Skip to main content
Erschienen in: Clinical Pharmacokinetics 14/2004

01.12.2004 | Review Article

Avoidance of Bleeding During Surgery in Patients Receiving Anticoagulant and/or Antiplatelet Therapy

Pharmacokinetic and Pharmacodynamic Considerations

verfasst von: Prof. Sebastian Harder, Ute Klinkhardt, John M. Alvarez

Erschienen in: Clinical Pharmacokinetics | Ausgabe 14/2004

Einloggen, um Zugang zu erhalten

Abstract

Perioperative management of chronically anticoagulated patients and/or patients treated with antiplatelet therapy is a complex medical problem. This review considers the pharmacokinetic and pharmacodynamic properties of commonly used antiplatelet and anticoagulant drugs with special emphasis on loss of effects after discontinuation and possible counteracting (or antidote) strategies. These drugs are aspirin (acetylsalicylic acid), ticlopidine/clopidogrel, abciximab, tirofiban and eptifibatide, heparin (unfractionated and low-molecular-weight), warfarin and direct thrombin inhibitors. Since the pharmacological mechanisms of some of these drugs are based on irreversible or slowly reversible effects, their pharmacokinetic profiles are not necessarily predictive for their pharmacodynamic profiles. A close and direct relationship between plasma concentrations and effects is seen only for the glycoprotein (GP) IIb/IIIa inhibitors tirofiban and eptifibatide with a fast off-rate for dissociation from the GPIIb/IIIa receptor, and for direct thrombin inhibitors (hirudin and argatroban). For other compounds, drug concentrations in plasma and pharmacodynamic effects are not closely correlated because of, for example, irreversible binding to their target (aspirin, Clopidogrel and abciximab), inhibition of the generation of a subset of clotting factors with differing regeneration and degradation rates (coumarins) or sustained binding to the vascular wall (heparins).
Surgery in patients on anticoagulant and/or antiplatelet therapy may be categorised as: (i) elective versus urgent; and (ii) cardiopulmonary bypass (CPB) versus non-CPB. Monotherapy with Clopidogrel or aspirin need not be discontinued in elective non-CPB surgery, and temporary discontinuation of warfarin should be accompanied by preoperative intravenous heparin only in selected high-risk patients. Vitamin K as an antidote for warfarin should only be used subcutaneously and solely in urgent/emergency surgery. In elective surgery requiring CPB (coronary artery bypass grafting), it is recommended to discontinue aspirin 7 days preoperatively in patients with a low risk profile. Patients requiring urgent CPB surgery (e.g. after failure of a percutaneous coronary angioplasty with or without coronary stent deployment) are usually pretreated with several antiplatelet agents (e.g. aspirin and Clopidogrel, together with a GPIIb/IIIa inhibitor) together with unfractionated or low-molecular-weight heparin. With judicious planning, urgent/emergency cardiac surgery can be safely performed on these patients. Delaying surgery (e.g. for 12 hours in patients treated with abciximab) should be considered if possible. Standard heparin doses should be given to achieve optimal anticoagulation for CPB. Prophylactic use of aprotinin (intraand/or postoperatively), aminocaproic acid or tranexamic acid should be considered. Early (in the operating theatre prior to chest closure) and judicious use of replacement blood products (platelets) should be commenced when clinically indicated.
Literatur
1.
Zurück zum Zitat Takahashi T, Kawamata T, Namiki A. A case of postoperative acute myocardial infarction due to the interruption of anticoagulant therapy. Masui 2002; 51: 280–2PubMed Takahashi T, Kawamata T, Namiki A. A case of postoperative acute myocardial infarction due to the interruption of anticoagulant therapy. Masui 2002; 51: 280–2PubMed
2.
Zurück zum Zitat Schanbacher CF, Bennett RG. Postoperative stroke after stopping warfarin for cutaneous surgery. Dermatol Surg 2000; 26: 785–9PubMedCrossRef Schanbacher CF, Bennett RG. Postoperative stroke after stopping warfarin for cutaneous surgery. Dermatol Surg 2000; 26: 785–9PubMedCrossRef
3.
Zurück zum Zitat Palareti G, Legnani C. Warfarin withdrawal: pharmacokineticpharmacodynamic considerations. Clin Pharmacokinet 1996; 30: 300–13PubMedCrossRef Palareti G, Legnani C. Warfarin withdrawal: pharmacokineticpharmacodynamic considerations. Clin Pharmacokinet 1996; 30: 300–13PubMedCrossRef
4.
Zurück zum Zitat Ferraris VA, Gildengorin V. Predictors of excessive blood use after coronary artery bypass grafting: a multivariate analysis. J Thorac Cardiovasc Surg 1989; 98: 492–7PubMed Ferraris VA, Gildengorin V. Predictors of excessive blood use after coronary artery bypass grafting: a multivariate analysis. J Thorac Cardiovasc Surg 1989; 98: 492–7PubMed
5.
6.
Zurück zum Zitat Yende S, Wunderink RG. Effect of Clopidogrel on bleeding after coronary artery bypass surgery. Crit Care Med 2001; 29: 2271–4PubMedCrossRef Yende S, Wunderink RG. Effect of Clopidogrel on bleeding after coronary artery bypass surgery. Crit Care Med 2001; 29: 2271–4PubMedCrossRef
7.
Zurück zum Zitat Gammie JS, Zenati M, Kormos RL, et al. Abciximab and excessive bleeding in patients undergoing emergency cardiac operations. Ann Thorac Surg 1998; 65: 465–9PubMedCrossRef Gammie JS, Zenati M, Kormos RL, et al. Abciximab and excessive bleeding in patients undergoing emergency cardiac operations. Ann Thorac Surg 1998; 65: 465–9PubMedCrossRef
8.
Zurück zum Zitat Juergens CP, Yeung AC, Oesterle SN. Routine platelet transfusion in patients undergoing emergency coronary bypass surgery after receiving abciximab. Am J Cardiol 1997; 80: 74–5PubMedCrossRef Juergens CP, Yeung AC, Oesterle SN. Routine platelet transfusion in patients undergoing emergency coronary bypass surgery after receiving abciximab. Am J Cardiol 1997; 80: 74–5PubMedCrossRef
9.
Zurück zum Zitat Arjomand H, Mascarenhas DA, Morgan RJ. Abciximab and the risk of bleeding during emergency cardiac operations. Ann Thorac Surg 1999; 67: 292–3PubMedCrossRef Arjomand H, Mascarenhas DA, Morgan RJ. Abciximab and the risk of bleeding during emergency cardiac operations. Ann Thorac Surg 1999; 67: 292–3PubMedCrossRef
10.
Zurück zum Zitat Silvestry SC, Smith PK. Current status of cardiac surgery in the abciximab-treated patient. Ann Thorac Surg 2000; 70 (2Suppl.): S12–9CrossRef Silvestry SC, Smith PK. Current status of cardiac surgery in the abciximab-treated patient. Ann Thorac Surg 2000; 70 (2Suppl.): S12–9CrossRef
11.
Zurück zum Zitat Alvarez JM. Emergency coronary bypass grafting for failed percutaneous coronary artery stenting: increased costs and platelet transfusion requirements after the use of abciximab. J Thorac Cardiovasc Surg 1998; 115: 472–3PubMedCrossRef Alvarez JM. Emergency coronary bypass grafting for failed percutaneous coronary artery stenting: increased costs and platelet transfusion requirements after the use of abciximab. J Thorac Cardiovasc Surg 1998; 115: 472–3PubMedCrossRef
12.
Zurück zum Zitat Alvarez JM. Coronary stenting and use of abciximab. Lancet 1998; 17: 1311–2CrossRef Alvarez JM. Coronary stenting and use of abciximab. Lancet 1998; 17: 1311–2CrossRef
13.
Zurück zum Zitat Singh M, Nuttall GA, Ballman KV, et al. Effect of abciximab on the outcome of emergency coronary artery bypass grafting after failed percutaneous coronary intervention. Mayo Clin Proc 2001; 76: 784–8PubMedCrossRef Singh M, Nuttall GA, Ballman KV, et al. Effect of abciximab on the outcome of emergency coronary artery bypass grafting after failed percutaneous coronary intervention. Mayo Clin Proc 2001; 76: 784–8PubMedCrossRef
14.
Zurück zum Zitat Vahl CF, Kayhan N, Thomas G, et al. Myocardial revascularization after pretreatment with the GPIIb/IIIa receptor blocker abciximab. Z Kardiol 2001; 90: 889–97PubMedCrossRef Vahl CF, Kayhan N, Thomas G, et al. Myocardial revascularization after pretreatment with the GPIIb/IIIa receptor blocker abciximab. Z Kardiol 2001; 90: 889–97PubMedCrossRef
15.
Zurück zum Zitat Bizzarri F, Scolletta S, Tucci E, et al. Perioperative use of tirofiban hydrochloride (Aggrastat) does not increase surgical bleeding after emergency or urgent coronary artery bypass grafting. J Thorac Cardiovasc Surg 2001; 122: 1181–5PubMedCrossRef Bizzarri F, Scolletta S, Tucci E, et al. Perioperative use of tirofiban hydrochloride (Aggrastat) does not increase surgical bleeding after emergency or urgent coronary artery bypass grafting. J Thorac Cardiovasc Surg 2001; 122: 1181–5PubMedCrossRef
16.
Zurück zum Zitat Dyke CM, Bhatia D, Lorenz TJ, et al. Immediate coronary artery bypass surgery after platelet inhibition with eptifibatide: results from PURSUIT (Platelet Glycoprotein IIb/IIIa in Unstable Angina: Receptor Suppression Using Integrelin Therapy). Ann Thorac Surg 2000; 70: 866–71PubMedCrossRef Dyke CM, Bhatia D, Lorenz TJ, et al. Immediate coronary artery bypass surgery after platelet inhibition with eptifibatide: results from PURSUIT (Platelet Glycoprotein IIb/IIIa in Unstable Angina: Receptor Suppression Using Integrelin Therapy). Ann Thorac Surg 2000; 70: 866–71PubMedCrossRef
17.
Zurück zum Zitat Horlocker TT. Low molecular weight heparin and neuraxial anesthesia. Thromb Res 2001; 101: V141–54PubMedCrossRef Horlocker TT. Low molecular weight heparin and neuraxial anesthesia. Thromb Res 2001; 101: V141–54PubMedCrossRef
18.
Zurück zum Zitat Horlocker TT, Wedel DJ, Schroeder DR, et al. Preoperative antiplatelet therapy does not increase the risk of spinal hematoma associated with regional anesthesia. Anesth Analg 1995; 80: 303–9PubMed Horlocker TT, Wedel DJ, Schroeder DR, et al. Preoperative antiplatelet therapy does not increase the risk of spinal hematoma associated with regional anesthesia. Anesth Analg 1995; 80: 303–9PubMed
19.
Zurück zum Zitat Urmey WF, Rowlingson J. Do antiplatelet agents contribute to the development of perioperative spinal hematoma? Reg Anesth Pain Med 1998; 23 Suppl. 2: 146–51CrossRef Urmey WF, Rowlingson J. Do antiplatelet agents contribute to the development of perioperative spinal hematoma? Reg Anesth Pain Med 1998; 23 Suppl. 2: 146–51CrossRef
20.
Zurück zum Zitat Neilipovitz DT, Bryson GL, Nichol G. The effect of perioperative aspirin therapy in peripheral vascular surgery: a decision analysis. Anesth Analg 2001; 93: 573–80PubMedCrossRef Neilipovitz DT, Bryson GL, Nichol G. The effect of perioperative aspirin therapy in peripheral vascular surgery: a decision analysis. Anesth Analg 2001; 93: 573–80PubMedCrossRef
21.
Zurück zum Zitat Kearon C, Hirsh J. Management of anticoagulation before and after elective surgery. N Engl J Med 1997; 336: 1506–11PubMedCrossRef Kearon C, Hirsh J. Management of anticoagulation before and after elective surgery. N Engl J Med 1997; 336: 1506–11PubMedCrossRef
22.
23.
Zurück zum Zitat Hull RD, Raskob GE, Hirsh J, et al. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N Engl J Med 1986; 315: 1109–14PubMedCrossRef Hull RD, Raskob GE, Hirsh J, et al. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N Engl J Med 1986; 315: 1109–14PubMedCrossRef
24.
Zurück zum Zitat De Swart CAM, Nijmeyer B, Roelofs JMM, et al. Kinetics of intravenously administered heparin in normal humans. Blood 1982; 60: 1251–8PubMed De Swart CAM, Nijmeyer B, Roelofs JMM, et al. Kinetics of intravenously administered heparin in normal humans. Blood 1982; 60: 1251–8PubMed
25.
Zurück zum Zitat Hirsh J, Warkentin TE, Shaughnessy SG, et al. Heparin and low-molecular-weight heparin: mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety. Chest 2001; 119: 64–94SCrossRef Hirsh J, Warkentin TE, Shaughnessy SG, et al. Heparin and low-molecular-weight heparin: mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety. Chest 2001; 119: 64–94SCrossRef
26.
Zurück zum Zitat Levine MN, Hirsh J, Kelton JG. Heparin induced bleeding. In: Lane DA, Lindahl U, editors. Heparin: chemical and biological properties, clinical applications. London: Edward Arnold, 1989: 517–32 Levine MN, Hirsh J, Kelton JG. Heparin induced bleeding. In: Lane DA, Lindahl U, editors. Heparin: chemical and biological properties, clinical applications. London: Edward Arnold, 1989: 517–32
27.
Zurück zum Zitat Morabia A. Heparin doses and major bleedings. Lancet 1986; I: 1278–9CrossRef Morabia A. Heparin doses and major bleedings. Lancet 1986; I: 1278–9CrossRef
28.
Zurück zum Zitat Levy JH. Pharmacologic preservation of the hemostatic system during cardiac surgery. Ann Thorac Surg 2001; 72: 1814–20CrossRef Levy JH. Pharmacologic preservation of the hemostatic system during cardiac surgery. Ann Thorac Surg 2001; 72: 1814–20CrossRef
29.
Zurück zum Zitat Young E, Wells P, Holloway S, et al. Ex-vivo and in-vitro evidence that low molecular weight heparins exhibit less binding to plasma proteins than unfractionated heparin. Thromb Haemostasis 1994; 71: 300–4 Young E, Wells P, Holloway S, et al. Ex-vivo and in-vitro evidence that low molecular weight heparins exhibit less binding to plasma proteins than unfractionated heparin. Thromb Haemostasis 1994; 71: 300–4
30.
Zurück zum Zitat Kessler CM, Esparraguera IM, Jacobs HM, et al. Monitoring the anticoagulant effects of a low molecular weight heparin preparation: correlation of assays in orthopedic surgery patients receiving ardeparin sodium for prophylaxis of deep venous thrombosis. Am J Clin Pathol 1995; 103: 642–8PubMedCrossRef Kessler CM, Esparraguera IM, Jacobs HM, et al. Monitoring the anticoagulant effects of a low molecular weight heparin preparation: correlation of assays in orthopedic surgery patients receiving ardeparin sodium for prophylaxis of deep venous thrombosis. Am J Clin Pathol 1995; 103: 642–8PubMedCrossRef
31.
Zurück zum Zitat Kronemann H, Eikelboom BC, Knot EA, et al. Pharmacokinetics of low-molecular-weight heparin and unfractionated heparin during elective aortobifemoral bypass grafting. J Vasc Surg 1991; 14: 208–14CrossRef Kronemann H, Eikelboom BC, Knot EA, et al. Pharmacokinetics of low-molecular-weight heparin and unfractionated heparin during elective aortobifemoral bypass grafting. J Vasc Surg 1991; 14: 208–14CrossRef
32.
Zurück zum Zitat Holst J, Lindblad B, Bergqvist D, et al. Protamine neutralization of intravenous and subcutaneous low-molecular-weight heparin (tinzaparin): an experimental investigation in healthy volunteers. Blood Coagul Fibrinolysis 1994; 5: 795–803PubMedCrossRef Holst J, Lindblad B, Bergqvist D, et al. Protamine neutralization of intravenous and subcutaneous low-molecular-weight heparin (tinzaparin): an experimental investigation in healthy volunteers. Blood Coagul Fibrinolysis 1994; 5: 795–803PubMedCrossRef
33.
Zurück zum Zitat Bauer KA. Fondaparinux sodium: a selective inhibitor of factor Xa. Am J Health Syst Pharm 2001; 58 Suppl. 2: S14–7PubMed Bauer KA. Fondaparinux sodium: a selective inhibitor of factor Xa. Am J Health Syst Pharm 2001; 58 Suppl. 2: S14–7PubMed
34.
Zurück zum Zitat Bijsterveld NR, Moons AH, Boekhold SM, et al. Ability of recombinant factor VIIa to reverse the anticoagulant effect of the pentasaccharide fondaparinux in healthy volunteers. Circulation 2002; 106: 2550–4PubMedCrossRef Bijsterveld NR, Moons AH, Boekhold SM, et al. Ability of recombinant factor VIIa to reverse the anticoagulant effect of the pentasaccharide fondaparinux in healthy volunteers. Circulation 2002; 106: 2550–4PubMedCrossRef
36.
Zurück zum Zitat Weitz JI, Leslie B, Hudoba M. Thrombin binds to soluble fibrin degradation products where it is protected from inhibition by heparin-antithrombin but susceptible to inactivation by antithrombin-independent inhibitors. Circulation 1998; 97: 544–52PubMedCrossRef Weitz JI, Leslie B, Hudoba M. Thrombin binds to soluble fibrin degradation products where it is protected from inhibition by heparin-antithrombin but susceptible to inactivation by antithrombin-independent inhibitors. Circulation 1998; 97: 544–52PubMedCrossRef
37.
Zurück zum Zitat Weitz JI, Harry RB. Direct thrombin inhibitors in acute coronary syndromes: present and future. Circulation 2002; 105: 1004–11PubMedCrossRef Weitz JI, Harry RB. Direct thrombin inhibitors in acute coronary syndromes: present and future. Circulation 2002; 105: 1004–11PubMedCrossRef
38.
Zurück zum Zitat Stringer KA, Lindenfeld J. Hirudins: antithrombin anticoagulants. Ann Pharmacother 1992; 26: 1535–40PubMedCrossRef Stringer KA, Lindenfeld J. Hirudins: antithrombin anticoagulants. Ann Pharmacother 1992; 26: 1535–40PubMedCrossRef
39.
Zurück zum Zitat Zoldhelyi P, Webster MW, Fuster V, et al. Recombinant hirudin in patients with chronic, stable coronary artery disease: safety, half-life, and effect on coagulation parameters. Circulation 1993; 88: 2015–22PubMedCrossRef Zoldhelyi P, Webster MW, Fuster V, et al. Recombinant hirudin in patients with chronic, stable coronary artery disease: safety, half-life, and effect on coagulation parameters. Circulation 1993; 88: 2015–22PubMedCrossRef
40.
Zurück zum Zitat Robson R, White H, Aylward P, et al. Bivalirudin pharmacokinetics and pharmacodynamics: effect of renal function, dose, and gender. Clin Pharmacol Ther 2002; 71: 433–9PubMedCrossRef Robson R, White H, Aylward P, et al. Bivalirudin pharmacokinetics and pharmacodynamics: effect of renal function, dose, and gender. Clin Pharmacol Ther 2002; 71: 433–9PubMedCrossRef
41.
Zurück zum Zitat Fitzgerald D, Murphy N. Argatroban: a synthetic thrombin inhibitor of low relative molecular mass. Coron Artery Dis 1996; 7: 455–8PubMedCrossRef Fitzgerald D, Murphy N. Argatroban: a synthetic thrombin inhibitor of low relative molecular mass. Coron Artery Dis 1996; 7: 455–8PubMedCrossRef
43.
Zurück zum Zitat Gustafsson D, Elg M. The pharmacodynamics and pharmacokinetics of the oral direct thrombin inhibitor ximelagatran and its active metabolite melagatran: a mini-review. Thromb Res 2003; 109 Suppl. 1: S9–15PubMedCrossRef Gustafsson D, Elg M. The pharmacodynamics and pharmacokinetics of the oral direct thrombin inhibitor ximelagatran and its active metabolite melagatran: a mini-review. Thromb Res 2003; 109 Suppl. 1: S9–15PubMedCrossRef
44.
Zurück zum Zitat Harder S, Graff J, Klinkhardt U, et al. Transition from argatroban to oral anticoagulation with phenprocoumon or acenocoumarol: effects on Prothrombin time, activated partial thromboplastin time, and Ecarin clotting time. Thromb Haemost 2004; 91: 1137–45PubMed Harder S, Graff J, Klinkhardt U, et al. Transition from argatroban to oral anticoagulation with phenprocoumon or acenocoumarol: effects on Prothrombin time, activated partial thromboplastin time, and Ecarin clotting time. Thromb Haemost 2004; 91: 1137–45PubMed
45.
Zurück zum Zitat Hirsh J, Dalen JE, Anderson DR, et al. Oral anticoagulants: mechanism of action, clinical effectiveness, and optimal therapeutic range. Chest 2001; 119: 8–21CrossRef Hirsh J, Dalen JE, Anderson DR, et al. Oral anticoagulants: mechanism of action, clinical effectiveness, and optimal therapeutic range. Chest 2001; 119: 8–21CrossRef
46.
Zurück zum Zitat Breckenridge AM. Oral anticoagulant drugs: pharmacokinetic aspects. Semin Hematol 1978; 15: 19–26PubMed Breckenridge AM. Oral anticoagulant drugs: pharmacokinetic aspects. Semin Hematol 1978; 15: 19–26PubMed
47.
Zurück zum Zitat O’Reilly RA. Warfarin metabolism and drug-drug interactions. In: Wessler S, Becker CG, Nemerson Y, editors. The new dimensions of warfarin prophylaxis: advances in experimental medicine and biology. New York: Plenum, 1986: 205–12 O’Reilly RA. Warfarin metabolism and drug-drug interactions. In: Wessler S, Becker CG, Nemerson Y, editors. The new dimensions of warfarin prophylaxis: advances in experimental medicine and biology. New York: Plenum, 1986: 205–12
49.
Zurück zum Zitat Harder S, Thurmann P. Clinically important drug interactions with anticoagulants: an update. Clin Pharmacokinet 1996; 30: 416–44PubMedCrossRef Harder S, Thurmann P. Clinically important drug interactions with anticoagulants: an update. Clin Pharmacokinet 1996; 30: 416–44PubMedCrossRef
50.
Zurück zum Zitat White RH, McKittrick T, Hutchinson R, et al. Temporary discontinuation of warfarin therapy: changes in the international normalized ratio. Ann Intern Med 1995; 122: 40–2PubMedCrossRef White RH, McKittrick T, Hutchinson R, et al. Temporary discontinuation of warfarin therapy: changes in the international normalized ratio. Ann Intern Med 1995; 122: 40–2PubMedCrossRef
52.
Zurück zum Zitat Schroder H, Schror K. Clinical pharmacology of acetylsalicylic acid. Z Kardiol 1992; 81: 171–5PubMed Schroder H, Schror K. Clinical pharmacology of acetylsalicylic acid. Z Kardiol 1992; 81: 171–5PubMed
53.
Zurück zum Zitat Cryer B, Feldman M. Cyclooxygenase-1 and cyclooxygenase-2 selectivity of widely used nonsteroidal anti-inflammatory drugs. Am J Med 1998; 104: 413–21PubMedCrossRef Cryer B, Feldman M. Cyclooxygenase-1 and cyclooxygenase-2 selectivity of widely used nonsteroidal anti-inflammatory drugs. Am J Med 1998; 104: 413–21PubMedCrossRef
54.
Zurück zum Zitat Antiplatelet Trialists’ Collaboration. Collaborative overview of randomised trials of antiplatelet therapy: I: prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients. BMJ 1994; 308: 81–106CrossRef Antiplatelet Trialists’ Collaboration. Collaborative overview of randomised trials of antiplatelet therapy: I: prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients. BMJ 1994; 308: 81–106CrossRef
55.
Zurück zum Zitat Benedek IH, Joshi AS, Pieniaszek HJ, et al. Variability in the pharmacokinetics and pharmacodynamics of low dose aspirin in healthy male volunteers. J Clin Pharmacol 1995; 35: 1181–6PubMedCrossRef Benedek IH, Joshi AS, Pieniaszek HJ, et al. Variability in the pharmacokinetics and pharmacodynamics of low dose aspirin in healthy male volunteers. J Clin Pharmacol 1995; 35: 1181–6PubMedCrossRef
56.
Zurück zum Zitat Feldman M, Shewmake K, Cryer B. Time course inhibition of gastric and platelet COX activity by acetylsalicylic acid in humans. Am J Physiol Gastrointest Liver Physiol 2000; 279: 1113–20 Feldman M, Shewmake K, Cryer B. Time course inhibition of gastric and platelet COX activity by acetylsalicylic acid in humans. Am J Physiol Gastrointest Liver Physiol 2000; 279: 1113–20
57.
58.
Zurück zum Zitat Savi P, Combalbert J, Gaich C, et al. The antiaggregating activity of Clopidogrel is due to a metabolic activation by the hepatic cytochrome P450-1A. Thromb Haemost 1994; 26: 347–55 Savi P, Combalbert J, Gaich C, et al. The antiaggregating activity of Clopidogrel is due to a metabolic activation by the hepatic cytochrome P450-1A. Thromb Haemost 1994; 26: 347–55
59.
Zurück zum Zitat Savi P, Pereillo JM, Uzabiaga MF, et al. Identification and biological activity of the active metabolite of Clopidogrel. Thromb Haemost 2000; 84: 891–6PubMed Savi P, Pereillo JM, Uzabiaga MF, et al. Identification and biological activity of the active metabolite of Clopidogrel. Thromb Haemost 2000; 84: 891–6PubMed
60.
Zurück zum Zitat Klinkhardt U, Kirchmaier CM, Westrup D, et al. Ex vivo-in vitro interaction between aspirin, Clopidogrel, and the glycoprotein IIb/IIIa inhibitors abciximab and SR121566A. Clin Pharmacol Ther 2000; 67: 305–13PubMedCrossRef Klinkhardt U, Kirchmaier CM, Westrup D, et al. Ex vivo-in vitro interaction between aspirin, Clopidogrel, and the glycoprotein IIb/IIIa inhibitors abciximab and SR121566A. Clin Pharmacol Ther 2000; 67: 305–13PubMedCrossRef
61.
Zurück zum Zitat Heptinstall S, May JA, Glenn JR, et al. Effects of ticlopidine administered to healthy volunteers on platelet function in whole blood. Thromb Haemost 1995; 74: 1310–5PubMed Heptinstall S, May JA, Glenn JR, et al. Effects of ticlopidine administered to healthy volunteers on platelet function in whole blood. Thromb Haemost 1995; 74: 1310–5PubMed
62.
Zurück zum Zitat Cattaneo M, Akkawat B, Lecchi A, et al. Ticlopidine selectively inhibits human platelet responses to adenosine diphosphate. Thromb Haemost 1991; 66: 694–9PubMed Cattaneo M, Akkawat B, Lecchi A, et al. Ticlopidine selectively inhibits human platelet responses to adenosine diphosphate. Thromb Haemost 1991; 66: 694–9PubMed
63.
Zurück zum Zitat Weber AA, Braun M, Hohfeld T, et al. Recovery of platelet function after discontinuation of Clopidogrel treatment in healthy volunteers. Br J Clin Pharmacol 2001; 52: 333–6PubMedPubMedCentralCrossRef Weber AA, Braun M, Hohfeld T, et al. Recovery of platelet function after discontinuation of Clopidogrel treatment in healthy volunteers. Br J Clin Pharmacol 2001; 52: 333–6PubMedPubMedCentralCrossRef
64.
Zurück zum Zitat Yusuf S, Zhao F, Mehta SR, et al. Effects of Clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation. N Engl J Med 2001; 345: 494–502PubMedCrossRef Yusuf S, Zhao F, Mehta SR, et al. Effects of Clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation. N Engl J Med 2001; 345: 494–502PubMedCrossRef
65.
Zurück zum Zitat Kleiman NS. Pharmacokinetics and pharmacodynamics of glycoprotein IIb-IIIa inhibitors. Am Heart J 1999; 138: 263–75PubMedCrossRef Kleiman NS. Pharmacokinetics and pharmacodynamics of glycoprotein IIb-IIIa inhibitors. Am Heart J 1999; 138: 263–75PubMedCrossRef
66.
Zurück zum Zitat Klinkhardt U, Graff J, Westrup D, et al. Pharmacodynamic characterization of the interaction between abciximab or tirofiban with unfractionated or a low molecular weight heparin in healthy subjects. Br J Clin Pharmacol 2000; 52: 297–305CrossRef Klinkhardt U, Graff J, Westrup D, et al. Pharmacodynamic characterization of the interaction between abciximab or tirofiban with unfractionated or a low molecular weight heparin in healthy subjects. Br J Clin Pharmacol 2000; 52: 297–305CrossRef
67.
Zurück zum Zitat Faulds D, Sorkin EM. Abciximab (c7E3 Fab): a review of its pharmacology and therapeutic potential in ischaemic heart disease. Drugs 1994; 48: 583–98PubMedCrossRef Faulds D, Sorkin EM. Abciximab (c7E3 Fab): a review of its pharmacology and therapeutic potential in ischaemic heart disease. Drugs 1994; 48: 583–98PubMedCrossRef
68.
Zurück zum Zitat Tcheng JE, Ellis SG, George BS, et al. Pharmacodynamics of chimeric glycoprotein IIb/IIIa integrin antiplatelet antibody Fab 7E3 in high-risk coronary angioplasty. Circulation 1994; 90: 1757–64PubMedCrossRef Tcheng JE, Ellis SG, George BS, et al. Pharmacodynamics of chimeric glycoprotein IIb/IIIa integrin antiplatelet antibody Fab 7E3 in high-risk coronary angioplasty. Circulation 1994; 90: 1757–64PubMedCrossRef
69.
Zurück zum Zitat Harder S, Kirchmaier CM, Krzywanek HJ, et al. Pharmacokinetics and pharmacodynamic effects of a new antibody glycoprotein IIb/IIIa inhibitor (YM337) in healthy subjects. Circulation 1999; 100: 1175–81PubMedCrossRef Harder S, Kirchmaier CM, Krzywanek HJ, et al. Pharmacokinetics and pharmacodynamic effects of a new antibody glycoprotein IIb/IIIa inhibitor (YM337) in healthy subjects. Circulation 1999; 100: 1175–81PubMedCrossRef
70.
Zurück zum Zitat Lefkovits J, Topol EJ. Platelet glycoprotein IIb/IIIa receptor antagonists in coronary artery disease. Eur Heart J 1996; 17: 9–18PubMedCrossRef Lefkovits J, Topol EJ. Platelet glycoprotein IIb/IIIa receptor antagonists in coronary artery disease. Eur Heart J 1996; 17: 9–18PubMedCrossRef
71.
Zurück zum Zitat Tcheng JE, Talley JD, O’shea JC, et al. Clinical pharmacology of higher dose eptifibatide in percutaneous coronary intervention (the PRIDE study). Am J Cardiol 2001; 88: 1097–102PubMedCrossRef Tcheng JE, Talley JD, O’shea JC, et al. Clinical pharmacology of higher dose eptifibatide in percutaneous coronary intervention (the PRIDE study). Am J Cardiol 2001; 88: 1097–102PubMedCrossRef
72.
Zurück zum Zitat Theroux P, White H, David D, et al. A heparin-controlled study of MK-383 in unstable angina [abstract]. Circulation 1994; 90 Suppl. 1: I–231 Theroux P, White H, David D, et al. A heparin-controlled study of MK-383 in unstable angina [abstract]. Circulation 1994; 90 Suppl. 1: I–231
73.
Zurück zum Zitat Barrett JS, Murphy G, Peerlinck K, et al. Pharmacokinetics and pharmacodynamics of MK-383, a selective non-peptide platelet glycoprotein-IIb/IIIa receptor antagonist, in healthy men. Clin Pharmacol Ther 1994; 56: 377–88PubMedCrossRef Barrett JS, Murphy G, Peerlinck K, et al. Pharmacokinetics and pharmacodynamics of MK-383, a selective non-peptide platelet glycoprotein-IIb/IIIa receptor antagonist, in healthy men. Clin Pharmacol Ther 1994; 56: 377–88PubMedCrossRef
74.
Zurück zum Zitat Thompson CM, Steinhubl SR. Monitoring of platelet function in the setting of glycoprotein IIb/IIIa inhibitor therapy. J Interv Cardiol 2002; 15: 61–70PubMedCrossRef Thompson CM, Steinhubl SR. Monitoring of platelet function in the setting of glycoprotein IIb/IIIa inhibitor therapy. J Interv Cardiol 2002; 15: 61–70PubMedCrossRef
75.
Zurück zum Zitat Poullis M, Manning R, Haskard D, et al. Reopro removal during cardiopulmonary bypass using a hemoconcentrator. J Thorac Cardiovasc Surg 1999; 117: 1032–4PubMedCrossRef Poullis M, Manning R, Haskard D, et al. Reopro removal during cardiopulmonary bypass using a hemoconcentrator. J Thorac Cardiovasc Surg 1999; 117: 1032–4PubMedCrossRef
76.
Zurück zum Zitat Lemmer Jr JH. Abciximab (ReoPro) removal with a hemoconcentrator during cardiopulmonary bypass. J Thorac Cardiovasc Surg 1999; 118: 980–1PubMedCrossRef Lemmer Jr JH. Abciximab (ReoPro) removal with a hemoconcentrator during cardiopulmonary bypass. J Thorac Cardiovasc Surg 1999; 118: 980–1PubMedCrossRef
77.
Zurück zum Zitat Steinhubl SR, Moore SA, Lincoff AM. Abciximab (ReoPro) removal during cardiopulmonary bypass with a hemoconcentrator. J Thorac Cardiovasc Surg 2000; 119: 401–2PubMedCrossRef Steinhubl SR, Moore SA, Lincoff AM. Abciximab (ReoPro) removal during cardiopulmonary bypass with a hemoconcentrator. J Thorac Cardiovasc Surg 2000; 119: 401–2PubMedCrossRef
78.
Zurück zum Zitat Poullis M. Abciximab (ReoPro) removal during cardiopulmonary bypass with a hemoconcentrator. J Thorac Cardiovasc Surg 2000; 119: 401–2PubMedCrossRef Poullis M. Abciximab (ReoPro) removal during cardiopulmonary bypass with a hemoconcentrator. J Thorac Cardiovasc Surg 2000; 119: 401–2PubMedCrossRef
79.
Zurück zum Zitat Royston D. Aprotinin versus lysine analogues: the debate continues. Ann Thorac Surg 1998; 65: S9–19PubMedCrossRef Royston D. Aprotinin versus lysine analogues: the debate continues. Ann Thorac Surg 1998; 65: S9–19PubMedCrossRef
80.
Zurück zum Zitat Jacobs LG, Nusbaum N. Perioperative management and reversal of antithrombotic therapy. Clin Geriatr Med 2001; 17: 189–202PubMedCrossRef Jacobs LG, Nusbaum N. Perioperative management and reversal of antithrombotic therapy. Clin Geriatr Med 2001; 17: 189–202PubMedCrossRef
81.
Zurück zum Zitat Sindet-Pedersen S, Ramstrom G, Bernvil S, et al. Hemostatic effect of tranexamic acid mouthwash in anticoagulant-treated patients undergoing oral surgery. N Engl J Med 1989; 320: 840–3PubMedCrossRef Sindet-Pedersen S, Ramstrom G, Bernvil S, et al. Hemostatic effect of tranexamic acid mouthwash in anticoagulant-treated patients undergoing oral surgery. N Engl J Med 1989; 320: 840–3PubMedCrossRef
82.
Zurück zum Zitat Douketis JD. Perioperative anticoagulation management in patients who are receiving oral anticoagulant therapy: a practical guide for clinicians. Thromb Res 2002; 108: 3–13PubMedCrossRef Douketis JD. Perioperative anticoagulation management in patients who are receiving oral anticoagulant therapy: a practical guide for clinicians. Thromb Res 2002; 108: 3–13PubMedCrossRef
83.
Zurück zum Zitat Eagle KA, Guyton RA, Davidoff R, et al. ACC/AHA guidelines for coronary artery bypass graft surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Revise the 1991 Guidelines for Coronary Artery Bypass Graft Surgery). J Am Coll Cardiol 1999; 34: 1262–347PubMedCrossRef Eagle KA, Guyton RA, Davidoff R, et al. ACC/AHA guidelines for coronary artery bypass graft surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Revise the 1991 Guidelines for Coronary Artery Bypass Graft Surgery). J Am Coll Cardiol 1999; 34: 1262–347PubMedCrossRef
84.
Zurück zum Zitat Mangano DT, the Multicenter Study of Perioperative Ischemia Research Group. Aspirin and mortality from coronary bypass surgery. N Engl J Med 2002; 347: 1309–17PubMedCrossRef Mangano DT, the Multicenter Study of Perioperative Ischemia Research Group. Aspirin and mortality from coronary bypass surgery. N Engl J Med 2002; 347: 1309–17PubMedCrossRef
85.
Zurück zum Zitat Alvarez JM, Chen L, Sinclair IN. Acute stent thrombosis following off pump coronary bypass surgery: a new and avoidable complication? J Thorac Cardiovasc Surg 2003; 125: 1544–6PubMedCrossRef Alvarez JM, Chen L, Sinclair IN. Acute stent thrombosis following off pump coronary bypass surgery: a new and avoidable complication? J Thorac Cardiovasc Surg 2003; 125: 1544–6PubMedCrossRef
86.
Zurück zum Zitat Alvarez JM, Harper RW, Peverill RE. Emergency coronary artery bypass grafting (CABG) after failed coronary artery intervention: caution regarding the combined use of aspirin, ticlopidine and abciximab. Aust N Z J Med 1998; 28: 463–4PubMedCrossRef Alvarez JM, Harper RW, Peverill RE. Emergency coronary artery bypass grafting (CABG) after failed coronary artery intervention: caution regarding the combined use of aspirin, ticlopidine and abciximab. Aust N Z J Med 1998; 28: 463–4PubMedCrossRef
87.
Zurück zum Zitat Alvarez JM, Jackson LR, Chatwin C, et al. Low dose postoperative aprotinin reduces mediastinal drainage and blood transfusion requirements in primary CABG patients on aspirin: a prospective, double-blind, placebo-controlled trial. J Thorac Cardiovasc Surg 2001; 112: 457–63CrossRef Alvarez JM, Jackson LR, Chatwin C, et al. Low dose postoperative aprotinin reduces mediastinal drainage and blood transfusion requirements in primary CABG patients on aspirin: a prospective, double-blind, placebo-controlled trial. J Thorac Cardiovasc Surg 2001; 112: 457–63CrossRef
88.
Zurück zum Zitat Christenson JT, Maurice J, Simonet F, et al. Open chest and delayed sternal closure after cardiac surgery. Eur J Cardiothorac Surg 1996; 10: 305–11PubMedCrossRef Christenson JT, Maurice J, Simonet F, et al. Open chest and delayed sternal closure after cardiac surgery. Eur J Cardiothorac Surg 1996; 10: 305–11PubMedCrossRef
89.
Zurück zum Zitat Bouboulis N, Rivas LF, Kuo J, et al. Packing the chest: a useful technique for intractable bleeding after open heart operation. Ann Thorac Surg 1994; 57: 856–60PubMedCrossRef Bouboulis N, Rivas LF, Kuo J, et al. Packing the chest: a useful technique for intractable bleeding after open heart operation. Ann Thorac Surg 1994; 57: 856–60PubMedCrossRef
90.
Zurück zum Zitat O’Regan DJ, Giannopoulos N, Mediretta N, et al. Topical aprotinin in cardiac operations. Ann Thorac Surg 1994; 58: 778–81PubMedCrossRef O’Regan DJ, Giannopoulos N, Mediretta N, et al. Topical aprotinin in cardiac operations. Ann Thorac Surg 1994; 58: 778–81PubMedCrossRef
91.
Zurück zum Zitat Peters DC, Noble S. Aprotinin: an update of its pharmacology and therapeutic use in open heart surgery and coronary artery bypass surgery. Drugs 1999; 57: 233–60PubMedCrossRef Peters DC, Noble S. Aprotinin: an update of its pharmacology and therapeutic use in open heart surgery and coronary artery bypass surgery. Drugs 1999; 57: 233–60PubMedCrossRef
92.
Zurück zum Zitat Munoz JJ, Birkemeyer NJ, Birkemeyer JD, et al. Is epsilonaminocaproic acid as effective as aprotinin in reducing bleeding with cardiac surgery?. A meta analysis. Circulation 1999; 99: 81–9PubMedCrossRef Munoz JJ, Birkemeyer NJ, Birkemeyer JD, et al. Is epsilonaminocaproic acid as effective as aprotinin in reducing bleeding with cardiac surgery?. A meta analysis. Circulation 1999; 99: 81–9PubMedCrossRef
93.
Zurück zum Zitat Laupacis A, Fergusson D. Drugs to minimize perioperative blood loss in cardiac surgery: meta-analyses using perioperative blood transfusion as the outcome. The International Study of Peri-operative Transfusion (ISPOT) investigators. Anesth Analg 1997; 85: 1258–67PubMedCrossRef Laupacis A, Fergusson D. Drugs to minimize perioperative blood loss in cardiac surgery: meta-analyses using perioperative blood transfusion as the outcome. The International Study of Peri-operative Transfusion (ISPOT) investigators. Anesth Analg 1997; 85: 1258–67PubMedCrossRef
94.
Zurück zum Zitat Levi M, Cromheecke ME, de Jonge E, et al. Pharmacological strategies to decrease excessive blood loss in cardiac surgery: a meta-analysis of clinically relevant endpoints. Lancet 1999; 345: 1940–7CrossRef Levi M, Cromheecke ME, de Jonge E, et al. Pharmacological strategies to decrease excessive blood loss in cardiac surgery: a meta-analysis of clinically relevant endpoints. Lancet 1999; 345: 1940–7CrossRef
95.
Zurück zum Zitat Alvarez JM, Quiney NF, McMillan D, et al. The use of ultralow-dose aprotinin to reduce blood loss in cardiac surgery. J Cardiothorac Vasc Anesth 1995 Feb; 9(1): 29–33PubMedCrossRef Alvarez JM, Quiney NF, McMillan D, et al. The use of ultralow-dose aprotinin to reduce blood loss in cardiac surgery. J Cardiothorac Vasc Anesth 1995 Feb; 9(1): 29–33PubMedCrossRef
96.
Zurück zum Zitat Westaby S. Aprotinin in perspective. Ann Thorac Surg 1993; 44: 1033–41CrossRef Westaby S. Aprotinin in perspective. Ann Thorac Surg 1993; 44: 1033–41CrossRef
97.
Zurück zum Zitat Ciçek S, Demirkiliç U, Özal E, et al. Postoperative use of aprotinin in cardiac operations: an alternative to its prophylactic use. J Thorac Cardiovasc Surg 1996; 112: 1462–7PubMedCrossRef Ciçek S, Demirkiliç U, Özal E, et al. Postoperative use of aprotinin in cardiac operations: an alternative to its prophylactic use. J Thorac Cardiovasc Surg 1996; 112: 1462–7PubMedCrossRef
98.
Zurück zum Zitat Ciçek S, Demirkiliç U, Özal E, et al. Postoperative aprotinin: effect on blood loss and transfusion requirements in cardiac operations. Ann Thorac Surg 1996; 61: 1372–6PubMedCrossRef Ciçek S, Demirkiliç U, Özal E, et al. Postoperative aprotinin: effect on blood loss and transfusion requirements in cardiac operations. Ann Thorac Surg 1996; 61: 1372–6PubMedCrossRef
99.
Zurück zum Zitat Forestier F, B’elisle S, Robitaille D, et al. Low-dose aprotinin is ineffective to treat excessive bleeding after cardiopulmonary bypass. Ann Thorac Surg 2000; 69: 452–6PubMedCrossRef Forestier F, B’elisle S, Robitaille D, et al. Low-dose aprotinin is ineffective to treat excessive bleeding after cardiopulmonary bypass. Ann Thorac Surg 2000; 69: 452–6PubMedCrossRef
100.
Zurück zum Zitat Alvarez JM, Goldstein J, Mezzatesta J, et al. Fatal intraoperative pulmonary thrombosis after graft replacement of an aneurysm of the arch and descending aorta in association with deep hypothermic circulatory arrest and aprotinin therapy. J Thorac Cardiovasc Surg 1998; 115: 723–4PubMedCrossRef Alvarez JM, Goldstein J, Mezzatesta J, et al. Fatal intraoperative pulmonary thrombosis after graft replacement of an aneurysm of the arch and descending aorta in association with deep hypothermic circulatory arrest and aprotinin therapy. J Thorac Cardiovasc Surg 1998; 115: 723–4PubMedCrossRef
101.
Zurück zum Zitat Alvarez JM, Chandraratna H, Newman MA. Intraoperative coronary thrombosis in association with low-dose aprotinin therapy. J Cardiothorac Vasc Anesth 1999; 13: 623–8PubMedCrossRef Alvarez JM, Chandraratna H, Newman MA. Intraoperative coronary thrombosis in association with low-dose aprotinin therapy. J Cardiothorac Vasc Anesth 1999; 13: 623–8PubMedCrossRef
102.
Zurück zum Zitat Alderman EL, Levy JH, Rich JB, et al. Analyses of coronary graft patency after aprotinin use: results from the International Multicenter Aprotinin Graft Patency Experience (IMAGE) trial. J Thorac Cardiovasc Surg 1998; 116: 716–30PubMedCrossRef Alderman EL, Levy JH, Rich JB, et al. Analyses of coronary graft patency after aprotinin use: results from the International Multicenter Aprotinin Graft Patency Experience (IMAGE) trial. J Thorac Cardiovasc Surg 1998; 116: 716–30PubMedCrossRef
103.
Zurück zum Zitat Hébert PC, Wells G, Blajchman MA, et al. The Transfusion Requirements in Critical Care Investigators for the Canadian Critical Care Trials Group: a multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. N Engl J Med 1999; 340: 409–17PubMedCrossRef Hébert PC, Wells G, Blajchman MA, et al. The Transfusion Requirements in Critical Care Investigators for the Canadian Critical Care Trials Group: a multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. N Engl J Med 1999; 340: 409–17PubMedCrossRef
104.
Zurück zum Zitat Weightman WM, Gibbs NM, Weidmann CR, et al. The effect of preoperative aspirin-free interval on red blood cell transfusion requirements in cardiac surgical patients. J Cardiothorac Vasc Anesth 2002; 16: 54–8PubMedCrossRef Weightman WM, Gibbs NM, Weidmann CR, et al. The effect of preoperative aspirin-free interval on red blood cell transfusion requirements in cardiac surgical patients. J Cardiothorac Vasc Anesth 2002; 16: 54–8PubMedCrossRef
105.
Zurück zum Zitat Hedner U. NovoSeven as a universal haemostatic agent. Blood Coagul Fibrinolysis 2000; 11 Suppl. 1: S107–11PubMedCrossRef Hedner U. NovoSeven as a universal haemostatic agent. Blood Coagul Fibrinolysis 2000; 11 Suppl. 1: S107–11PubMedCrossRef
106.
Zurück zum Zitat Al Douri M, Shafi T, Al Khudairi D, et al. Effect of the administration of recombinant activated factor VII (rFVIIa; NovoSeven) in the management of severe uncontrolled bleeding in patients undergoing heart valve replacement surgery. Blood Coagul Fibrinolysis 2000; 11 Suppl. 1: S121–7PubMedCrossRef Al Douri M, Shafi T, Al Khudairi D, et al. Effect of the administration of recombinant activated factor VII (rFVIIa; NovoSeven) in the management of severe uncontrolled bleeding in patients undergoing heart valve replacement surgery. Blood Coagul Fibrinolysis 2000; 11 Suppl. 1: S121–7PubMedCrossRef
Metadaten
Titel
Avoidance of Bleeding During Surgery in Patients Receiving Anticoagulant and/or Antiplatelet Therapy
Pharmacokinetic and Pharmacodynamic Considerations
verfasst von
Prof. Sebastian Harder
Ute Klinkhardt
John M. Alvarez
Publikationsdatum
01.12.2004
Verlag
Springer International Publishing
Erschienen in
Clinical Pharmacokinetics / Ausgabe 14/2004
Print ISSN: 0312-5963
Elektronische ISSN: 1179-1926
DOI
https://doi.org/10.2165/00003088-200443140-00002

Weitere Artikel der Ausgabe 14/2004

Clinical Pharmacokinetics 14/2004 Zur Ausgabe