Evidence map›Paper›PMID 41556483›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Diagnostic Yield of Repeat Blood Cultures and Risk Factors for Bloodstream Infection in Persistent Febrile Neutropenia.

Emily A Rosen, Elizabeth M Krantz, Allison Thibodeau, Keara Kennedy, Leah H Yoke, Frank Tverdek, Zahra Kassamali Escobar, Jason P Cooper, Masumi Ueda Oshima, Paul Hendrie and 2 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2026. 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. Drawing conclusions: blood culture yield across clinical scenarios in hematologic malignancy.Antimicrobial stewardship & healthcare epidemiology : ASHE · 2026
    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

12 authors.

Emily A RosenVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-1378-8859
Elizabeth M KrantzVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0009-0000-0029-8511
Allison ThibodeauClinical Analytics, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0009-0003-7503-4504
Keara KennedyVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0009-0002-5139-6167
Leah H YokeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Frank TverdekDepartment of Pharmacy, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0001-7510-5470
Zahra Kassamali EscobarDepartment of Pharmacy, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jason P CooperDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-0023-8054
Masumi Ueda OshimaDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0003-2277-1976
Paul HendrieDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA, USA.
Marco MielcarekDivision of Hematology and Oncology, Department of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-5680-8688
Catherine LiuVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-7532-4822

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Training Program in Infectious Diseases in the Immunocompromised HostT32AI118690 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BOECKH, MICHAEL J · 2016 to 2025
$4.0M
NCI NIH HHS P30 CA015704NIAID NIH HHS T32 AI118690
6 · The paper itself

Abstract

backgroundThe optimal frequency of repeat blood cultures in persistent febrile neutropenia (FN) remains unknown. This study aims to identify opportunities for blood culture diagnostic stewardship in persistent FN.

methodsThis is a retrospective cohort study of patients with hematology/oncology diagnoses and an FN episode >3 days. Generalized estimating equation logistic regression models were used to evaluate risk factors for new bloodstream infection (BSI) after FN day 3.

resultsAmong 620 patients, median FN duration was 5 days and median blood culture bottles collected per patient was 12. On FN day 1, 25% of patients had a positive blood culture; on FN days 2-9, <5% of patients per day had a new organism isolated. Among 31 new organisms isolated after FN day 3, 8 (26%) were contaminants. Of 503 patients with ≥1 blood culture collected after FN day 3, 19 (4%) had a new BSI after FN day 3. FN onset in the peri-hematopoietic cell transplant (HCT) period (day -7 to +30) was associated with lower odds of new BSI after FN day 3 (OR 0.18; 95%CI [0.04-0.71]; p=0.01).Thirty-six patients died within 30 days after FN day 3, including 4 with a new BSI after FN day 3; 1 death was attributable to BSI after FN day 3.

conclusionsDetection of new BSI after FN day 3 was uncommon, demonstrating low diagnostic yield of repeat blood cultures after FN day 3. FN episodes in the peri-HCT period may be a potential focus for blood culture diagnostic stewardship initiatives.

Indexed as

blood culturesdiagnostic stewardshipFebrile neutropenia

Identifiers

PMID41556483
PMCPMC13536489

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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.