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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

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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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