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Updated: Aug 6, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
A guide for diagnosis of patients with arterial and venous thrombosis
1Michigan State University, East Lansing, MI, USA.
Insights
Coagulation laboratories diagnose thrombosis by reviewing hemostatic system components and platelet functions. This review covers assays for clot formation, platelet activity, and molecular markers for thrombosis diagnosis and treatment guidance.
Area of Science:
- Hematology
- Clinical Pathology
- Thrombosis Research
Background:
- Coagulation laboratories are crucial for diagnosing venous and arterial thrombosis.
- Understanding the hemostatic system's components is vital for accurate diagnosis.
Purpose of the Study:
- To provide a comprehensive review of hemostatic system components in relation to thrombosis diagnosis.
- To include information on antiplatelet and antithrombotic therapies.
- To discuss various coagulation assays and molecular markers.
Main Methods:
- Review of biological properties and functions of hemostatic components.
- Inclusion of data on antiplatelet and antithrombotic therapy.
- Description of clot-based assays, chromogenic substrate assays, and antibody-based measurements.
- Discussion of genetic testing and screening assays like PT, APTT, and TT.
- Explanation of molecular markers for hemostasis and fibrinolysis.
Main Results:
- Coagulation testing includes assays for clot potential, platelet number, and function.
- Screening assays (PT, APTT, TT) are fundamental for specialized factor activity tests.
- Molecular markers, identified by antibodies, are increasingly used, with d-dimer being a key exception in clinical research.
Conclusions:
- Coagulation laboratories play a central role in diagnosing thrombosis and guiding therapy.
- A wide array of assays, from basic screening to molecular markers, are available for hemostasis evaluation.
- Continued research is expanding the utility of molecular markers in clinical settings.
Abstract:
Inasmuch as coagulation laboratories are involved in providing a diagnosis for underlying causes of venous and arterial thrombosis, we present a comprehensive review of the biological properties and functions of the components of the hemostatic system as they relate to the diagnosis of arterial and venous thrombosis. Moreover, as coagulation laboratories are necessary to evaluate the success of initial treatment modalities and to provide guidance for supplemental therapeutic intervention, we include information on antiplatelet and antithrombotic therapy. Included in clinical coagulation testing are assays that evaluate the potential of blood to form clots and tests for platelet numbers and platelet functions. Clot-based assays directly detect the biological activity of procoagulant factors and fibrinogen; chromogenic substrate assays evaluate proteolytic activities of clotting as well as fibrinolysis enzymes; and specific antibodies measure the concentrations of coagulation and fibrinolysis enzymes in plasma. Genetic testing is rapidly becoming incorporated into the clinical routine. The prothrombin time (PT), activated partial prothrombin time (APTT), and thrombin time (TT) are screening assays that measure the clotting times of recalcified whole blood or platelet-poor plasma. In addition to their function as screening assays, PT, APTT, and TT are the backbone of all the specialized clot-based assays for factor activities and for the indirect measurement of inhibitory antithrombin and protein C activities. Molecular markers related to hemostasis and fibrinolysis consist of proteins or peptides that indicate an ongoing physiological or abnormal process related to clot formation, thrombosis, vascular damage, or drug effect. Molecular markers are currently identified by means of specific antibodies prepared against them. The list of hemostatic molecular markers is rapidly growing. Most of the assays developed for molecular marker measurement, with the notable exception of the d-dimer assay, are typically used in clinical research.
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