PROSPECTIVE EVALUATION OF A PROSTACYCLIN-SPARING ASPIRIN FORMULATION AND HEPARIN WARFARIN IN ASPIRIN USERS WITH UNSTABLE ANGINA OR NON-Q-WAVE MYOCARDIAL-INFARCTION AT REST

被引:9
作者
COHEN, M
PARRY, G
ADAMS, PC
XIONG, J
CHAMBERLAIN, D
WIECZOREK, I
FOX, KAA
KRONMAL, R
FUSTER, V
机构
[1] HAHNEMANN UNIV,DEPT MED,DIV CARDIOL,PHILADELPHIA,PA 19102
[2] ROYAL VICTORIA INFIRM,DEPT CARDIOL,NEWCASTLE TYNE NE1 4LP,TYNE & WEAR,ENGLAND
[3] ROYAL SUSSEX CTY HOSP,DEPT CARDIOL,BRIGHTON BN2 5BE,E SUSSEX,ENGLAND
[4] UNIV EDINBURGH,CARDIOVASC RES UNIT,EDINBURGH EH8 9YL,MIDLOTHIAN,SCOTLAND
[5] STAT & EPIDEMIOL RES CORP,SEATTLE,WA
[6] MT SINAI HOSP,DIV CARDIOL,NEW YORK,NY
关键词
MYOCARDIAL ISCHEMIA; ASPIRIN; ANTICOAGULATION;
D O I
10.1093/oxfordjournals.eurheartj.a060653
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this trial was to compare the efficacy of combination antithrombotic therapy with a prostacyclin-sparing aspirin plus anticoagulation versus conventional aspirin plus anticoagulation, when added to antianginal therapy, in patients with unstable angina or non-Q wave myocardial infarction already being treated with aspirin. In a double-blind (for the aspirin) study, 144 prior aspirin users were randomized; 72 patients received controiled-release, prostacyclin-sparing aspirin 75 mg daily plus anticoagulation (intravenous heparin followed by warfarin to maintain the international normalized ratio at 2-3), and 72 patients received conventional aspirin 75 mg daily plus the same anticoagulation. Controlled-release aspirin was formulated to preserve endothelial cell prostacyclin synthesis. Trial therapy was begun by 13.2 ± 12.3 h of qualifying pain, and continued for 12 weeks.The frequency of recurrent angina with electrocardiographic changes, myocardial infarction, or death, was analysed by intention to treat. At 12 weeks, events were. © 1994 The European Society of Cardiology.
引用
收藏
页码:1196 / 1203
页数:8
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