Evidence map›Paper›PMID 35761790›Full record

ArticleJournal of hospital medicine2022

Associations between comorbidity-related functional limitations and pneumonia outcomes.

Chastity Greene, Hui Nian, Yuwei Zhu, James W Antoon, Katherine L Freundlich, Krow Ampofo, Laura F Sartori, Jakobi Johnson, Donald H Arnold, Per Gesteland and 5 more

Abstract read
In one paragraph

Article in Journal of hospital medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Validation of Childhood Pneumonia Prognostic Models for Use in Emergency Care Settings.Journal of the Pediatric Infectious Diseases Society · 2023
    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

15 authors.

Chastity GreeneMeharry Medical College, Nashville, Tennessee, USA.
Hui NianDepartment of Biostatistics, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Yuwei ZhuDepartment of Biostatistics, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
James W AntoonDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Katherine L FreundlichDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Krow AmpofoDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Laura F SartoriDepartment of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Jakobi JohnsonDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Donald H ArnoldDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Per GestelandDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Justine StassunDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-2645-0339
Jeff RobisonDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Andrew T PaviaDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Carlos G GrijalvaDepartment of Health Policy, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Derek J WilliamsDepartment of Pediatrics, Division of Hospital Medicines, Vanderbilt University School of Medicine and Vanderbilt University Medical Center, Nashville, Tennessee, USA.

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
National Institute of Allergy and Infectious Diseases R01 AI125642NCATS NIH HHS UL1 TR002243NIAID NIH HHS R01 AI125642
6 · The paper itself

Abstract

backgroundUnderlying comorbidities are common in children with pneumonia.

objectiveTo determine associations between comorbidity-related functional limitations and risk for severe pneumonia outcomes. DESIGN, SETTING, AND

participantsWe prospectively enrolled children <18 years with and without comorbidities presenting to the emergency department with clinical and radiographic pneumonia at two institutions. Comorbidities included chronic conditions requiring daily medications, frequent healthcare visits, or which limited age-appropriate activities. Among children with comorbidities, functional limitations were defined as none or mild, moderate, and severe. MAIN OUTCOMES AND MEASURES: Outcomes included an ordinal severity outcome, categorized as very severe (mechanical ventilation, shock, or death), severe (intensive care without very severe features), moderate (hospitalization without severe features), or mild (discharged home), and length of stay (LOS). Multivariable ordinal logistic regression was used to examine associations between comorbidity-related functional limitations and outcomes, while accounting for relevant covariates.

resultsA cohort of 1116 children, including 452 (40.5%) with comorbidities; 200 (44.2%) had none or mild functional limitations, 93 (20.6%) moderate, and 159 (35.2%) had severe limitations. In multivariable analysis, comorbidity-related functional limitations were associated with the ordinal severity outcome and LOS (p < .001 for both). Children with severe functional limitations had tripling of the odds of a more severe ordinal (adjusted odds ratio [aOR]: 3.01, 95% confidence interval [2.05, 4.43]) and quadrupling of the odds for longer LOS (aOR: 4.72 [3.33, 6.70]) as compared to children without comorbidities.

conclusionComorbidity-related functional limitations are important predictors of disease outcomes in children with pneumonia. Consideration of functional limitations, rather than the presence of comorbidity alone, is critical when assessing risk of severe outcomes.

Indexed as

PneumoniaChildComorbidityHospitalizationHumansLength of StayRespiration, Artificial

Identifiers

PMID35761790
PMCPMC9872961

What OpenQuestion holds

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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.