Evidence map›Paper›PMID 30475852›Full record

ArticlePloS one2018

Interleukin-27 as a candidate diagnostic biomarker for bacterial infection in immunocompromised pediatric patients.

Lauren Jacobs, Zachary Berrens, Erin K Stenson, Matthew Zackoff, Lara Danziger-Isakov, Patrick Lahni, Hector R Wong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
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

7 authors at 4 institutions in 1 country.

Lauren JacobsDepartment of Pediatrics, Division of Pediatric Critical Care, Texas Children's Hospital, Houston, Texas, United States of America.ORCID 0000-0003-1770-2861
Zachary BerrensDepartment of Pediatrics, Division of Pediatric Critical Care, Riley Hospital for Children at the University of Indiana Health, Indianapolis, Indiana, United States of America.
Erin K StensonDepartment of Pediatrics, Division of Pediatric Critical Care, Children's Hospital of Colorado, Aurora, Colorado, United States of America.
Matthew ZackoffDepartment of Pediatrics, Division of Pediatric Critical Care, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United states of America.
Lara Danziger-IsakovDepartment of Pediatrics, Division of Pediatric Infectious Disease, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
Patrick LahniDepartment of Pediatrics, Division of Pediatric Critical Care, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United states of America.
Hector R WongDepartment of Pediatrics, Division of Pediatric Critical Care, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United states of America.
Cincinnati Children's Hospital Medical Center · USChildren's Hospital Colorado · USRiley Hospital for Children · USTexas Children's Hospital · US

Funding

Novel diagnostic and stratification tools for septic shockR01GM108025 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI WONG, HECTOR R. · 2014 to 2017
$2.3M
NIGMS NIH HHS R01 GM108025
6 · The paper itself

Abstract

backgroundImmunocompromised pediatric patients constitute a growing population that is particularly vulnerable to bacterial infection, necessitating prompt recognition and treatment. This study assessed the utility of interleukin-27 (IL-27) and procalcitonin (PCT) as biomarkers of bacterial infection among immunocompromised pediatric subjects.

methodsThis is a single-center prospective cohort study conducted from July 2016 through September 2017, drawing subjects from the inpatient units at Cincinnati Children's Hospital Medical Center (CCHMC), a large, tertiary care children's hospital. Patients were included if they fit the definition of immunocompromised and were under clinical suspicion for infection, defined by the acquisition of a blood culture at any point during the admission. The primary analysis assessed the accuracy of IL-27 to diagnose bacterial infection in immunocompromised pediatric patients, using PCT as a comparator.

results293 patients were recruited, representing 400 episodes of suspected bacterial infection. The median age was 7.8 years (IQR 3.1-13.8 years). Fifty-three percent (n = 213) of the population had a primary oncologic diagnosis, 24% (n = 95) had received a bone marrow transplant, and 21% (n = 85) had received a solid organ transplant. The overall infection rate was 37%, with 70% of those patients having some form of culture positivity. Twenty-eight-day mortality was 5%, 60-day mortality was 9%, with 87% of patients surviving to hospital discharge. The AUC's of the ROC curve to diagnose bacterial infection were 0.62 (0.5-0.68) for IL-27 and 0.65 (0.6-0.73) for PCT. Using the previously determined cutoff of 5.0 ng/mL, the specificity of IL-27 to diagnose bacterial infection reached 94%, with a negative predictive value of 64%.

conclusionsDespite prior work demonstrating IL-27 and PCT as possible biomarkers of bacterial infection in immunocompromised pediatric patients, we were unable to validate these findings. This illustrates the challenges associated with developing reliable biomarkers of bacterial infection in this vulnerable population.

Indexed as

AdolescentArea Under CurveBacteriaBacterial InfectionsBiomarkersBone Marrow TransplantationChildChild, PreschoolFemaleHumansImmunocompromised HostInfantInterleukin-27MaleProcalcitoninProspective StudiesBiomarkersInterleukin-27Procalcitonin

Identifiers

PMID30475852
PMCPMC6261028
OpenAlexW2903211732

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.