Evidence map›Paper›PMID 42189672›Full record

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

Early Discontinuation of Empiric Antibiotics in Pediatric Haploidentical Hematopoietic Cell Transplant Recipients with Febrile Neutropenia.

Sandra Castejon-Ramirez, Diego R Hijano, Rachel L Wattier, Jose Ferrolino, Megan Peterson, Pamela Merritt, Amber Davis, Amanda Cole, Kim J Alison, Ashleigh Gowen and 5 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. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

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5 · Who and what money

Authors and funding

15 authors.

Sandra Castejon-RamirezDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-8979-1819
Diego R HijanoDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-2903-666X
Rachel L WattierDepartment of Pediatrics, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-5271-4705
Jose FerrolinoDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-4008-5507
Megan PetersonDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
Pamela MerrittDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
Amber DavisDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0009-0007-1226-4344
Amanda ColeDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
Kim J AlisonDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ashleigh GowenDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ronald DallasDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-3259-6801
Li TangDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
Jiaming LiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0002-2017-3377
Brandon TriplettDepartment of Transplant Cellular Therapy, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0001-8220-9980
Gabriela MaronDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0001-5247-5399

Funding

UCSF-Kaiser Urological Epidemiology Research Career Development ProgramK12DK111028 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUANG, ALISON · 2016 to 2025
$5.3M
NIDDK NIH HHS K12 DK111028
6 · The paper itself

Abstract

backgroundFebrile neutropenia (FN) is common in children, adolescents, and young adults (CAYA) undergoing hematopoietic cell transplant (HCT), particularly following allogeneic haploidentical HCT (haplo-HCT). Optimal empiric antibiotic duration for FN is not well established in this population.

methodsA retrospective quasi-experimental study was conducted among CAYA undergoing haplo-HCT between 2010 and 2022 who experienced FN. In 2017 a guideline was implemented for discontinuation of empiric antibiotics within 72 hours of FN in patients without identified infection regardless of persistence of fever. We compared patients who underwent haplo-HCT pre-implementation (Pre-I) vs. post-implementation (Post-I) of this guideline. The primary outcome was days of therapy (DOT). Secondary outcomes included incidence of bloodstream infections (BSI), ICU admission, and mortality from 72 hours of FN onset until neutrophil engraftment. A Desirability of Outcome Ranking (DOOR) with a modified Response Adjusted for Duration of Antibiotic Risk (RADAR) approach using DOT was applied to comprehensively assess outcomes.

resultsPatients in Post-I (n=82) had fewer DOT compared to Pre-I (n=90) with a median difference of 8 days (p<0.01). There were no significant differences in BSI incidence, ICU admission, or mortality between groups. The DOOR-modified RADAR analysis demonstrated Post-I was associated with a 70% (95% CI = 61, 78%) probability of experiencing a more favorable clinical outcome compared to the Pre-I group (p <0.01).

conclusionsEarly antibiotic discontinuation appears safe and feasible in CAYA haplo-HCT recipients with FN, significantly reducing antibiotic exposure without increasing adverse outcomes. Large prospective multicenter trials are needed to confirm these findings.

Indexed as

adolescentsand young adults (CAYA)childrenDesirability of Outcome Ranking (DOOR)Early antibiotic discontinuation strategyFebrile neutropenia (FN)hematopoietic cell transplant from haploidentical donor (haplo-HCT)Response Adjusted for Duration of Antibiotic Risk (RADAR)

Identifiers

PMID42189672
PMCPMC13671421

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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.