Evidence map›Paper›PMID 41452892›Full record

ArticlePloS one2025

Drivers of prognosis and clinical trajectories differ between COVID and non-COVID acute hypoxic respiratory failure.

Shaun Pienkos, Andrew R Moore, Jonasel Roque, Alexandria Jensen, Ana Pacheco-Navarro, Katherine M Lebold, Caitlin Parmer-Chow, Pablo A Sanchez, Haley Morin, Christian O'Donnell and 5 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Shaun PienkosPulmonary and Critical Care Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0009-0001-8409-4803
Andrew R MoorePulmonary and Critical Care Medicine, Stanford University, Stanford, California, United States of America.
Jonasel RoqueStanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0001-7818-6958
Alexandria JensenStanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0001-6337-9079
Ana Pacheco-NavarroPulmonary and Critical Care Medicine, Stanford University, Stanford, California, United States of America.
Katherine M LeboldDivision of Pulmonary, Allergy and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon, United States of America.
Caitlin Parmer-ChowDivision of Hospital Medicine, Stanford University, Stanford, California, United States of America.
Pablo A SanchezCritical Care Medicine, Stanford, California, United States of America.
Haley MorinStanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0003-1967-7890
Christian O'DonnellCritical Care Medicine, Stanford, California, United States of America.
Tara RamaswamyCritical Care Medicine, Stanford, California, United States of America.
William CollinsDivision of Hospital Medicine, Stanford University, Stanford, California, United States of America.
Jennifer G WilsonCritical Care Medicine, Stanford, California, United States of America.
Angela J RogersPulmonary and Critical Care Medicine, Stanford University, Stanford, California, United States of America.
Joseph E LevittPulmonary and Critical Care Medicine, Stanford University, Stanford, California, United States of America.

Funding

Stanford Training Program in Lung BiologyT32HL129970 · NHLBI · STANFORD UNIVERSITY · PI CORNFIELD, DAVID N., NICOLLS, MARK ROBERT · 2016 to 2025
$3.2M
Metabolic derangements in ARDSK23HL125663 · NHLBI · STANFORD UNIVERSITY · PI ROGERS, ANGELA J · 2015 to 2018
$744k
NHLBI NIH HHS K23 HL125663NHLBI NIH HHS T32 HL129970
6 · The paper itself

Abstract

purposeExamine non-respiratory comorbidities that may affect prognosis in acute hypoxic respiratory failure (AHRF) and respiratory trajectories, comparing those with COVID and non-COVID etiologies of AHRF.

methodsThis is a retrospective cohort study of patients with AHRF from COVID and non-COVID etiologies treated with high flow oxygen, noninvasive ventilation, or endotracheal intubation in ICUs in two United States hospitals.

resultsWe compared drivers of prognosis and respiratory trajectories between 241 patients with AHRF from COVID and 99 patients with non-COVID AHRF. Patients with COVID had a lower prevalence of major comorbidities or terminal illness (OR 0.14), neurologic disease (OR 0.19), goals of care limitations (OR 0.54), and shock (OR 0.11). A lower proportion of the COVID group were managed with invasive mechanical ventilation (IMV) early in their AHRF course (OR 0.15); however, fewer COVID patients had improvement in AHRF in the first 7 days (OR 0.49), and a greater proportion of COVID patients required IMV on day 14 (OR 2.57). Additionally, fewer COVID patients died or transitioned to comfort care within 14 days following AHRF onset (OR 0.24), and more COVID patients had severe hypoxemia at end-of-life (OR 2.42).

conclusionsPatients with AHRF from COVID had fewer non-respiratory comorbidities or goals of care limitations, more prolonged respiratory failure and higher risk of mortality related to hypoxemia. These differences could explain why patients with COVID AHRF may experience greater benefit from disease-specific therapies targeting AHRF compared to patients with non-COVID AHRF.

Indexed as

COVID-19HypoxiaRespiratory InsufficiencyAgedComorbidityFemaleHumansIntensive Care UnitsMaleMiddle AgedPrognosisRespiration, ArtificialRetrospective StudiesSARS-CoV-2

Identifiers

PMID41452892
PMCPMC12742738

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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.