Evidence map›Paper›PMID 40745148›Full record

ArticleJournal of medical toxicology : official journal of the American College of Medical Toxicology2025

Trends in Fomepizole Use for Acetaminophen Poisoning in the United States; 2013-2024.

Mitchell D'Aloia, Dale Smith, Randy Boley, Emily Schamber, Dillon Thorpe, Trevonne M Thompson, Neeraj Chhabra

Abstract read
In one paragraph

Article in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Trial
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

7 authors.

Mitchell D'AloiaDivision of Medical Toxicology, Department of Emergency Medicine, University of Illinois Chicago, Chicago, IL, USA.
Dale SmithAI.Health4All Center, College of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Randy BoleyAI.Health4All Center, College of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Emily SchamberAI.Health4All Center, College of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Dillon ThorpeAI.Health4All Center, College of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Trevonne M ThompsonDivision of Medical Toxicology, Department of Emergency Medicine, University of Illinois Chicago, Chicago, IL, USA.
Neeraj ChhabraDivision of Medical Toxicology, Department of Emergency Medicine, University of Illinois Chicago, Chicago, IL, USA. neeraj1@uic.edu.ORCID http://orcid.org/0000-0002-0945-1233

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFomepizole has been suggested as adjunctive therapy for severe acetaminophen poisoning though clinical efficacy is unknown. We sought to determine trends in the use of fomepizole for acetaminophen poisoning.

methodsThis is a cross-sectional analysis of hospitalized patients with acetaminophen poisoning from January 2013 through December 2024, using Epic Cosmos, a research database of 298 million patients nationally. We identified encounters involving acetaminophen poisoning by International Classification of Diseases, version 10 (ICD-10-CM) code. Data extracted included administration of N-acetylcysteine (NAC) and fomepizole, demographic data, and outcomes of death and liver transplantation. Data were analyzed using descriptive statistics to identify trends and multivariable logistic regression to determine associations with death.

resultsThere were 114,111 hospital encounters involving acetaminophen poisoning with 64,957 (56.92%) receiving NAC, and 1,552 (1.36%) receiving fomepizole. In 2013, 0.44% of NAC-treated acetaminophen poisoning cases also received fomepizole. This rose to 6.27% in 2024. From 2013 to 2019, the proportion of NAC-treated acetaminophen cases receiving fomepizole was stable, but from 2019 to 2024, there was a 1029.64% increase in fomepizole use. Regression modeling indicated increased odds for death (OR = 5.88, aOR = 5.32 [95% CI: 4.52, 6.27]) among those who received fomepizole in addition to NAC, indicating increased fomepizole use in patients with severe toxicity.

conclusionFomepizole use in acetaminophen poisoning has risen dramatically since 2019, particularly among patients at highest risk for death and liver transplantation. It is of critical importance to determine the efficacy of fomepizole for acetaminophen poisoning.

Indexed as

AcetaminophenAnalgesics, Non-NarcoticAntidotesFomepizolePractice Patterns, Physicians'AcetylcysteineAdolescentAdultAgedChemical and Drug Induced Liver InjuryCross-Sectional StudiesDatabases, FactualFemaleHumansMaleMiddle AgedAcetaminophenAcetylcysteineAnalgesics, Non-NarcoticAntidotesFomepizoleAcetaminophenAcetaminophen PoisoningAcetaminophen ToxicityFomepizolePoisoning

Identifiers

PMID40745148
PMCPMC12511483

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Registered trials

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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.