Hirudin monitoring using the TAS ecarin clotting time in patients with heparin-induced thrombocytopenia type II

To assess the reliability of the TAS/ecarin clotting time (ECT) for on-line monitoring of r-hirudin in cardiovascular surgery with and without cardiopulmonary bypass (CPB). Samples were spiked with r-hirudin (0 to 5 microg/mL) and calibration curves constructed. Reproducibility was evaluated by meas...

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Veröffentlicht in:Journal of cardiothoracic and vascular anesthesia 2000-06, Vol.14 (3), p.249-252
Hauptverfasser: KOSTER, A, HANSEN, R, GRAUHAN, O, HAUSMANN, H, BAUER, M, HETZER, R, KUPPE, H, MERTZLUFFT, F
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container_end_page 252
container_issue 3
container_start_page 249
container_title Journal of cardiothoracic and vascular anesthesia
container_volume 14
creator KOSTER, A
HANSEN, R
GRAUHAN, O
HAUSMANN, H
BAUER, M
HETZER, R
KUPPE, H
MERTZLUFFT, F
description To assess the reliability of the TAS/ecarin clotting time (ECT) for on-line monitoring of r-hirudin in cardiovascular surgery with and without cardiopulmonary bypass (CPB). Samples were spiked with r-hirudin (0 to 5 microg/mL) and calibration curves constructed. Reproducibility was evaluated by measurement of the sample five times at each concentration. The influence of variations in hematocrit, plasma factors, and platelet count on the test results was examined. Samples were obtained from patients during cardiovascular surgery with CPB (n = 8), without CPB (n = 3), and from volunteers (n = 5) and compared with the laboratory reference tests. All tests were performed in duplicate. Deutsches Herzzentrum Berlin. Five healthy volunteers and 11 patients undergoing cardiovascular surgery. None. The TAS/ECT showed linearity and reliability to an r-hirudin concentration of 5 microg/mL and was not influenced (p < 0.005) by the varying conditions of the in vitro setup. The correlation to the laboratory method was 0.74 for the CPB group and 0.87 for the non-CPB group. The TAS/ECT is a reliable assay for monitoring r-hirudin at the point of care. With this information, the use of r-hirudin during surgery or angioplasty should become more effective and safer.
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Samples were spiked with r-hirudin (0 to 5 microg/mL) and calibration curves constructed. Reproducibility was evaluated by measurement of the sample five times at each concentration. The influence of variations in hematocrit, plasma factors, and platelet count on the test results was examined. Samples were obtained from patients during cardiovascular surgery with CPB (n = 8), without CPB (n = 3), and from volunteers (n = 5) and compared with the laboratory reference tests. All tests were performed in duplicate. Deutsches Herzzentrum Berlin. Five healthy volunteers and 11 patients undergoing cardiovascular surgery. None. The TAS/ECT showed linearity and reliability to an r-hirudin concentration of 5 microg/mL and was not influenced (p &lt; 0.005) by the varying conditions of the in vitro setup. The correlation to the laboratory method was 0.74 for the CPB group and 0.87 for the non-CPB group. The TAS/ECT is a reliable assay for monitoring r-hirudin at the point of care. 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subjects Adult
Aged
Anticoagulants - blood
Biological and medical sciences
Cardiopulmonary Bypass
Drug Monitoring
Female
Heparin - adverse effects
Hirudins - blood
Humans
Immunomodulators
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Recombinant Proteins - blood
Reproducibility of Results
Thrombocytopenia - chemically induced
Whole Blood Coagulation Time
title Hirudin monitoring using the TAS ecarin clotting time in patients with heparin-induced thrombocytopenia type II
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