Laboratory Monitoring of Anticoagulation: Where Do We Stand?

被引:22
作者
Tripodi, Armando [2 ,3 ]
van den Besselaar, Antonius [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, Leiden, Netherlands
[2] Univ Med Sch, Dept Internal Med, Angelo Bianchi Bonomi Hemophilia & Thrombosis Ctr, Milan, Italy
[3] Mangiagalli & Regina Elena Fdn, Osped Maggiore Policlin, IRCCS, Milan, Italy
关键词
Heparin; low-molecular-weight heparin; vitamin K antagonists; fondaparinux; new anticoagulant drugs; MOLECULAR-WEIGHT HEPARIN; INTERNATIONAL SENSITIVITY INDEX; DEEP-VEIN THROMBOSIS; PROTHROMBIN TIME MONITOR; ANTI-XA ASSAYS; PULMONARY-EMBOLISM; QUALITY ASSESSMENT; CLOTTING TIME; THERAPY; CALIBRATION;
D O I
10.1055/s-0029-1214146
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The treatment of choice for acute venous thromboembolism is anticoagulant therapy with fast-acting drugs (Unfractionated or low-molecular-weight heparin or fondaparinux) aimed at preventing thrombus extension, followed by extended prophylaxis with vitamin K antagonists aimed at preventing recurrence. Experience accumulated over the years has demonstrated that strict laboratory monitoring is required for unfractionated heparin and vitamin K antagonists, making use of these drugs problematic for patients and physicians and prompting researchers to develop new anticoagulants equally effective but without the requirement for laboratory monitoring. The results of clinical trials to date, albeit limited, suggest that these new drugs will probably keep their promise. However, the definitive answer will come subsequent to these clinical trials, when clinicians will start to use these drugs to treat patients in the real world. It is likely that some sort of laboratory monitoring will be required at least for selected categories of patients. Accordingly, clinical laboratories should still be prepared to monitor patients, although the numbers may hopefully decrease sharply in the next decade or so.
引用
收藏
页码:34 / 41
页数:8
相关论文
共 63 条
[1]   Thrombin generation for the control of heparin treatment, comparison with the activated partial thromboplastin time [J].
Al Dieri, R ;
Alban, S ;
Béguin, S ;
Hemker, HC .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (08) :1395-1401
[2]  
BARA L, 1987, HAEMOSTASIS, V17, P127
[3]   PROSPECTIVE STUDY OF VALUE OF MONITORING HEPARIN TREATMENT WITH ACTIVATED PARTIAL THROMBOPLASTIN TIME [J].
BASU, D ;
CADE, J ;
GALLUS, A ;
HIRSH, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1972, 287 (07) :324-+
[4]  
Bauer K. A., 2006, NEW ANTICOAGULANTS, P450
[5]  
BLOMBACK M, 1994, THROMB HAEMOSTASIS, V71, P375
[6]  
BONEU B, 1994, THROMB HAEMOSTASIS, V72, P330
[7]  
BONEU B, 1991, NOUV REV FR HEMATOL, V33, P287
[8]   Is laboratory monitoring of low-molecular-weight heparin therapy necessary? No [J].
Bounameaux, H ;
De Moerloose, P .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (04) :551-554
[9]   Performance evaluation of the new CoaguChek XS system compared with the established CoaguChek system by patients experienced in INR-self management [J].
Braun, Siegmund ;
Watzke, Herbert ;
Hasenkam, J. Michael ;
Schwab, Michael ;
Wolf, Tanja ;
Dovifat, Clemens ;
Voeller, Heinz .
THROMBOSIS AND HAEMOSTASIS, 2007, 97 (02) :310-314
[10]  
Cai ZJ, 1999, WHO TECH REP SER, V887, P1