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Relationship between microvascular obstruction and adverse events following primary percutaneous coronary
Suzanne de Waha1,2, Manesh R Patel3, Christopher B Granger3
1University Heart Centre Luebeck, University Hospital Schleswig-Holstein, Ratzeburger Allee 160, 23538 Luebeck, Germany.
Aims:
Microvascular obstruction (MVO) is the underlying cause for the no-reflow phenomenon in ST-segment elevation myocardial infarction (STEMI). The association between MVO assessed by cardiac magnetic resonance imaging (CMR) and prognosis has not been convincingly demonstrated. We sought to determine the relationship between MVO assessed early after primary percutaneous coronary intervention (PCI) in STEMI and all-cause mortality, hospitalization for heart failure (HF), and reinfarction.
Methods And Results:
We performed a pooled analysis using individual patient data from seven randomized primary PCI trials in which MVO was assessed within 7 days after reperfusion by CMR using late gadolinium enhancement imaging (n = 1688). Clinical follow-up was performed for at least 6 months after the index event. Median time to CMR after STEMI was 3 days [interquartile range (IQR) 2-4], and median duration of clinical follow-up was 365 days (IQR 188-374). Microvascular obstruction was present in 960 (56.9%) of patients, and median MVO (percent left ventricular myocardial mass) was 0.47% (IQR 0.00-2.54). A graded response was present between the extent of MVO (per 1.0% absolute increase) and subsequent mortality [Cox adjusted hazard ratio (HR) 1.14, 95% confidence interval (CI) 1.09-1.19, P < 0.0001] and hospitalization for HF (Cox adjusted HR 1.08, 95% CI 1.05-1.12, P < 0.0001). Microvascular obstruction remained significantly associated with all-cause mortality even after further adjustment for infarct size (Cox adjusted HR 1.09, 95% CI 1.01-1.17, P = 0.03). MVO was not significantly related to subsequent reinfarction (P = 0.29).
Conclusions:
The presence and extent of MVO measured by CMR after primary PCI in STEMI are strongly associated with mortality and hospitalization for HF within 1 year.
Insights
Microvascular obstruction (MVO) after ST-segment elevation myocardial infarction (STEMI) is linked to higher mortality and heart failure hospitalizations. Early assessment of MVO using cardiac magnetic resonance imaging (CMR) can predict patient outcomes within one year.
Area of Science:
- Cardiology
- Medical Imaging
- Clinical Research
Background:
- Microvascular obstruction (MVO) is a key factor in the no-reflow phenomenon following ST-segment elevation myocardial infarction (STEMI).
- The prognostic significance of MVO, particularly when assessed early via cardiac magnetic resonance imaging (CMR), requires further clarification.
Purpose of the Study:
- To investigate the association between early MVO assessment by CMR and clinical outcomes in STEMI patients post-primary percutaneous coronary intervention (PCI).
- Specifically, to determine the relationship between MVO and all-cause mortality, heart failure (HF) hospitalization, and reinfarction.
Main Methods:
- A pooled analysis of individual patient data from seven randomized primary PCI trials was conducted.
- MVO was assessed using CMR with late gadolinium enhancement within 7 days of reperfusion in 1688 STEMI patients.
- Clinical follow-up data for at least 6 months post-event were analyzed.
Main Results:
- Microvascular obstruction was identified in 56.9% of patients, with a median extent of 0.47% of left ventricular myocardial mass.
- A significant, graded association was observed between the extent of MVO and increased risk of all-cause mortality (HR 1.14) and HF hospitalization (HR 1.08).
- MVO remained a significant predictor of mortality even after adjusting for infarct size, but was not significantly associated with reinfarction.
Conclusions:
- The presence and extent of MVO, as measured by CMR shortly after primary PCI in STEMI, are robustly associated with increased mortality and HF hospitalization within one year.
- Early CMR assessment of MVO provides valuable prognostic information for STEMI patients.
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