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Figure 1 Event-Free Survival After Randomization
Two-year adverse events in patients allocated to tirofiban + sirolimus-eluting stent (tirofiban + sirolimus-eluting stent [SES] group) and in patients randomized to abciximab infusion plus bare-metal stenting (abciximab + bare-metal stent [BMS] group). Cumulative risk of major adverse events (A), death or myocardial infarction (B), and target vessel revascularization (C).
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