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Author Spotlight: Enhancing Coronary Artery Revascularization
Published on: September 15, 2023
Strategies to attenuate micro-vascular obstruction during P-PCI: the randomized reperfusion facilitated by local
Sheraz A Nazir1, Gerry P McCann1, John P Greenwood2
1Department of Cardiovascular Sciences, University of Leicester and NIHR Leicester Cardiovascular Biomedical Research Unit, Glenfield Hospital, Groby Road, Leicester LE3 9QP, UK.
Background:
Microvascular obstruction (MVO) following primary percutaneous coronary intervention (PPCI) treatment of ST-segment elevation myocardial infarction (STEMI) contributes to infarct expansion, left ventricular (LV) remodelling, and worse clinical outcomes. The REFLO-STEMI trial tested whether intra-coronary (IC) high-dose adenosine or sodium nitroprusside (SNP) reduce infarct size and/or MVO determined by cardiac magnetic resonance (CMR).
Methods And Results:
REFLO-STEMI, a prospective, open-label, multi-centre trial with blinded endpoints, randomized (1:1:1) 247 STEMI patients with single vessel disease presenting within 6 h of symptom onset to IC adenosine (2-3 mg total) or SNP (500 microg total) immediately following thrombectomy and again following stenting, or to standard PPCI. The primary endpoint was infarct size % LV mass (%LVM) on CMR undertaken 24-96 h after PPCI (n = 197). Clinical follow-up was to 6 months. There was no significant difference in infarct size (%LVM, median, interquartile range, IQR) between adenosine (10.1, 4.7-16.2), SNP (10.0, 4.2-15.8), and control (8.3, 1.9-14.0), P = 0.062 and P = 0.160, respectively, vs.
Control:
MVO (% LVM, median, IQR) was similar across groups (1.0, 0.0-3.7, P = 0.205 and 0.6, 0.0-2.4, P = 0.244 for adenosine and SNP, respectively, vs. control 0.3, 0.0-2.8). On per-protocol analysis, infarct size (%LV mass, 12.0 vs. 8.3, P = 0.031), major adverse cardiac events (hazard ratio, HR, 5.39 [1.18-24.60], P = 0.04) at 30 days and 6 months (HR 6.53 [1.46-29.2], P = 0.01) were increased and ejection fraction reduced (42.5 ± 7.2% vs. 45.7 ± 8.0%, P = 0.027) in adenosine-treated patients compared with control.
Conclusions:
High-dose IC adenosine and SNP during PPCI did not reduce infarct size or MVO measured by CMR. Furthermore, adenosine may adversely affect mid-term clinical outcome.
Clinical Trial Registration:
ClinicalTrials.gov Identifier: NCT01747174; https://clinicaltrials.gov/ct2/show/NCT01747174.
Insights
Intra-coronary adenosine and sodium nitroprusside did not reduce infarct size or microvascular obstruction in ST-elevation myocardial infarction patients. Adenosine treatment was associated with increased adverse events and reduced ejection fraction.
Area of Science:
- Cardiology
- Interventional Cardiology
- Cardiovascular Research
Background:
- Microvascular obstruction (MVO) after primary percutaneous coronary intervention (PPCI) for ST-segment elevation myocardial infarction (STEMI) worsens outcomes.
- Assessing novel treatments to mitigate MVO and infarct size is crucial for improving patient prognosis.
Purpose of the Study:
- To evaluate the efficacy of intra-coronary (IC) high-dose adenosine or sodium nitroprusside (SNP) in reducing infarct size and MVO.
- To assess the impact of these treatments on clinical outcomes up to 6 months post-STEMI.
Main Methods:
- REFLO-STEMI trial: a prospective, open-label, multi-center study randomizing 247 STEMI patients (1:1:1) to IC adenosine, IC SNP, or standard PPCI.
- Primary endpoint: infarct size (% LV mass) measured by cardiac magnetic resonance (CMR) 24-96 hours post-PPCI.
- Secondary endpoints included MVO and clinical outcomes at 6 months.
Main Results:
- No significant difference in infarct size or MVO was observed between adenosine, SNP, and control groups.
- Per-protocol analysis showed increased infarct size in the adenosine group (12.0% vs. 8.3%, P=0.031).
- Adenosine treatment was linked to higher major adverse cardiac events and reduced ejection fraction at 6 months.
Conclusions:
- High-dose IC adenosine and SNP administered during PPCI do not reduce infarct size or MVO in STEMI patients.
- Adenosine treatment may be associated with adverse mid-term clinical outcomes, warranting caution.
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