Evidence map›Paper›PMID 33991456›Full record

ArticlePhysiological reports2021

A novel swine model of the acute respiratory distress syndrome using clinically relevant injury exposures.

Mohamad H Tiba, Brendan M McCracken, Danielle C Leander, Carmen I Colmenero, Jean A Nemzek, Michael W Sjoding, Kristine E Konopka, Thomas L Flott, J Scott VanEpps, Rodney C Daniels and 3 more

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Mohamad H TibaDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6789-7532
Brendan M McCrackenDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Danielle C LeanderDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Carmen I ColmeneroDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Jean A NemzekMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
Michael W SjodingMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
Kristine E KonopkaMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
Thomas L FlottMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
J Scott VanEppsDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Rodney C DanielsMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
Kevin R WardDepartment of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Kathleen A StringerMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.
Robert P DicksonMichigan Center for Integrative Research in Critical Care, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6875-4277
University of Michigan · US

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Microfluidic Tissue Engineering of Small Airway InjuriesR01HL136141 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI GROTBERG, JAMES BERNARD, NEMZEK, JEAN A · 2017 to 2020
$2.9M
Translational Metabolomics in Critical CareR35GM136312 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KATHLEEN A STRINGER · 2020 to 2026
$2.8M
The role of the lung microbiome in oxygen-induced lung injuryR01HL144599 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DICKSON, ROBERT PICKETT · 2019 to 2023
$2.1M
Direct mechanisms of fibrocyte immunotherapy in sepsisR01GM112799 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NEMZEK, JEAN A · 2015 to 2018
$1.2M
L-Carnitine Pharmacometabolomics in Sepsis (CaPS)R01GM111400 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STRINGER, KATHLEEN A · 2016 to 2019
$1.2M
SCH: Leveraging Clinical Time Series to Learn Optimal Treatment of Acute Dyspnea R01LM013325 · NLM · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SJODING, MICHAEL WILLIAM, WIENS, JENNA · 2019 to 2022
$935k
Data-Driven Identification of the Acute Respiratory Distress SyndromeK01HL136687 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SJODING, MICHAEL WILLIAM · 2017 to 2021
$862k
Antimicrobial mechanisms of action zinc oxide nanoparticlesK08AI128006 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VANEPPS, J SCOTT · 2017 to 2020
$778k
NCATS NIH HHS UL1 TR002240NHLBI NIH HHS K01 HL136687NHLBI NIH HHS R01 HL136141NHLBI NIH HHS R01 HL144599NIAID NIH HHS K08 AI128006NIGMS NIH HHS R01 GM111400NIGMS NIH HHS R01 GM112799NIGMS NIH HHS R35 GM136312NIH HHS K01HL136687NIH HHS K08AI128006NIH HHS K23HL13064NIH HHS R01GM111400NIH HHS R01GM112799NIH HHS R01HL136141NIH HHS R01HL144599NIH HHS R01LM013325NIH HHS R35GM136312NIH HHS UL1TR002240NLM NIH HHS R01 LM013325
6 · The paper itself

Abstract

To date, existing animal models of the acute respiratory distress syndrome (ARDS) have failed to translate preclinical discoveries into effective pharmacotherapy or diagnostic biomarkers. To address this translational gap, we developed a high-fidelity swine model of ARDS utilizing clinically relevant lung injury exposures. Fourteen male swine were anesthetized, mechanically ventilated, and surgically instrumented for hemodynamic monitoring, blood, and tissue sampling. Animals were allocated to one of three groups: (1) Indirect lung injury only: animals were inoculated by direct injection of Escherichia coli into the kidney parenchyma, provoking systemic inflammation and distributive shock physiology; (2) Direct lung injury only: animals received volutrauma, hyperoxia, and bronchoscope-delivered gastric particles; (3) Combined indirect and direct lung injury: animals were administered both above-described indirect and direct lung injury exposures. Animals were monitored for up to 12 h, with serial collection of physiologic data, blood samples, and radiographic imaging. Lung tissue was acquired postmortem for pathological examination. In contrast to indirect lung injury only and direct lung injury only groups, animals in the combined indirect and direct lung injury group exhibited all of the physiological, radiographic, and histopathologic hallmarks of human ARDS: impaired gas exchange (mean PaO

Indexed as

Disease Models, AnimalAnimalsEscherichia coliLungMalePulmonary Gas ExchangeRespiratory Distress SyndromeSwineacute lung injuryacute respiratory distress syndromecritical carediffuse alveolar damagedirect lung injuryindirect lung injuryporcine modelssepsisseptic shock

Identifiers

PMID33991456
PMCPMC8123544
OpenAlexW3160415356

What OpenQuestion holds

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Registered trials

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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.