Bivalirudin versus Unfractionated Heparin for Prevention of Hemofilter Occlusion During Continuous Renal Replacement Therapy

被引:18
作者
Kiser, Tyree H. [1 ]
MacLaren, Robert [1 ]
Fish, Douglas N. [1 ]
Hassell, Kathryn L. [2 ]
Teitelbaum, Isaac [2 ]
机构
[1] Univ Colorado, Sch Pharm, Dept Clin Pharm, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dept Med, Aurora, CO 80045 USA
来源
PHARMACOTHERAPY | 2010年 / 30卷 / 11期
关键词
bivalirudin; hirulog; direct thrombin inhibitor; anticoagulation; bleeding; thrombus; continuous renal replacement therapy; CRRT; hemofilter; dialysis; continuous venovenous hemofiltration; CVVH; CONTINUOUS VENOVENOUS HEMOFILTRATION; REGIONAL CITRATE ANTICOAGULATION; MOLECULAR-WEIGHT HEPARIN; INDUCED THROMBOCYTOPENIA; ANTITHROMBIN-III; FAILURE; PATIENT; TRIAL; COAGULATION; ACTIVATION;
D O I
10.1592/phco.30.11.1117
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study Objective. To evaluate the safety and efficacy of bivalirudin compared with heparin for preventing hemofilter occlusion during continuous venovenous hemofiltration (CVVH). Design. Prospective, randomized, double-blind study Setting. University-affiliated hospital. Patients. Ten critically ill adults (median age 58 yrs, 70% male) with acute renal failure who, without anticoagulation, experienced hemofilter survival time of 24 hours or less during CVVH. Intervention. Patients were randomized to receive bivalirudin 2 mg/hour (five patients) or heparin 400 units/hour (five patients) administered prefilter into the extracorporeal circuit. Measurements and Main Results. Patients had a median Acute Physiology and Chronic Health Evaluation (APACHE) II score of 24, Sequential Organ Failure Assessment (SOFA) score of 11, and reduced antithrombin activity (75.5 units/dl). Baseline characteristics were not significantly different between groups. Study drug was administered in 40 hemofilters (18 from bivalirudin-treated patients, 22 from heparin-treated patients). The primary efficacy outcome was hemofilter survival time, defined as the interval of time between commencement of CVVH with a new extracorporeal circuit (hemofilter) and hemofilter failure. Compared with no anticoagulation, the addition of bivalirudin or heparin significantly improved hemofilter survival time (mean +/- SD 10 +/- 5 hrs with no anticoagulation vs 22 +/- 18 hrs with anticoagulation, p=0.0005). Hemofilter survival time was significantly increased in patients receiving bivalirudin versus those receiving heparin (29.6 +/- 20.7 vs 16.5 +/- 13.6 hrs, p=0.045). Independent predictors of hemofilter survival were use of bivalirudin therapy and increased antithrombin III activity. No patients randomized to bivalirudin experienced any bleeding or thrombosis events; one patient who received heparin developed alveolar hemorrhage, and one developed a lower extremity deep vein thrombosis. Conclusion. Compared with heparin, bivalirudin was more efficacious in prolonging hemofilter survival time and was well tolerated. Additional studies of bivalirudin for prevention of hemofilter occlusion during continuous renal replacement therapy are warranted.
引用
收藏
页码:1117 / 1126
页数:10
相关论文
共 44 条
[1]  
BASTIEN O, 1995, CONTRIB NEPHROL, V116, P154
[2]   Acute renal failure - definition, outcome measures, animal models, fluid therapy and information technology needs: the Second International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group [J].
Bellomo, R ;
Ronco, C ;
Kellum, JA ;
Mehta, RL ;
Palevsky, P .
CRITICAL CARE, 2004, 8 (04) :R204-R212
[3]   Activation of the tissue factor pathway occurs during continuous venovenous hemofiltration [J].
Cardigan, RA ;
McGloin, H ;
Mackie, IJ ;
Machin, SJ ;
Singer, M .
KIDNEY INTERNATIONAL, 1999, 55 (04) :1568-1574
[4]   Argatroban for heparin-induced thrombocytopenia in hepato-renal failure and CVVHD [J].
Dager, WE ;
White, RH .
ANNALS OF PHARMACOTHERAPY, 2003, 37 (09) :1232-1236
[6]   Treatment with recombinant human activated protein C obviates additional anticoagulation during continuous venovenous hemofiltration in patients with severe sepsis [J].
de Pont, ACJM ;
Bouman, CSC ;
de Jonge, E ;
Vroom, MB ;
Büller, HR ;
Levi, M .
INTENSIVE CARE MEDICINE, 2003, 29 (07) :1205-1205
[7]   Antithrombin supplementation for anticoagulation during continuous hemofiltration in critically ill patients with septic shock: a case-control study [J].
du Cheyron, Damien ;
Bouchet, Bruno ;
Bruel, Cedric ;
Daubin, Cedric ;
Ramakers, Michel ;
Charbonneau, Pierre .
CRITICAL CARE, 2006, 10 (02)
[8]   Antithrombin III in patients with severe sepsis - A randomized, placebo-controlled, double-blind multicenter trial plus a meta-analysis on all randomized, placebo-controlled, double-blind trials with antithrombin III in severe sepsis [J].
Eisele, B ;
Lamy, M ;
Thijs, LG ;
Keinecke, HO ;
Schuster, HP ;
Matthias, FR ;
Fourrier, F ;
Heinrichs, H ;
Delvos, U .
INTENSIVE CARE MEDICINE, 1998, 24 (07) :663-672
[9]   Citrate anticoagulation in continuous venovenous hemodiafiltration:: a metabolic challenge [J].
Gabutti, L ;
Marone, C ;
Colucci, G ;
Duchini, F ;
Schönholzer, C .
INTENSIVE CARE MEDICINE, 2002, 28 (10) :1419-1425
[10]  
Greaves M, 2002, THROMB HAEMOSTASIS, V87, P163