European Heart Journal Advance Access originally published online on March 17, 2009
European Heart Journal 2009 30(8):882-884; doi:10.1093/eurheartj/ehp105
Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org
Aspirin following PCI: too much of a good thing?
1 Geisinger Clinic, Danville, Pennsylvania, USA
2 The Medicines Company, 8058 Zurich-Flughafen, Switzerland
* Corresponding author. Tel: +41 44 810 0956, Fax: +41 43 813 3337, Email: steve.steinhubl@themedco.com
This editorial refers to Effects of aspirin dose on ischaemic events and bleeding after percutaneous coronary intervention: insights from the PCI-CURE study
, by S.S. Jolly et al., on page 900
| The first 10% of the full text of this article appears below. |
There is only one cardiovascular medication with a 4-fold difference in the routine daily dose approved by regulatory bodies, recommended by guideline committees, and suggested by clinicians.1 That medication is acetylsalicylic acid (ASA), or aspirin. When considering any drug routinely used in the treatment of the patient with cardiovascular disease—statins, thienopyridines, angiotensin-converting enzyme (ACE) inhibitors, β-blockers—are there any in which a 4-fold difference in dose would not be expected to lead to significant differences in efficacy, safety, and tolerability? Yet with aspirin, the most widely used drug worldwide for cardiovascular disease prevention, the choice of dose is frequently based more on habit than on science. In fact, market research suggests that, among US cardiologists,
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EHJ 2009 30: 900-907.[Abstract] [Full Text]