Prognostic implications of left ventricular dyssynchrony early after non-ST elevation myocardial infarction without
Arnold C T Ng1, Da T Tran, Christine Allman
1Department of Cardiology, Liverpool Hospital, University of New South Wales, Elizabeth Street, Liverpool, Sydney, NSW 2170, Australia.
Insights
Left ventricular (LV) dyssynchrony after non-ST elevation myocardial infarction (NSTEMI) is predicted by proximal left circumflex artery stenosis and poor LV function. A composite dyssynchrony score predicts long-term LV dysfunction.
Area of Science:
- Cardiology
- Cardiac Imaging
- Heart Failure Research
Background:
- Left ventricular (LV) dyssynchrony is a significant complication following non-ST elevation myocardial infarction (NSTEMI).
- Predicting long-term LV dysfunction after NSTEMI remains a clinical challenge.
Purpose of the Study:
- To identify independent predictors of LV dyssynchrony post-NSTEMI.
- To evaluate the prognostic value of combining dyssynchrony parameters for predicting long-term LV dysfunction.
Main Methods:
- 100 NSTEMI patients underwent LV dyssynchrony assessments.
- A composite dyssynchrony score was utilized.
- Patients were followed for 1 year to assess long-term LV function.
Main Results:
- Proximal left circumflex artery (LCx) stenosis and global systolic dysfunction independently predicted early LV dyssynchrony.
- Absence of early dyssynchrony, fewer diseased vessels, and revascularization were associated with improved LV volumes and ejection fraction over time.
- The composite dyssynchrony score independently predicted persistent LV dilation and low ejection fraction at follow-up.
Conclusions:
- Proximal LCx stenosis and impaired LV function are independent predictors of LV dyssynchrony after NSTEMI.
- The composite dyssynchrony score demonstrates prognostic value, identifying patients at risk for persistent LV dilation and dysfunction.
Aims:
To determine independent predictors of left ventricular (LV) dyssynchrony after non-ST elevation myocardial infarction (NSTEMI) and prognostic value of combining dyssynchrony parameters for long-term LV dysfunction.
Methods And Results:
Left ventricular dyssynchrony assessments were performed in 100 NSTEMI patients followed-up for 1 year using a composite dyssynchrony score. Early LV dyssynchrony was independently predicted by the presence of significant proximal left circumflex artery (LCx) stenosis and global systolic dysfunction. Left ventricular end-diastolic volume index decreased with time and was independently determined by a lower number of diseased vessels and the absence of early dyssynchrony. Left ventricular end-systolic volume index decreased with time and was independently determined by the absence of early dyssynchrony, lower number of diseased vessels, and revascularization. Left ventricular ejection fraction increased with time and was independently determined by the absence of early dyssynchrony, lower number of diseased vessels, and revascularization. The composite dyssynchrony score was an independent determinant of a persistently dilated LV and low LVEF at follow-up.
Conclusion:
After NSTEMI, proximal LCx stenosis and impaired LV function independently predicted LV dyssynchrony. The composite dyssynchrony score had prognostic value and identified patients with persistently dilated and impaired LV on follow-up.
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