Literature DB >> 24656240

Low-molecular-weight heparin is more effective than aspirin in preventing early neurologic deterioration and improving six-month outcome.

Xingyang Yi1, Jing Lin2, Chun Wang1, Biao Zhang1, Wanzhang Chi3.   

Abstract

BACKGROUND: We evaluated the efficacy of low-molecular-weight heparin (LMWH) relative to aspirin in preventing early neurologic deterioration (END), venous thromboembolism (VTE), and outcomes at 6 months.
METHODS: Patients were randomly assigned to receive either subcutaneous enoxaparin 4000 anti-factor Xa IU/0.4 mL twice daily or oral aspirin 200 mg daily for 10 days. After day 10, all subjects received aspirin 100 mg once daily for 6 months. We assessed whether LMWH was superior to aspirin in preventing END and VTE within the first 10 days after index stroke and evaluated 6-month outcomes.
FINDINGS: Of the total 1368 patients, 7.89% suffered from END, and 2.85% suffered from deep-vein thrombosis during the first 10 days, with a significance difference between the LMWH group and aspirin group (3.95%, 1.46% versus 11.82%, 4.23%, respectively). At 6 months, there was a significant difference in the frequency of good outcomes among patients over the median age of 70 years (LMWH 63.8% versus aspirin 44.6%). The benefit of LMWH was also significant in patients with symptomatic stenosis of the posterior circulation and basilar artery (75.2% and 82% for LMWH versus 40.5% and 48% for aspirin, respectively).
CONCLUSIONS: For patients with acute ischemic stroke, treatment with LMWH within 48 hours of stroke until 10 days later may reduce END and deep-vein thrombosis during the first 10 days. LMWH appears to have advantages over aspirin in certain subgroups, such as elderly patients and patients with posterior circulation and basilar artery stenosis.
Copyright © 2014 National Stroke Association. All rights reserved.

Entities:  

Keywords:  Acute ischemic stroke; anticoagulation; neurologic degeneration; outcomes; venous thromboembolism

Mesh:

Substances:

Year:  2014        PMID: 24656240     DOI: 10.1016/j.jstrokecerebrovasdis.2013.12.036

Source DB:  PubMed          Journal:  J Stroke Cerebrovasc Dis        ISSN: 1052-3057            Impact factor:   2.136


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