Evidence map›Paper›PMID 39057766›Full record

ArticlePathogens (Basel, Switzerland)2024

Evaluation of Type I Interferon Treatment in Hospitalized COVID-19 Patients: A Retrospective Cohort Study.

Vivian Y Tat, Pinghan Huang, Kamil Khanipov, Nathan Y Tat, Chien-Te Kent Tseng, George Golovko

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Vivian Y TatDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Pinghan HuangDepartment of Microbiology & Immunology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
Kamil KhanipovDepartment of Pharmacology & Toxicology, The University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0002-3881-737X
Nathan Y TatTaking Our Best Shot, Galveston, TX 77555, USA.ORCID 0009-0008-7764-1427
Chien-Te Kent TsengDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555, USA.
George GolovkoDepartment of Pharmacology & Toxicology, The University of Texas Medical Branch, Galveston, TX 77555, USA.

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
West African Center for Emerging Infectious DiseasesU01AI151801 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Robert W Cross, Scott C Weaver · 2020 to 2026
$10.1M
NCATS NIH HHS UL1 TR001439NIAID NIH HHS U01 AI151801
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) continues to cause morbidity and mortality worldwide; therefore, effective treatments remain crucial to controlling it. As interferon-alpha (IFN-α) and -beta (β) have been proposed as COVID-19 treatments, we sought to assess their effectiveness on respiratory, cardiovascular, neurological, and psychiatric signs and symptoms, as well as PASC and death, in hospitalized COVID-19 patients without multiple sclerosis (MS). Using a federated data research network (TriNetX), we performed a retrospective cohort study of hospitalized COVID-19 patients without MS who received IFN-α or -β treatment, comparing them to a similar cohort who did not receive treatment. Following propensity-score matched analyses, we demonstrate that hospitalized COVID-19 patients who were treated with IFN-α or -β had significantly higher odds of death. In contrast, there was no significant difference in any other outcomes between 1-30 days or 1 day to anytime afterward. Overall, hospitalized COVID-19 patients without MS who were treated with IFN-α or -β had similar short- and long-term sequelae (except for mortality) as those who did not receive treatment. The potential benefits of utilizing IFN-α or -β treatment as therapeutics remain to be realized, and our research highlights the need to explore repurposing drugs for COVID-19 using real-world evidence.

Indexed as

Antiviral AgentsCOVID-19COVID-19 Drug TreatmentHospitalizationSARS-CoV-2AdultAgedFemaleHumansInterferon-alphaInterferon-betaInterferon Type IMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntiviral AgentsInterferon-alphaInterferon-betaInterferon Type ICOVID-19interferonssequelaetreatments

Identifiers

PMID39057766
PMCPMC11280121

What Socratic 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 Socratic graph.