Evidence map›Paper›PMID 39919086›Full record

ArticlePloS one2025

Association between red blood cell distribution width-to-albumin ratio at admission and all-cause mortality in patients with acute pancreatitis based on the MIMIC-III database.

Qingsong Wu, Lianyi Liao, Qingjun Deng

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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

The trial behind it

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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

6 citing papers in PubMed.

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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

3 authors.

Qingsong WuDepartment of Critical Care Medicine, Chongqing Red Cross Hospital (People's Hospital of Jiangbei District), Chongqing, China.ORCID https://orcid.org/0000-0002-4311-7474
Lianyi LiaoDepartment of Scientific Research and Education, Chongqing Red Cross Hospital (People's Hospital of Jiangbei District), Chongqing, China.
Qingjun DengDepartment of Critical Care Medicine, Chongqing Red Cross Hospital (People's Hospital of Jiangbei District), Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe association between red blood cell distribution width-to-albumin (RDW/ALB) ratio (RAR) and all-cause mortality in patients with acute pancreatitis has not been fully delineated. The purpose of this study was to investigate the impact of RAR at admission on 28-day all-cause mortality in patients with acute pancreatitis.

designThis investigation was conducted as a retrospective analysis utilizing data from the Medical Information Mart for Intensive Care (MIMIC)-III database.

participantsPatients with acute pancreatitis were selected from the MIMIC-III database according to predefined eligibility criteria. OUTCOME: The outcome was the all-cause mortality rates within 28 days.

resultsUpon screening and excluding ineligible participants, a total of 931 patients with acute pancreatitis who met the inclusion criteria were analyzed. The overall mortality at 28 days was 11.71%. The receiver operating characteristic (ROC) analysis indicated that RAR had a moderate predictive value for all-cause mortality at 28 days, with an area under the curve (AUC) of 0.669 (95%CI, 0.617-0.720; p<0.05), and the cutoff value was 4.39. Divide the patients into a high RAR group and a low RAR group based on the cutoff value. Kaplan-Meier survival analysis demonstrated a statistically significant increase in 28-day mortality among patients in the high RAR group compared to those in the low RAR group. Multivariate analysis indicated that potassium levels, total bilirubin, blood urea nitrogen, lactate, partial thromboplastin time, neutrophil and RAR were independently associated with the 28-day mortality. Multivariate Cox regression analysis confirmed that an elevated RAR was independently associated with increased mortality at 28 day (HR, 2.72; 95% CI, 1.64-4.52; p < 0.001).

conclusionsThis study demonstrated that RAR at admission functioned as a significant prognostic indicator for mortality in patients with acute pancreatitis.

Indexed as

Erythrocyte IndicesPancreatitisSerum AlbuminAcute DiseaseAdultAgedDatabases, FactualFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesROC CurveSerum Albumin

Identifiers

PMID39919086
PMCPMC11805432

What Socratic holds

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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.