Evidence map›Paper›PMID 36250865›Full record

ArticleMicrobiology spectrum2022

Using a 29-mRNA Host Response Classifier To Detect Bacterial Coinfections and Predict Outcomes in COVID-19 Patients Presenting to the Emergency Department.

Nikhil Ram-Mohan, Angela J Rogers, Catherine A Blish, Kari C Nadeau, Elizabeth J Zudock, David Kim, James V Quinn, Lixian Sun, Oliver Liesenfeld, Stanford COVID-19 Biobank Study Group and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Nikhil Ram-MohanDepartment of Emergency Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.ORCID 0000-0002-7761-2772
Angela J RogersDepartment of Medicine-Pulmonary, Allergy & Critical Care Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Catherine A BlishDepartment of Medicine/Infectious Diseases, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Kari C NadeauDepartment of Medicine-Pulmonary, Allergy & Critical Care Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Elizabeth J ZudockDepartment of Emergency Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
David KimDepartment of Emergency Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
James V QuinnDepartment of Emergency Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Lixian SunInflammatix, Inc., Burlingame, California, USA.
Oliver LiesenfeldInflammatix, Inc., Burlingame, California, USA.
Stanford COVID-19 Biobank Study Group
Samuel YangDepartment of Emergency Medicine, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.ORCID 0000-0003-1123-9036
Stanford University · US

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
Changing Cultures in Sepsis: Rapid single-cell pathogen identification and antibiotic susceptibility testing directly from whole bloodR01AI153133 · NIAID · STANFORD UNIVERSITY · PI WONG, PAK KIN, YANG, SAMUEL · 2020 to 2024
$3.7M
A "Culture" Shift: Integrated Bacterial Screening and Antibacterial Susceptibility Test on Microfluidic Digital Array for Bloodstream InfectionsR01AI137272 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WANG, TZA-HUEI JEFF, YANG, SAMUEL · 2018 to 2022
$3.6M
NIAID NIH HHS R01 AI137272NIAID NIH HHS R01 AI153133NIAID NIH HHS U19 AI057229
6 · The paper itself

Abstract

Clinicians in the emergency department (ED) face challenges in concurrently assessing patients with suspected COVID-19 infection, detecting bacterial coinfection, and determining illness severity since current practices require separate workflows. Here, we explore the accuracy of the IMX-BVN-3/IMX-SEV-3 29 mRNA host response classifiers in simultaneously detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and bacterial coinfections and predicting clinical severity of COVID-19. A total of 161 patients with PCR-confirmed COVID-19 (52.2% female; median age, 50.0 years; 51% hospitalized; 5.6% deaths) were enrolled at the Stanford Hospital ED. RNA was extracted (2.5 mL whole blood in PAXgene blood RNA), and 29 host mRNAs in response to the infection were quantified using Nanostring nCounter. The IMX-BVN-3 classifier identified SARS-CoV-2 infection in 151 patients with a sensitivity of 93.8%. Six of 10 patients undetected by the classifier had positive COVID tests more than 9 days prior to enrollment, and the remaining patients oscillated between positive and negative results in subsequent tests. The classifier also predicted that 6 (3.7%) patients had a bacterial coinfection. Clinical adjudication confirmed that 5/6 (83.3%) of the patients had bacterial infections, i.e., Clostridioides difficile colitis (

Indexed as

Bacterial InfectionsCoinfectionCOVID-19BacteriaFemaleHumansMaleMiddle AgedRNA, MessengerSARS-CoV-2RNA, Messengerbacterial superinfectioncoinfectionCOVID-19diagnosisemergency departmenthost response classifiermortality predictionprognosis

Identifiers

PMID36250865
PMCPMC9769905
OpenAlexW4306409796

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.