Semin Thromb Hemost 2008; 34: 081-086
DOI: 10.1055/s-0028-1086086
© Thieme Medical Publishers

Drug Monitoring of Argatroban Using the Ecarin Chromogenic Assay

Götz Nowak1 , Ute Lange2 , Elke Bucha2
  • 1University Medical Center Jena, Research Unit, Pharmacological Haemostaseology, Drackendorfer Str. 1, 07747 Jena, Germany
  • 2JenAffin GmbH, Winzerlaer Str. 2, 07745 Jena, Germany
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Publikationsverlauf

Publikationsdatum:
28. Oktober 2008 (online)

ABSTRACT

The ecarin chromogenic assay (HaemoSys ECA; JenAffin GmbH, Jena, Germany) was developed for quantitative determination of direct thrombin inhibitors. As a further development of the ecarin clotting time (ECT), the ECA is based on the same principle of measurement: the activation of prothrombin by ecarin, a snake venom from Echis carinatus. In the ECA, the prothrombin activation products meizothrombin and meizothrombin-des-F1 cleave a chromogenic substrate. The activity of meizothrombin/meizothrombin-des-F1 is inhibited in a concentration-dependent manner by direct thrombin inhibitors. The ECA-T is an assay for quantitative determination of active site directed synthetic thrombin inhibitors. For argatroban ECA-T, there is a very precise and sensitive method of quantitative drug monitoring. Only very low interindividual variations were found compared with activated partial thromboplastin time and even ECT. ECA-T is independent of variations in prothrombin levels of the plasma samples. Heparin does not influence the measuring result. ECA-T is performed on manual coagulation analyzers with an option for optical measurement but can also be applied to automated laboratory systems. By the use of ECA-T as a drug-monitoring method, the drug safety of argatroban, most of all in critically ill patients, can be increased.

REFERENCES

Prof. Dr. Götz Nowak

University Medical Center Jena, Research Group, Pharmacological Haemostaseology

Drackendorfer Str. 1, 07747 Jena, Germany

eMail: AGPHH@med.uni-jena.de