Evidence map›Paper›PMID 35677819›Full record

ArticleFrontiers in medicine2022

Characterizing the Severity of SARS-CoV-2 Variants at a Single Pediatric Center.

Aslam Khan, Caroline Ichura, Hannah Wang, Izabela Rezende, Malaya K Sahoo, ChunHong Huang, Daniel Solis, Mamdouh Sibai, Fumiko Yamamoto, Sindiso Nyathi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

13 authors at 1 institution in 1 country.

Aslam KhanDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Caroline IchuraDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Hannah WangDepartment of Pathology, Stanford University, Stanford, CA, United States.
Izabela RezendeDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Malaya K SahooDepartment of Pathology, Stanford University, Stanford, CA, United States.
ChunHong HuangDepartment of Pathology, Stanford University, Stanford, CA, United States.
Daniel SolisDepartment of Pathology, Stanford University, Stanford, CA, United States.
Mamdouh SibaiDepartment of Pathology, Stanford University, Stanford, CA, United States.
Fumiko YamamotoDepartment of Pathology, Stanford University, Stanford, CA, United States.
Sindiso NyathiDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Bethel BayrauDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Benjamin A PinskyDepartment of Pathology, Stanford University, Stanford, CA, United States.
A Desiree LaBeaudDepartment of Pediatrics, Division of Infectious Diseases, Stanford University, Stanford, CA, United States.
Stanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since March 2020, SARS-CoV-2 has plagued the world with COVID-19 and individuals of all ages have experienced varying symptoms of disease. Older adults were experiencing more severe disease compared to children and were prioritized by vaccination efforts. While biologic therapies and vaccinations were implemented, there were changes in public health restrictions with subsequent surges resulting in more infected children. During these surges there was a rise of different SARS-CoV-2 variants with the dominant variant initially alpha (B.1.1.7 and other Pango lineages) and epsilon (B.1.427/B.1.429) in early 2021 and a dramatic shift to delta (B.1.617.2 and other Pango lineages) by mid-summer 2021. In this study we aimed to characterize the clinical severity and host factors associated with disease by SARS-CoV-2 variant and evaluate if there are differences in disease severity by circulating variant. We retrospectively included all individuals 0-25 years of age who presented to our center and had a positive SARS-CoV-2 RT-PCR, SARS-CoV-2 variant mutation testing, and documented clinical notes from 1 January 2021 through 31 December 2021. We identified 745 individuals who met inclusion criteria and found the delta variant was associated with severe/critical disease compared to the other variants studied. The results of the model showed that underlying respiratory disease and diabetes were risk factors for progression to severe disease. These insights are important when evaluating public health measures and treatment options for children as more variants arise.

Indexed as

COVID-19pediatricsSARS-CoV-2SARS-COV-2 variantsseverityvariants

Identifiers

PMID35677819
PMCPMC9168367
OpenAlexW4281288581

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.