Key result
Intracoronary abciximab significantly reduced mortality (2.7% vs 10.0%, p=0.004), target vessel revascularization, and myocardial infarction at 1 year compared to intravenous abciximab in STEMI.
Why the study?
Does intracoronary bolus abciximab reduce mortality, TVR, and MI in STEMI patients undergoing primary PCI compared to intravenous bolus abciximab?
RCT (n=355)
Does intracoronary bolus abciximab reduce mortality, TVR, and MI in STEMI patients undergoing primary PCI compared to intravenous bolus abciximab?
Absolute Event Rate: 2.7% vs 10%
p-value: p=0.004
Intracoronary administration of abciximab bolus significantly reduces mortality, TVR, and MI at 1 year compared to intravenous administration in STEMI patients undergoing primary PCI.
Supports intracoronary abciximab in STEMI primary PCI; extends randomized evidence on bolus route versus intravenous.
OBJECTIVES: Administration of the glycoprotein IIb/IIIa inhibitor abciximab to patients with ST segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI) improves outcome. Data have suggested that an intracoronary (IC) bolus might be superior to the standard intravenous (IV) administration. We have previously reported reduced short-term mortality and need for target vessel revascularization (TVR) with the IC route. We now present long-term data from our randomized trial on IC versus IV abciximab in pPCI-treated STEMI patients. METHODS: A total of 355 pPCI-treated STEMI patients were randomized to either IC or IV bolus abciximab followed by a 12-hour IV infusion. Patients were followed for 1 year to observe mortality, TVR or myocardial infarction (MI) and the combination of these. RESULTS: The two treatment arms (IV, n = 170; IC, n = 185) were similar with regard to baseline characteristics. Mortality was reduced from 10% in the IV group to 2.7% in the IC group (p = 0.004). TVR and MI were also reduced with IC administration (TVR: 14.1 vs. 7.6%, p = 0.04; MI: 11.8 vs. 5.4%, p = 0.03). Consequently, patients in the IC treatment arm had a relative risk reduction of 55% for the combined endpoint after 1 year (p = 0.002) compared to the IV treatment arm. CONCLUSIONS: In pPCI-treated STEMI patients treated with abciximab, IC bolus administration resulted in a significant reduction in mortality, TVR and MI compared to IV bolus administration.
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Iversen et al. (2011) conducted an RCT in ST segment elevation myocardial infarction (STEMI) (n=355). Intracoronary abciximab vs. Intravenous abciximab was evaluated on Mortality (p=0.004). Intracoronary abciximab significantly reduced mortality (2.7% vs 10.0%, p=0.004), target vessel revascularization, and myocardial infarction at 1 year compared to intravenous abciximab in STEMI.
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