Evidence map›Paper›PMID 35392677›Full record

ArticleThe American surgeon2022

Unmasking the Confounder: The Inherent Physiologic Variability of Swine During an Automated Experimental Model of Ischemia-Reperfusion Injury.

Symonne C Martin, Nathaniel Hauser, Antonio C Renaldo, Magan Lane, James E Jordan, Hisham I Qadri, Nicholas Mouser, Elaheh Rahbar, Timothy K Williams, Lucas P Neff

Abstract read
In one paragraph

Article in The American surgeon, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Symonne C Martin12279Wake Forest School of Medicine, Winston-Salem, NC, USA.ORCID https://orcid.org/0000-0001-9123-1055
Nathaniel HauserDepartment of Biomedical Engineering, 12279Wake Forest School of Medicine, Winston-Salem, NC, USA.
Antonio C RenaldoDepartment of Biomedical Engineering, 12279Wake Forest School of Medicine, Winston-Salem, NC, USA.
Magan LaneDepartment of Vascular and Endovascular Surgery, 12280Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.ORCID https://orcid.org/0000-0003-2874-5787
James E JordanDepartment of Cardiothoracic Surgery, 12280Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.
Hisham I Qadri12279Wake Forest School of Medicine, Winston-Salem, NC, USA.ORCID https://orcid.org/0000-0002-5697-3421
Nicholas Mouser12279Wake Forest School of Medicine, Winston-Salem, NC, USA.
Elaheh RahbarDepartment of Biomedical Engineering, 12279Wake Forest School of Medicine, Winston-Salem, NC, USA.
Timothy K WilliamsDepartment of Vascular and Endovascular Surgery, 12280Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.
Lucas P NeffDepartment of General Surgery, 12280Atrium Health Wake Forest Baptist, Winston-Salem, NC, USA.

Funding

Development of a Multi-scale closed loop model for hemorrhagic shock: a platform to assess REBOA performanceR01HL162633 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Elaheh Rahbar · 2022 to 2026
$3.2M
NHLBI NIH HHS R01 HL162633
6 · The paper itself

Abstract

backgroundWe sought to determine the magnitude of the inherent inter-animal physiologic variability by automating a porcine Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) protocol to minimize external influences that might alter physiology and confound experimental results.

methodsSwine (n = 42) underwent a controlled 30% blood volume hemorrhage followed by 30 minutes of REBOA (ie, ischemic phase). The animals were weaned from REBOA autonomously over 15 minutes, beginning the reperfusion phase, while continuing to provide partial flow balloon support to maintain a target proximal mean arterial pressure (pMAP) of 65 mmHg. Simultaneously, shed blood was re-transfused as part of the resuscitation efforts. Physiologic data were continuously recorded, and serum samples were serially collected. Baseline characteristics, variance in vital signs, and 8-isoprostane levels were quantified during hemorrhage, REBOA, and reperfusion phases.

resultsThere was no significant difference in baseline physiology across animals ( DISCUSSION: Despite subjecting animals to a highly consistent ischemia-reperfusion injury through automation, we noted significant variability in the hemodynamic and biochemical response. These findings illustrate the inherent physiologic variability and potential limitations of porcine large animal models for the study of shock.

Indexed as

Balloon OcclusionEndovascular ProceduresReperfusion InjuryShock, HemorrhagicAnimalsDisease Models, AnimalHemorrhageResuscitationSwine8-isoprostanehemorrhageischemia-reperfusionphysiologic variabilityREBOAswine

Identifiers

PMID35392677
PMCPMC10320810

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.