HMGB-1 as a predictor of major bleeding requiring activation of a massive transfusion protocol in severe trauma
Language English Country Great Britain, England Media electronic
Document type Journal Article
Grant support
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
(FNOs/2019)
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
39920329
PubMed Central
PMC11806012
DOI
10.1038/s41598-025-89139-1
PII: 10.1038/s41598-025-89139-1
Knihovny.cz E-resources
- Keywords
- Bleeding, HMGB-1, Major trauma, Massive transfusion protocol,
- MeSH
- Biomarkers blood MeSH
- Adult MeSH
- Blood Transfusion * methods MeSH
- Hemorrhage * blood therapy etiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Prospective Studies MeSH
- HMGB1 Protein * blood MeSH
- Wounds and Injuries * blood therapy complications MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Injury Severity Score MeSH
- Emergency Service, Hospital MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- HMGB1 protein, human MeSH Browser
- HMGB1 Protein * MeSH
Massive bleeding causes approximately 50% of deaths in patients with major trauma. Most patients die within 6 h of injury, which is preventable in at least 10% of cases. For these patients, early activation of the massive transfusion protocol (MTP) is a critical survival factor. With severe trauma, high-mobility group box 1 (HMGB-1, i.e., amphoterin) is released into the blood, and its levels correlate with the development of a systemic inflammatory response, traumatic coagulopathy, and fibrinolysis. Previous work has shown that higher levels of HMGB-1 are associated with a higher use of red blood cell transfusions. We conducted a retrospective analysis of previous prospective single-center study to assess the value of admission HMGB-1 levels in predicting activation of MTP in the emergency department. From July 11, 2019, to April 23, 2022, a total of 104 consecutive adult patients with severe trauma (injury severity score > 16) were enrolled. A blood sample was taken at admission, and HMGB-1 was measured. MTP activation in the emergency department was recorded in the study documentation. The total amount of blood products and fibrinogen administered to patients within 6 h of admission was monitored. Among those patients with massive bleeding requiring MTP activation, we found significantly higher levels of HMGB-1 compared to patients without MTP activation (median [interquartile range]: 84.3 µg/L [34.2-145.9] vs. 21.1 µg/L [15.7-30.4]; p < 0.001). HMGB-1 level showed good performance in predicting MTP activation, with an area under the receiver operating characteristic curve of 0.84 (95% CI 0.75-0.93) and a cut-off value of 30.55 µg/L. HMGB-1 levels correlated significantly with the number of red blood cell units (rs [95% CI] 0.46 [0.28-0.61]; p < 0.001), units of fresh frozen plasma (rs 0.46 [0.27-0.61]; p < 0.001), platelets (rs 0.48 [0.30-0.62]; p < 0.001), and fibrinogen (rs 0.48 [0.32-0.62]; p < 0.001) administered in the first 6 h after hospital admission. Admission HMGB-1 levels reliably predict severe bleeding requiring MTP activation in the emergency department and correlate with the amount of blood products and fibrinogen administered during the first 6 h of hemorrhagic shock resuscitation.Trial registration: NCT03986736. Registration date: June 4, 2019.
Department of Science and Research Faculty of Medicine University of Ostrava Ostrava Czech Republic
Institute of Laboratory Diagnostics University Hospital Ostrava Ostrava Czech Republic
See more in PubMed
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ClinicalTrials.gov
NCT03986736