Effect of argatroban on the activated partial thromboplastin time: a comparison of 21 commercial reagents

被引:31
作者
Francis, JL
Hursting, MJ
机构
[1] Florida Hosp, Ctr Thrombosis & Hemostasis, Orlando, FL 32804 USA
[2] Clin Sci Consulting, Potomac, MD USA
关键词
argatroban; thrombin; antagonists and inhibitors; anticoagulation; activated partial thromboplastin time; reagents; heparin-induced thrombocytopenia;
D O I
10.1097/01.mbc.0000169217.15926.d0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Argatroban is a direct thrombin inhibitor used for the treatment of heparin-induced thrombocytopenia. The drug is administered by continuous infusion, at a recommended initial dose of 2 mu g/kg per min, to achieve activated partial thromboplastin times (aPTTs) 1.5-3.0 times baseline. We evaluated the effect of argatroban, at clinically relevant concentrations, on aPTTs using 21 commercially available reagents. The aPTTs of plasma containing argatroban at 0.125-8.0 mu g/ml (final concentration) were assessed using each reagent and an ACL 3000+ coagulation analyzer. Argatroban increased aPTTs (and aPTT ratios relative to control) in a broadly comparable fashion among reagents. Concentration - aPTT ratio profiles linearized well using logarithmic - logarithmic transformation (r(2) > 0.98), with the regression slope taken as the reagent's sensitivity to argatroban. Sensitivity ranged from 0.304 +/- 0.006 to 0.364 +/- 0.007. Only the least and two most sensitive reagents (all now unavailable in the United States) differed significantly in sensitivity from the other reagents (P< 0.05). aPTT ratios of 2.25 occurred for all reagents at 0.41 +/- 0.92 mu g/ml argatroban, and for 14 (67%) reagents at 0.53-0.67 mu g/ml. This corresponds to a similar to 0.5 mu g/kg per min dose difference in healthy subjects. We conclude that most aPTT reagents are similarly sensitive to argatroban, and reagent choice is unlikely to significantly affect argatroban monitoring in patients with heparin-induced thrombocytopenia. (C) Lippincott Williams & Wilkins
引用
收藏
页码:251 / 257
页数:7
相关论文
共 23 条
[1]   HIRUDIN IN ACUTE MYOCARDIAL-INFARCTION - SAFETY REPORT FROM THE THROMBOLYSIS AND THROMBIN INHIBITION IN MYOCARDIAL-INFARCTION (TIMI)-9A TRIAL [J].
ANTMAN, EM .
CIRCULATION, 1994, 90 (04) :1624-1630
[2]   ESTABLISHING A THERAPEUTIC RANGE FOR HEPARIN-THERAPY [J].
BRILLEDWARDS, P ;
GINSBERG, JS ;
JOHNSTON, M ;
HIRSH, J .
ANNALS OF INTERNAL MEDICINE, 1993, 119 (02) :104-109
[3]   Lepirudin (recombinant hirudin) for parenteral anticoagulation in patients with heparin-induced thrombocytopenia [J].
Greinacher, A ;
Janssens, U ;
Berg, G ;
Böck, M ;
Kwasny, H ;
Kemkes-Matthes, B ;
Eichler, P ;
Völpel, H ;
Pötzsch, B ;
Luz, M .
CIRCULATION, 1999, 100 (06) :587-593
[4]   Recombinant hirudin (Lepirndin) provides safe and effective anticoagulation in patients with heparin-induced thrombocytopenia -: A prospective study [J].
Greinacher, A ;
Völpel, H ;
Janssens, U ;
Hach-Wunderle, V ;
Kemkes-Matthes, B ;
Eichler, P ;
Mueller-Velten, HG ;
Pötzsch, B .
CIRCULATION, 1999, 99 (01) :73-80
[5]  
Greinacher A, 2001, HEPARIN INDUCED THRO, P349
[6]   Novastan® (brand of argatroban):: A small-molecule, direct thrombin inhibitor [J].
Hursting, MJ ;
Alford, KL ;
Becker, JCP ;
Brooks, RL ;
Joffrion, JL ;
Knappenberger, GD ;
Kogan, PW ;
Kogan, TP ;
McKinney, AA ;
Schwarz, RP .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1997, 23 (06) :503-516
[7]  
Jang IK, 2003, J AM COLL CARDIOL, V41, p68A
[8]   A multicenter, randomized study of argatroban versus heparin as adjunct to tissue plasminogen activator (TPA) in acute myocardial infarction: Myocardial infarction with novastan and TPA (MINT) study [J].
Jang, IK ;
Brown, DFM ;
Giugliano, RP ;
Anderson, HV ;
Losordo, D ;
Nicolau, JC ;
Dutra, OP ;
Bazzino, O ;
Viamonte, VM ;
Norbady, R ;
Liprandi, AS ;
Massey, TJ ;
Dinsmore, R ;
Schwarz, RP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (07) :1879-1885
[9]  
Kitchen S, 1996, THROMB HAEMOSTASIS, V75, P734
[10]   Argatroban anticoagulation in patients with acute ischemic stroke (ARGIS-1) - A randomized, placebo-controlled safety study [J].
LaMonte, MP ;
Nash, ML ;
Wang, DZ ;
Woolfenden, AR ;
Schultz, J ;
Hursting, MJ ;
Brown, PM .
STROKE, 2004, 35 (07) :1677-1682