Intracoronary Eptifibatide During Primary Percutaneous Coronary Intervention in Early Versus Late Presenters with ST

Ayman Elbadawi1,2, Gerald Gasioch3, Islam Y Elgendy4

  • 1Department of Internal Medicine, Rochester General Hospital, Rochester, NY, USA.

Cardiology and Therapy
|November 16, 2016
PubMed

Insights

Intracoronary eptifibatide improved reperfusion markers in ST-elevation myocardial infarction patients undergoing primary PCI, particularly those presenting later. Further research is recommended for late presenters to confirm clinical benefits.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Pharmacology

Background:

  • The efficacy of intracoronary (IC) eptifibatide in primary percutaneous coronary intervention (PPCI) for ST-elevation myocardial infarction (STEMI) remains unclear, especially concerning the impact of patient presentation time.
  • This study aimed to assess the benefits of IC eptifibatide during PPCI in early versus late STEMI presenters.

Purpose of the Study:

  • To evaluate the effectiveness of IC eptifibatide in improving reperfusion during PPCI for STEMI.
  • To determine if the timing of patient presentation influences the benefit of IC eptifibatide.

Main Methods:

  • Seventy STEMI patients eligible for PPCI were randomized to receive either IC eptifibatide or standard care.
  • Patients were categorized as early (<3 hours) or late (≥3 hours) presenters based on symptom-to-door time.
  • Primary endpoint was myocardial blush grade (MBG); secondary endpoints included corrected TIMI frame count (cTFC), ST segment resolution (STR), and peak CKMB.

Main Results:

  • In late presenters, IC eptifibatide significantly improved MBG (100% vs. 50%, p=0.001).
  • IC eptifibatide use was associated with improved cTFC and reduced peak CKMB in both early and late presenters compared to controls.
  • No significant difference in STR was observed between groups.

Conclusions:

  • IC eptifibatide may enhance reperfusion markers in STEMI patients undergoing PPCI, particularly those presenting after 3 hours.
  • A large randomized trial is warranted to confirm the clinical benefits of IC eptifibatide in late presenters.
Abstract

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