Evidence map›Paper›PMID 34745093›Full record

Trial reportFrontiers in immunology2021

Non-Randomized Trial of Dornase Alfa for Acute Respiratory Distress Syndrome Secondary to Covid-19.

Zachary M Holliday, Alexander P Earhart, Mohammed M Alnijoumi, Armin Krvavac, Lee-Ann H Allen, Adam G Schrum

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04402970 (Inhaled Dornase Alfa for Treatment of ARDS in Patients With SARS-CoV-2), which is not on this map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.1field-weighted citation impact, top 3% 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.

NCT04402970 phase3completednot on this map

Inhaled Dornase Alfa for Treatment of ARDS in Patients With SARS-CoV-2

TypeinterventionalSponsorUniversity of Missouri-ColumbiaRan2020 to 2020Enrolled30ConditionsSARS-CoV 2, ARDSArmsDornase Alfa Inhalation Solution
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
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  4. Review
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  6. Review
  7. Training the Lung, Taming the NETs.Frontiers in cellular and infection microbiology · 2026
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Neutrophil diversity and function in health and disease.Signal transduction and targeted therapy · 2024
    Review
  15. Review
  16. Neutrophil extracellular traps in homeostasis and disease.Signal transduction and targeted therapy · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. Review
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 at 1 institution in 1 country.

Zachary M HollidayDepartment of Medicine, University of Missouri, Columbia, MO, United States.
Alexander P EarhartMolecular Pathogenesis and Therapeutics Program, University of Missouri, Columbia, MO, United States.
Mohammed M AlnijoumiDepartment of Medicine, University of Missouri, Columbia, MO, United States.
Armin KrvavacDepartment of Medicine, University of Missouri, Columbia, MO, United States.
Lee-Ann H AllenDepartment of Molecular Microbiology and Immunology, University of Missouri, Columbia, MO, United States.
Adam G SchrumDepartment of Molecular Microbiology and Immunology, University of Missouri, Columbia, MO, United States.
University of Missouri · US

Funding

Measuring multiprotein assemblies that drive biological signalsR01GM103841 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI SCHRUM, ADAM G. · 2013 to 2023
$3.3M
NIGMS NIH HHS R01 GM103841
6 · The paper itself

Abstract

Background: The most severe cases of Coronavirus-Disease-2019 (COVID-19) develop into Acute Respiratory Distress Syndrome (ARDS). It has been proposed that oxygenation may be inhibited by extracellular deoxyribonucleic acid (DNA) in the form of neutrophil extracellular traps (NETs). Dornase alfa (Pulmozyme, Genentech) is recombinant human deoxyribonuclease I that acts as a mucolytic by cleaving and degrading extracellular DNA. We performed a pilot study to evaluate the effects of dornase alfa in patients with ARDS secondary to COVID-19. Methods: We performed a pilot, non-randomized, case-controlled clinical trial of inhaled dornase for patients who developed ARDS secondary to COVID-19 pneumonia. Results: Improvement in arterial oxygen saturation to inhaled fraction of oxygen ratio (PaO Conclusion: Treatment with dornase alfa was associated with improved oxygenation and decreased DNA : MPO complexes in BALF. The positive effects, however, were limited to the time of drug delivery. These data suggest that degradation of extracellular DNA associated with NETs or other structures by inhaled dornase alfa can be beneficial. We propose a more extensive clinical trial is warranted. Clinical Trial Registration: ClinicalTrials.gov, Identifier: NCT04402970.

Indexed as

COVID-19 Drug TreatmentAdministration, InhalationAdultAgedAged, 80 and overCase-Control StudiesDeoxyribonuclease IDNAExtracellular TrapsFemaleHumansMaleMiddle AgedOxygen ConsumptionPeroxidasePilot ProjectsDeoxyribonuclease IDNAdornase alfaPeroxidaseRecombinant ProteinsARDSCOVID - 19pneumoniarespiratory failureviral

Identifiers

PMID34745093
PMCPMC8564175
OpenAlexW3207022961

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.