Evidence map›Paper›PMID 38193076›Full record

ArticleFrontiers in immunology2023

Utilizing predictive machine-learning modelling unveils feature-based risk assessment system for hyperinflammatory patterns and infectious outcomes in polytrauma.

Melanie Fachet, Raghava Vinaykanth Mushunuri, Christian B Bergmann, Ingo Marzi, Christoph Hoeschen, Borna Relja

Abstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Patterns of sex-specific outcomes and mortality in polytrauma: a demographic and epidemiologic analysis by injury severity score.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2025
    Observational
  3. Article
  4. Article
  5. Article
  6. Observational
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.

Melanie FachetInstitute for Medical Technology, Medical Systems Technology, Faculty of Electrical Engineering and Information Technology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
Raghava Vinaykanth MushunuriInstitute for Medical Technology, Medical Systems Technology, Faculty of Electrical Engineering and Information Technology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
Christian B BergmannTranslational and Experimental Trauma Research, Department of Trauma, Hand, Plastic and Reconstructive Surgery, Ulm University Medical Center, University Ulm, Ulm, Germany.
Ingo MarziDepartment of Trauma, Hand and Reconstructive Surgery, Medical Faculty, Goethe University Frankfurt, Frankfurt, Germany.
Christoph HoeschenInstitute for Medical Technology, Medical Systems Technology, Faculty of Electrical Engineering and Information Technology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
Borna ReljaTranslational and Experimental Trauma Research, Department of Trauma, Hand, Plastic and Reconstructive Surgery, Ulm University Medical Center, University Ulm, Ulm, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Earlier research has identified several potentially predictive features including biomarkers associated with trauma, which can be used to assess the risk for harmful outcomes of polytraumatized patients. These features encompass various aspects such as the nature and severity of the injury, accompanying health conditions, immune and inflammatory markers, and blood parameters linked to organ functioning, however their applicability is limited. Numerous indicators relevant to the patients` outcome are routinely gathered in the intensive care unit (ICU) and recorded in electronic medical records, rendering them suitable predictors for risk assessment of polytraumatized patients. Methods: 317 polytraumatized patients were included, and the influence of 29 clinical and biological features on the complication patterns for systemic inflammatory response syndrome (SIRS), pneumonia and sepsis were analyzed with a machine learning workflow including clustering, classification and explainability using SHapley Additive exPlanations (SHAP) values. The predictive ability of the analyzed features within three days after admission to the hospital were compared based on patient-specific outcomes using receiver-operating characteristics. Results: A correlation and clustering analysis revealed that distinct patterns of injury and biomarker patterns were observed for the major complication classes. A k-means clustering suggested four different clusters based on the major complications SIRS, pneumonia and sepsis as well as a patient subgroup that developed no complications. For classification of the outcome groups with no complications, pneumonia and sepsis based on boosting ensemble classification, 90% were correctly classified as low-risk group (no complications). For the high-risk groups associated with development of pneumonia and sepsis, 80% of the patients were correctly identified. The explainability analysis with SHAP values identified the top-ranking features that had the largest impact on the development of adverse outcome patterns. For both investigated risk scenarios (infectious complications and long ICU stay) the most important features are SOFA score, Glasgow Coma Scale, lactate, GGT and hemoglobin blood concentration. Conclusion: The machine learning-based identification of prognostic feature patterns in patients with traumatic injuries may improve tailoring personalized treatment modalities to mitigate the adverse outcomes in high-risk patient clusters.

Indexed as

Communicable DiseasesMultiple TraumaPneumoniaSepsisHumansLactic AcidMachine LearningRisk AssessmentSystemic Inflammatory Response SyndromeLactic Acidbiomarkerbloodclassificationclinical decision makingexplainabilityrisk assessmentSHAP values

Identifiers

PMID38193076
PMCPMC10773821

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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.