Literature DB >> 9211628

Monitoring of recombinant hirudin: assessment of a plasma-based ecarin clotting time assay.

B Pötzsch1, S Hund, K Madlener, C Unkrig, G Müller-Berghaus.   

Abstract

Assay conditions of a plasma-based ecarin clotting time (ECT) were evaluated and the precision of the ECT in monitoring plasma levels of r-hirudin assessed. The snake venom enzyme ecarin converts prothrombin to meizothrombin possessing only weak coagulant but strong esterase activity. In r-hirudin containing plasma samples, meizo thrombin is rapidly neutralized by r-hirudin resulting in a dose-dependent prolongation of the clotting times. Among the different assay conditions tested, addition of 50 microliters of ecarin (4 U/ml) to 100 microliters of undiluted citrate-anticoagulated plasma gave optimal results with respect to precision and reproducibility. The measuring range of the ECT performed in this way is about 0.02-5.0 micrograms/ml r-hirudin. In vitro studies performed on r-hirudin-spiked plasma samples of 50 healthy individuals demonstrate remarkably low interindividual differences in r-hirudin responsiveness as indicated by CV-values below 5% and 7% at r-hirudin concentrations between 0-3 micrograms/ml and 4-5 micrograms/ml, respectively. The specificity for r-hirudin of the ECT is further demonstrated by the strong correlation (r = 0.94) between the results of a chromogenic assay and the ECT-measured r-hirudin concentrations obtained on 67 ex vivo blood samples. Depending on the concentration of r-hirudin the ECT is sensitive to plasma levels of prothrombin. In the absence of r-hirudin the critical prothrombin concentration was found to be 20% but increasing to 60% in the presence of 2.0 micrograms/ml r-hirudin. A fibrinogen concentration of 50 mg/dl was found to be the minimal concentration independent of the r-hirudin concentration. The precision of the ECT in measuring plasma levels of r-hirudin is not influenced by treatment with heparin, aprotinin or oral anticoagulants. The data demonstrate that the ECT is a rapid and easily perfor mable clotting assay which allows accurate measurement of r-hirudin plasma levels. ECT-monitored hirudin treatment will help to establish optimal dose regimens that are more efficacious but still as safe as heparin.

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Year:  1997        PMID: 9211628     DOI: 10.1016/s0049-3848(97)00082-0

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  12 in total

Review 1.  Management of patients with heparin-induced thrombocytopenia: focus on recombinant hirudin.

Authors:  N Lubenow; A Greinacher
Journal:  J Thromb Thrombolysis       Date:  2000-11       Impact factor: 2.300

Review 2.  Laboratory diagnosis of heparin-induced thrombocytopenia and monitoring of alternative anticoagulants.

Authors:  Albrecht Leo; Susanne Winteroll
Journal:  Clin Diagn Lab Immunol       Date:  2003-09

3.  Comparison of two different ecarin clotting time methods.

Authors:  Tivadar Fenyvesi; Job Harenberg; Christel Weiss; Ingrid Jörg
Journal:  J Thromb Thrombolysis       Date:  2005-08       Impact factor: 2.300

Review 4.  Thrombin inhibitors and cardiopulmonary bypass.

Authors:  Alan Merry
Journal:  J Extra Corpor Technol       Date:  2006-03

5.  Neutralization of EP217609, a new dual-action FIIa/FXa anticoagulant, by its specific antidote avidin: a phase I study.

Authors:  P Gueret; S Combe; C Krezel; E Fuseau; P L M van Giersbergen; M Petitou; E Neuhart
Journal:  Eur J Clin Pharmacol       Date:  2016-10-15       Impact factor: 2.953

Review 6.  Hirudin-based anticoagulant strategies for patients with suspected heparin-induced thrombocytopenia undergoing percutaneous coronary interventions and bypass grafting.

Authors:  R C Becker
Journal:  J Thromb Thrombolysis       Date:  2000-11       Impact factor: 2.300

7.  Ecarin clotting time but not aPTT correlates with PEG-hirudin plasma activity.

Authors:  M Moser; J Ruef; K Peter; B Kohler; D C Gulba; N Paterna; T Nordt; W Kübler; C Bode
Journal:  J Thromb Thrombolysis       Date:  2001-10       Impact factor: 2.300

Review 8.  Measurement and reversal of the direct oral anticoagulants.

Authors:  Bethany T Samuelson; Adam Cuker
Journal:  Blood Rev       Date:  2016-09-02       Impact factor: 8.250

9.  First in man study of EP217609, a new long-acting, neutralisable parenteral antithrombotic with a dual mechanism of action.

Authors:  Pierre Gueret; S Combe; C Krezel; E Fuseau; P L M van Giersbergen; M Petitou; E Neuhart
Journal:  Eur J Clin Pharmacol       Date:  2016-06-03       Impact factor: 2.953

10.  Lepirudin in the management of patients with heparin-induced thrombocytopenia.

Authors:  Sirak Petros
Journal:  Biologics       Date:  2008-09
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