Evidence map›Paper›PMID 41448710›Full record

ArticleBMJ open2025

Time-dependent predictive performance of inflammatory markers for 30-day all-cause mortality in patients with suspected infection in a Japanese emergency department: a retrospective cohort study.

Moeko Omiya, Toshihiko Takada, Tetsuhiro Yano, Kotaro Fujii, Ryuto Fujiishi, Shunichi Fukuhara

Abstract read
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

6 authors.

Moeko OmiyaDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University, Fukushima, Fukushima Prefecture, Japan momiya1014@gmail.com.ORCID http://orcid.org/0000-0002-1091-8355
Toshihiko TakadaDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University, Fukushima, Japan.ORCID http://orcid.org/0000-0002-8032-6224
Tetsuhiro YanoDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University, Fukushima, Japan.
Kotaro FujiiDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University, Fukushima, Japan.
Ryuto FujiishiDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University, Fukushima, Japan.
Shunichi FukuharaDepartment of General Medicine, Shirakawa Satellite for Teaching And Research (STAR), Fukushima Medical University School of Medicine, Fukushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo evaluate the time-dependent predictive performance of inflammatory markers for 30-day all-cause mortality in patients with suspected infection.

designRetrospective cohort study.

settingThe ambulatory care division of the department of general medicine or the emergency department of a single acute care hospital in Japan, from April 2015 to March 2017.

participantsThe participants were 977 consecutive adult patients with suspected infection defined as those who underwent at least two sets of blood culture. PRIMARY OUTCOME MEASURES: The primary outcome, ascertained from electronic medical records, was 30-day all-cause mortality. The predictive performance of three inflammatory markers (C-reactive protein (CRP), neutrophil-to-lymphocyte ratio and red cell distribution width (RDW)) was assessed across four time intervals from symptom onset to hospital presentation: ≤6, >6 to ≤24, >24 to ≤72, and >72 hours.

resultsTime from symptom onset to hospital presentation influenced the predictive performance of inflammatory markers for 30-day all-cause mortality, and CRP ≥15 mg/dL was the most useful for identifying patients at higher risk of mortality within 6 hours (positive likelihood ratio (LR+) 7.7); however, this association weakened over time (LR+ 1.3 at >72 hours). Conversely, RDW ≥16% became more informative later in the course (LR+ 4.1 at >72 hours). For identifying patients at lower risk of 30-day all-cause mortality, CRP <5 mg/dL showed some utility after 6 hours (negative likelihood ratio (LR-) 0.5-0.7), while RDW <14% was more predictive after 72 hours (LR- 0.3).

conclusionThese findings suggest the potential utility of CRP for ruling in high-risk patients within 6 hours from symptom onset, and of RDW for both ruling in and ruling out patients after 72 hours, thereby suggesting that time-dependent variations are important when interpreting inflammatory markers in emergency care settings. However, caution is needed when interpreting these findings because of the retrospective design of this study and potential selection bias.

Indexed as

C-Reactive ProteinEmergency Service, HospitalInfectionsInflammationAdultAgedAged, 80 and overBiomarkersEast Asian PeopleErythrocyte IndicesFemaleHumansJapanMaleMiddle AgedNeutrophilsBiomarkersC-Reactive ProteinEmergency DepartmentsINFECTIOUS DISEASESPrognosis

Identifiers

PMID41448710
PMCPMC12742116

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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.