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Anticoagulation in Acute Ischemic Stroke

Clinical Trials of Anticoagulation in Stroke

Recently Published Clinical Trials

Trial Format

 

IST

HK

TOAST

Entry

<48 hrs

<48 hrs

<24 hrs

Endpoint

Dead/Dependent

Dead/Dependent

Good

Duration

6 months

6 months

3 months

Drug

Heparin

Nadroparin

ORG 10172

Class

 

LMWH

Heparinoid

Dose

5000 SC BID
12,500 SC BID

4100 SC QD
4100 SC BID

7200 IV/day

Time

14 days

10 days

7 days

 

Recurrent Ischemic Stroke

  

IST

HK

TOAST

Time

14 days

10 days

7 days

HD

3.2%

2%

1.1%

LD

2.6%

1%

     

Control

3.8%

1%

1.1%

 

Percent with Poor Outcome

   

IST

HK

TOAST

HD

62.6%

45%

24.8%*

LD

63.1%

52%

   

Control

62.9%

65%

26.3*  

Results

Negative

p=.007

Negative

 

Intracranial Hemorrhage   

  

IST

HK

TOAST

Time

14 days

10 days

10 days

HD

1.8%

0%

2.2%

LD

0.7%

2%

  

Control

0.4%*

1.0%

0.6%

 

*p<.05

Major Extracranial Hemorrhage   

  

IST

HK

TOAST

Time

14 days

10 days

10 days

HD

2%

0%

5%

LD

0.6%

0%

  

Control

0.4%*

1%

1.6%

 

*p<.05 HK data for major GI hemorrhages only 

 

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This presentation was written by Dr. William J. Powers, co-director of the Stroke Center at Barnes-Jewish Hospital and the Washington University School of Medicine.

Last Revised: March 26, 2001

 

 

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