Evidence map›Paper›PMID 33050737›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2021

Hyperoxia and modulation of pulmonary vascular and immune responses in COVID-19.

Dusan Hanidziar, Simon C Robson

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  7. Review
  8. Anticoagulation during extracorporeal membrane oxygenation.The Cochrane database of systematic reviews · 2024
    Article
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  15. CD73: Friend or Foe in Lung Injury.International journal of molecular sciences · 2023
    Review
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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

2 authors at 2 institutions in 1 country.

Dusan HanidziarDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.ORCID 0000-0001-6769-1908
Simon C RobsonDepartment of Anesthesia, Critical Care and Pain Medicine, Center for Inflammation Research, Beth Israel Deaconess Medical Center, Boston, Massachusetts.ORCID 0000-0001-6374-0194
Beth Israel Deaconess Medical Center · USMassachusetts General Hospital · US

Funding

Purinergic Modulation of NKT Cells Ameliorates Hyperoxic Lung InjuryK08HL141694 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HANIDZIAR, DUSAN · 2019 to 2023
$864k
HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI)NHLBI NIH HHS K08 HL141694U.S. Department of Defense (DOD)
6 · The paper itself

Abstract

Oxygen is the most commonly used therapy in hospitalized patients with COVID-19. In those patients who develop worsening pneumonia and acute respiratory distress syndrome (ARDS), high concentrations of oxygen may need to be administered for prolonged time periods, often together with mechanical ventilation. Hyperoxia, although lifesaving and essential for maintaining adequate oxygenation in the short term, may have adverse long-term consequences upon lung parenchymal structure and function. How hyperoxia per se impacts lung disease in COVID-19 has remained largely unexplored. Numbers of experimental studies have previously established that hyperoxia is associated with deleterious outcomes inclusive of perturbations in immunologic responses, abnormal metabolic function, and alterations in hemodynamics and alveolar barrier function. Such changes may ultimately progress into clinically evident lung injury and adverse remodeling and result in parenchymal fibrosis when exposure is prolonged. Given that significant exposure to hyperoxia in patients with severe COVID-19 may be unavoidable to preserve life, these sequelae of hyperoxia, superimposed on the cytopathic effects of SARS-CoV-2 virus, may well impact pathogenesis of COVID-19-induced ARDS.

Indexed as

COVID-19HemodynamicsHumansImmunityLungOxygenRespiration, ArtificialRespiratory Distress SyndromeSARS-CoV-2OxygenCOVID-19hyperoxialung injurymicrocirculation

Identifiers

PMID33050737
PMCPMC7816427
OpenAlexW3092361660

What OpenQuestion holds

Textmetadata
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.