Key result
Postoperative troponin release ≥150 ng/L after noncardiac surgery was strongly associated with one-year MACE compared to levels <14 ng/L (40.6% vs 3.4%; HR 10.24, 95% CI 5.91-17.75).
Why the study?
Troponin elevations after noncardiac surgery predict mortality, but their prognostic value for early and late major adverse cardiovascular events (MACE) is less well investigated.
Does postoperative troponin release predict major adverse cardiovascular events in patients aged ≥60 years undergoing intermediate-to-high risk noncardiac surgery?
Cohort (n=3,085)
No
Does postoperative troponin release predict major adverse cardiovascular events in patients aged ≥60 years undergoing intermediate-to-high risk noncardiac surgery?
Hazard Ratio: 10.24 (95% CI 5.91–17.75)
Absolute Event Rate: 40.6% vs 3.4%
Postoperative high-sensitivity troponin T elevation demonstrates a strong, graded association with the occurrence of MACE and all-cause mortality in the first year after intermediate-to-high risk noncardiac surgery.
May flag high-risk patients for closer monitoring after noncardiac surgery; leaves open whether troponin-guided interventions reduce MACE.
Introduction Troponin elevations after intermediate-to-high risk noncardiac surgery are common and can predict mortality. However, the prognostic value for early and late major adverse cardiovascular events (MACE) is less well investigated. The authors evaluated the relationship between postoperative troponin release and MACE in the first year after noncardiac surgery. Methods This observational cohort registry comprised data of patients aged ≥60 years undergoing intermediate-to-high risk noncardiac surgery between July 2012 and 2015, at the Erasmus University Medical Center, Rotterdam, the Netherlands. High-sensitivity troponin T was measured on day 1 to 3 after surgery. Peak troponin values were divided into four categories: <14 ng·L −1 , 14–49 ng·L −1 , 50–149 ng·L −1 and ≥150 ng·L −1 . The primary endpoint MACE was defined as the occurrence of myocardial infarction, angina, revascularization therapy or cerebrovascular accident in the first year after surgery. The incidence of MACE and all-cause mortality was calculated using Kaplan-Meier estimates. Cox regression was used to estimate risks for both endpoints. Results In total, 3085 patients were included for analyses and peak troponin elevation above 14 ng·L −1 was present in 1678 (54.4%) patients. The overall incidence for one-year MACE was 5.8% (3.4%, 6.1%, 10.4% and 40.6% per increasing troponin category) with adjusted HR (95% CI) 1.32 (0.85–2.06), 2.53 (1.42–4.53) and 10.24 (5.91–17.75) for the consecutive increasing categories. One-year mortality occurred in 14.6% and showed a similar stepwise increase with adjusted HR (95% CI) 1.25 (0.98–1.60), 2.39 (1.72–3.32) and 3.79 (2.60–5.54). Conclusion Our dataset demonstrates a graded relationship between postoperative troponin release and occurrence of MACE in the first year after intermediate-to-high risk noncardiac surgery.
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Mol et al. (2019) conducted a cohort in intermediate-to-high risk noncardiac surgery (n=3,085). Postoperative troponin release (≥150 ng/L) vs. Troponin <14 ng/L was evaluated on Major adverse cardiovascular events (MACE) defined as myocardial infarction, angina, revascularization therapy or cerebrovascular accident in the first year after surgery (HR 10.24, 95% CI 5.91-17.75). Postoperative troponin release ≥150 ng/L after noncardiac surgery was strongly associated with one-year MACE compared to levels <14 ng/L (40.6% vs 3.4%; HR 10.24, 95% CI 5.91-17.75).
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