Aktaş, HalilKaypaklı, OnurÖzmen, ÇağlarGül, MuratYıldırım, Oğuzİnci, SinanDeniz, AliDemirtaş, Mustafa2021-05-252021-05-252021https:/dx.doi.org/10.33678/coL2020.082https://hdl.handle.net/20.500.12451/7965Aktaş, Halil ( Aksaray, Yazar )Objective: Several studies have investigated different cardiac biomarkers as predictors of the prognosis after percutaneous coronary interventions (PCI) in patients with chronic ischemic heart disease; nevertheless, the results of these studies are conflicting. High sensitive troponin T (Hs-TnT) measurement is a novel and sensitive method. The aim of this study was to investigate if Hs-TnT levels are a predictor of major adverse cardiovascular events (MACE) in the first year after a successful elective PCI in patients with stable angina pectoris (SAP). Material and methods: 100 patients who presented with SAP and underwent successfully elective PCI were included in the study. Patients with elevated troponin I levels (>0.1 ng/mL) before the procedure excluded from the study. Hs-TnT levels were measured before the procedure and at 3-4 hours (h) (early period) and 12-24 hours (late period) after the procedure and Hs-TnT level >14 pg/mL was considered positive. The incidence of MACE during the first year was recorded. Results: Hs-TnT levels were positive in 36% of the patients in the early period and in 54% of the patients in the late period. The incidence rate of MACE for the first year was significantly higher in the patients with positive Hs-TnT levels in the early period but not the late period (36.1% vs. 15.6%; p = 0.026) and logistic regression analysis yielded an odds ratio of 3.36. Conclusion: Hs-TnT levels measured 3-4 h after a successful elective PCI in patients with SAP can predict the incidence of MACE within the first year. Nonetheless, these results must be corroborated by other larger studies.eninfo:eu-repo/semantics/openAccessChronic Ischemic Heart DiseaseHigh Sensitive Troponin TMajor Adverse Cardiovascular EventsPercutaneous Coronary InterventionPrognosisArticle631323910.33678/coL2020.082N/AN/A