Why the study?
Does early administration of glycoprotein IIb/IIIa agents reduce long-term overall mortality/re-infarction in STEMI patients undergoing primary PCI?
Does early administration of glycoprotein IIb/IIIa agents reduce long-term overall mortality/re-infarction in STEMI patients undergoing primary PCI?
Early administration of glycoprotein IIb/IIIa agents before arrival at the catheterization laboratory is associated with reduced long-term mortality and re-infarction in STEMI patients undergoing primary PCI, particularly in high-risk subgroups.
Answers are grounded in this paper and cite their sources.
May support earlier GP IIb/IIIa use in STEMI networks; extends observational data but leaves open need for randomized confirmation.
AIMS: To evaluate the clinical impact of early administration of glycoprotein IIb/IIIa agents (IIb/IIIa agents) in the context of a dedicated hub and spoke network allowing very prompt pharmacological/mechanical interventions. METHODS AND RESULTS: Using a prospective database, we conducted a cohort study of ST-elevation myocardial infarction (STEMI) patients (n = 1124) undergoing primary percutaneous coronary interventions (PPCIs) and IIb/IIIa agents administration (period, 2003-2006). Comparisons were planned between patients receiving early IIb/IIIa agents administration (in hub/spoke centre emergency departments or during ambulance transfer; early group, n = 380) or delayed administration (in the catheterization laboratory; late group, n = 744). The primary outcome measure was long-term overall mortality/re-infarction. Baseline characteristics of the two groups were largely comparable. Angiographically, early group patients more often achieved pre-PPCI TIMI Grade 2-3 and TIMI Grade 3 flow. Clinically, the early administration group experienced lower 2-year risk of unadjusted mortality/re-infarction (17 vs. 23%; P = 0.01). After adjustment for potential confounders, early administration was associated with favourable outcome in the overall population (HR = 0.71, P = 0.03) and in high-risk subgroups (TIMI risk index >25, HR = 0.64, P = 0.02; Killip class >1, HR = 0.54, P = 0.01). CONCLUSION: In patients treated by PPCI within a STEMI network setting, early administration of IIb/IIIa agents may provide long-term clinical benefits. Notably, these results appeared magnified in high-risk patients.
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Ortolani et al. (2008) studied this question.
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