2019
DOI: 10.1016/j.surg.2019.05.011
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Clot activators do not expedite the time to predict massive transfusion in trauma patients analyzed with tissue plasminogen activator thrombelastography

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Cited by 6 publications
(4 citation statements)
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“…A substantial amount of plasmin (> 10% total plasmin generation potential) can be buffered by the peripheral blood before it causes significant coagulation changes in healthy individuals. 37 Therefore, PAP levels while reflective of plasmin generation do not define fibrinolysis status, as plasmin can be activated for Fig. 1 Activation of coagulation and fibrinolysis following hemorrhagic shock.…”
Section: Low Fibrinolytic States Early After Injury: Fibrinolysis Shumentioning
confidence: 99%
“…A substantial amount of plasmin (> 10% total plasmin generation potential) can be buffered by the peripheral blood before it causes significant coagulation changes in healthy individuals. 37 Therefore, PAP levels while reflective of plasmin generation do not define fibrinolysis status, as plasmin can be activated for Fig. 1 Activation of coagulation and fibrinolysis following hemorrhagic shock.…”
Section: Low Fibrinolytic States Early After Injury: Fibrinolysis Shumentioning
confidence: 99%
“…This clinical pharmacist facilitated COVID-19 patients' ultrasound screening, diagnosis, and monitoring of prophylactic and full anticoagulation treatment. [18][19][20][21]47 This multidisciplinary team was adapted from previous programs that utilized a similar dynamic for management of trauma-related anticoagulation…”
Section: Discussionmentioning
confidence: 99%
“…prophylaxis and treatment (46,47). Nine of thirty-one (29%) COVID-19 patients had radiographic evidence of VTE despite no clinical symptoms on initial presentation.…”
mentioning
confidence: 99%
“…44 Finally, one of the most challenging yet important aspects for advancing VHA and other global hemostasis analytics for real-time decision making is shortening the length of time it takes to get information on fibrinolysis. To that end, the present authors have worked extensively on rapid fibrinolysis diagnostics through a variety of modifications to the assayed blood samples, such as adding exogenous tPA, 135 plasmin, 133 or both 136 to VHA assays as a way to challenge the system and see if patients have already exhausted their native ability to inhibit fibrinolysis, essentially releasing the brakes on the system. These assay results, in essence, can rapidly identify patients (<15 minutes) in whom any further insults, such as hypotension, that cause tPA release would cause a major clinical bleed and warrant prompt treatment with TXA or other antifibrinolytic therapy.…”
Section: Future Directions and Conclusionmentioning
confidence: 99%