Evidence map›Paper›PMID 35362055›Full record

ArticleHospital pediatrics2022

Association Between Procalcitonin and Antibiotics in Children With Community-Acquired Pneumonia.

Mert Sekmen, Jakobi Johnson, Yuwei Zhu, Laura F Sartori, Carlos G Grijalva, Justine Stassun, Donald H Arnold, Krow Ampofo, Jeff Robison, Per H Gesteland and 2 more

Abstract read
In one paragraph

Article in Hospital pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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.

Mert SekmenaDepartments of Pediatrics.
Jakobi JohnsonaDepartments of Pediatrics.
Yuwei ZhubBiostatistics, Vanderbilt University School of Medicine, Nashville Tennessee.
Laura F SartoriaDepartments of Pediatrics.
Carlos G GrijalvacDepartment of Health Policy, Vanderbilt University Medical Center; Nashville, Tennessee.
Justine StassunaDepartments of Pediatrics.
Donald H ArnoldcDepartment of Health Policy, Vanderbilt University Medical Center; Nashville, Tennessee.
Krow AmpofodDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Jeff RobisondDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Per H GestelanddDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Andrew T PaviadDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah.
Derek J WilliamsaDepartments of Pediatrics.

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Risk Stratification and Decision Support to Improve Care and Outcomes in Children with PneumoniaR01AI125642 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WILLIAMS, DEREK J. · 2017 to 2021
$3.3M
NCATS NIH HHS UL1 TR002243NIAID NIH HHS R01 AI125642
6 · The paper itself

Abstract

objectiveTo determine whether empirical antibiotic initiation and selection for children with pneumonia was associated with procalcitonin (PCT) levels when results were blinded to clinicians.

methodsWe enrolled children <18 years with radiographically confirmed pneumonia at 2 children's hospitals from 2014 to 2019. Blood for PCT was collected at enrollment (blinded to clinicians). We modeled associations between PCT and (1) antibiotic initiation and (2) antibiotic selection (narrow versus broad-spectrum) using multivariable logistic regression models. To quantify potential stewardship opportunities, we calculated proportions of noncritically ill children receiving antibiotics who also had a low likelihood of bacterial etiology (PCT <0.25 ng/mL) and those receiving broad-spectrum therapy, regardless of PCT level.

resultsWe enrolled 488 children (median PCT, 0.37 ng/mL; interquartile range [IQR], 0.11-2.38); 85 (17%) received no antibiotics (median PCT, 0.32; IQR, 0.09-1.33). Among the 403 children receiving antibiotics, 95 (24%) received narrow-spectrum therapy (median PCT, 0.24; IQR, 0.08-2.52) and 308 (76%) received broad-spectrum (median PCT, 0.46; IQR, 0.12-2.83). In adjusted analyses, PCT values were not associated with antibiotic initiation (odds ratio [OR], 1.02, 95% confidence interval [CI], 0.97%-1.06%) or empirical antibiotic selection (OR 1.07; 95% CI, 0.97%-1.17%). Of those with noncritical illness, 246 (69%) were identified as potential targets for antibiotic stewardship interventions.

conclusionNeither antibiotic initiation nor empirical antibiotic selection were associated with PCT values. Whereas other factors may inform antibiotic treatment decisions, the observed discordance between objective likelihood of bacterial etiology and antibiotic use suggests important opportunities for stewardship.

Indexed as

Community-Acquired InfectionsPneumoniaAnti-Bacterial AgentsCalcitoninChildHumansProcalcitoninAnti-Bacterial AgentsCalcitoninProcalcitonin

Identifiers

PMID35362055
PMCPMC10332340

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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.