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Original Article
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Volume 333:1588-1594 December 14, 1995 Number 24
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Low-Molecular-Weight Heparin for the Treatment of Acute Ischemic Stroke
Richard Kay, M.D., Ka Sing Wong, M.B., B.S., Yuk Ling Yu, M.D., Yuk Wah Chan, M.Med., Tak Hong Tsoi, M.B., B.S., Anil T. Ahuja, M.D., Fu Luk chan, M.B., B.S., Ka Yeung Fong, M.B., B.S., Chun Bong Law, M.B., Ch.B., Agatha Wong, R.N., and Jean Woo, M.D.

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ABSTRACT

Background Despite doubts about their efficacy and concern about their safety, antithrombotic agents are often used to treat acute ischemic stroke. Recent experience in patients with other thromboembolic disorders suggests that low-molecular-weight heparin, which requires only subcutaneous administration once or twice daily, may be more effective and safer than standard (unfractionated) heparin.

Methods We conducted a randomized, double-blind, placebo-controlled trial comparing two dosages of low-molecular-weight heparin with placebo in the treatment of ischemic stroke. Patients were randomly assigned within 48 hours of the onset of symptoms to receive high-dose nadroparin (4100 anti–factor Xa IU twice daily), low-dose nadroparin (4100 IU once daily), or placebo subcutaneously for 10 days. The primary measure of outcome was death or dependency regarding activities of daily living six months after randomization. Secondary outcomes were death, hemorrhagic transformation of the infarction, and other complications at 10 days, and death or dependency at 3 months.

Results A total of 2750 patients were screened for the study. Among 312 patients randomized, 306 had outcomes that were analyzed at six months. Forty-five patients (45 percent) in the high-dose group, 53 patients (52 percent) in the low-dose group, and 68 patients (65 percent) in the placebo group died or became dependent. There was a significant dose-dependent effect among the three study groups in favor of low-molecular-weight heparin (P = 0.005 by the chi-square test for trend). No significant differences among the groups in the occurrence of secondary outcomes were observed at 10 days.

Conclusions For patients with ischemic stroke treated within 48 hours of the onset of symptoms, low-molecular-weight heparin was effective in improving outcomes at six months.


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From the Departments of Medicine (R.K., K.S.W., A.W., J.W.) and Diagnostic Radiology and Organ Imaging (A.T.A.), Prince of Wales Hospital; the Departments of Medicine (Y.L.Y., K.Y.F.) and Diagnostic Radiology (F.L.C.), Queen Mary Hospital; the Department of Medicine and Geriatrics, Kwong Wah Hospital (Y.W.C., C.B.L.); and the Department of Medicine, Pamela Youde Nethersole Eastern Hospital (T.H.T.) — all in Hong Kong.

Address reprint requests to Dr. Kay at the Department of Medicine, Prince of Wales Hospital, Shatin, Hong Kong.

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Related Letters:

Low-Molecular-Weight Heparin for the Treatment of Acute Ischemic Stroke
Bloom J. M., Kay R., Wong K. S., Woo J.
Extract | Full Text  
N Engl J Med 1996; 334:1407, May 23, 1996. Correspondence

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