Evidence map›Paper›PMID 41413861›Full record

ArticleBMC gastroenterology2025

Aspirin reduces short-term mortality risk in critically ill patients with liver cirrhosis: a propensity-score matched retrospective analysis using the MIMIC-IV database.

Yu Yi, Yinghua Chen, Yawen Luo

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Article in BMC gastroenterology, 2025. 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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1 · What the graph read from it

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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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yu Yi *Department of Infectious Diseases, The Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou Province, China.
Yinghua Chen *Department of Infectious Diseases, The Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou Province, China.
Yawen LuoDepartment of Infectious Diseases, The Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou Province, China. 17718064215@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver cirrhosis not only leads to high mortality but also imposes significant economic burdens and health losses. Aspirin is a drug with potential indications for liver disease, but its benefits in cirrhosis have primarily been demonstrated in outpatient settings. This study aimed to determine whether aspirin therapy confers protective effects on the prognosis of critically ill cirrhosis patients.

methodsCirrhosis patients were identified from the Medical Information Mart for Critical Care Medicine IV (MIMIC-IV) database. Propensity score matching (PSM) was used to balance baseline differences. Multivariate Cox regression models assessed the association between aspirin therapy and 30-day and 90-day mortality, while multivariable logistic regression models evaluated its relationship with in-hospital mortality. Due to a lack of relevant data, this study could not assess aspirin-related bleeding events.

resultsThe study included 3,105 patients, of whom 348 received aspirin and 2,757 did not. After propensity score matching, 334 matched pairs were successfully identified. The 30-day mortality rate among aspirin users was 15.27%, and the 90-day mortality rate was 16.77%, both lower than those among non-users. Multivariate Cox regression analysis demonstrated that aspirin use was associated with reduced 30-day mortality (HR 0.69, 95% CI 0.48–0.99) and 90-day mortality (HR 0.65, 95% CI 0.46–0.92). Multivariable logistic regression analysis indicated that aspirin use was associated with reduced in-hospital mortality (OR = 0.66, 95% CI 0.44–0.99). There was no significant difference in intensive care unit length of stay between the two groups. However, due to most participants (81.0%) receiving the 81 mg/d dose, the significant disparity in sample sizes between the high- and low-dose groups and the baseline imbalance precluded reliable dose-response comparisons in this study.

conclusionThis single-Centre retrospective study found that aspirin use was associated with reduced mortality in critically ill patients with liver cirrhosis. However, the overall net therapeutic effect remains to be further validated due to the lack of data on bleeding risk. The relationship between aspirin dosage and specific outcomes requires clarification in future studies with larger sample sizes and more prospective designs.

Indexed as

AspirinCritical IllnessLiver CirrhosisPlatelet Aggregation InhibitorsAgedDatabases, FactualFemaleHospital MortalityHumansLogistic ModelsMaleMiddle AgedPrognosisPropensity ScoreProportional Hazards ModelsRetrospective StudiesAspirinPlatelet Aggregation InhibitorsAspirinIntensive care unitLiver cirrhosisMIMIC-IV databaseMortality

Identifiers

PMID41413861
PMCPMC12784597

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.