Key result
Postoperative troponin I linked to ~23% higher 30-day major cardiovascular events risk per ng/mL after elective CABG.
Why the study?
Although myocardial injury is almost universal after CABG, the prognostic significance of the postoperative rise in cardiac troponin I for 30-day MACE remains uncertain, particularly in Southeast Asian populations.
Does postoperative delta troponin I predict 30-day major adverse cardiovascular events in patients with coronary artery disease undergoing elective coronary artery bypass grafting?
Cohort (n=60)
No
Does postoperative delta troponin I predict 30-day major adverse cardiovascular events in patients with coronary artery disease undergoing elective coronary artery bypass grafting?
Postoperative delta troponin I (cut-off 2.225 ng/mL) and absolute postoperative troponin I demonstrate moderate discrimination for predicting 30-day MACE—particularly cardiovascular death and type 5 MI—following elective CABG in an Indonesian cohort.
Answers are grounded in this paper and cite their sources.
Postoperative troponin I may aid 30-day MACE risk stratification after CABG; leaves open validation of delta thresholds in prospective cohorts.
Introduction: Myocardial injury is almost universal after coronary artery bypass grafting (CABG), yet the prognostic significance of the postoperative rise in cardiac troponin I remains uncertain, particularly in Southeast Asian populations. To evaluate the association and prognostic performance of postoperative delta (Δ) troponin I for 30-day major adverse cardiovascular events (MACE) after elective CABG. Methods: This retrospective cohort study enrolled 60 consecutive patients who underwent elective CABG at Haji Adam Malik General Hospital, Medan, Indonesia, between January 2025 and May 2026. Δ troponin I was calculated as postoperative (≤72 h) minus preoperative (≤24 h) troponin I. MACE comprised malignant arrhythmia, acute heart failure, stroke, type 5 myocardial infarction, and cardiovascular death within 30 days. Analyses included Mann–Whitney tests, multivariable logistic regression, and receiver operating characteristic (ROC) curves. Results: The mean age was 59.7 ± 7.5 years, and 71.7% were men. MACE occurred in 36 patients (60.0%). Median Δ troponin I was higher in patients with MACE than in those without (7.45 vs. 0.81 ng/mL; p = 0.002). Δ troponin I yielded an area under the curve of 0.742 (95% CI 0.610–0.875); a cut-off of 2.225 ng/mL provided 77.8% sensitivity, 79.2% specificity, and positive and negative predictive values of 84.8% and 70.4%, respectively. Postoperative troponin I independently predicted MACE (odds ratio 1.231 per ng/mL; 95% CI 1.087–1.395; p = 0.001). Conclusion: Postoperative Δ troponin I showed moderate discrimination for 30-day MACE after elective CABG and may complement early postoperative risk stratification pending external validation in larger prospective cohorts.
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Putri et al. (2026) conducted a cohort in Coronary artery disease undergoing elective coronary artery bypass grafting (CABG) (n=60). Postoperative troponin I / Delta troponin I elevation vs. Lower postoperative / Delta troponin I levels (or No MACE group) was evaluated on 30-day major adverse cardiovascular events (MACE: composite of malignant arrhythmia, acute heart failure, stroke, type 5 myocardial infarction, and cardiovascular death) (OR 1.231 per ng/mL, 95% CI 1.087-1.395, p=0.001). Postoperative troponin I independently predicted 30-day major cardiovascular events after elective CABG, while delta troponin I showed moderate discrimination.
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