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1. |
A Special Thanks to our Reviewers for 2002 |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 827-832
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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2. |
Immune Activation to Underlie Moderate Hyperhomocysteinemia in Stroke and Dementia?Response |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 833-834
Stephen,
McIlroy A.,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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3. |
Carotid Angioplasty and Stenting in High-Risk Patients With Severe Symptomatic Carotid Stenosis |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 834-835
Enzo,
Ballotta Giuseppe,
Giau Claudio,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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4. |
CTA Source Images in Acute Stroke |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 835-836
Michael,
Hill Shelagh,
Coutts J.H.,
Pexman Andrew,
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PDF (57KB)
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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5. |
CTA Source Images in Acute StrokeResponse |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 836-837
Peter,
Schramm Peter,
Schellinger Jochen,
Fiebach Werner,
Hacke Klaus,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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6. |
Banning Anticoagulation in Stroke or Consequence of Poor Study Design |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 837-838
E.,
Grips M.,
Daffertshofer M.,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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7. |
Banning Anticoagulation in Stroke or Consequence of Poor Study DesignResponse |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 838-839
Harold,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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8. |
C-Reactive Protein and Blood Pressure in the Acute Phase After an Ischemic Stroke |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 839-839
Mario,
Di Napoli Francesca,
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ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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9. |
Comparison of Triflusal and Aspirin for Prevention of Vascular Events in Patients After Cerebral InfarctionThe TACIP Study: A Randomized, Double-Blind, Multicenter Trial |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 840-847
Jordi,
Matías-Guiu José,
Ferro José,
Alvarez-Sabín Ferran,
Torres M.,
Jiménez Aida,
Lago Teresa,
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摘要:
Background and Purpose—The efficacy of the antiplatelet agent triflusal for prevention of vascular events after stroke has been reported in a pilot study. However, there is a need to confirm those results in a larger study.Methods—We performed a randomized, double-blind, multicenter study to test the efficacy of triflusal (600 mg/d) versus aspirin (325 mg/d) for prevention of vascular events in patients with stroke or transient ischemic attack (Triflusal versus Aspirin in Cerebral Infarction Prevention [TACIP]). We assessed a combined end point (incidence of nonfatal ischemic stroke, nonfatal acute myocardial infarction, or vascular death) as well as the incidence of these events separately and the incidence of major hemorrhage.Results—Of 2113 patients, 1058 received triflusal and 1055 aspirin. The mean follow-up period was 30.1 months. The incidence of combined end point (13.1% for triflusal, 12.4% for aspirin) as well the survival analysis (hazard ratio [HR] for triflusal versus aspirin, 1.09; 95% CI, 0.85 to 1.38) showed no differences between groups. The incidence of nonfatal stroke (HR, 1.09; 95% CI, 0.82 to 1.44), nonfatal acute myocardial infarction (HR, 0.95; 95% CI, 0.46 to 1.98,) and vascular death (HR, 1.22; 95% CI, 0.75 to 1.96) was also similar. A significantly higher incidence of major hemorrhages in the aspirin group was recorded (HR, 0.48; 95% CI, 0.28 to 0.82). The overall incidence of hemorrhage was significantly lower in the triflusal group (16.7% versus 25.2%) (odds ratio, 0.76; 95% CI, 0.67 to 0.86;P<0.001).Conclusions—This study failed to show significantly superior efficacy of triflusal over aspirin in the long-term prevention of vascular events after stroke, but triflusal was associated with a significantly lower rate of hemorrhagic complications.
ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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10. |
Platelet Function Under Aspirin, Clopidogrel, and Both After Ischemic StrokeA Case-Crossover Study |
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Stroke: Journal of the American Heart Association,
Volume 34,
Issue 4,
2003,
Page 849-854
Armin,
Grau Sven,
Reiners Christoph,
Lichy Florian,
Buggle Andreas,
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摘要:
Background and Purpose—Combined antiplatelet agents may offer additive protection over single drugs after stroke. We investigated whether platelet activation is reduced under combined aspirin and clopidogrel compared with each drug alone.Methods—In a case-crossover study, 31 patients with previous atherothrombotic or lacunar stroke who were treated with aspirin (100 to 300 mg/d) received clopidogrel (75 mg/d) and both aspirin and clopidogrel for 4 weeks. Platelet function in whole blood was studied after each treatment period and in healthy control subjects to assess activation-dependent antigens CD62p and CD63 by flow cytometry and collagen/epinephrine (CEPI-CT) and collagen/ADP (CADP-CT) closure times with the platelet function analyzer PFA-100, which investigates platelet-related function under shear stress.Results—CD62p expression and CD63 expression were not different under the 3 treatment regimens. CD63 but not CD62p expression was lower in control subjects than in stroke patients regardless of the antiplatelet treatment (P<0.05). CEPI-CT was prolonged under aspirin and aspirin plus clopidogrel compared with clopidogrel monotherapy (P<0.0001). CADP-CT was longer under combination therapy than under aspirin (P=0.0009) or clopidogrel (P=0.0074) or in control subjects (P=0.0010), mainly because of strong prolongation in a patient subgroup (28%).Conclusions—CD63 expression reflecting the release of platelet lysosomes is consistently increased after stroke and incompletely suppressed by treatment with aspirin, clopidogrel, or both. The strong prolongation of CADP-CT under combined aspirin and clopidogrel in a patient subgroup may indicate a lower risk of thrombosis but also a higher risk of hemorrhage. The predictive value of platelet activation parameters requires investigation in prospective studies.
ISSN:0039-2499
出版商:OVID
年代:2003
数据来源: OVID
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