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2214 Part XII: Hemostasis and Thrombosis Chapter 129: Disseminated Intravascular Coagulation 2215
and purpura fulminans, intravenous bolus injection of 5000 to 10,000 14. Lasch HG, Heene DL, Huth K, et al: Pathophysiology, clinical manifestations and ther-
U heparin may be given simultaneously with replacement therapy with apy of consumption-coagulopathy (“Verbrauchskoagulopathie”). Am J Cardiol 20:381,
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blood products. Some experts would not administer a bolus dose of 15. Merskey C, Johnson AJ, Kleiner GJ, et al: The defibrination syndrome: Clinical features
heparin even under these circumstances. Continuous infusion of 500 and laboratory diagnosis. Br J Haematol 13:528, 1967.
to 1000 U/h heparin may be necessary to maintain the benefit until the 16. Robboy SJ, Major MC, Colman RW, et al: Pathology of disseminated intravascular
coagulation (DIC). Analysis of 26 cases. Hum Pathol 3:327, 1972.
underlying disease responds to treatment. 339 17. Wilde JT, Roberts KM, Greaves M, et al: Association between necropsy evidence of dis-
Theoretically, the most logical anticoagulant agent to use in DIC is seminated intravascular coagulation and coagulation variables before death in patients
directed against TF activity. Potential agents include recombinant TFPI, in intensive care units. J Clin Pathol 41:138, 1988.
inactivated factor VIIa, and recombinant nematode anticoagulant pro- 18. Kim HS, Suzuki M, Lie JT, et al: Clinically unsuspected disseminated intravascular
coagulation (DIC): An autopsy survey. Am J Clin Pathol 66:31, 1976.
tein c2 (NAPc2), a potent and specific inhibitor of the ternary complex 19. Watanabe T, Imamura T, Nakagaki K, et al: Disseminated intravascular coagulation
of TF–factor VIIa and factor Xa. Phase II trials of recombinant TFPI in autopsy cases. Its incidence and clinicopathologic significance. Pathol Res Pract
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341
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did not show an overall survival benefit in patients who were treated 20. Shimamura K, Oka K, Nakazawa M, et al: Distribution patterns of microthrombi in
disseminated intravascular coagulation. Arch Pathol Lab Med 107:543, 1983.
with TFPI. 341,342 21. Levi M, van der Poll T, ten Cate H, et al: The cytokine-mediated imbalance between
Recombinant human soluble thrombomodulin binds to thrombin coagulant and anticoagulant mechanisms in sepsis and endotoxaemia. Eur J Clin Invest
27:3, 1997.
to form a complex that inactivates thrombin’s coagulant activity and 22. Levi M, van der Poll T, Buller HR: The bidirectional relationship between coagulation
activates protein C, and thus, is a potential drug for the treatment of and inflammation. Circulation 109:2698, 2004.
patients with DIC. In a phase III randomized double-blind clinical trial 23. Aird WC: Vascular bed-specific hemostasis: Role of endothelium in sepsis pathogene-
in patients with DIC, administration of the soluble thrombomodulin sis. Crit Care Med 29:S28, 2001.
had a significantly better effect on bleeding manifestations and coagula- 24. Weinbaum S, Zhang X, Han Y, et al: Mechanotransduction and flow across the endothe-
lial glycocalyx. Proc Natl Acad Sci U S A 100:7988, 2003.
343
tion parameters than heparin. Ongoing trials with soluble thrombo- 25. Maczewski M, Duda M, Pawlak W, et al: Endothelial protection from reperfusion
modulin focus on DIC, organ failure, and mortality rate. injury by ischemic preconditioning and diazoxide involves a SOD-like anti-O -mecha-
2
nism. J Physiol Pharmacol 55:537, 2004.
26. Vink H, Constantinescu AA, Spaan JA: Oxidized lipoproteins degrade the endothelial
INHIBITORS OF FIBRINOLYSIS surface layer: Implications for platelet-endothelial cell adhesion. Circulation 101:1500,
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Patients with DIC should not be treated with antifibrinolytic agents 27. Nieuwdorp M, van Haeften TW, Gouverneur MC, et al: Loss of endothelial glycocalyx
such as ε-aminocaproic acid or tranexamic acid because these drugs during acute hyperglycemia coincides with endothelial dysfunction and coagulation
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block fibrinolysis that preserves tissue perfusion in patients with DIC. 28. Levi M, van der Poll T, ten Cate H: Tissue factor in infection and severe inflammation.
Use of these agents in patients with DIC has been complicated by severe Semin Thromb Hemost 32:33, 2006.
thrombosis. 344,345 29. Taylor FBJ, Chang A, Ruf W, et al: Lethal E. coli septic shock is prevented by blocking
tissue factor with monoclonal antibody. Circ Shock 33:127, 1991.
A different situation prevails in patients with DIC accompanied by 30. Levi M, ten Cate H, Bauer KA, et al: Inhibition of endotoxin-induced activation of
primary fibrino(geno)lysis, as in some cases of APL, giant hemangioma, coagulation and fibrinolysis by pentoxifylline or by a monoclonal anti-tissue factor
heat stroke, amniotic fluid embolism, some forms of liver disease, and antibody in chimpanzees. J Clin Invest 93:114, 1994.
metastatic carcinoma of the prostate. In these conditions, the use of 31. van der Poll T, Levi M, Hack CE, et al: Elimination of interleukin 6 attenuates coagula-
tion activation in experimental endotoxemia in chimpanzees. J Exp Med 179:1253, 1994.
fibrinolytic inhibitors can be considered, provided (1) the patient is 32. Osterud B, Rao LV, Olsen JO: Induction of tissue factor expression in whole blood—
346
bleeding profusely and has not responded to replacement therapy and Lack of evidence for the presence of tissue factor expression on granulocytes. Thromb
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(2) excessive fibrino(geno)lysis is observed, that is, rapid whole blood 33. Franco RF, de Jonge E, Dekkers PE, et al: The in vivo kinetics of tissue factor messenger
clot lysis or a very short euglobulin lysis time. In such circumstances, RNA expression during human endotoxemia: Relationship with activation of coagula-
use of antifibrinolytic agents should be preceded by replacement of tion. Blood 96:554, 2000.
depleted blood components and continuous heparin infusion (see 34. Rauch U, Bonderman D, Bohrmann B, et al: Transfer of tissue factor from leukocytes to
platelets is mediated by CD15 and tissue factor. Blood 96:170, 2000.
Fig. 129–4). 35. Osterud B, Bjorklid E: Sources of tissue factor. Semin Thromb Hemost 32:11, 2006.
36. van Deventer SJ, Buller HR, ten Cate JW, et al: Experimental endotoxemia in humans:
Analysis of cytokine release and coagulation, fibrinolytic, and complement pathways.
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