CO110 | FLOW-BASED WHOLE-BLOOD THROMBUS PROFILING DISCRIMINATES ANTITHROMBOTIC DRUG EFFECTS AND UNCOVERS PLATELET-DEPENDENT COAGULATION DEFECTS AFTER CARDIOPULMONARY BYPASS
Abstract
Background and Aims. Conventional coagulation tests and viscoelastic assays assess isolated enzymatic pathways or fibrin-weighted clot mechanics and often fail to capture thrombus formation as a dynamic process arising from platelet–coagulation interactions under flow. Most methods also rely on exogenous activators or inhibitors that may alter physiological responses. These limitations are relevant in complex settings such as cardiopulmonary bypass (CPB), where coagulopathy is multifactorial and not fully reflected by routine assays. We evaluated a flow-based whole-blood approach to quantify integrated thrombus formation under native conditions and assess its sensitivity to antithrombotic therapies and CPB-related hemostatic alterations. Methods. Whole blood from healthy donors (n=62), patients on antiplatelet therapy (ASA n=24; P2Y12 inhibitors n=11; DAPT n=32), anticoagulants (DOACs n=18; VKAs n=12), and CPB patients (Pre-CPB n=21; Post-CPB t0 (immediately after protamine infusion) n=5; Post-CPB ICU (within ≈ 1.5h from protamine) n=21) was analyzed. Pre-CPB patients received low-dose aspirin (75–100 mg/day). Recalcified citrated blood was perfused over collagen at arterial shear (γ̇=300 s-1) without exogenous activators or inhibitors. Dual-channel epifluorescence imaging enabled real-time quantification of platelet aggregation and fibrin(ogen) formation. Time series of integrated density (ID) were modeled to derive pseudo-volumes (AUC ID) for platelets, fibrinogen, and total thrombus. Platelet aggregate size was assessed at early (50–100 s) and late (200–450 s) phases; fibrin lag time was assessed by Kaplan–Meier analysis. Results. The assay resolved distinct pharmacodynamic signatures. ASA reduced fibrin(ogen) and total thrombus more than platelet signal, whereas P2Y12 inhibition markedly impaired platelet-dependent thrombus growth; DAPT showed the strongest inhibition. Anticoagulants mainly reduced fibrin(ogen) and total thrombus, with greater suppression in VKAs at higher INR. In CPB patients (Table 1), platelet (−66%), fibrinogen (−71%), and total thrombus (−70%) pseudo-volumes were markedly reduced at ICU despite near-normal INR and aPTT. Early platelet adhesion (50–100 s) was preserved, indicating intact initial interaction with collagen. In contrast, aggregate growth was impaired in the late phase (200–450 s), when thrombin normally amplifies platelet recruitment and fibrin formation. Consistently, fibrin lag time was prolonged (219→332 s). These findings indicate that, despite preserved adhesion, insufficient development of a platelet-dependent procoagulant surface limits thrombin generation, resulting in reduced fibrin formation and smaller thrombus structures. Conclusions. Flow-based whole-blood thrombus profiling discriminates functional signatures of anticoagulant and antiplatelet therapies and identifies a platelet-dependent coagulation defect after CPB not detected by conventional assays. The dissociation between preserved early adhesion and impaired thrombus growth reflects defective support of thrombin generation during the propagation phase of coagulation. By integrating platelet and fibrin dynamics under physiological flow without exogenous substances, this approach provides a mechanistic assessment of hemostatic function and may improve identification of clinically relevant bleeding risk in complex settings.
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BibTeX
@article{mazzucato2026co110,
title = {{CO110 | FLOW-BASED WHOLE-BLOOD THROMBUS PROFILING DISCRIMINATES ANTITHROMBOTIC DRUG EFFECTS AND UNCOVERS PLATELET-DEPENDENT COAGULATION DEFECTS AFTER CARDIOPULMONARY BYPASS}},
author = {Mario Mazzucato},
journal = {Bleeding, Thrombosis and Vascular Biology},
year = {2026},
month = oct,
url = {https://www.btvb.org/btvb/article/view/812},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - CO110 | FLOW-BASED WHOLE-BLOOD THROMBUS PROFILING DISCRIMINATES ANTITHROMBOTIC DRUG EFFECTS AND UNCOVERS PLATELET-DEPENDENT COAGULATION DEFECTS AFTER CARDIOPULMONARY BYPASS
AU - Mario Mazzucato
PY - 2026
DA - 2026/10/26
JO - Bleeding, Thrombosis and Vascular Biology
UR - https://www.btvb.org/btvb/article/view/812
AB - Background and Aims. Conventional coagulation tests and viscoelastic assays assess isolated enzymatic pathways or fibrin-weighted clot mechanics and often fail to capture thrombus formation as a dynamic process arising from platelet–coagulation interactions under flow. Most methods also rely on exogenous activators or inhibitors that may alter physiological responses. These limitations are relevant in complex settings such as cardiopulmonary bypass (CPB), where coagulopathy is multifactorial and not fully reflected by routine assays. We evaluated a flow-based whole-blood approach to quantify integrated thrombus formation under native conditions and assess its sensitivity to antithrombotic therapies and CPB-related hemostatic alterations. Methods. Whole blood from healthy donors (n=62), patients on antiplatelet therapy (ASA n=24; P2Y12 inhibitors n=11; DAPT n=32), anticoagulants (DOACs n=18; VKAs n=12), and CPB patients (Pre-CPB n=21; Post-CPB t0 (immediately after protamine infusion) n=5; Post-CPB ICU (within ≈ 1.5h from protamine) n=21) was analyzed. Pre-CPB patients received low-dose aspirin (75–100 mg/day). Recalcified citrated blood was perfused over collagen at arterial shear (γ̇=300 s-1) without exogenous activators or inhibitors. Dual-channel epifluorescence imaging enabled real-time quantification of platelet aggregation and fibrin(ogen) formation. Time series of integrated density (ID) were modeled to derive pseudo-volumes (AUC ID) for platelets, fibrinogen, and total thrombus. Platelet aggregate size was assessed at early (50–100 s) and late (200–450 s) phases; fibrin lag time was assessed by Kaplan–Meier analysis. Results. The assay resolved distinct pharmacodynamic signatures. ASA reduced fibrin(ogen) and total thrombus more than platelet signal, whereas P2Y12 inhibition markedly impaired platelet-dependent thrombus growth; DAPT showed the strongest inhibition. Anticoagulants mainly reduced fibrin(ogen) and total thrombus, with greater suppression in VKAs at higher INR. In CPB patients (Table 1), platelet (−66%), fibrinogen (−71%), and total thrombus (−70%) pseudo-volumes were markedly reduced at ICU despite near-normal INR and aPTT. Early platelet adhesion (50–100 s) was preserved, indicating intact initial interaction with collagen. In contrast, aggregate growth was impaired in the late phase (200–450 s), when thrombin normally amplifies platelet recruitment and fibrin formation. Consistently, fibrin lag time was prolonged (219→332 s). These findings indicate that, despite preserved adhesion, insufficient development of a platelet-dependent procoagulant surface limits thrombin generation, resulting in reduced fibrin formation and smaller thrombus structures. Conclusions. Flow-based whole-blood thrombus profiling discriminates functional signatures of anticoagulant and antiplatelet therapies and identifies a platelet-dependent coagulation defect after CPB not detected by conventional assays. The dissociation between preserved early adhesion and impaired thrombus growth reflects defective support of thrombin generation during the propagation phase of coagulation. By integrating platelet and fibrin dynamics under physiological flow without exogenous substances, this approach provides a mechanistic assessment of hemostatic function and may improve identification of clinically relevant bleeding risk in complex settings.
SN - 2785-5309
ER -