Evidence map›Paper›PMID 41952331›Full record

ArticleWorld journal of surgery2026

Is the COBRA-OS 4 French Aortic Occlusion Device Feasible for Partial REBOA?

Adam Power, Asha Parekh, Samuel Jessula, Joao Rezende-Neto, Laura J Moore

Abstract read
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Article in World journal of surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Adam PowerDepartment of Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.ORCID https://orcid.org/0009-0004-8311-1837
Asha ParekhSchool of Biomedical Engineering, Western University, London, Ontario, Canada.
Samuel JessulaDepartment of Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.
Joao Rezende-NetoTrauma and Acute Care General Surgery, Department of Surgery, St. Michael's Hospital, Toronto, Ontario, Canada.
Laura J MooreDepartment of Surgery, The University of Texas McGovern Medical School, Houston, Texas, USA.

Funding

Front Line Medical Technologies Inc
6 · The paper itself

Abstract

backgroundNoncompressible torso hemorrhage is a leading cause of preventable death. Resuscitative endovascular balloon occlusion of the aorta (REBOA) is used to control hemorrhage but full aortic occlusion is limited by distal ischemia. Partial REBOA (pREBOA) allows some distal perfusion to prolong occlusion, but precise balloon titration is difficult with standard devices. The COBRA-OS 4 French (Fr) aortic occlusion catheter was evaluated in vitro and in vivo for partial REBOA.

methodsBench-top (in vitro) and porcine (in vivo) models were used. The titration window of the device was evaluated in a non-hemorrhage porcine model and in a pulsatile aortic model. The ability of the device to maintain a targeted distal aortic pressure (20 mmHg) for an extended period (3 h) was tested in a porcine model of hemorrhagic shock (40% blood volume), with a corresponding in vitro experiment using a pulsatile aortic model.

resultsThe COBRA-OS demonstrated a 3-4 mL linear titration window with 1-1.5 mL deflation volume to reach a target distal aortic pressure of 20 mm Hg in vitro and in vivo. During 3 h of prolonged partial REBOA, the device maintained a stable distal target with a set-and-forget strategy (21 +/- 2 mmHg in vitro and 22 +/-7 mmHg in vivo).

conclusionsThe COBRA-OS 4 Fr device enabled precise, stable partial aortic occlusion in this preclinical model. This is the first demonstration of a 4 Fr REBOA catheter achieving prolonged, controlled partial occlusion in a large-animal hemorrhagic shock model, supporting the feasibility of this device for pREBOA. LEVEL OF EVIDENCE: Basic Science, Animal study.

Indexed as

AortaBalloon OcclusionEndovascular ProceduresHemorrhageResuscitationShock, HemorrhagicAnimalsDisease Models, AnimalEquipment DesignFeasibility StudiesSwineaortic occlusionhemorrhagic shockpartial REBOAREBOAtrauma resuscitation

Identifiers

PMID41952331
PMCPMC13206285

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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.