Intracoronary versus intravenous bolus abciximab application in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention: 6-month effects on infarct size and left ventricular function: The randomised Leipzig Immediate PercutaneouS Coronary Intervention Abciximab i.v. versus i.c. in ST-Elevation Myocardial Infarction Trial (LIPSIAbciximab-STEMI)
Background Administration of abciximab during primary percutaneous coronary intervention (PCI) reduces major adverse cardiac events (MACE) in patients with ST-elevation myocardial infarction (STEMI). Intracoronary (IC) abciximab bolus application during PCI results in high local drug concentration,...
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Veröffentlicht in: | Clinical research in cardiology 2011-05, Vol.100 (5), p.425-432 |
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Sprache: | eng |
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Zusammenfassung: | Background
Administration of abciximab during primary percutaneous coronary intervention (PCI) reduces major adverse cardiac events (MACE) in patients with ST-elevation myocardial infarction (STEMI). Intracoronary (IC) abciximab bolus application during PCI results in high local drug concentration, improved perfusion, reduction of infarct size, and less microvascular obstruction early after infarction. Aim of this study was to investigate whether the early benefits of an IC abciximab administration in STEMI patients undergoing PCI are sustained at 6 months.
Methods
We performed 6-month follow-up of 154 STEMI patients undergoing PCI, who were randomised to either IC (
n
= 77) or intravenous (IV) (
n
= 77) bolus abciximab administration with subsequent 12-h intravenous infusion. The primary endpoint was infarct size at 6-month follow-up as assessed by delayed enhancement magnetic resonance imaging. Clinical end points were MACEs within 6 months after infarction.
Results
The median infarct size after 6 months was significantly reduced in the IC abciximab group (16.7 vs. 24.1%,
p
= 0.002). A significant recovery of LV function was only observed in the IC abciximab group (
p
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ISSN: | 1861-0684 1861-0692 |
DOI: | 10.1007/s00392-010-0260-5 |