Evidence map›Paper›PMID 42856642›Full record

ArticleFrontiers in medicine2026

A three-parameter complete blood count triage tool for monocytosis to prioritize hematology evaluation: development in MIMIC-IV and external validation in two independent cohorts.

Lingyun Xu, Jing Wu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Lingyun Xu *Department of Hematology, Fuyang People's Hospital (The Affiliated Fuyang People's Hospital of Anhui Medical University), Fuyang, Anhui, China.
Jing Wu *Department of Hematology, The Second Affiliated Hospital of Chengdu Medical College, China National Nuclear Corporation 416 Hospital, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Monocytosis is a common complete blood count (CBC) abnormality, but in non-hematology settings it may be difficult to distinguish reactive causes from patterns warranting urgent evaluation for acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS). We aimed to develop and externally validate a simple, report-level CBC triage model to prioritize hematology assessment in patients with monocytosis. Methods: MonoxGB was developed using admission-level data from MIMIC-IV v2.2 and three routinely reported CBC variables: absolute monocyte count, monocyte percentage, and platelet count. No proprietary analyzer signals, scattergram-derived parameters, morphology flags, or manufacturer-specific cell-population data were used. External validation included a retrospective Fuyang cohort of 91 eligible patients with monocytosis, all of whom underwent bone marrow examination, and an eICU Collaborative Research Database cohort of 73,650 intensive care admissions with monocytosis. Results: In fivefold cross-validation within MIMIC-IV, the mean area under the receiver operating characteristic curve (AUC) was 0.931 ± 0.022. In the Fuyang cohort, 29 of 91 patients had AML/MDS; the AUC was 0.840 (95% confidence interval, 0.753-0.915), and average precision was 0.682. In eICU-CRD, the AUC was 0.886 (95% confidence interval, 0.839-0.928). At an exploratory local high-sensitivity threshold of 0.0028, sensitivity was 0.966, specificity was 0.500, and negative predictive value was 0.969. Across cohorts, AML/MDS was associated with a higher monocyte burden and lower platelet counts; platelet count monocyte percentage, and absolute monocyte count were the dominant model features. Discussion: MonoxGB is a three-parameter, CBC report-based triage tool that may help non-hematologists prioritize patients with monocytosis for earlier smear review or hematology assessment. It is not a diagnostic substitute for bone marrow evaluation or specialist judgment. Prospective workflow-based validation using a prespecified deployment threshold is required before routine implementation.

Indexed as

acute myeloid leukemiacomplete blood countexternal validationhematology triagemonocytosismyelodysplastic syndromes

Identifiers

PMID42856642
PMCPMC13649514

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.