Evidence map›Paper›PMID 35079694›Full record

ArticleSN comprehensive clinical medicine2022

Efficacy of Combination Therapy with the JAK Inhibitor Baricitinib in the Treatment of COVID-19.

Brendan L Thoms, Jeanne Gosselin, Bonita Libman, Benjamin Littenberg, Ralph C Budd

Open access · hybridAbstract read
In one paragraph

Article in SN comprehensive clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The JAK-STAT Signaling Pathway in Epilepsy.Current neuropharmacology · 2023
    Review
  5. Review
  6. Understanding COVID-19-associated coagulopathy.Nature reviews. Immunology · 2022
    Review
  7. COVID-19: Some unresolved issues.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2022
    Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Brendan L ThomsDivision of Rheumatology and Clinical Immunology, Department of Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Burlington, VT 05401 USA.
Jeanne GosselinDivision of Rheumatology and Clinical Immunology, Department of Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Burlington, VT 05401 USA.
Bonita LibmanRheumatology and Clinical Immunology Division, Department of Medicine, The Larner College of Medicine at the University of Vermont, Burlington, VT 05405 USA.
Benjamin LittenbergDivision of General Internal Medicine Research, Department of Medicine, The University of Vermont Larner College of Medicine, Burlington, VT 05405 USA.
Ralph C BuddRheumatology and Clinical Immunology Division, Department of Medicine, The Larner College of Medicine at the University of Vermont, Burlington, VT 05405 USA.
University of Vermont · USUniversity of Vermont Medical Center · US

Funding

Vermont Immunology/Infectious Diseases CenterP30GM118228 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2016 to 2021
$6.8M
NIGMS NIH HHS P30 GM118228
6 · The paper itself

Abstract

Coronavirus disease-19 (COVID-19), resulting from infection with SARS-CoV-2, spans a wide spectrum of illness. In severely ill patients, highly elevated serum levels of certain cytokines and considerable cytolytic T cell infiltrates in the lungs have been observed. These same patients may bear low to negligible viral burdens suggesting that an overactive immune response, often termed cytokine storm, contributes to the severity of COVID-19. We report the safety and efficacy of baricitinib combined with remdesivir and dexamethasone in a retrospective review of 45 hospitalized patients with COVID-19 pneumonia at a tertiary academic medical center. Patients received 7-day course of baricitinib, 5-day course of remdesivir, and 10-day course of dexamethasone. Clinical status and biomarkers were obtained daily. Outcomes assessed include mortality, duration of hospitalization, presence of shock, need for supplemental oxygen, need for non-invasive ventilation, need for mechanical ventilation, and development of thrombosis. Obesity and multiple medical comorbidities were associated with hospitalization in the setting of COVID-19. Treated patients demonstrated rapid declines of C-reactive protein (CRP), ferritin and D-dimer with gradual improvement in hemoglobin, platelet counts, and clinical status. Only 2 of 45 (4.4%) treated patients required mechanical ventilation after initiating treatment, and there were six deaths (13.3%). Only 2 of 45 (4.4%) treated patients required mechanical ventilation after initiating treatment. There were six deaths (13.3%) and these were associated with lower BMI. These findings support the utility of immunosuppression via JAK inhibition in moderate to severe COVID-19 pneumonia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42399-022-01121-4.

Indexed as

BaricitinibCoronavirus disease-19 (COVID-19)Critical careCytokine stormJAK inhibitor

Identifiers

PMID35079694
PMCPMC8776555
OpenAlexW4226111233

What Socratic holds

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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.