Clinical Study

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

Table 4

Events stratified by postoperative troponin peak level during the follow-up period.

All patients  
(%)
Troponin ≥ 0.04 µg/L 
(%)
Troponin < 0.04 µg/L 
(%)
OR (95% CI)

Primary outcome16 (11.3)15 (31.9)1 (1.1)44.06 (5.60–346.9)<0.001
 Cardiac death2 (1.4)2 (4.3)010.5 (0.5–218.97)*0.19
 Nonfatal cardiac arrest2 (1.4)1 (2.1)1 (1.1)2.04 (0.12–33.40)1.00
 Nonfatal MI14 (9.9)14 (29.8)082.67 (4.87–1402.27)*<0.001
Secondary outcome28 (19.7)17 (36.2)11 (11.6)4.32 (1.82–10.28)0.001
 Death9 (6.3)6 (12.8)3 (3.2)4.48 (1.07–18.82)0.06
 Nonfatal stroke5 (3.5)05 (5.3)0.17 (0.01–3.11)*0.17
 Congestive heart failure12 (8.5)9 (19.1)3 (3.2)7.26 (1.86–28.30)0.002
 Atrial fibrillation7 (4.9)6 (12.8)1 (1.1)13.75 (1.60–117.92)0.005
 Coronary revascularization1 (0.7)1 (2.1)06.16 (0.25–150.94)*0.33

OR: odds ratio; CI: confidence interval; MI: myocardial infarction. value indicates differences between patients with and without troponin elevation. Adjusted by adding 0.5 in each cell in case of zero frequency.