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  • Percutaneous coronary intervention for acute coronary syndrome: no difference in 48-h bleeding rate or vascular access-site complications with low- or standard-dose unfractionated heparin in patients initially treated with fondaparinux

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Therapeutics
Randomised controlled trial
Percutaneous coronary intervention for acute coronary syndrome: no difference in 48-h bleeding rate or vascular access-site complications with low- or standard-dose unfractionated heparin in patients initially treated with fondaparinux

http://dx.doi.org/10.1136/ebm1174

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    Footnotes

    • Competing interests AML has received research funding and consulting honoraria from Roche, Bristol-Myers Squibb and Schering Plough. AK has no disclosures to report.

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