Evidence map›Paper›PMID 41857443›Full record

Observational studyJournal of medical toxicology : official journal of the American College of Medical Toxicology2026

N-Acetylcysteine Dose and Treatment Duration in High-Risk Acetaminophen Ingestions Treated Within Eight Hours: A Retrospective Cohort Study.

C James Watson, Michael D Simpson, Nishita Saraiya, Christopher A Wilkosz, Michael B Yu, Michele M Burns, Mark J Neavyn, Karen E Simone, Tania D Strout

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

C James WatsonDepartment of Emergency Medicine, Maine Medical Center Portland, 22 Bramhall Street, Portland, ME, 04102, USA. james.watson@mainehealth.org.
Michael D SimpsonDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Nishita SaraiyaAlleghany General Hospital, Pittsburgh, PA, USA.
Christopher A WilkoszNorthern New England Poison Center, Portland, ME, USA.
Michael B YuNorthern New England Poison Center, Portland, ME, USA.
Michele M BurnsMassachusetts and Rhode Island Poison Center, Boston, MA, USA.
Mark J NeavynDepartment of Emergency Medicine, Maine Medical Center Portland, 22 Bramhall Street, Portland, ME, 04102, USA.
Karen E SimoneNorthern New England Poison Center, Portland, ME, USA.
Tania D StroutDepartment of Emergency Medicine, Maine Medical Center Portland, 22 Bramhall Street, Portland, ME, 04102, USA.

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Susan L SANTANGELO · 2017 to 2026
$51.6M
CTSA K12 Program at Tufts UniversityK12TR004384 · NCATS · TUFTS UNIVERSITY BOSTON · PI Karen Freund, Lesley Ann Inker · 2023 to 2026
$6.1M
Training Program in Resuscitation ScienceT32HL155020 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Michael William Donnino, Robert Yeh · 2021 to 2026
$2.6M
NCATS NIH HHS K12 TR004384NHLBI NIH HHS T32 HL155020NIGMS NIH HHS U54 GM115516NIH HHS K12TR004384NIH HHS T32HL155020NIH HHS U54GM115516
6 · The paper itself

Abstract

introductionToxicologists may use high dose n-acetylcysteine (HD-NAC) for early-treated high-risk acetaminophen ingestions (EHRAI) given concerns over standard NAC (S-NAC) dosing’s efficacy. We utilize the novel, clinically relevant outcome of mean additional 16-hour NAC maintenance infusions (NMI) to evaluate differences in treatment duration for EHRAI patients treated with S-NAC versus HD-NAC.

methodsRetrospective multistate poison center study from 1/1/2019-7/4/2024 of patients ≥ 13-years-old who were treated with S-NAC or HD-NAC within eight hours of a high-risk acetaminophen ingestion. The primary outcome was mean additional NMI. Secondary outcomes were NAC infusion duration, hepatotoxicity, coagulopathy, transplant, and death. Sensitivity analyses evaluated for robustness of findings.

resultsOf 127 included cases, 52.0% (66/127) received HD-NAC. 7.1% (9/127) had anti-peristaltic co-ingestions. HD-NAC cases received more fomepizole (23.1% versus 1.6%; difference 21.1%). Acetaminophen concentrations controlled for time since ingestion were similar (mean acetaminophen ratio for HD-NAC: 2.7, IQR: 2.3, 3.3 versus S-NAC: 2.4, IQR: 2.2, 2.7; difference − 0.3). 26.0% (33/127) received NMI solely for residual detectable serum acetaminophen. There was no difference in mean additional NMI (HD-NAC: 0.53 versus S-NAC: 0.38; p = 0.240). Median NAC infusion durations were equal across groups (21.0; IQR: 21.0, 37.0; difference 0.0) (p = 0.137). One patient per group developed hepatotoxicity; there were no transplants or deaths. Sensitivity analyses yielded similar results.

conclusionsWe found no difference in mean NMI for EHRAI based on NAC dose. These findings support additional NMI as an objective, common, clinically relevant outcome for acetaminophen toxicity research.

Indexed as

AcetaminophenAcetylcysteineAnalgesics, Non-NarcoticAntidotesDrug OverdoseAdolescentAdultChemical and Drug Induced Liver InjuryDrug Administration ScheduleFemaleHumansMaleMiddle AgedPoison Control CentersRetrospective StudiesTime FactorsAcetaminophenAcetylcysteineAnalgesics, Non-NarcoticAntidotesAcetaminophenAcetylcysteineDuration of therapyPoisoning

Identifiers

PMID41857443
PMCPMC13076740

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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.