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. 2020 Jun 30;34(2):635–656. doi: 10.1007/s12028-020-01037-8

Table 7.

Viscoelastic assays

Reference Study design TBI type Age category Patients (n) Antithrombotic treatment (n, %) Hemostatic comorbidities Sampling times First sample Results
Fair [31] Prospective observational Isolated TBI Adults 141 20 (14%) ASA Excluded those with known coagulation disorders On admission and 6, 12, 24, 48 h after injury N/A Normal TEG LY30 during time studied
Wang [33] Interventional Isolated moderate TBI Adults 83 0 (0%) Excluded those with known coagulation disorders NO admission, 12, 24, 48, 72 h after injury N/A Normal ROTEM CT, CFT or MCF during time studied
Leeper [50] Prospective observational Severe TBI Pediatric 39 N/A Excluded those with preexisting coagulation disorders On admission and 1, 2, 3, 4 days after injury N/A Normal LY30 on admission that decreased to fibrinolysis shutdown ranges starting on postinjury day 1 and continuing to postinjury day 3
Leeper [49] Prospective observational Severe TBI Pediatric 91 N/A Excluded those with preexisting coagulation disorders N/A N/A Elevated TEG LY30 within the first hour after injury, followed by a decrease toward fibrinolysis shutdown which had become the predominant phenotype already 3 h after trauma
Massaro [57] Prospective observational Moderate to severe TBI Adults 25 0 (0%) Alcohol use in 68% On admission and 1–2, 2–3, 3–4, 4–5 days after injury Mean 18 h after injury TEG MA, TG and G higher at late stage (> 48 h) compared to early stage (0–48 h) after injury

CFT clot formation time; CT clotting time; h hours; MA maximum amplitude; MCF maximum clot firmness; G G-value; TBI traumatic brain injury; TEG thromboelastography; TG thrombin generation; ROTEM rotational thromboelastometry