Evidence map›Paper›PMID 40924914›Full record

Observational studyCritical care explorations2025

Monocyte Anisocytosis Can Discriminate Between Sepsis and Sterile Inflammation, but not Mortality, in Critically Ill Surgical/Trauma Patients: A Secondary Prospective Analysis.

Miguel Hernández-Ríos, Ruoxuan Wu, Valerie A Polcz, Rachel D Burnside, Lael M Yonker, Daniel Irimia, Feifei Xiao, Jaimar C Rincon, Tyler J Loftus, Lyle L Moldawer and 3 more

Abstract readObservational Study
In one paragraph

Observational study in Critical care explorations, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Miguel Hernández-RíosSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Ruoxuan WuDepartment of Biostatistics, University of Florida Colleges of Medicine and Public Health and Health Professions, Gainesville, FL.
Valerie A PolczSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Rachel D BurnsideDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL.
Lael M YonkerDepartment of Pediatrics, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
Daniel IrimiaDepartment of Surgery, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
Feifei XiaoDepartment of Biostatistics, University of Florida Colleges of Medicine and Public Health and Health Professions, Gainesville, FL.
Jaimar C RinconSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Tyler J LoftusSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Lyle L MoldawerSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Robert MaileSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Philip A EfronSepsis and Critical Illness Research Center, Department of Surgery, University of Florida College of Medicine, Gainesville, FL.
Muxuan LiangDepartment of Biostatistics, University of Florida Colleges of Medicine and Public Health and Health Professions, Gainesville, FL.

Funding

Renewal: Dysfunctional Myelopoiesis and Myeloid-Derived Suppressor Cells in Sepsis PathobiologyRM1GM139690 · NIGMS · UNIVERSITY OF FLORIDA · PI Philip A Efron, Michael Paul Kladde · 2021 to 2026
$10.3M
Molecular Biology in Burns and TraumaT32GM008721 · NIGMS · UNIVERSITY OF FLORIDA · PI Philip A Efron · 1999 to 2026
$5.0M
Stratifying Patient Immune Endotypes in Sepsis (SPIES Study)R01GM139046 · NIGMS · UNIVERSITY OF FLORIDA · PI MAILE, ROBERT · 2020 to 2024
$4.2M
Defining neutrophil pathobiology in pediatric Long COVIDR01HL173059 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Lael Yonker · 2024 to 2026
$2.4M
R35 Equipment SupplementR35GM140806 · NIGMS · UNIVERSITY OF FLORIDA · PI EFRON, PHILIP A · 2021 to 2025
$2.2M
NHLBI NIH HHS R01 HL173059NIGMS NIH HHS R01 GM139046NIGMS NIH HHS R35 GM140806NIGMS NIH HHS RM1 GM139690NIGMS NIH HHS T32 GM008721
6 · The paper itself

Abstract

OBJECTIVES

backgroundMonocyte anisocytosis (monocyte distribution width [MDW]) has been previously validated to predict sepsis and outcome in patients presenting in the emergency department and mixed-population ICUs. Determining sepsis in a critically ill surgical/trauma population is often difficult due to concomitant inflammation and stress. We examined whether MDW could identify sepsis among patients admitted to a surgical/trauma ICU and predict clinical outcome.

designSecondary analysis of three prospective observational clinical studies.

settingSingle institution ICU. PATIENTS/SUBJECTS: Two hundred thirty-eight participants were included in this study: 107 patients who were admitted to the ICU and adjudicated to have sepsis, 80 patients who were considered critically ill nonseptic (CINS), and 51 healthy control participants.

interventionsMDW was measured among hospitalized patients admitted to the ICU with the diagnosis of sepsis or CINS patients at risk of developing sepsis. Blood samples were collected at admission and at intervals during ICU admission. MEASUREMENTS AND MAIN

resultsMDW significantly differed between septic and CINS patients on ICU admission (26.4, interquartile range [IQR, 23.5-30.8] vs. 20.1 [IQR, 17.9-21.9]; p < 0.001) and could discriminate with an area under the receiver operating characteristic curve of 0.85 (95% CI, 0.79-0.91; p < 0.001). An MDW of greater than 22.0 at admission to the ICU could identify sepsis with a 78% specificity and a 90% sensitivity but could not discriminate in-hospital, 30-day, or 90-day mortality. LIMITATIONS: Small sample size from a single institution. Our analysis did not include other relevant biomarkers such as procalcitonin, C-reactive protein, and interleukin-6. In the imputation of missing values, linear mixed-effect models were used, risking model misspecification and the violation of the missing-at-random assumption.

conclusionsAmong surgical/trauma ICU patients, MDW can discriminate between sepsis and nonseptic inflammation, but it is a weak predictor of mortality.

Indexed as

Critical IllnessInflammationLeukocytosisMonocytesSepsisWounds and InjuriesAdultAgedFemaleHumansIntensive Care UnitsMaleMiddle AgedProspective StudiesROC Curveinflammationmonocyte distribution widthsepsissurgical patients

Identifiers

PMID40924914
PMCPMC12422779

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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.