Link between aortic valve sclerosis and myocardial no-reflow in ST-segment elevation myocardial infarction
1Department of Cardiology, Ahi Evren Cardiovascular and Thoracic Surgery Training and Research Hospital, Trabzon, Turkey, l.korkmaz@yahoo.com.
Insights
Aortic valve sclerosis (AVS) is linked to myocardial no-reflow in ST-segment elevation myocardial infarction (STEMI) patients. This finding may help predict and prevent no-reflow, improving outcomes for STEMI patients.
Area of Science:
- Cardiology
- Cardiovascular Research
- Interventional Cardiology
Background:
- The no-reflow phenomenon negatively impacts prognosis in ST-segment elevation myocardial infarction (STEMI) patients.
- Predicting and preventing no-reflow is critical for improving STEMI patient outcomes.
- Aortic valve sclerosis (AVS) is a condition affecting the aortic valve.
Purpose of the Study:
- To investigate the association between aortic valve sclerosis (AVS) and myocardial no-reflow in patients with STEMI.
- To identify potential predictors of the no-reflow phenomenon in STEMI.
Main Methods:
- Consecutive enrollment of patients diagnosed with STEMI for the first time.
- No-reflow defined by specific coronary flow and blush criteria.
- AVS diagnosed via echocardiography, characterized by valve thickening and calcification.
Main Results:
- No-reflow occurred in 41 patients.
- Univariate analysis showed associations with age, male gender, smoking, Syntax score, and hypertension.
- Multivariate analysis identified age, AVS, Syntax score, and symptom-to-balloon time as independent determinants of no-reflow.
Conclusions:
- Aortic valve sclerosis is a significant and independent predictor of myocardial no-reflow in STEMI patients.
- Identifying AVS may aid in risk stratification and management strategies for STEMI.
Objective:
The"no-reflow" phenomenon is associated with a worse prognosis at follow-up for patients with acute ST-segment elevation myocardial infarction (STEMI). Predicting and preventing no-reflow is therefore a crucial step in improving the prognosis of STEMI patients. The purpose of this study was to investigate the association between aortic valve sclerosis (AVS) and myocardial no-reflow in patients with STEMI.
Patients And Methods:
Patients with a first-time diagnosis of STEMI were enrolled consecutively. No-reflow was defined as a final TIMI 3 flow with a myocardial blush of grade < 2, temporary epicardial coronary no-reflow, and distal coronary occlusion. AVS was defined by echocardiography as thickening and calcification of the normal trileaflet aortic valve without obstruction to the left ventricular outflow.
Results:
No-reflow developed in 41 patients. In univariate analysis, age, male gender, smoking, culprit lesion Syntax score (SX score), and hypertension were significantly associated with no-reflow. Multivariate binary logistic regression analyses demonstrated age [95 % confidence interval (CI), 1.024-1.096; p=0.001), AVS (95 % CI, 1.002-1.100; p=0.039], culprit lesion SX score (95 % CI, 1.08-1.021 p=0.008), and symptom-to-balloon time (95 % CI, 1.020-1.097; p=0.002) as independent determinants of myocardial no-reflow.
Conclusion:
AVS was significantly and independently associated with myocardial no-reflow in STEMI patients.
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