogramparacetamolpoisoning

Identifiers

PMID39068527
PMCPMC11287716

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.