The potential impact of coagulation factor XIII in trauma-induced coagulopathy – a retrospective case series analysis

Background The role of factor XIII (FXIII) in trauma-induced coagulopathy (TIC) is not fully understood. Methods We evaluated FXIII supplementation in severely injured patients with persistent bleeding. This was a retrospective case series analysis. Results Twenty-four patients received FXIII concen...

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Veröffentlicht in:European journal of trauma and emergency surgery (Munich : 2007) 2023-06, Vol.49 (3), p.1517-1523
Hauptverfasser: Wilhelmi, Michaela, Albrecht, Alexander, Macke, Christian, Wilhelmi, Mathias, Omar, Mohammed, Winkelmann, Marcel, Clausen, Jan-Dierk
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container_issue 3
container_start_page 1517
container_title European journal of trauma and emergency surgery (Munich : 2007)
container_volume 49
creator Wilhelmi, Michaela
Albrecht, Alexander
Macke, Christian
Wilhelmi, Mathias
Omar, Mohammed
Winkelmann, Marcel
Clausen, Jan-Dierk
description Background The role of factor XIII (FXIII) in trauma-induced coagulopathy (TIC) is not fully understood. Methods We evaluated FXIII supplementation in severely injured patients with persistent bleeding. This was a retrospective case series analysis. Results Twenty-four patients received FXIII concentrate within 24 h of admission for bleeding that continued after transfusion of > 6 U red blood cells (RBCs); control patients ( n  = 27) did not receive FXIII concentrate. Both study groups were similar regarding injury severity score and global coagulation tests, but FXIII activity levels were significantly higher and lactate levels significantly lower in the control group, respectively. The differences in FXIII activity between the groups could be attributed to a more severe trauma-induced coagulopathy in FXIII-deficient patients, as demonstrated by lower fibrinogen and higher lactate levels. The median dose of FXIII concentrate within 24 h of admission was 2500 IU (IQR: 1250–4375). Median 24-h transfusion of RBCs (primary study endpoint) was significantly higher in the FXIII group versus controls (10.0 U, IQR 5–14 U vs. 2, IQR 0–6 U; p  
doi_str_mv 10.1007/s00068-023-02221-z
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Methods We evaluated FXIII supplementation in severely injured patients with persistent bleeding. This was a retrospective case series analysis. Results Twenty-four patients received FXIII concentrate within 24 h of admission for bleeding that continued after transfusion of &gt; 6 U red blood cells (RBCs); control patients ( n  = 27) did not receive FXIII concentrate. Both study groups were similar regarding injury severity score and global coagulation tests, but FXIII activity levels were significantly higher and lactate levels significantly lower in the control group, respectively. The differences in FXIII activity between the groups could be attributed to a more severe trauma-induced coagulopathy in FXIII-deficient patients, as demonstrated by lower fibrinogen and higher lactate levels. The median dose of FXIII concentrate within 24 h of admission was 2500 IU (IQR: 1250–4375). Median 24-h transfusion of RBCs (primary study endpoint) was significantly higher in the FXIII group versus controls (10.0 U, IQR 5–14 U vs. 2, IQR 0–6 U; p  &lt; 0.01). Subsequently, while patients were in the intensive care unit, there was no statistically significant difference regarding RBC transfusion anymore and the overall clinical outcomes were similar in both patient groups. Conclusions The substitution of FXIII in patients who were more seriously compromised due to higher lactate levels and who presented with initially more severe bleedings than patients in the control group, resulted in a comparable transfusion necessity after 24 h. Thus, we guess that the substitution of FXIII in severely injured patients with ongoing bleeding might have an impact on their clinical outcome.</description><identifier>ISSN: 1863-9933</identifier><identifier>EISSN: 1863-9941</identifier><identifier>DOI: 10.1007/s00068-023-02221-z</identifier><identifier>PMID: 36670303</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Blood ; Blood platelets ; Coagulation ; Critical Care Medicine ; Emergency Medicine ; Intensive ; Intensive care ; Length of stay ; Medicine ; Medicine &amp; Public Health ; Original ; Original Article ; Patients ; Sports Medicine ; Surgery ; Surgical Orthopedics ; Trauma ; Traumatic Surgery</subject><ispartof>European journal of trauma and emergency surgery (Munich : 2007), 2023-06, Vol.49 (3), p.1517-1523</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. 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Methods We evaluated FXIII supplementation in severely injured patients with persistent bleeding. This was a retrospective case series analysis. Results Twenty-four patients received FXIII concentrate within 24 h of admission for bleeding that continued after transfusion of &gt; 6 U red blood cells (RBCs); control patients ( n  = 27) did not receive FXIII concentrate. Both study groups were similar regarding injury severity score and global coagulation tests, but FXIII activity levels were significantly higher and lactate levels significantly lower in the control group, respectively. The differences in FXIII activity between the groups could be attributed to a more severe trauma-induced coagulopathy in FXIII-deficient patients, as demonstrated by lower fibrinogen and higher lactate levels. The median dose of FXIII concentrate within 24 h of admission was 2500 IU (IQR: 1250–4375). Median 24-h transfusion of RBCs (primary study endpoint) was significantly higher in the FXIII group versus controls (10.0 U, IQR 5–14 U vs. 2, IQR 0–6 U; p  &lt; 0.01). Subsequently, while patients were in the intensive care unit, there was no statistically significant difference regarding RBC transfusion anymore and the overall clinical outcomes were similar in both patient groups. Conclusions The substitution of FXIII in patients who were more seriously compromised due to higher lactate levels and who presented with initially more severe bleedings than patients in the control group, resulted in a comparable transfusion necessity after 24 h. Thus, we guess that the substitution of FXIII in severely injured patients with ongoing bleeding might have an impact on their clinical outcome.</description><subject>Blood</subject><subject>Blood platelets</subject><subject>Coagulation</subject><subject>Critical Care Medicine</subject><subject>Emergency Medicine</subject><subject>Intensive</subject><subject>Intensive care</subject><subject>Length of stay</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Original</subject><subject>Original Article</subject><subject>Patients</subject><subject>Sports Medicine</subject><subject>Surgery</subject><subject>Surgical Orthopedics</subject><subject>Trauma</subject><subject>Traumatic Surgery</subject><issn>1863-9933</issn><issn>1863-9941</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kctu1DAUhq0KRC_wAl0gS2y6CfiSOM6qQhUtI1ViUyR21olzZsZVEqe2UzRd9R36hjwJhhmGy4KFZcvnO_-5_ISccvaWM1a_i4wxpQsmZD5C8OLhgBxxrWTRNCV_tn9LeUiOY7zNNFOVeEEOpVI1k0weka83a6STTzgmBz11wwQ2Ub-k1sNq7iE5P9Jl_vOBflksFtSNNAWYByjc2M0Wux3pJ0jrDf32-ESBBkzBxwltcvdILUSkEYPDSGGEfhNdfEmeL6GP-Gp3n5DPlx9uLj4W15-uFhfvrwtbCpUKrMpOKFZ1DehGKiuErQBaUEzqBjpRVpoDclbL2ra5TWiR8bZrrEahG9HKE3K-1Z3mdsDO5jkD9GYKboCwMR6c-TsyurVZ-XvD80obpauscLZTCP5uxpjM4KLFvocR_RyNqJUWZVlLndE3_6C3fg554kxpwTSXSpeZElvK5h3FgMt9N5yZH8aarbEmG2t-GmsectLrP-fYp_xyMgNyC8QcGlcYftf-j-x3s0OyZA</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Wilhelmi, Michaela</creator><creator>Albrecht, Alexander</creator><creator>Macke, Christian</creator><creator>Wilhelmi, Mathias</creator><creator>Omar, Mohammed</creator><creator>Winkelmann, Marcel</creator><creator>Clausen, Jan-Dierk</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7814-6526</orcidid></search><sort><creationdate>20230601</creationdate><title>The potential impact of coagulation factor XIII in trauma-induced coagulopathy – a retrospective case series analysis</title><author>Wilhelmi, Michaela ; 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Methods We evaluated FXIII supplementation in severely injured patients with persistent bleeding. This was a retrospective case series analysis. Results Twenty-four patients received FXIII concentrate within 24 h of admission for bleeding that continued after transfusion of &gt; 6 U red blood cells (RBCs); control patients ( n  = 27) did not receive FXIII concentrate. Both study groups were similar regarding injury severity score and global coagulation tests, but FXIII activity levels were significantly higher and lactate levels significantly lower in the control group, respectively. The differences in FXIII activity between the groups could be attributed to a more severe trauma-induced coagulopathy in FXIII-deficient patients, as demonstrated by lower fibrinogen and higher lactate levels. The median dose of FXIII concentrate within 24 h of admission was 2500 IU (IQR: 1250–4375). Median 24-h transfusion of RBCs (primary study endpoint) was significantly higher in the FXIII group versus controls (10.0 U, IQR 5–14 U vs. 2, IQR 0–6 U; p  &lt; 0.01). Subsequently, while patients were in the intensive care unit, there was no statistically significant difference regarding RBC transfusion anymore and the overall clinical outcomes were similar in both patient groups. Conclusions The substitution of FXIII in patients who were more seriously compromised due to higher lactate levels and who presented with initially more severe bleedings than patients in the control group, resulted in a comparable transfusion necessity after 24 h. Thus, we guess that the substitution of FXIII in severely injured patients with ongoing bleeding might have an impact on their clinical outcome.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36670303</pmid><doi>10.1007/s00068-023-02221-z</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7814-6526</orcidid><oa>free_for_read</oa></addata></record>
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subjects Blood
Blood platelets
Coagulation
Critical Care Medicine
Emergency Medicine
Intensive
Intensive care
Length of stay
Medicine
Medicine & Public Health
Original
Original Article
Patients
Sports Medicine
Surgery
Surgical Orthopedics
Trauma
Traumatic Surgery
title The potential impact of coagulation factor XIII in trauma-induced coagulopathy – a retrospective case series analysis
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