Assessment of No-Reflow in Patients With STEMI After Intracoronary Tirofiban After Opening of the Vessel

Mohammed Ali Mohammed Hammad1, Wael Anwar Elshahat Hassib1, Mohamed Kamal Ibrahim Salama1

  • 1Cardiology Department, Faculty of Medicine, Kafr Elsheikh University, Kafr Elsheikh, Egypt.

Cardiology Research
|March 13, 2026
PubMed

Insights

Intracoronary tirofiban effectively reduces the no-reflow phenomenon (NRP) after primary percutaneous coronary intervention (PPCI) in ST-segment elevation myocardial infarction (STEMI) patients, improving coronary flow and reducing major adverse cardiac events (MACE).

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Pharmacology

Background:

  • No-reflow phenomenon (NRP) is a critical complication after primary percutaneous coronary intervention (PPCI) in ST-segment elevation myocardial infarction (STEMI).
  • Successful epicardial recanalization does not always prevent NRP, leading to adverse outcomes.
  • Identifying effective strategies to mitigate NRP is crucial for improving STEMI patient prognosis.

Purpose of the Study:

  • To evaluate the efficacy of intracoronary (IC) tirofiban in preventing NRP following PPCI in STEMI patients.
  • To assess the impact of IC tirofiban on coronary flow restoration and clinical outcomes.
  • To determine the safety profile of IC tirofiban, including bleeding complications.

Main Methods:

  • A randomized controlled double-blind study involving 60 STEMI patients undergoing successful PPCI.
  • Patients with suboptimal coronary flow (TIMI grade < 3) received either IC tirofiban (25 ug/kg) or placebo (0.9% saline).
  • Outcomes assessed included TIMI flow grade, NRP incidence, ST-T normalization, bleeding complications, and major adverse cardiac events (MACE) at 30 days.

Main Results:

  • The tirofiban group showed significantly higher rates of TIMI 3 flow (80% vs. 46.67%) and lower NRP incidence (20% vs. 53.33%) compared to placebo (P = 0.007 for both).
  • Minor bleeding complications were higher in the tirofiban group (26.67% vs. 3.33%, P = 0.026), with no significant difference in major bleeding.
  • In-hospital MACE were substantially reduced in the tirofiban group (3.33% vs. 30%, P = 0.012).

Conclusions:

  • Intracoronary tirofiban is effective in reducing NRP and improving coronary flow after PPCI in STEMI.
  • IC tirofiban administration leads to a significant reduction in MACE.
  • While associated with increased minor bleeding, IC tirofiban offers a favorable risk-benefit profile for managing NRP in STEMI.
Abstract

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