Recombinant human antithrombin III restores heparin responsiveness and decreases activation of coagulation in heparin-resistant patients during cardiopulmonary bypass

被引:103
作者
Avidan, MS
Levy, JH
van Aken, H
Feneck, RO
Latimer, RD
Ott, E
Martin, E
Birnbaum, DE
Bonfiglio, LJ
Kajdasz, DK
Despotis, GJ
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Cardiotharac Surg, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO USA
[4] Washington Univ, Sch Med, Dept Surg, St Louis, MO USA
[5] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[6] Emory Univ, Sch Med, Dept Anesthesiol, Atlanta, GA 30322 USA
[7] Emory Healthcare, Div Cardiothorac Anesthesiol & Crit Care, Atlanta, GA USA
[8] Univ Munster, Klin Anasthesiol, Munster, Germany
[9] St Thomas Hosp, Dept Anaesthesia, London, England
[10] Papworth Hosp, Dept Anaesthesia, Cambridge, England
[11] Univ Klinikum Grosshadern, Dept Anesthesiol, Munich, Germany
[12] Inst Anasthesiol, Munich, Germany
[13] Heidelberg Univ, Dept Anesthesiol, Heidelberg, Germany
[14] Klinikum Univ Regensburg, Dept Anesthesiol, Regensburg, Germany
[15] GTC Biotherapeut Inc, Clin Res, Farmington, CT USA
[16] Lilly Corp Ctr, Indianapolis, IN USA
[17] Eli Lilly & Co, Indianapolis, IN USA
关键词
D O I
10.1016/j.jtcvs.2004.10.045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: We sought to evaluate the efficacy of recombinant human antithrombin III for restoration of heparin responsiveness in heparin-resistant patients scheduled for cardiac surgery. Methods: This was a multicenter, randomized, double-blind, placebo-controlled study in heparin-resistant patients undergoing elective cardiac surgery. Patients were considered heparin resistant if the activated clotting time was less than 480 seconds after 400 U/kg heparin. Fifty-two heparin-resistant patients were randomized into 2 cohorts. One cohort received a single bolus (75 U/kg) of recombinant human antithrombin III (n = 28), and the other, the placebo group (n = 24), received a normal saline bolus. If the activated clotting time remained less than 480 seconds, this was defined as treatment failure, and 2 units of fresh frozen plasma were transfused. Patients were monitored for adverse events during hospitalization. Results: Six (21%) of the patients in the recombinant human antithrombin III group received fresh frozen plasma transfusions compared with 22 (92%) of the placebo-treated patients (P < .001). Two units of fresh frozen plasma did not restore heparin responsiveness. There was no increased incidence of adverse events associated with recombinant human antithrombin III administration. Postoperative 24-hour chest tube bleeding was not different in the 2 groups. Surrogate measures of hemostatic activation suggested that there was less activation of the hemostatic system during cardiopulmonary bypass in the recombinant human antithrombin III group. Conclusion: Treatment with recombinant human antithrombin III in a dose of 75 U/kg is effective in restoring heparin responsiveness and promoting therapeutic anticoagulation for cardiopulmonary bypass in the majority of heparin-resistant patients. Two units of fresh frozen plasma were insufficient to restore heparin responsiveness. There was no apparent increase in bleeding associated with recombinant human antithrombin III.
引用
收藏
页码:107 / 113
页数:7
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