Kinetics and dynamics of ionized calcium in a porcine major trauma model

BACKGROUND: Disturbances in ionized calcium (iCa²⁺) are common after major trauma and correlate parabolically with coagulopathy, transfusion, and mortality. However, the mechanisms underlying iCa²⁺ changes during trauma and resuscitation remain poorly understood. This exploratory study aimed to develop an experimental animal model to characterize the dynamics and kinetics of iCa²⁺ during trauma and resuscitation. METHODS: A controlled porcine polytrauma model (PT, n=6)-including thoracic, abdominal, musculoskeletal trauma, controlled hemorrhage, and ischemia-reperfusion-was compared with nontrauma controls (C, n=4). Continuous hemodynamic monitoring and serial blood sampling during trauma, hemorrhage, ischemia-reperfusion, damage control resuscitation (DCR), transfusion, and observation enabled analysis of iCa²⁺ in relation to hemodynamic and acid-base status, ion interactions, and endocrine parameters. RESULTS: Two animals in the polytrauma group died during the experiment and were excluded from analysis. Baseline iCa²⁺ levels were comparable between groups (C: 1.38 [95% CI: 1.36-1.41] vs. PT: 1.42 [95% CI: 1.35-1.49] mmol/L, p =0.211) and remained stable in controls. In the polytrauma group, iCa²⁺ initially increased with early respiratory acidosis following thoracic trauma, then progressively decreased during hemorrhagic shock and ischemia-reperfusion. A further rapid decrease followed transfusion of citrated autologous whole blood ( p <0.001). Phosphate, lactate, and magnesium increased during shock, while bicarbonate and albumin decreased. Parathyroid hormone peaked, whereas calcitonin and 25-hydroxy-Vit D reached their lowest levels at the nadir of hypocalcemia. iCa²⁺ recovered during DCR, returning to baseline by the end of observation ( t =240 min, 1.39 [1.30-1.47] mmol/L, p =0.593). CONCLUSIONS: iCa²⁺ changes dynamically during trauma and resuscitation, in parallel with alterations in acid-base status, circulating ions, transfusion, and endocrine responses. iCa²⁺ can spontaneously recover to baseline with adequate resuscitation without calcium supplementation. This exploratory study can contribute to the development of a robust experimental model for future translational research. ( J Trauma Acute Care Surg . 2026;00:00-00. Copyright © 2026 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Surgery of Trauma.).

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Journal
The Journal of Trauma: Injury, Infection, and Critical Care
Published
2026-04-06
DOI
https://doi.org/10.1097/ta.0000000000004997
Primary Topic
Trauma, Hemostasis, Coagulopathy, Resuscitation
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article
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article

Kinetics and dynamics of ionized calcium in a porcine major trauma model

Dries Helsloot, Dieter Van Beersel, Arne Neyrinck, Simon F. De Meyer et al.
The Journal of Trauma: Injury, Infection, and Critical Care
Trauma, Hemostasis, Coagulopathy, Resuscitation
article

Kinetics and dynamics of ionized calcium in a porcine major trauma model

Dries Helsloot, Dieter Van Beersel, Arne Neyrinck, Simon F. De Meyer, Carlo Missant, Hans Pottel, Belgium Epidemiological Virology. Leuven, Deniz D. Özman, Mark Fitzgerald, Chris Groombridge, Joseph K. Mathew
article en

Abstract

BACKGROUND: Disturbances in ionized calcium (iCa²⁺) are common after major trauma and correlate parabolically with coagulopathy, transfusion, and mortality. However, the mechanisms underlying iCa²⁺ changes during trauma and resuscitation remain poorly understood. This exploratory study aimed to develop an experimental animal model to characterize the dynamics and kinetics of iCa²⁺ during trauma and resuscitation. METHODS: A controlled porcine polytrauma model (PT, n=6)-including thoracic, abdominal, musculoskeletal trauma, controlled hemorrhage, and ischemia-reperfusion-was compared with nontrauma controls (C, n=4). Continuous hemodynamic monitoring and serial blood sampling during trauma, hemorrhage, ischemia-reperfusion, damage control resuscitation (DCR), transfusion, and observation enabled analysis of iCa²⁺ in relation to hemodynamic and acid-base status, ion interactions, and endocrine parameters. RESULTS: Two animals in the polytrauma group died during the experiment and were excluded from analysis. Baseline iCa²⁺ levels were comparable between groups (C: 1.38 [95% CI: 1.36-1.41] vs. PT: 1.42 [95% CI: 1.35-1.49] mmol/L, p =0.211) and remained stable in controls. In the polytrauma group, iCa²⁺ initially increased with early respiratory acidosis following thoracic trauma, then progressively decreased during hemorrhagic shock and ischemia-reperfusion. A further rapid decrease followed transfusion of citrated autologous whole blood ( p <0.001). Phosphate, lactate, and magnesium increased during shock, while bicarbonate and albumin decreased. Parathyroid hormone peaked, whereas calcitonin and 25-hydroxy-Vit D reached their lowest levels at the nadir of hypocalcemia. iCa²⁺ recovered during DCR, returning to baseline by the end of observation ( t =240 min, 1.39 [1.30-1.47] mmol/L, p =0.593). CONCLUSIONS: iCa²⁺ changes dynamically during trauma and resuscitation, in parallel with alterations in acid-base status, circulating ions, transfusion, and endocrine responses. iCa²⁺ can spontaneously recover to baseline with adequate resuscitation without calcium supplementation. This exploratory study can contribute to the development of a robust experimental model for future translational research. ( J Trauma Acute Care Surg . 2026;00:00-00. Copyright © 2026 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Surgery of Trauma.).

The Journal of Trauma: Injury, Infection, and Critical Care
KU Leuven (BE)
Good health and well-being
Openalex Percentile: Top 29%
Trauma, Hemostasis, Coagulopathy, Resuscitation
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