Differentiating Pathologic from Physiologic Fibrinolysis: Not as Simple as Conventional Thrombelastography

Author:

Moore Hunter B1,Barrett Christopher D2,Moore Ernest E3,Pieracci Fredric M3,Sauaia Angela4

Affiliation:

1. From the Department of Surgery, Transplant Institution, AdventHealth at Porter Hospital, Denver, CO (HB Moore)

2. Department of Surgery, University of Nebraska School of Medicine, Omaha, NE (Barrett)

3. Department of Surgery, Ernest E Moore Shock Trauma Center at Denver Health, Denver, CO (EE Moore, Pieracci)

4. Department of Public Health, University of Colorado School of Public Health, Aurora, CO (Sauaia).

Abstract

BACKGROUND: Conventional rapid thrombelastography (rTEG) cannot differentiate fibrinolysis shutdown from hypofibrinolysis, as both of these patient populations have low fibrinolytic activity. Tissue plasminogen activator (tPA) TEG can identify depletion of fibrinolytic inhibitors, and its use in combination with rTEG has the potential to differentiate all 3 pathologic fibrinolytic phenotypes after trauma. We hypothesize tPA-TEG and rTEG in combination can further stratify fibrinolysis phenotypes postinjury to better stratify risk for mortality. STUDY DESIGN: Adult trauma patients (981) with both rTEG and tPA-TEG performed less than 2 hours postinjury were included. rTEG lysis at 30 minutes after maximum amplitude (LY30) was used to initially define fibrinolysis phenotypes (hyperfibrinolysis >3%, physiologic 0.9% to 3%, and shutdown <0.9%), with Youden Index then used to define pathologic extremes of tPA-TEG LY30 (tPA sensitive [depletion of fibrinolytic inhibitors] vs resistant) resulting in 9 groups that were assessed for risk of death. RESULTS: The median New Injury Severity Score was 22, 21% were female, 45% had penetrating injury, and overall mortality was 13%. The tPA-TEG LY30 inflection point for increased mortality was >35.5% (tPA sensitive, odds ratio mortality 9.2, p < 0.001) and <0.3% (tPA resistance, odds ratio mortality 6.3, p = 0.04). Of the 9 potential fibrinolytic phenotypes, 5 were associated with increased mortality. Overall, the 9 phenotypes provided a significantly better prediction of mortality than rTEG or tPA-TEG alone (areas under the operating characteristics curves = 0.80 vs 0.63 and 0.75, respectively, p < 0.0001). These could be condensed to 3 pathologic phenotypes (true hyperfibrinolysis, early fibrinolysis shutdown, and hypofibrinolysis). CONCLUSIONS: The combination of rTEG and tPA-TEG increases the ability to predict mortality and suggests patient-specific strategies for improved outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference49 articles.

1. Trauma-induced coagulopathy.;Moore;Nat Rev Dis Primers,2021

2. Coagulation and fibrinolysis in injured patients.;Innes;J Clin Pathol,1964

3. Primary fibrinolysis is integral in the pathogenesis of the acute coagulopathy of trauma.;Kashuk;Ann Surg,2010

4. Hyperfibrinolysis after major trauma: differential diagnosis of lysis patterns and prognostic value of thrombelastometry.;Schochl;J Trauma,2009

5. Hyperfibrinolysis at admission is an uncommon but highly lethal event associated with shock and prehospital fluid administration.;Cotton;J Trauma Acute Care Surg,2012

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