Caspers, Michael, Schaefer, Nadine, Froehlich, Matthias, Bauerfeind, Ursula, Bouillon, Bertil, Mutschler, Manuel and Maegele, Marc (2018). How do external factors contribute to the hypocoagulative state in trauma-induced coagulopathy? - In vitro analysis of the lethal triad in trauma. Scand. J. Trauma Resusc. Emerg. Med., 26. LONDON: BMC. ISSN 1757-7241

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Abstract

Background: External factors following trauma and iatrogenic intervention influence blood coagulation and particularly clot formation. In particular, three external factors (in detail dilution via uncritical volume replacement, acidosis and hypothermia), in combination, referred to as the lethal triad, substantially aggravate the hypocoagulative state after trauma. Contribution of these external factors to the resulting hypocoagulative state in trauma and especially their influence on primary haemostasis has still not been investigated systematically. This study aims to assess this contribution to the aggravating hypocoagulative state in trauma-induced coagulopathy (TIC) using an in vitro simulation assay. Emphasis is given to platelet contribution to clot formation and to the investigation of how platelet activation alters under the respective conditions. Methods: To simulate the conditions of lethal triad in vitro, whole blood samples taken from five healthy volunteers were introduced to the respective conditions. Besides standard coagulation testing, thrombelastometric analysis and differentiated platelet mapping were performed. Results: All three simulated conditions induced significant impairments of clot formation (clot formation time, CFT; alpha-angle) and propagation (maximum clot firmness, MCF; Diameter A5-A25), with the highest impact under hypothermia and dilution. Consistently, lethal triad resulted in an additive effect of all conditions. None of the simulated conditions induced a statistically relevant change in coagulation initiation assessed by EXTEM and FIBTEM thrombelastometry. Platelet contribution to clot formation decreased gradually under the respective conditions, reaching statistical significance for simulated dilution, and attaining its greatest extent under the conditions of lethal triad (Delta trias/baseline 0.59; p = 0.01). Consistent, reduced CD62 expression levels were observed under experimental acidosis (Delta acidosis/baseline 0.32; p = 0.006), dilution (Delta dilution/baseline 0.34; p = 0.01) and lethal triad (Delta lethal triad/baseline 0.24; p = 0.01). Conclusion: The respective external factors of lethal triad play a pivotal role in the development of coagulopathy, essentially influencing the kinetics of clot formation, and to a varying extent clot diameter, as measured by thrombelastometry. Moreover, impairment of platelet function under the conditions of lethal triad plays a key role in the pathophysiology of TIC, resulting in reduced responsiveness to stimulation with ADP that might also be present after trauma. Our data indicate that impairment of primary haemostasis contribute to the hypocoagulative state in TIC after trauma aggravated by external factors of lethal triad.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Caspers, MichaelUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schaefer, NadineUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Froehlich, MatthiasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bauerfeind, UrsulaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bouillon, BertilUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mutschler, ManuelUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Maegele, MarcUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-176382
DOI: 10.1186/s13049-018-0536-8
Journal or Publication Title: Scand. J. Trauma Resusc. Emerg. Med.
Volume: 26
Date: 2018
Publisher: BMC
Place of Publication: LONDON
ISSN: 1757-7241
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PLATELET DYSFUNCTION; IMPAIR COAGULATION; HYPOTHERMIA; ACIDOSIS; TEMPERATURE; MORTALITY; AGGREGATION; ACTIVATION; FIBRINOGEN; PATTERNSMultiple languages
Emergency MedicineMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/17638

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