Evidence map›Paper›PMID 33209953›Full record

ArticleOpen forum infectious diseases2020

Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997-2017).

Sarah M Heston, Rebecca R Young, Hwanhee Hong, Ibukunoluwa C Akinboyo, John S Tanaka, Paul L Martin, Richard Vinesett, Kirsten Jenkins, Lauren E McGill, Kevin C Hazen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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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 at 3 institutions in 1 country.

Sarah M HestonDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0001-6150-1149
Rebecca R YoungDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.
Hwanhee HongDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0002-3736-6327
Ibukunoluwa C AkinboyoDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.
John S TanakaDuke University School of Medicine, Durham, North Carolina, USA.
Paul L MartinDivision of Pediatric Transplant and Cellular Therapy, Duke University Medical Center, Durham, North Carolina, USA.
Richard VinesettDivision of Pediatric Transplant and Cellular Therapy, Duke University Medical Center, Durham, North Carolina, USA.
Kirsten JenkinsDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.
Lauren E McGillDivision of Pediatric Transplant and Cellular Therapy, Duke University Medical Center, Durham, North Carolina, USA.
Kevin C HazenPathology, Duke University Medical Center, Durham, North Carolina, USA.
Patrick C SeedDivision of Pediatric Infectious Diseases, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Matthew S KellyDivision of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.
Duke Medical Center · USDuke University · USLurie Children's Hospital · US

Funding

Unified Program for Therapeutics in Children (UPTiC)T32HD094671 · NICHD · DUKE UNIVERSITY · PI Ian J Davis, Kanecia Obie Zimmerman · 2019 to 2026
$2.9M
Nasopharyngeal Microbiome and Risk of Bacterial Pathogen Colonization in InfantsK23AI135090 · NIAID · DUKE UNIVERSITY · PI KELLY, MATTHEW SCOTT · 2018 to 2022
$860k
NIAID NIH HHS K23 AI135090NICHD NIH HHS T32 HD094671
6 · The paper itself

Abstract

backgroundBloodstream infections (BSIs) occur frequently after hematopoietic stem cell transplantation (HSCT). We examined the microbiology of BSI in pediatric HSCT recipients over a 2-decade period at our institution to inform empirical antimicrobial prescribing and infection prevention strategies.

methodsWe conducted a retrospective cohort study of children (<18 years) who underwent HSCT at Duke University between 1997 and 2015. We used recurrent-event gap-time Cox proportional hazards models to determine the hazards of all-cause and cause-specific BSI according to HSCT year. We compared the median time to BSI by causative organism type and evaluated for temporal trends in the prevalence of antibiotic resistance among causative organisms.

resultsA total of 865 BSI occurred in 1311 children, including 412 (48%) Gram-positive bacterial, 196 (23%) Gram-negative bacterial, 56 (6%) fungal, 23 (3%) mycobacterial, and 178 (21%) polymicrobial BSI. The hazard of all BSIs did not change substantially over time during the study period, but the hazard of fungal BSIs declined over time during the study period (

conclusionsDespite expanded practices for BSI prevention over the past several decades, the incidence of BSI remains high in pediatric HSCT recipients at our institution. Additional strategies are urgently needed to effectively prevent BSIs in this high-risk population.

Indexed as

antibiotic resistancebloodstream infectionshematopoietic stem cell transplantationimmunocompromised hostpediatrics

Identifiers

PMID33209953
PMCPMC7652097
OpenAlexW3091352011

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LicenceCC BY-NC-ND
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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.