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Volume 99, Issue 2, Pages 186-188 (15 January 2007)


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Comparison of Effectiveness of Enoxaparin Versus Unfractionated Heparin to Reduce Silent and Clinically Apparent Acute Myocardial Infarction in Patients Presenting With Non–ST-Segment Elevation Acute Coronary Syndrome

Sanjit Jolly, MDb, Mary Tana, Aurora Mendelsohna, David Fitchett, MDab, Paul W. Armstrong, MDc, Anatoly Langer, MDab, Shaun G. Goodman, MDabCorresponding Author Informationemail address

Received 15 February 2006; received in revised form 25 July 2006; accepted 25 July 2006. published online 17 November 2006.

Electrocardiographic (ECG) estimates of myocardial infarct size based on the Selvester ECG score have been shown to predict mortality and left ventricular function after acute myocardial infarction (AMI). This score has also been used to identify not clinically apparent AMI (“silent” AMI) and to determine treatment effect, suggesting it could serve as a clinical trial end point. The objective of this study was to compare the rate of silent AMI as measured by the Selvester QRS score in patients with a non–ST-segment elevation acute coronary syndrome treated with enoxaparin versus intravenous unfractionated heparin who were participating in a continuous ECG monitoring substudy of the Efficacy and Safety of Subcutaneous Enoxaparin in Non–Q-wave Coronary Events study (ESSENCE) and INTegrelin and Enoxaparin Randomized Assessment of acute Coronary syndrome Treatment trial (INTERACT). Enoxaparin was associated with a 56% relative risk decrease in silent AMI at 96 hours compared with unfractionated heparin (2.7% vs 6.1% p = 0.03). Similarly, enoxaparin decreased Holter-detected myocardial ischemia compared with unfractionated heparin (18.7% vs 35.9%, p = 0.03). In conclusion, enoxaparin significantly decreased the composite of silent AMI or clinical AMI and death at 1 year (9.3% vs 21%, p = 0.0001).

a Canadian Heart Research Centre, Division of Cardiology, St. Michaelx2019;s Hospital, University of Toronto, Toronto, Ontario, Canada

b Terrence Donnelly Heart Centre, Division of Cardiology, St. Michaelx2019;s Hospital, University of Toronto, Toronto, Ontario, Canada

c Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.

Corresponding Author InformationCorresponding author: Tel: 416-864-5722; fax: 416-864-5407.

 The ESSENCE study and ESSENCE ECG substudy were sponsored by Aventis Pharma, USA. The INTERACT study was sponsored by the Canadian Heart Research Centre, Toronto, Ontario, Canada; Key Pharmaceuticals, Division of Schering Canada, Inc., Kirkland, Quebec, Canada; and Millienium Pharmaceuticals, Inc., Cambridge, Massachusetts.

PII: S0002-9149(06)01996-5

doi:10.1016/j.amjcard.2006.07.078


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