Evidence map›Paper›PMID 40880351›Full record

ArticlePloS one2025

User experience and hemostatic efficacy: Comparative analysis of commercial agents in junctional and hepatic hemorrhage models.

Kyle Patterson, Adelle M Dagher, Meredith Lackie, Lauren M Heyda, Zain Baig, John Mares, Justin Hutzler, J T Green, Woo Do, Jason S Radowsky and 4 more

Abstract readComparative Study
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.

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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

14 authors.

Kyle PattersonBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.ORCID https://orcid.org/0009-0005-6644-5787
Adelle M DagherBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Meredith LackieBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Lauren M HeydaBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Zain BaigBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
John MaresBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Justin HutzlerBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
J T GreenBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.ORCID https://orcid.org/0000-0001-5947-9464
Woo DoBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Jason S RadowskyBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Matthew BradleyBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Brandon PropperBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
David M BurmeisterBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Patrick WalkerBattlefield Shock and Organ Support Laboratory, The Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.ORCID https://orcid.org/0000-0002-0871-2702

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesHemorrhage is associated with most preventable combat-related deaths. Management of non-compressible truncal and junctional hemorrhage remains challenging, especially with prolonged evacuations. This study evaluated the efficacy of commercial topical hemostatic agents in uncontrolled hemorrhage models under coagulopathic conditions, examining differences based on applicator experience.

methodsSixty Yorkshire swine were randomized to 5 groups: Combat Gauze (CG), Celox Rapid (CR), ChitoSAM 100 (CS), EVARREST® Fibrin Sealant Patch (EP), and X-Stat 30 (XS). After 50% hemodilution, a 5 mm femoral arteriotomy or 6 cm liver laceration was created, and the agents were applied as per device instructions. Hemostatic agents were placed by experienced (≥5 previous applications) or non-experienced (<5 previous applications) users. Animals were then monitored for rebleeding for 60 minutes.

resultsIn the junctional hemorrhage model, only ChitoSAM required more applications by novice applicators (2.3 vs. 1, p = 0.0104). No significant differences in rebleed rates among devices (CG 0%, CS 33%, CR 17%, EP 17%, XS 33%, p = 0.73) or by user experience were observed. No differences in perfusion were noted on angiography. In the hepatic laceration model, no significant differences in applications or rebleed rates for any agent (CG 0%, CS 50%, CR 17%, EP 17%, XS 0%, p = 0.21) or by user experience were found. Overall survival did not significantly vary by device.

conclusionAll 5 hemostatic agents showed similar efficacy in controlling junctional and intra-abdominal hemorrhage, with no significant differences in hemostasis, rebleed rate, or survival by experience level. However, more ChitoSAM applications were needed for junctional hemorrhage control in the absence of experience. All tested dressings show promise for rapid hemorrhage control.

Indexed as

HemorrhageHemostaticsLiverAnimalsBandagesDisease Models, AnimalSwineHemostatics

Identifiers

PMID40880351
PMCPMC12396726

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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.