Title of article :
Association Between the Platelet-to-Lymphocyte Ratio and the No-Reflow Phenomenon and Thrombolysis in Myocardial Infarction Flow 3 After Primary Percutaneous Coronary Intervention in Patients With ST-Segment Elevation Myocardial Infarction
Author/Authors :
Amirpour, Afshin Department of cardiology - School of Medicine - Isfahan University of Medical Sciences, Isfahan, IR Iran. , Zavar, Reihane Department of cardiology - School of Medicine - Isfahan University of Medical Sciences, Isfahan, IR Iran. , Ramezani Nejad, Ali Department of cardiology - School of Medicine - Isfahan University of Medical Sciences, Isfahan, IR Iran.
Pages :
9
From page :
12
To page :
20
Abstract :
Background: Atherosclerosis is one of the major causes of cardiovascular mortality. Inflammation has been proven to have a role in this process, and inflammatory markers can predict the prognosis of atherosclerotic events such as acute coronary syndrome and ST-elevation myocardial infarction. Method: We sought to assess the prognostic value of the blood cell count and its components— platelets, C-reactive protein, cholesterol, triglycerides, creatinine, and troponin—in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention. Results: Significant prognostic values were found for the neutrophil count, platelet count, fasting blood sugar, cholesterol, triglycerides, low-density lipoprotein, creatinine, and C-reactive protein. Conclusions: The platelet-to-lymphocyte ratio had prognostic value for predicting reflow after primary percutaneous coronary intervention. Nevertheless, C-reactive protein, platelet count, fasting blood sugar, cholesterol, triglycerides, low-density lipoprotein, and creatinine were more valuable in terms of predicting the outcome of percutaneous coronary intervention in patients with ST-elevation myocardial infarction.
Keywords :
Platelet , Lymphocyte , No-reflow , STEMI , TIMI
Journal title :
Astroparticle Physics
Serial Year :
2017
Record number :
2441489
Link To Document :
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