Increased D-dimers at admission of COVID-19 infected patients entering hospital due to a severe disease is a risk factor for death. Understanding this acquired coagulopathy is a prerequisite before specific interventional studies. The study investigators aim to apply a normalized and automated thrombin generation test (TGT), developed for testing the thrombotic risk (triggered by 5 pM Tissue Factor, with a purified thrombomodulin (TM) challenge) and to study its association with survival.
Accumulating data describe, in COVID-19 severely infected patients necessitating hospitalized medical support, the development of an acquired coagulopathy, from a sepsis-induced coagulopathy to an overt-DIC, which is a strong risk factor for death. Understanding this coagulopathy is a prerequisite before specific interventional studies. Conventional coagulation tests, like prothrombin time PT and aPTT, only reflect 5% of the total thrombin generation and are insensitive to the patients' natural anticoagulants. The investigators thus wish to analyze the coagulopathy of SARS-CoV-2 using a global analytical test reflecting the full complexity of thrombin generation then inhibition, the thrombin generation test (TGT), in its version designed to analyze the thrombotic risk (initiation by an intermediate concentration of human Tissue: 5 pM), in its fully automated and standardized technical version. This test analyzes not only the generation of thrombin and its various informative phases (initiation phase, propagation phase culminating at the peak of formation, inhibition phase with natural anticoagulants) but also the capacity for an exogenous addition of purified thrombomodulin (TM), which quantifies the anticoagulant activity of the patient's protein C activated by thrombin, to inhibit this generation of thrombin. The aim is to assay this TGT version in a centralized way, on the patients' plasma obtained at hospital admission, just after checking the positive COVID-19 testing , together with the traditional blood tests including platelet counts, PT, D-dimers (DDi) and soluble fibrin monomers (FMs). The various quantitative biological parameters describing the results of the TGT assay, together with relevant covariates, will be tested using multivariate analysis for their capacity to be risk factors for clinically-relevant qualitative outcomes.
Study Type
OBSERVATIONAL
Enrollment
175
lag time, initial velocity, time-to-peak, thrombin peak, total thrombin generation time, extrinsic thrombin potential (ETP). Crude quantitative values and relative values (%, by reference to the one obtained with an invariant reference plasma). Both without the addition of purified thrombomodulin (TM-) and with the addition of purified thrombomodulin (TM+). The ability of TM to inhibit thrombin generation will be calculated as follows: \[ETP (%)(TM+) / ETP (%)(TM-)\].
D-dimers (coagulation plus fibrinolysis), soluble fibrin monomers (coagulation only)
CHU de Bordeaux
Bordeaux, France
CHU de Limoges
Limoges, France
CHU de Montpellier
Montpellier, France
CHU de Nimes
Nîmes, France
28-day survival rate
Death yes/no during hopstilization, 28 days after admittence
Time frame: 1 month
Absolute thrombin generation test latent period
Seconds; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test latent period compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Absolute thrombin generation test initial velocity
nmol/s; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test initial velocity compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test peak thrombin compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Absolute thrombin generation test peak thrombin
nmol/L; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Absolute thrombin generation test peak thrombin time
Seconds; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test peak thrombin time compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Absolute thrombin generation test total thrombin generation time
seconds; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test total thrombin generation time compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Absolute thrombin generation test endogenous thrombin potential
Seconds; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
Relative thrombin generation test endogenous thrombin potential compared to reference plasma
%; without (TM-) and with (TM+) purified thrombomodulin
Time frame: Day 0
3-month survival rate
Death yes/no
Time frame: 3 months
Transfer to intensive care unit during hospitalization
Yes/no
Time frame: 3 months
Thrombotic complication during hospitalization
Yes/no (deep vein thrombosis, pulmonary embolism, atherothrombosis flare, arterial thrombosis)
Time frame: 3 months
Plasma concentrations of D-dimers
µg / L, assayed by automated enzyme linked fluorescent assay (Vidas® D-dimers Exclusion ™ II)
Time frame: Day 0
Plasma concentrations of soluble fibrin monomers
mg / L, measured by automated immunoagglutination (STA®-Liatest® FM)
Time frame: Day 0
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