Evidence map›Paper›PMID 40551190›Full record

ArticleEuropean journal of medical research2025

Early acetaminophen use is associated with the reduced mortality risk in patients with sepsis-associated encephalopathy: a retrospective study.

Fengzhen Huang, Jiping Yi, Tieqiao Zhou, Xiaoxiang Gong

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Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Fengzhen HuangDepartment of Neurology, The First People's Hospital of Chenzhou affiliated to the University of South China, Chenzhou, 423000, Hunan, China.
Jiping YiDepartment of Neurology, The First People's Hospital of Chenzhou affiliated to the University of South China, Chenzhou, 423000, Hunan, China.
Tieqiao ZhouDepartment of Laboratory Medicine, The First People's Hospital of Chenzhou affiliated to the University of South China, Chenzhou, 423000, Hunan, China.
Xiaoxiang GongDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China. gongxiaoxiang@csu.edu.cn.

Funding

Department of Science and Technology of Hunan Province in China 2023SK4018Natural Science Foundation of Hunan Province 2022JJ40684Natural Science Foundation of Hunan Province 2023JJ50382Natural Science Foundation of Hunan Province 2025JJ70556Scientific research project of Hunan Provincial Health Commission D202303077714Scientific research project of Xiangnan University 2020XJ88
6 · The paper itself

Abstract

backgroundSepsis-associated encephalopathy (SAE), a severe neurological complication of systemic infection, carries substantial morbidity and mortality risks. This study aims to examine the relationship between early acetaminophen use and survival rates in critically ill SAE patients.

methodsUsing data from the MIMIC-IV database, we conducted a retrospective cohort study on patients with SAE, stratified by acetaminophen exposure within 48 h of ICU admission. Among the 4111 eligible patients (1689 acetaminophen recipients versus 2422 non-recipients), propensity score matching resulted in 3124 matched subjects (1562 per cohort). The primary outcome was 90-day mortality, while secondary outcomes included mortality rates at 30, 60, 180, and 365 days. Survival analyses utilized Cox proportional hazards regression and Kaplan-Meier curves, supplemented by subgroup analyses for 90-day mortality.

resultsAcetaminophen exposure was correlated with reduced 30-day mortality rate (HR = 0.78, 95%CI [0.65-0.94], p < 0.05), as well as decreased 60-day (HR = 0.71, 95%CI [0.60-0.83], p < 0.001), 90-day (HR = 0.70, 95%CI [0.60-0.81], p < 0.001), 180-day (HR = 0.70, 95%CI [0.60-0.80], p < 0.001) and 365-day (HR = 0.69, 95%CI [0.61-0.79], p < 0.001) mortality rate after PSM. The Kaplan-Meier analysis demonstrated significantly higher survival rates in the acetaminophen group compared to the non-acetaminophen group, with a persistent trend at 30, 90, 180, and 365 days (log-rank p < 0.05). The protective effect was consistent across subgroups except acetaminophen dosage ≥ 650 mg.

conclusionEarly administration of acetaminophen is associated with reduced short- and long-term mortality in SAE patients. These findings support a potential therapeutic role for acetaminophen in SAE and warrant further mechanistic and prospective validation.

Indexed as

AcetaminophenAnalgesics, Non-NarcoticSepsis-Associated EncephalopathyAgedFemaleHumansKaplan-Meier EstimateMaleMiddle AgedRetrospective StudiesRisk FactorsAcetaminophenAnalgesics, Non-NarcoticAcetaminophenMIMIC IV databaseMortalitySepsisSepsis-associated encephalopathy

Identifiers

PMID40551190
PMCPMC12183892

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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 Socratic graph.