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

**Authors:** Mohammed Ali Mohammed Hammad, Wael Anwar Elshahat Hassib, Mohamed Kamal Ibrahim Salama, Husna Irfan Thalib, Mohammed Moanes, Muhammad Reihan

PMC · DOI: 10.14740/cr2180 · 2026-02-28

## TL;DR

This study shows that giving tirofiban directly into the coronary artery after heart attack treatment improves blood flow and reduces complications, though it increases minor bleeding.

## Contribution

The study demonstrates the effectiveness of intracoronary tirofiban in reducing no-reflow phenomenon in STEMI patients after successful vessel opening.

## Key findings

- Tirofiban improved TIMI 3 flow in 80% of patients versus 46.67% in controls.
- NRP occurred in 20% of tirofiban cases versus 53.33% in controls.
- Tirofiban reduced in-hospital MACE to 3.33% versus 30% in controls.

## Abstract

No-reflow phenomenon (NRP) following primary percutaneous coronary intervention (PPCI) remains a critical determinant of adverse outcomes in ST-segment elevation myocardial infarction (STEMI) cases despite successful epicardial recanalization. The core purpose of this study was to establish the value of intracoronary (IC) tirofiban, delivered via the IC route, in mitigating the occurrence of NRP for STEMI cases subsequent to successful vessel reopening.

This randomized controlled double-blind study enrolled 60 STEMI cases. Following successful PCI, cases with thrombolysis in myocardial infarction (TIMI) flow grade less than 3 were randomized to receive either IC tirofiban (25 ug/kg) or saline 0.9% as placebo, in addition to standard pre-procedural therapy with aspirin, heparin, and ticagrelor. TIMI flow grade and incidence of NRP were evaluated. Additionally, ST-T normalization in electrocardiogram (ECG) was assessed. Bleeding complications and major adverse cardiac events (MACEs) were recorded during hospitalization and at 30-day follow-up.

The tirofiban group demonstrated notably superior coronary flow restoration with 80% achieving TIMI 3 flow versus 46.67% in controls (P = 0.007). NRP occurred in 20% of tirofiban cases compared to 53.33% in controls (P = 0.007). Minor bleeding complications increased in the tirofiban group (26.67% versus 3.33%, P = 0.026), while major bleeding remained absent in both groups. Total in-hospital MACEs were notably reduced with tirofiban treatment compared to controls (3.33% versus 30%, P = 0.012).

In STEMI cases following PPCI, IC tirofiban administration effectively reduces NRP, improves coronary flow restoration, and reduces MACE despite increased minor bleeding risk.

## Linked entities

- **Chemicals:** tirofiban (PubChem CID 60947), aspirin (PubChem CID 2244), ticagrelor (PubChem CID 9871419)
- **Diseases:** ST-segment elevation myocardial infarction (MONDO:0041656)

## Full-text entities

- **Diseases:** ST-segment elevation myocardial infarction (MESH:D000072657), bleeding (MESH:D006470), Bleeding complications (MESH:D008107), TIMI (MESH:D009203)
- **Chemicals:** aspirin (MESH:D001241), Tirofiban (MESH:D000077466), heparin (MESH:D006493), ticagrelor (MESH:D000077486)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12978383/full.md

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Source: https://tomesphere.com/paper/PMC12978383