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Myocardial Infarction and Functional Outcome Assessment in Pigs
Published on: April 25, 2014
Determinants and Prognoses of Visual-Functional Mismatches After Mechanical Reperfusion in ST-Elevation Myocardial
Jieliang Liu1, Junguo Jin1, Bingyan Yu2
1Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, 510080, People's Republic of China.
Insights
Visual-functional mismatch in ST-elevation myocardial infarction (STEMI) patients undergoing PCI is linked to microcirculatory resistance. This mismatch indicates a worse prognosis, highlighting the importance of assessing both anatomy and physiology.
Area of Science:
- Cardiology
- Interventional Cardiology
- Myocardial Infarction Research
Background:
- Discordance between coronary anatomy and physiology is crucial in stable coronary disease management.
- Its significance in ST-elevation myocardial infarction (STEMI) requires further elucidation.
Purpose of the Study:
- To investigate the clinical implications of visual-functional mismatches in STEMI patients.
- To assess the role of angiography-derived microcirculatory resistance (AMR) in these mismatches.
- To evaluate the prognostic impact of these mismatches on major adverse cardiovascular events (MACE).
Main Methods:
- Retrospective study of 310 STEMI patients undergoing percutaneous coronary intervention (PCI).
- Quantitative coronary angiography (QCA) and quantitative flow ratio (QFR) assessments stratified patients into four groups based on visual and functional severity.
- Multivariable logistic regression and Kaplan-Meier analyses were used to identify factors associated with mismatches and estimate MACE-free survival.
Main Results:
- 68 patients showed visual-functional mismatch, and 51 showed reverse mismatch.
- Mismatch was associated with higher angiography-derived microcirculatory resistance (AMR).
- Reverse mismatch was linked to larger area stenosis, lower coronary flow velocity, and lower AMR.
- The mismatch group exhibited the worst 18-month MACE-free survival.
Conclusions:
- AMR significantly contributes to visual-functional mismatches between QCA-DS and QFR in STEMI.
- Patients with mismatch demonstrate the poorest prognosis regarding MACE.
Background:
Discordance between the anatomy and physiology of the coronary has important implications for managing patients with stable coronary disease, but its significance in ST-elevation myocardial infarction has not been fully elucidated.
Methods:
The retrospective study involved patients diagnosed with ST-elevation myocardial infarction (STEMI) who underwent percutaneous coronary intervention (PCI), along with quantitative coronary angiography (QCA) and quantitative flow ratio (QFR) assessments. Patients were stratified into four groups regarding the severity of the culprit vessel, both visually and functionally: concordantly negative (QCA-diameter stenosis [DS] ≤ 50% and QFR > 0.80), mismatch (QCA-DS > 50% and QFR > 0.80), reverse mismatch (QCA-DS ≤ 50% and QFR ≤ 0.80), and concordantly positive (QCA-DS > 50% and QFR ≤ 0.80). Multivariable logistic regression analyses were conducted to identify the clinical factors linked to visual-functional mismatches. Kaplan‒Meier analysis was conducted to estimate the 18-month adverse cardiovascular events (MACE)-free survival between the four groups.
Results:
The study involved 310 patients, with 68 presenting visual-functional mismatch, and 51 exhibiting reverse mismatch. The mismatch was associated with higher angiography-derived microcirculatory resistance (AMR) (adjusted odds ratio [aOR]=1.016, 95% CI: 1.010-1.022, P<0.001). Reverse mismatch was associated with larger area stenosis (aOR=1.044, 95% CI: 1.004-1.086, P=0.032), lower coronary flow velocity (aOR=0.690, 95% CI: 0.567-0.970, P<0.001) and lower AMR (aOR=0.947, 95% CI: 0.924-0.970, P<0.001). Additionally, the mismatch group showed the worst 18-month MACE-free survival among the four groups (Log rank test p = 0.013).
Conclusion:
AMR plays a significant role in the occurrence of visual-functional mismatches between QCA-DS and QFR, and the mismatch group showed the worst prognosis.
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