Evidence map›Paper›PMID 42859300›Full record

ArticleIntensive care medicine experimental2026

The impact of ventilation mode on systemic inflammation and organ dysfunction in a porcine model of abdominal sepsis-associated acute respiratory distress syndrome.

James G Williams, Michaela Kollisch-Singule, Nirmeen Elmadany, Nader M Habashi, Gary F Nieman, Brian M Varisco

Abstract read
In one paragraph

Article in Intensive care medicine experimental, 2026. 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

6 authors.

James G Williams *Division of Critical Care Medicine and Department of Pediatrics, University of Arkansas for Medical Sciences, 13 Children's Way, Slot 512-36, Little Rock, 72205, AR, USA. Jwilliams4@uams.edu.ORCID http://orcid.org/0000-0002-3790-8413
Michaela Kollisch-Singule *Department of Pediatric Surgery, University of Arkansas for Medical Sciences, Little Rock, 72205, AR, USA.
Nirmeen ElmadanyDivision of Critical Care Medicine and Department of Pediatrics, University of Arkansas for Medical Sciences, 13 Children's Way, Slot 512-36, Little Rock, 72205, AR, USA.
Nader M HabashiAdams Cowley Shock Trauma Center, University of Maryland Medical Center, Baltimore, 21201, MD, USA.
Gary F NiemanDepartment of Surgery, SUNY Upstate Medical University, Syracuse, 13210, NY, USA.
Brian M VariscoDivision of Critical Care Medicine and Department of Pediatrics, University of Arkansas for Medical Sciences, 13 Children's Way, Slot 512-36, Little Rock, 72205, AR, USA.

Funding

Supplement for Google cloud build-outR24GM137786 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Alan Tackett · 2020 to 2026
$15.4M
Expanding Translational Science in ArkansasUM1TR004909 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI Laura P James · 2024 to 2026
$11.7M
Electroporation-mediated Pulmonary Gene Transfer for Acute Lung InjuryR21HL092801 · NHLBI · UNIVERSITY OF ROCHESTER · PI DEAN, DAVID A · 2008 to 2012
$2.9M
CTSA K12 Program at the University of Arkansas for Medical SciencesK12TR004924 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI Jason Eli Farrar, Joshua Kennedy · 2024 to 2026
$2.3M
Mathematical Modeling of Inflammation in ARDSR33HL089076 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI NIEMAN, GARY F · 2008 to 2010
$1.4M
NCATS NIH HHS 1K12TR004924NCATS NIH HHS K12 TR004924NCATS NIH HHS UM1 TR004909NCATS NIH HHS UM1TR004909NHLBI NIH HHS R21 HL092801NHLBI NIH HHS R21HL092801NHLBI NIH HHS R33 HL089076NHLBI NIH HHS R33HL089076NIGMS NIH HHS R24 GM137786
6 · The paper itself

Abstract

introductionSepsis commonly causes acute respiratory distress syndrome (ARDS), and immune hyperactivation may be a causal link. Ventilator-induced lung injury (VILI) is common in ARDS, and VILI may potentiate organ dysfunction in severe sepsis. We used a porcine model of abdominal sepsis-associated ARDS to test whether ventilation strategy could impact systemic inflammation and organ dysfunction.

methodsFemale Yorkshire pigs (6-8 months) underwent ischemia-reperfusion (I/R) injury of the small bowel and fecal clot implantation or sham laparotomy. The abdominal sepsis animals were ventilated with a volume-controlled (VC) mode using the ARDS-Net low tidal volume (LVt) method to set and adjust the mode, and applied at two time points. Late LVt, was applied once PaO

resultsSham animals showed no evidence of sepsis or ARDS, whereas all experimental animals developed septic shock, requiring fluid resuscitation and vasopressors. Both LVt groups developed ARDS as measured by PaO

conclusionIn a porcine model of abdominal septic shock we found that animals ventilated with a higher mean airway pressure strategy (APRV) had decreased plasma proteomic signatures of inflammation compared to those ventilated with a conventional low tidal volume strategy. Our findings are hypothesis generating and not directly translatable to the clinical setting. Future studies should focus on further elucidating a link between VILI and its effect on systemic inflammation and organ dysfunction.

Indexed as

Acute respiratory distress syndrome (ARDS)Critical careProteomicsSepsisSystems biology

Identifiers

PMID42859300
PMCPMC13653911

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.