High-sensitivity Troponin in Cardiac Surgery
Heart; Dysfunction Postoperative, Cardiac Surgery, Myocardial Infarction, Myocardial Injury
About this trial
This is an interventional screening trial for Heart; Dysfunction Postoperative, Cardiac Surgery focused on measuring High-sensitivity Cardiac Troponin, Creatinin Kinase MB, Cardiac Surgery, Myocardial injury, Myocardial infarction, Concentration change
Eligibility Criteria
Inclusion Criteria:
- Each participant must be older than 18 years
- Undergoing cardiac surgery
- Each participant must have the mental capacity to decide whether he takes part in the trial or not.
- Each participant must voluntarily give his written informed consent.
Exclusion Criteria:
- Patients with severe or end-stage renal insufficiency.
- Insertion of assist devices.
- Surgery on urgent basis, that is, the same day after their coronary angiogram.
Sites / Locations
- Intensive Care Unit, OLV Hospital Aalst, Belgium
Arms of the Study
Arm 1
Experimental
Cardiac biomarkers concentration changes
In 2012 the Third Global MI Task Force has presented a third universal definition of MI implying that MI associated with CABG is arbitrarily defined by elevation of cardiac biomarkers values > 10x99th percentile URL in patients with normal baseline cTn values (≤ 99th percentile URL), in addition with either (i) new pathological Q waves or new LBBB (left bundle branch block), or (ii) angiographic documented new graft or new native coronary artery occlusion, or (iii) imaging evidence of new loss of viable myocardium or new regional wall motion abnormality. In this study we will measure the concentration changes over time of cardiac biomarkers (hs-cTN and CK-MB) and establish a threshold value for myocardial injury, diagnosed by ECG and approved -if necessary- by echocardiography.