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The incidence of combined major and minor vascular access site bleeding in nonabciximab (heparin plus placebo) patients progressively decreased from EPIC (8.2%) to EPILOG (2.9%) to EPISTENT (1.7%; <jats:italic>P<\/jats:italic> &lt; 0.001). Combined major and minor vascular access site bleeding in abciximab (heparin plus abciximab) patients decreased from EPIC (20%) to EPILOG (5.8%) to EPISTENT (2.2%; <jats:italic>P<\/jats:italic> &lt; 0.001). There were more major vascular access site bleeds with abciximab compared to placebo in EPIC (odds ration 3.2; <jats:italic>P<\/jats:italic> &lt; 0.001) but not in EPILOG or EPISTENT. Modified abciximab and heparin dosing and improved vascular access site management strategies have decreased the risk of vascular access bleeding during coronary intervention and have essentially eliminated the excess access site bleeding associated with abciximab. 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