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Медицинская библиотека · Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis · 1993

The prolonged activated clotting time (ACT) with aprotinin depends on the type of activator used for measurement.

Wendel H P, Heller W, Gallimore M J, Bantel H, Müller-Beissenhirtz H, Hoffmeister H E

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Аннотация

In cardiopulmonary bypass (CPB) surgery high dose heparin is necessary to inhibit the clotting cascade which is activated through damage to the vessels (extrinsic pathway) as well as contact activation of the blood with the various artificial surfaces of the CPB machine (intrinsic pathway). In most European heart surgery centres, the fibrinolytic activation that always occurs in CPB due to contact activation is reduced by the proteinase inhibitor aprotinin. Monitoring of anticoagulation during CPB is performed with the activated whole blood clotting time (ACT). The two machines commonly used for this purpose, Hemotec and Hemochron, use different contact system activators, kaolin and celite. These activators displayed highly significant differences, in both in vitro tests (modified APTT with whole blood in a neutral coagulometer), and ACT in both machines where aprotinin and heparin were used, as well as with parallel measurements with the two machines with blood from patients undergoing CPB with high dose aprotinin therapy (P < 0.001). The Hemotec machine with kaolin as activator was not affected by aprotinin throughout surgery, while the Hemochron clotting times almost doubled as soon as aprotinin and heparin were combined. Our studies show that for the determination of ACT in CPB were high dose aprotinin therapy is used only ACT determinations with machines using kaolin as activator yield accurate results.

Для цитирования: Wendel H P, Heller W, Gallimore M J, Bantel H, Müller-Beissenhirtz H, Hoffmeister H E. The prolonged activated clotting time (ACT) with aprotinin depends on the type of activator used for measurement.. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis. 1993.

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