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1:
N Engl J Med.
2003 Apr 10;348(15):1425-34. Epub 2003 Feb 24.
Related Articles
,
Links
Comment in:
ACP J Club. 2003 Sep-Oct;139(2):42.
CMAJ. 2003 Apr 29;168(9):1160-1.
J Fam Pract. 2003 Aug;52(8):588, 591.
N Engl J Med. 2003 Apr 10;348(15):1478-80.
N Engl J Med. 2003 Aug 14;349(7):675-83.
N Engl J Med. 2003 Jul 24;349(4):398-400; author reply 398-400.
N Engl J Med. 2003 Jul 24;349(4):398-400; author reply 398-400.
N Engl J Med. 2003 Jul 24;349(4):398-400; author reply 398-400.
N Engl J Med. 2003 Jul 24;349(4):398-400; author reply 398-400.
N Engl J Med. 2003 Jul 24;349(4):398-400; author reply 398-400.
Rev Cardiovasc Med. 2004 Spring;5(2):135-8.
Long-term, low-intensity warfarin therapy for the prevention of recurrent venous thromboembolism.
Ridker PM
,
Goldhaber SZ
,
Danielson E
,
Rosenberg Y
,
Eby CS
,
Deitcher SR
,
Cushman M
,
Moll S
,
Kessler CM
,
Elliott CG
,
Paulson R
,
Wong T
,
Bauer KA
,
Schwartz BA
,
Miletich JP
,
Bounameaux H
,
Glynn RJ
;
PREVENT Investigators
.
Center for Cardiovascular Disease Prevention and the Division of Preventive Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston 02215, USA. pridker@partners.org
BACKGROUND: Standard therapy to prevent recurrent venous thromboembolism includes 3 to 12 months of treatment with full-dose warfarin with a target international normalized ratio (INR) between 2.0 and 3.0. However, for long-term management, no therapeutic agent has shown an acceptable benefit-to-risk ratio. METHODS: Patients with idiopathic venous thromboembolism who had received full-dose anticoagulation therapy for a median of 6.5 months were randomly assigned to placebo or low-intensity warfarin (target INR, 1.5 to 2.0). Participants were followed for recurrent venous thromboembolism, major hemorrhage, and death. RESULTS: The trial was terminated early after 508 patients had undergone randomization and had been followed for up to 4.3 years (mean, 2.1). Of 253 patients assigned to placebo, 37 had recurrent venous thromboembolism (7.2 per 100 person-years), as compared with 14 of 255 patients assigned to low-intensity warfarin (2.6 per 100 person-years), a risk reduction of 64 percent (hazard ratio, 0.36 [95 percent confidence interval, 0.19 to 0.67]; P<0.001). Risk reductions were similar for all subgroups, including those with and those without inherited thrombophilia. Major hemorrhage occurred in two patients assigned to placebo and five assigned to low-intensity warfarin (P=0.25). Eight patients in the placebo group and four in the group assigned to low-intensity warfarin died (P=0.26). Low-intensity warfarin was thus associated with a 48 percent reduction in the composite end point of recurrent venous thromboembolism, major hemorrhage, or death. According to per-protocol and as-treated analyses, the reduction in the risk of recurrent venous thromboembolism was between 76 and 81 percent. CONCLUSIONS: Long-term, low-intensity warfarin therapy is a highly effective method of preventing recurrent venous thromboembolism. Copyright 2003 Massachusetts Medical Society
Publication Types:
Clinical Trial
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
PMID: 12601075 [PubMed - indexed for MEDLINE]
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