Clinical Study

Clinical Use of Ultrasensitive Cardiac Troponin I Assay in Intermediate- and High-Risk Surgery Patients

Figure 3

Primary endpoint (%) according to the combination of preoperative N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels less than (−) or greater than (+) 917 pg/mL and postoperative cardiac troponin I (cTnI) peak levels less than (−) or greater than (+) 0.04 μg/L during the 30-day postoperative follow-up period.
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