Medium intensity oral anticoagulants versus aspirin after cerebral ischaemia of arterial origin (ESPRIT): a randomised controlled trial

被引:150
作者
Halkes, P. H. A. [1 ]
van Gijn, J. [1 ]
Kappelle, L. J. [1 ]
Koudstaal, P. J. [1 ]
Algra, A. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Neurol, Rudolf Magnus Inst Neurosci, NL-3508 GA Utrecht, Netherlands
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1474-4422(06)70685-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Oral anticoagulants are better than aspirin for secondary prevention after myocardial infarction and after cerebral ischaemia in combination with non-rheumatic atrial fibrillation. The European/Australasian Stroke Prevention in Reversible Ischaemia Trial (ESPRIT) aimed to determine whether oral anticoagulation with medium intensity is more effective than aspirin in preventing future vascular events in patients with transient ischaemic attack or minor stroke of presumed arterial origin. Methods In this international, multicentre trial, patients were randomly assigned within 6 months after a transient ischaemic attack or minor stroke of presumed arterial origin either anticoagulants (target INR range 2.0-3.0; n=536) or aspirin (30-325 mg daily; n=532). The primary outcome was the composite of death from all vascular causes, non-fatal stroke, non-fatal myocardial infarction, or major bleeding complication, whichever occurred first. In a post hoc analysis anticoagulants were compared with the combination of aspirin and dipyridamole (200 mg twice daily). Treatment was open, but auditing of outcome events was blinded. Primary analysis was by intention to treat. This study is registered as an International Standard Randomised Controlled Trial (number ISRCTN73824458) and with ClinicalTrials.gov (NCT00161070). Findings The anticoagulants versus aspirin comparison of ESPRIT was prematurely ended because ESPRIT reported previously that the combination of aspirin and dipyridamole was more effective than aspirin alone. Mean follow-up was 4.6 years (SD 2.2). The mean achieved INR was 2.57 (SD 0.86). A primary outcome event occurred in 99 (19%) patients on anticoagulants and in 98 (18%) patients on aspirin (hazard ratio [HR] 1.02, 95% CI 0.77-1.35). The HR for ischaemic events was 0.73 (0.52-1.01) and for major bleeding complications 2.56 (1.48-4.43). The HR for the primary outcome event comparing anticoagulants with the combination treatment of aspirin and dipyridamole was 1.31 (0.98-1.75). Interpretation Oral anticoagulants (target INR range 2.0-3.0) are not more effective than aspirin for secondary prevention after transient ischaemic attack or minor stroke of arterial origin. A possible protective effect against ischaemic events is offset by increased bleeding complications.
引用
收藏
页码:115 / 124
页数:10
相关论文
共 32 条
[11]   Comparison of warfarin and aspirin for symptomatic intracranial arterial stenosis [J].
Chimowitz, MI ;
Lynn, MJ ;
Howlett-Smith, H ;
Stern, BJ ;
Hertzberg, VS ;
Frankel, MR ;
Levine, SR ;
Chaturvedi, S ;
Kasner, SE ;
Benesch, CG ;
Sila, CA ;
Jovin, TG ;
Romano, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (13) :1305-1316
[12]   Clopidogrel plus aspirin versus oral anticoagulation for atrial fibrillation in the Atrial fibrillation Clopidogrel Trial with Irbesartan for prevention of Vascular Events (ACTIVE W): a randomised controlled trial [J].
Connolly, S. ;
Pogue, J. ;
Hart, R. ;
Pfeffer, M. ;
Hohnloser, S. ;
Chrolavicius, S. ;
Yusuf, S. .
LANCET, 2006, 367 (9526) :1903-1912
[13]   Population based study of early risk of stroke after transient ischaemic attack or minor stroke: implications for public education and organisation of services [J].
Coull, AJ ;
Lovett, JK ;
Rothwell, PM .
BMJ-BRITISH MEDICAL JOURNAL, 2004, 328 (7435) :326-328
[14]   Severity of cerebral white matter lesions and infarcts in patients with transient or moderately disabling cerebral ischaemia: reproducibility of grading by neurologists [J].
De Schryver, E. L. L. M. ;
van Gijn, J. ;
Kappelle, L. J. ;
Koudstaal, P. J. ;
Algra, A. .
EUROPEAN JOURNAL OF NEUROLOGY, 2006, 13 (08) :901-903
[15]   Type of stroke after transient monocular blindness or retinal infarction of presumed arterial origin [J].
De Schryver, ELLM ;
Algra, A ;
Donders, RCJM ;
van Gijn, J ;
Kappelle, LJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2006, 77 (06) :734-738
[16]   ESPRIT: Protocol change [J].
De Schryver, ELLM .
CEREBROVASCULAR DISEASES, 2001, 11 (03) :286-286
[17]   Design of ESPRIT: An international randomized trial for secondary prevention after non-disabling cerebral ischaemia of arterial origin [J].
De Schryver, ELLM .
CEREBROVASCULAR DISEASES, 2000, 10 (02) :147-150
[18]  
Franke CL, 1997, ANN NEUROL, V42, P857
[19]   A randomised, blinded, trial of clopidogrel versus aspirin in patients at risk of ischaemic events (CAPRIE) [J].
Gent, M ;
Beaumont, D ;
Blanchard, J ;
Bousser, MG ;
Coffman, J ;
Easton, JD ;
Hampton, JR ;
Harker, LA ;
Janzon, L ;
Kusmierek, JJE ;
Panak, E ;
Roberts, RS ;
Shannon, JS ;
Sicurella, J ;
Tognoni, G ;
Topol, EJ ;
Verstraete, M ;
Warlow, C .
LANCET, 1996, 348 (9038) :1329-1339
[20]   Major bleeding during anticoagulation after cerebral ischemia - Patterns and risk factors [J].
Gorter, JW .
NEUROLOGY, 1999, 53 (06) :1319-1327