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Pentraxin Level is the Key to Determine Primary Percutaneous Coronary Intervention (PCI) or Fibrinolysis
Habib Haybar1, Saeed Alipour Parsa2, Isa Khaheshi2
1Atherosclerosis research center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Insights
Pentraxin 3 (PTX3) levels can guide treatment for ST-Elevation Myocardial Infarction (STEMI). Patients with lower PTX3 levels benefit more from primary Percutaneous Coronary Intervention (PCI) over fibrinolysis, preserving left ventricular ejection fraction.
Area of Science:
- Cardiology
- Biomarkers
- Acute Myocardial Infarction
Background:
- Acute ST-Elevation Myocardial Infarction (STEMI) requires timely reperfusion therapy.
- Primary Percutaneous Coronary Intervention (PCI) and fibrinolysis are key treatments.
- Identifying patients who benefit most from each strategy is crucial.
Purpose of the Study:
- To investigate if pentraxin 3 (PTX3) can predict treatment response in STEMI patients.
- To determine if PTX3 modifies the benefit of primary PCI versus fibrinolysis.
- To assess PTX3's role in selecting optimal reperfusion therapy.
Main Methods:
- Patients with STEMI were recruited from centers with and without PCI facilities.
- Left ventricular ejection fraction (LVEF) was measured at baseline and 5 days post-admission.
- Regression models were used to analyze the impact of PTX3 on LVEF improvement after PCI vs. fibrinolysis.
Main Results:
- PTX3 levels influenced the functional advantage of PCI over fibrinolysis.
- Higher PTX3 levels were associated with attenuated or reversed LVEF improvement.
- Primary PCI significantly increased LVEF compared to fibrinolysis in patients with PTX3 < 7 ng/mL.
Conclusions:
- PTX3 levels can help guide the choice between primary PCI and fibrinolysis in STEMI.
- Patients with PTX3 ≤ 7 ng/mL show a clear benefit from primary PCI.
- PTX3 is a relevant biomarker for optimizing reperfusion therapy in STEMI.
Aims:
To examine if pentraxin can help identify patients benefitting most from primary Percutaneous Coronary Intervention (PCI) vs. fibrinolysis.
Methods:
Patients with acute ST-Elevation Myocardial Infarction (STEMI) were consecutively recruited from a community center without PCI and a tertiary center with PCI facilities. Left ventricular ejection fraction (LVEF) was determined echocardiographically at baseline and 5 days after the index admission; the difference between two measurements was considered as the magnitude of improvement. We used regression models to test the hypothesis that the magnitude of the advantage of PCI over fibrinolysis in preserving LVEF 5 days after STEMI is modified by pentraxin 3 (PTX3).
Results:
The functional advantage (LVEF) of the PCI over fibrinolysis has been determined by PTX3. LVEF was attenuated and even reversed as PTX3 level increased. The primary PCI of the participants with less than 7 ng.ml-1 PTX3 level, achieved a clinically significant increase in the LVEF as compared to fibrinolysis. At lower levels of PTX3, PCI shows a conspicuous advantage over fibrinolysis in terms of the probability of developing an LVEF <40%.
Conclusion:
We demonstrated not only the functional advantage of PCI over fibrinolysis performed within the recommended time frames but also the relative advantage of its relevance to the baseline PTX3 levels. PTX3 can play a role in determining the choice of best therapy. More than 75% of patients with STEMI who have PTX3 levels ≤7 ng.ml-1 imply the need of PCI.
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