Outpatient treatment of deep vein thrombosis: Translating clinical trials into practice

被引:30
作者
Dunn, AS [1 ]
Coller, B [1 ]
机构
[1] CUNY Mt Sinai Sch Med, Dept Med, New York, NY 10029 USA
关键词
D O I
10.1016/S0002-9343(99)00129-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To develop a rational approach to outpatient management, we review the pharmacologic properties of low-molecular-weight heparins and their efficacy in clinical trials of deep vein thrombosis treatment. Low-molecular-weight heparins have better bioavailability and more predictable anticoagulant activity than standard heparin and thus can be administered without routine laboratory monitoring. Randomized trials comparing subcutaneous low-molecular-weight heparin administered primarily at home with inpatient intravenous standard heparin have established the safety and efficacy of outpatient treatment of selected patients. However, many patients were excluded from these studies. The benefits demonstrated in carefully controlled clinical trials of outpatient treatment of deep vein thrombosis required a complex multidisciplinary organization of medical care that is not readily achievable in routine practice. A structured protocol is necessary to ensure that patient care is optimal. The essential components of an outpatient program include appropriate patient selection, adequate patient education, daily follow-up during therapy with low-molecular-weight heparin, and easy access to health-care professionals. Am J Med. 1999; 106:660-669. (C) 1999 by Excerpta Medica, Inc.
引用
收藏
页码:660 / 669
页数:10
相关论文
共 99 条
[1]   TREATMENT OF ACUTE VENOUS THROMBOEMBOLISM WITH LOW-MOLECULAR WEIGHT HEPARIN (FRAGMIN) - RESULTS OF A DOUBLE-BLIND RANDOMIZED STUDY [J].
ALBADA, J ;
NIEUWENHUIS, HK ;
SIXMA, JJ .
CIRCULATION, 1989, 80 (04) :935-940
[2]  
AMIRAL J, 1992, THROMB HAEMOSTASIS, V68, P95
[3]   Are the pharmacokinetic parameters of low molecular weight heparins predictive of their clinical efficacy? [J].
Andrassy, K ;
Eschenfelder, V .
THROMBOSIS RESEARCH, 1996, 81 (02) :S29-S35
[4]   LOW-MOLECULAR-WEIGHT HEPARIN (FRAGMIN(TM)) VERSUS HEPARIN FOR ANTICOAGULATION DURING CARDIOPULMONARY BYPASS IN OPEN-HEART-SURGERY, USING A PIG MODEL [J].
BAGGE, L ;
WAHLBERG, T ;
HOLMER, E ;
TYDEN, H ;
NYSTROM, SO ;
MALM, T .
BLOOD COAGULATION & FIBRINOLYSIS, 1994, 5 (02) :265-272
[5]   INCREASED ANTI-XA BIOAVAILABILITY FOR A LOW-MOLECULAR WEIGHT HEPARIN (PK-10169) COMPARED WITH UNFRACTIONATED HEPARIN [J].
BARA, L ;
BILLAUD, E ;
KHER, A ;
SAMAMA, M .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1985, 11 (03) :316-317
[6]  
BARA L, 1990, ACTA CHIR SCAND, P57
[7]   CORRELATION BETWEEN ANTI-XA AND OCCURRENCE OF THROMBOSIS AND HEMORRHAGE IN POSTSURGICAL PATIENTS TREATED WITH EITHER LOGIPARIN(R) (LMWH) OR UNFRACTIONATED HEPARIN [J].
BARA, L ;
LEIZOROVICZ, A ;
PICOLET, H ;
SAMAMA, M .
THROMBOSIS RESEARCH, 1992, 65 (4-5) :641-650
[8]   COMPARISON OF THE PLATELET PRO-AGGREGATORY EFFECT OF CONVENTIONAL UNFRACTIONATED HEPARINS AND A LOW-MOLECULAR-WEIGHT HEPARIN FRACTION (CY-222) [J].
BARRADAS, MA ;
MIKHAILIDIS, DP ;
EPEMOLU, O ;
JEREMY, JY ;
FONSECA, V ;
DANDONA, P .
BRITISH JOURNAL OF HAEMATOLOGY, 1987, 67 (04) :451-457
[9]   BINDING AND ENDOCYTOSIS OF HEPARIN BY HUMAN-ENDOTHELIAL CELLS IN CULTURE [J].
BARZU, T ;
MOLHO, P ;
TOBELEM, G ;
PETITOU, M ;
CAEN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 845 (02) :196-203
[10]  
BENDETOWICZ AV, 1994, THROMB HAEMOSTASIS, V71, P305