Evidence map›Paper›PMID 39368804›Full record

ArticleBlood advances2024

Identification of factors predicting low-risk febrile neutropenia admissions in adults with acute myeloid leukemia.

Khushboo V Pal, Megan Othus, Zahra Ali, Katherine Russell, Carole Shaw, Mary-Elizabeth M Percival, Paul C Hendrie, Jacob S Appelbaum, Roland B Walter, Anna B Halpern

Abstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Refining favorable-risk classification in pediatricBlood science (Baltimore, Md.) · 2026
    Article
  2. Article
  3. 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

10 authors.

Khushboo V PalDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.
Megan OthusPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA.
Zahra AliDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.
Katherine RussellDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.ORCID 0009-0003-2503-4207
Carole ShawClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Mary-Elizabeth M PercivalDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.
Paul C HendrieDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.ORCID 0000-0003-1902-5972
Jacob S AppelbaumDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.ORCID 0000-0002-4362-7773
Roland B WalterDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.ORCID 0000-0002-9268-3341
Anna B HalpernDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractFebrile neutropenia (FN) is the most common reason for hospital readmission after chemotherapy for acute myeloid leukemia (AML) and is a major driver of health care resource utilization. Although FN risk models exist, they have largely been developed and validated for solid tumors. We therefore examined whether baseline characteristics could predict which patients with AML and FN have a lower risk of progression to severe illness. We identified adults with high-grade myeloid neoplasms (≥10% blasts in the blood/marrow) who received intensive chemotherapy and who were admitted for FN between 2016 and 2023. We collected baseline clinical and disease variables. Outcomes were: infections identified, hospital length of stay (LOS), intensive care unit (ICU) admission, and survival. A lower-risk (LR) outcome was defined as LOS <72 hours without ICU admission or inpatient death. Univariate and multivariable (MV) logistic regression models were used to assess covariate associations with outcomes. We identified 397 FN admissions in 248 patients (median age, 61; [range, 29-77] years). The median hospital LOS was 6 days (range, 1-56) days; 10% required ICU admission, and 3.5% died inpatient. Only 15% of admissions were LR. Infection was identified in 59% of admissions. Physiologic parameters, including heart rate, blood pressure, and fever height, were the best predictors of LR admission and infection. We developed MV models to predict LR admission and infection with area under the curve (AUC) of 0.82 and 0.72, respectively. Established FN and critical illness models were not predictive of outcomes in AML, and we could not identify a LR group; thus, an AML-specific FN risk model requires further development and validation.

Indexed as

Febrile NeutropeniaLeukemia, Myeloid, AcuteAdultAgedFemaleHospitalizationHumansIntensive Care UnitsLength of StayMaleMiddle AgedPrognosisRisk Factors

Identifiers

PMID39368804
PMCPMC11696649

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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.