Evidence map›Paper›PMID 42228193›Full record

ArticleEuropean journal of trauma and emergency surgery : official publication of the European Trauma Society2026

Injury to the thorax is a dominant contributor to post-traumatic neutrophil mediated inflammatory response.

F J C van Eerten, L V Duebel, E J de Fraiture, M F Hanlo, E A Breuking, S R Brands, T D van den Bosch, K J P van Wessem, N Vrisekoop, L Koenderman and 1 more

Abstract read
In one paragraph

Article in European journal of trauma and emergency surgery : official publication of the European Trauma Society, 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

11 authors.

F J C van EertenDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands. F.J.C.vaneerten-3@umcutrecht.nl.
L V DuebelDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
E J de FraitureDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
M F HanloDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
E A BreukingDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
S R BrandsDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
T D van den BoschDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
K J P van WessemDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.
N VrisekoopDepartment of Respiratory Medicine and Center for Translational Immunology (CTI), University Medical Center Utrecht, Utrecht, The Netherlands.
L KoendermanDepartment of Respiratory Medicine and Center for Translational Immunology (CTI), University Medical Center Utrecht, Utrecht, The Netherlands.
F HietbrinkDepartment of Trauma Surgery, University Medical Center Utrecht, Utrecht, 3508 GA, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTraumatic injury induces a neutrophil associated inflammatory response mediated by the release of damage-associated molecular patterns (DAMPs). This response can be maladaptive, increasing risk of infection. Since blunt thoracic injuries are associated with high infection rates, we hypothesized that these injuries elicit a stronger neutrophil associated inflammatory response than injuries to other body regions.

methodsA cohort study was conducted in adult patients presenting at the trauma bay of a level 1 trauma center between March 2020 and November 2022. These patients underwent routine analysis of their neutrophil associated inflammatory response by phenotyping blood neutrophils using automated flow cytometry. Injury per body region was counted when the Abbreviated Injury Severity (AIS) scores were ≥3 to focus on substantial injuries. The primary outcome was an extensive post-traumatic inflammatory neutrophil response.

results861 patients were included. Blunt internal thoracic injuries showed the strongest association with severe neutrophil associated inflammation (OR 5.7), followed by abdominal (OR 2.6), pelvis (OR 2.5) and lower extremities (OR 2.3), even when corrected for ISS, age and hemodynamic instability. In multivariable analysis, only thoracic internal injuries remained a statistically significant contributor to excessive neutrophil associated inflammation (OR 5.4).

conclusionInjuries to internal thoracic organs elicit a more pronounced post-traumatic neutrophil associated inflammatory response than injuries of similar severity in other body regions. This might be due to greater release of DAMPs from the soft tissue of the lungs. Understanding the body region-specific activation of neutrophil associated inflammation may support more patient-tailored surgical strategies to lower the infection risk.

Indexed as

InflammationNeutrophilsThoracic InjuriesWounds, NonpenetratingAdultFemaleHumansInjury Severity ScoreMaleMiddle AgedInflammationInjuryNeutrophilThoraxTrauma

Identifiers

PMID42228193
PMCPMC13230304

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.