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Erschienen in: European Journal of Pediatrics 5/2007

01.05.2007 | Original Paper

Anticoagulant action of melagatran: a comparison between neonates and adults using calibrated automated thrombography (CAT)

verfasst von: Gerhard Cvirn, Christina Cimenti, Joerg Kutschera, Ulrika Ferstl, Thomas Wagner, Wolfgang Muntean, Gunther Jurgens, Siegfried Gallistl, Martin Koestenberger

Erschienen in: European Journal of Pediatrics | Ausgabe 5/2007

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Abstract

In the present study, we comparatively evaluated the anticoagulant efficacy of the new direct thrombin inhibitor melagatran in cord vs. adult plasma. In contrast to heparin, melagatran does not require antithrombin as a cofactor. Thus, anticoagulant treatment with melagatran is of special interest in neonatal patients, whose plasma is relatively deficient in antithrombin. We evaluated the anticoagulant action of increasing amounts of melagatran (0.1–2.0 μmol/l) in both cord and adult plasma by means of calibrated automated thrombography (CAT) with respect to the lag time until the onset of thrombin formation, time to thrombin peak maximum (TTP), endogenous thrombin potential (ETP), and thrombin peak height. Melagatran exhibited approximately the same ability to prolong lag times or TTPs in both cord and adult plasma. Similar concentrations (IC50) of melagatran were required to double the lag times (0.44±0.04 μmol/l vs. 0.52±0.05 μmol/l) or to double the TTPs (0.91±0.08 μmol/l vs. 1.06±0.09 μmol/l) in cord vs. adult plasma. Melagatran exhibited a higher ability to suppress ETPs or thrombin peak heights in cord vs. adult plasma. Markedly lower concentrations (IC50) of melagatran were required to suppress ETPs (0.27±0.03 μmol/l vs. 0.70±0.06 μmol/l) or thrombin peak heights by 50% (0.29±0.03 μmol/l vs. 0.53±0.04 μmol/l) in cord vs. adult plasma. We conclude that our results suggest a higher ability of melagatran to suppress thrombin formation in cord vs. adult plasma. Thus, lower amounts of melagatran might be required in neonates undergoing antithrombotic therapy.
Literatur
1.
Zurück zum Zitat Andrew M, David M, Adams M, Ali K, Anderson R, Barnard D, Bernstein M, Brisson L, Cairney B, Desai D, Grant R, Isreals S, Jardine L, Luke B, Massicotte P, Silva M (1994) Venous thromboembolic complications (VTE) in children: first analyses of the Canadian Registry of VTE. Blood 83(5):1251–1257PubMed Andrew M, David M, Adams M, Ali K, Anderson R, Barnard D, Bernstein M, Brisson L, Cairney B, Desai D, Grant R, Isreals S, Jardine L, Luke B, Massicotte P, Silva M (1994) Venous thromboembolic complications (VTE) in children: first analyses of the Canadian Registry of VTE. Blood 83(5):1251–1257PubMed
2.
Zurück zum Zitat Andrew M, Paes B, Milner R, Johnston M, Mitchell L, Tollefsen DM, Powers P (1987) Development of the human coagulation system in the full-term infant. Blood 70(1):165–172PubMed Andrew M, Paes B, Milner R, Johnston M, Mitchell L, Tollefsen DM, Powers P (1987) Development of the human coagulation system in the full-term infant. Blood 70(1):165–172PubMed
3.
Zurück zum Zitat Andrew M, Schmidt B, Mitchell L, Paes B, Ofoso F (1990) Thrombin generation in newborn plasma is critically dependent on the concentration of prothrombin. Thromb Haemost 63(1):27–30PubMed Andrew M, Schmidt B, Mitchell L, Paes B, Ofoso F (1990) Thrombin generation in newborn plasma is critically dependent on the concentration of prothrombin. Thromb Haemost 63(1):27–30PubMed
4.
Zurück zum Zitat Brighton TA (2004) The direct thrombin inhibitor melagatran/ximelagatran. Med J Aust 181(8):432–437PubMed Brighton TA (2004) The direct thrombin inhibitor melagatran/ximelagatran. Med J Aust 181(8):432–437PubMed
5.
Zurück zum Zitat Butenas S, van’t Veer C, Mann KG (1999) “Normal” thrombin generation. Blood 94(7):2169–2178PubMed Butenas S, van’t Veer C, Mann KG (1999) “Normal” thrombin generation. Blood 94(7):2169–2178PubMed
6.
Zurück zum Zitat Chan AK, Deveber G, Monagle P, Brooker LA, Massicotte PM (2003) Venous thrombosis in children. J Thromb Haemost 1(7):1443–1455PubMedCrossRef Chan AK, Deveber G, Monagle P, Brooker LA, Massicotte PM (2003) Venous thrombosis in children. J Thromb Haemost 1(7):1443–1455PubMedCrossRef
7.
Zurück zum Zitat Christersson C, Oldgren J, Bylock A, Wallentin L, Siegbahn A (2005) Long-term treatment with ximelagatran, an oral direct thrombin inhibitor, persistently reduces the coagulation activity after a myocardial infarction. J Thromb Haemost 3(10):2245–2253PubMedCrossRef Christersson C, Oldgren J, Bylock A, Wallentin L, Siegbahn A (2005) Long-term treatment with ximelagatran, an oral direct thrombin inhibitor, persistently reduces the coagulation activity after a myocardial infarction. J Thromb Haemost 3(10):2245–2253PubMedCrossRef
8.
Zurück zum Zitat Cvirn G, Gallistl S, Leschnik B, Muntean W (2003) Low tissue factor pathway inhibitor (TFPI) together with low antithrombin allows sufficient thrombin generation in the neonate. J Thromb Haemost 1(2):263–268PubMedCrossRef Cvirn G, Gallistl S, Leschnik B, Muntean W (2003) Low tissue factor pathway inhibitor (TFPI) together with low antithrombin allows sufficient thrombin generation in the neonate. J Thromb Haemost 1(2):263–268PubMedCrossRef
9.
Zurück zum Zitat Cvirn G, Gallistl S, Rehak T, Jürgens G, Muntean W (2003) Elevated thrombin-forming capacity of tissue factor-activated cord compared with adult plasma. J Thromb Haemost 1(8):1785–1790PubMedCrossRef Cvirn G, Gallistl S, Rehak T, Jürgens G, Muntean W (2003) Elevated thrombin-forming capacity of tissue factor-activated cord compared with adult plasma. J Thromb Haemost 1(8):1785–1790PubMedCrossRef
10.
Zurück zum Zitat Cvirn G, Koestenberger M, Leschnik B, Male C, Kutschera J, Ferstl U, Muntean W, Juergens G, Gallistl S (2005) Protein S modulates the anticoagulant action of recombinant human activated protein C: a comparison between neonates and adults. Brit J Pharmacol 146(8):1082–1086CrossRef Cvirn G, Koestenberger M, Leschnik B, Male C, Kutschera J, Ferstl U, Muntean W, Juergens G, Gallistl S (2005) Protein S modulates the anticoagulant action of recombinant human activated protein C: a comparison between neonates and adults. Brit J Pharmacol 146(8):1082–1086CrossRef
11.
Zurück zum Zitat Davie EW, Fujikawa K, Kisiel W (1991) The coagulation cascade: initiation, maintenance, and regulation. Biochemistry 30(43):10363–10370PubMedCrossRef Davie EW, Fujikawa K, Kisiel W (1991) The coagulation cascade: initiation, maintenance, and regulation. Biochemistry 30(43):10363–10370PubMedCrossRef
12.
Zurück zum Zitat Eriksson BI, Bergqvist D, Kalebo P, Dahl OE, Lindbratt S, Bylock A, Frison L, Eriksson UG, Welin L, Gustafsson D (2002) Ximelagatran and melagatran compared with dalteparin for prevention of venous thromboembolism after total hip or knee replacement: the METHRO II randomised trial. Lancet 360(9344):1441–1447PubMedCrossRef Eriksson BI, Bergqvist D, Kalebo P, Dahl OE, Lindbratt S, Bylock A, Frison L, Eriksson UG, Welin L, Gustafsson D (2002) Ximelagatran and melagatran compared with dalteparin for prevention of venous thromboembolism after total hip or knee replacement: the METHRO II randomised trial. Lancet 360(9344):1441–1447PubMedCrossRef
13.
Zurück zum Zitat Gulseth MP (2005) Ximelagatran: an orally active direct thrombin inhibitor. Am J Health Syst Ph 62(14):1451–1467CrossRef Gulseth MP (2005) Ximelagatran: an orally active direct thrombin inhibitor. Am J Health Syst Ph 62(14):1451–1467CrossRef
14.
Zurück zum Zitat Gustafsson D, Nystrom J, Carlsson S, Bredberg U, Eriksson U, Gyzander E, Elg M, Antonsson T, Hoffmann K, Ungell A, Sorensen H, Nagard S, Abrahamsson A, Bylund R (2001) The direct thrombin inhibitor melagatran and its oral prodrug H 376/95: intestinal absorption properties, biochemical and pharmacodynamic effects. Thromb Res 101(3):171–181PubMedCrossRef Gustafsson D, Nystrom J, Carlsson S, Bredberg U, Eriksson U, Gyzander E, Elg M, Antonsson T, Hoffmann K, Ungell A, Sorensen H, Nagard S, Abrahamsson A, Bylund R (2001) The direct thrombin inhibitor melagatran and its oral prodrug H 376/95: intestinal absorption properties, biochemical and pharmacodynamic effects. Thromb Res 101(3):171–181PubMedCrossRef
15.
Zurück zum Zitat Hemker HC, Beguin S (2000) Phenotyping the clotting system. Thromb Haemost 84(5):747–751PubMed Hemker HC, Beguin S (2000) Phenotyping the clotting system. Thromb Haemost 84(5):747–751PubMed
16.
Zurück zum Zitat Mann KG, Brummel K, Butenas S (2003) What is all that thrombin for? J Thromb Haemost 1(7):1504–1514PubMedCrossRef Mann KG, Brummel K, Butenas S (2003) What is all that thrombin for? J Thromb Haemost 1(7):1504–1514PubMedCrossRef
17.
Zurück zum Zitat Hemker HC, Giesen P, Al Dieri R, Regnault V, de Smedt E, Wagenvoord R, Lecompte T, Beguin S (2003) Calibrated automated thrombin generation measurement in clotting plasma. Pathophysiol Haemo Thromb 33(1):4–15CrossRef Hemker HC, Giesen P, Al Dieri R, Regnault V, de Smedt E, Wagenvoord R, Lecompte T, Beguin S (2003) Calibrated automated thrombin generation measurement in clotting plasma. Pathophysiol Haemo Thromb 33(1):4–15CrossRef
18.
Zurück zum Zitat Koestenberger M, Gallistl S, Cvirn G, Baier K, Leschnik B, Muntean W (2005) Anticoagulant action of melagatran, the active form of the oral direct thrombin inhibitor ximelagatran, in umbilical cord and adult plasma: an in vitro examination. Thromb Res 115(1–2):135–142PubMedCrossRef Koestenberger M, Gallistl S, Cvirn G, Baier K, Leschnik B, Muntean W (2005) Anticoagulant action of melagatran, the active form of the oral direct thrombin inhibitor ximelagatran, in umbilical cord and adult plasma: an in vitro examination. Thromb Res 115(1–2):135–142PubMedCrossRef
19.
Zurück zum Zitat Kuhle S, Male C, Mitchell L (2003) Developmental hemostasis: pro- and anticoagulant systems during childhood. Semin Thromb Hemost 29(4):329–337PubMedCrossRef Kuhle S, Male C, Mitchell L (2003) Developmental hemostasis: pro- and anticoagulant systems during childhood. Semin Thromb Hemost 29(4):329–337PubMedCrossRef
20.
Zurück zum Zitat Reverdiau-Moalic P, Delahousse B, Body G, Bardos P, Leroy J, Gruel Y (1996) Evolution of blood coagulation activators and inhibitors in the healthy human fetus. Blood 88(3):900–906PubMed Reverdiau-Moalic P, Delahousse B, Body G, Bardos P, Leroy J, Gruel Y (1996) Evolution of blood coagulation activators and inhibitors in the healthy human fetus. Blood 88(3):900–906PubMed
21.
Zurück zum Zitat Sorensen B, Johansen P, Christiansen K, Woelke M, Ingerslev J (2003) Whole blood coagulation thrombelastographic profiles employing minimal tissue factor activation. J Thromb Haemost 1(3):551–558PubMedCrossRef Sorensen B, Johansen P, Christiansen K, Woelke M, Ingerslev J (2003) Whole blood coagulation thrombelastographic profiles employing minimal tissue factor activation. J Thromb Haemost 1(3):551–558PubMedCrossRef
22.
Zurück zum Zitat Weitz JI (2004) New anticoagulants for treatment of venous thromboembolism. Circulation 110(Suppl 1):I19–I26PubMedCrossRef Weitz JI (2004) New anticoagulants for treatment of venous thromboembolism. Circulation 110(Suppl 1):I19–I26PubMedCrossRef
23.
Zurück zum Zitat Weitz JI, Hudoba M, Massel D, Maraganore J, Hirsh J (1990) Clot-bound thrombin is protected from inhibition by heparin-antithrombin III but is susceptible to inactivation by antithrombin-independent inhibitors. J Clin Invest 86:85–91 Weitz JI, Hudoba M, Massel D, Maraganore J, Hirsh J (1990) Clot-bound thrombin is protected from inhibition by heparin-antithrombin III but is susceptible to inactivation by antithrombin-independent inhibitors. J Clin Invest 86:85–91
Metadaten
Titel
Anticoagulant action of melagatran: a comparison between neonates and adults using calibrated automated thrombography (CAT)
verfasst von
Gerhard Cvirn
Christina Cimenti
Joerg Kutschera
Ulrika Ferstl
Thomas Wagner
Wolfgang Muntean
Gunther Jurgens
Siegfried Gallistl
Martin Koestenberger
Publikationsdatum
01.05.2007
Verlag
Springer-Verlag
Erschienen in
European Journal of Pediatrics / Ausgabe 5/2007
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-006-0253-6

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