Evidence map›Paper›PMID 31599813›Full record

ArticleCritical care medicine2019

Allergic Immune Diseases and the Risk of Mortality Among Patients Hospitalized for Acute Infection.

Philip A Verhoef, Sivasubramanium V Bhavani, Kyle A Carey, Matthew M Churpek

Open access · greenAbstract read
In one paragraph

Article in Critical care medicine, 2019. 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
0.5field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. IL-33-mediated Eosinophilia Protects against Acute Lung Injury.American journal of respiratory cell and molecular biology · 2021
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Philip A VerhoefDepartment of Medicine, University of Chicago, Chicago, IL.
Sivasubramanium V BhavaniDepartment of Medicine, University of Chicago, Chicago, IL.
Kyle A CareyDepartment of Medicine, University of Chicago, Chicago, IL.
Matthew M ChurpekDepartment of Medicine, University of Chicago, Chicago, IL.
University of Chicago · US

Funding

The Institute for Translational MedicineUL1TR002389 · NCATS · UNIVERSITY OF CHICAGO · PI Joshua J Jacobs, DAVID O MELTZER · 2017 to 2026
$71.6M
RESEARCH TRAINING IN RESPIRATORY BIOLOGYT32HL007605 · NHLBI · UNIVERSITY OF CHICAGO · PI Yun Fang, Gokhan M. Mutlu · 1985 to 2026
$18.1M
Sepsis Early Prediction and Subphenotype Illumination Study (SEPSIS)R01GM123193 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI CHURPEK, MATTHEW MICHAEL · 2017 to 2021
$1.9M
Predicting In-hospital Cardiac Arrest Using Electronic Health Record DataK08HL121080 · NHLBI · UNIVERSITY OF CHICAGO · PI CHURPEK, MATTHEW MICHAEL · 2014 to 2018
$751k
Type 2 Immune Responses Protect Against the Morbidity and Mortality of SepsisK08HL132109 · NHLBI · UNIVERSITY OF CHICAGO · PI VERHOEF, PHILIP A · 2016 to 2019
$656k
NCATS NIH HHS UL1 TR002389NHLBI NIH HHS K08 HL121080NHLBI NIH HHS K08 HL132109NHLBI NIH HHS T32 HL007605NIGMS NIH HHS R01 GM123193
6 · The paper itself

Abstract

objectivesThe immune response during sepsis remains poorly understood and is likely influenced by the host's preexisting immunologic comorbidities. Although more than 20% of the U.S. population has an allergic-atopic disease, the type 2 immune response that is overactive in these diseases can also mediate beneficial pro-resolving, tissue-repair functions. Thus, the presence of allergic immunologic comorbidities may be advantageous for patients suffering from sepsis. The objective of this study was to test the hypothesis that comorbid type 2 immune diseases confer protection against morbidity and mortality due to acute infection.

designRetrospective cohort study of patients hospitalized with an acute infection between November 2008 and January 2016 using electronic health record data.

settingSingle tertiary-care academic medical center. PATIENTS: Admissions to the hospital through the emergency department with likely infection at the time of admission who may or may not have had a type 2 immune-mediated disease, defined as asthma, allergic rhinitis, atopic dermatitis, or food allergy, as determined by International Classification of Diseases, 9th Revision, Clinical Modification codes.

interventionsNone. MEASUREMENTS AND MAIN

resultsOf 10,789 admissions for infection, 2,578 (24%) had a type 2 disease; these patients were more likely to be female, black, and younger than patients without type 2 diseases. In unadjusted analyses, type 2 patients had decreased odds of dying during the hospitalization (0.47; 95% CI, 0.38-0.59, p < 0.001), while having more than one type 2 disease conferred a dose-dependent reduction in the risk of mortality (p < 0.001). When adjusting for demographics, medications, types of infection, and illness severity, the presence of a type 2 disease remained protective (odds ratio, 0.55; 95% CI, 0.43-0.70; p < 0.001). Similar results were found using a propensity score analysis (odds ratio, 0.57; 95% CI, 0.45-0.71; p < 0.001).

conclusionsPatients with type 2 diseases admitted with acute infections have reduced mortality, implying that the type 2 immune response is protective in sepsis.

Indexed as

Acute DiseaseAdultAgedCohort StudiesFemaleHospitalizationHumansHypersensitivityInfectionsMaleMiddle AgedRetrospective StudiesRisk Assessment

Identifiers

PMID31599813
PMCPMC6861689
OpenAlexW2979829085

What OpenQuestion holds

Textmetadata
LicenceTDM
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.