Introduction

Perioperative serum cardiac troponin concentration has recently been accepted as a strong predictor of 30-day mortality after noncardiac surgery1,2. Based on robust clinical relevance, the diagnostic criteria for postoperative myocardial injury after noncardiac surgery (MINS) include the occurrence of postoperative troponin concentrations above the 99th-percentile upper reference limit (URL) within 30 days post-surgery, resulting from myocardial ischemia without the requirement of an ischemic feature3,4,5. Since the establishment of the MINS criteria, subsequent studies have mainly focused on postoperative troponin concentrations and used the 99th-percentile URL to reveal relevant risk factors or optimal treatments for MINS4,6,7.

Preoperative cardiac troponin concentrations have also been shown to be associated with postoperative outcomes8,9,10,11, but this phenomenon has garnered little attention, because it precedes an enormous metabolic stress from surgical manipulations. Although baseline measurements of some cardiac biomarkers that fall within normal values have shown prognostic value in asymptomatic patients12,13,14, the presence of preoperative troponin concentrations below the 99th-percentile URL has typically been considered normal5,15,16. However, as highlighted by the Fourth Universal Definition, perioperative myocardial injury shows distinct features that differentiate it from myocardial infarction5, and several factors other than heart injury are also related to the serum troponin concentration to varying degrees17. Given the 99th-percentile URL provided by the high-sensitivity cardiac troponin (hs-cTn) immunoassay manufacturer was established using data from healthy individuals, this URL may not be an optimal cut-off value for patients scheduled for surgery. In addition, the association between preoperative cardiac troponin concentrations below the 99th-percentile URL and postoperative outcome has not been fully evaluated. Therefore, we aimed to evaluate the prognostic impact of preoperative serum cardiac troponin concentrations above the lowest limit of detection (LOD) but below the 99th-percentile URL.

Results

Baseline characteristics

The 12,415 patients were divided into the two groups according to preoperative hs-cTn I concentration: 7958 (64.1%) patients were in the LOD group and 4457 (35.9%) patients were in the mild elevation group. The patient characteristics at baseline are summarized in Table 1. The mild elevation group tended to be older and showed higher incidences of past medical events and medication use. A total of 3869 pairs of data were generated by 1:1 individual matching without replacement using the propensity scores for preoperative variables. After propensity score matching, all preoperative variables were well balanced, and we found no significant difference between intraoperative variables (Table 1).

Table 1 Baseline characteristics.

Clinical outcomes

As we used mortality data validated from the National Population Registry of the Korea National Statistical Office, all study patients completed follow-up period of postoperative 30-day mortality. For in-hospital mortality, the median period was 8 days (interquartile range [IQR] 5–16). In the entire population, multivariate analyses showed significantly higher risks of 30-day and in-hospital mortalities for the mild elevation group (2.1% vs. 4.0%; hazard ratio [HR] 1.73; 95% confidence interval [CI] 1.39–2.16; p < 0.001 and 2.8% vs. 5.5%; HR 1.40; 95% CI 1.16–1.69; p = 0.001, respectively; Table 2). The propensity-score-matched analysis produced similar results (2.6% vs. 4.2%; HR 1.61; 95% CI 1.26–2.07; p < 0.001 and 3.6% vs. 5.7%; HR 1.38; 95% CI 1.12–1.71; p = 0.003, respectively) (Table 2). Survival curves for the entire and propensity-score-matched populations are shown in Fig. 1. Sensitivity of the effect of an unmeasured confounder on this association was calculated with an assumed prevalence of 40% for unmeasured confounder, and the association was consistently significant (Supplementary Table S1). The power of this study regarding the sample size was 0.97. In this study, the significant attributable fractions of the risk for 30-day mortality included emergency surgery (40.9%), preoperative hs-cTn I above the lowest LOD (21.2%), and high surgical risk (10.6%) (Supplementary Table S2).

Table 2 Clinical outcomes.
Figure 1
figure 1

Kaplan–Meier curves for (A) 30-day and (B) in-hospital mortalities of the minimum and minor elevation groups within the full study population, and Kaplan–Meier curves for (C) 30-day and (D) in-hospital mortalities of the minimum and minor elevation groups in the propensity-score-matched population.

The mild elevation group was further divided into two groups according to the median preoperative hs-cTn I concentration (14 ng/L). The baseline characteristics of the three groups are presented Supplementary Table S3. Each subgroup was compared to the LOD group in terms of 30-day and in-hospital mortalities. Both groups showed significantly greater 30-day mortality in the entire population (2.1% vs. 3.3%; HR 1.60; 95% CI 1.20–2.11; p = 0.001 for the below median group and 2.1% vs. 4.6%; HR 1.51; 95% CI 1.34–1.71; p < 0.001 for the above median group; Supplementary Table S4). In the propensity-score-matched population, the numerical values of the incidences showed graded elevations, but only the patients with hs-cTn concentrations above the median value were significantly different (2.6% vs. 5.0%; HR 1.93; 95% CI 1.47–2.53; p < 0.001) (Supplementary Table S4). Similar results were shown for in-hospital mortality. Both groups showed significantly greater mortality in the entire population (2.8% vs. 4.5%; HR 1.39; 95% CI 1.09–1.77; p = 0.01 for the below median group and 2.8% vs. 6.4%; HR 1.32; 95% CI 1.19–1.47; p < 0.001 for the above median group; Supplementary Table S4), but in the propensity-score-matched population, only the patients with hs-cTn concentrations above the median value showed significantly different results (3.6% vs. 6.7%; HR 1.55; 95% CI 1.23–1.97; p < 0.001) (Supplementary Table S4). Survival curves for the three groups are presented in Fig. 2.

Figure 2
figure 2

Kaplan–Meier curves of three groups according to the median preoperative high-sensitivity cardiac troponin I concentrations; (A) 30-day mortality in crude, (B) propensity-score-matched populations and (C) in-hospital mortality in crude, (D) propensity-score-matched populations.

Threshold of preoperative hs-cTn I

In the generation of repeated split samples, thresholds for preoperative hs-cTn I associated with 30-day mortality converged at 12 ng/L, and the estimated HR was 1.66 (IQR 1.6–1.7). The smoothed log-hazard ratio for the preoperative hs-cTn I threshold is shown in Fig. 3. By applying this threshold, 9647 (77.7%) patients were stratified into the < 12 ng/L group and 2768 (22.3%) into the ≥ 12 ng/L group (Supplementary Table S5). After an adjustment, the patients in the ≥ 12 ng/L group showed a significantly increased risk of 30-day and in-hospital mortality (2.2% vs. 4.6%; HR 1.54; 95% CI 1.23–1.93; p < 0.001 and 3.0% vs. 6.3%; HR 1.28; 95% CI 1.05–1.55; p = 0.01, respectively; Table 3). Survival curves according to the calculated threshold are demonstrated in Fig. 3.

Figure 3
figure 3

(A) Smoothed log-hazard ratio to calculate the threshold for preoperative high-sensitivity cardiac troponin I using a modified Mazumdar approach, (B) Kaplan–Meier curves for 30-day mortality according to the threshold, and (C) Kaplan–Meier curves for in-hospital mortality according to the threshold.

Table 3 Clinical outcomes according to the calculated threshold of hs-cTn I ≥ 12 ng/L.

Postoperative hs-cTn I & MINS

The peak hs-cTn I concentrations within 30 days post-surgery were available in 51.3% (4086/7958) of patients in the LOD group and 56.7% (2529/4457) in the mild elevation group. Comparisons of the baseline characteristics of the patients according to the availability of postoperative hs-cTn measurements are presented in the Supplementary Table S6. In patients with postoperative hs-cTn measurements, the median durations from surgery to the peak hs-cTn I concentration were 0 day (IQR 0–1) in the LOD group and 1 day (IQR 0–3) in the mild elevation group (p < 0.001). The peak concentration was significantly greater in the mild elevation group, as was the incidence of MINS in the analysis regarding the patients without postoperative hs-cTn as not having MINS. (242 ng/L vs. 1179 ng/L; p < 0.001 and 644 (8.1%) vs. 840 (18.8%); p < 0.001, Table 2). The two groups in the primary analysis were divided according to the diagnosis of MINS, and four groups were generated from the entire and propensity-score-matched populations (Supplementary Tables S7 and S8). The 30-day mortality was also increased for those with preoperative hs-cTn above the LOD in the comparison between the patients without MINS (1.4% vs. 2.5%; HR 1.87; 95% CI 1.41–2.49; p < 0.001), but the increase in 30-day mortality was more pronounced, regardless of preoperative hs-cTn concentration, for the patients who were diagnosed with MINS compared to the LOD group without MINS (1.4% vs. 10.1%; HR 7.83; 95% CI 5.72–10.70; p < 0.001 in the LOD group and 1.4% vs. 10.4%; HR 8.01; 95% CI 6.00–10.68; p < 0.001 in the mild elevation group; Table 4). Similar results were found in the propensity-score-matched population (1.7% vs. 2.7%; HR 1.61; 95% CI 1.16–2.25; p = 0.005, 1.7% vs. 11.2%; HR 7.06; 95% CI 4.76–10.47; p < 0.001, and 1.7% vs. 11.1%; HR 6.99; 95% CI 4.97–9.84; p < 0.001, respectively; Table 4). The same analyses comparing the four groups were conducted in patient with available postoperative hs-cTn I measurement (Supplementary Tables S9 and S10) and showed the similar results (1.7% vs. 2.9%; HR 1.76; 95% CI 1.10–2.81; p = 0.02, 1.7% vs. 11.2%; HR 7.11; 95% CI 4.44–11.38; p < 0.001, and 1.7% vs. 11.1%; HR 7.05; 95% CI 4.59–10.81; p < 0.001, respectively; Table 5). The survival curves of the four groups are presented in Fig. 4.

Table 4 Clinical outcomes according to the diagnosis of myocardial injury after noncardiac surgery in the entire population.
Table 5 Clinical outcomes according to the diagnosis of myocardial injury after noncardiac surgery in patients with postoperative hs-cTn I.
Figure 4
figure 4

Kaplan–Meier curves for 30-day mortality according to diagnosed MINS; (A) crude and (B) propensity-score-matched population.

Discussion

The main findings of this study are as follows: (1) preoperative hs-cTn concentrations above the lowest LOD but below the 99th-percentile URL were significantly associated with early mortality in patients, (2) this association was consistent regardless of the occurrence of MINS, (3) the incidence of MINS was also increased in patients with preoperative hs-cTn above the lowest LOD, and the patients who were diagnosed with MINS had an enormously increased risk of postoperative mortality regardless of preoperative hs-cTn, and (4) the calculated threshold at which mortality increased was a preoperative hs-cTn concentration of 12 ng/L, well below the 99th-percentile URL. These findings indicate that the risk of mortality may differ according to the preoperative hs-cTn concentration even when it is below the 99th-percentile URL. Based on these findings, we suggest that preoperative hs-cTn concentration below the 99th-percentile URL could be used to predict noncardiac surgical risk that might otherwise be overlooked.

In clinical practice, risk assessment of a patient’s cardiac troponin concentration has been generally comprised a binary “rule in” or “rule out” threshold at the 99th-percentile URL. This cut-off has allowed an early confident “ruling out” of myocardial infarction18, but “ruling in” of myocardial infarction solely on the basis elevated cardiac troponin often leads to a misinterpretation19. On the other hand, postoperative troponin elevation has shown a robust association with mortality, regardless of ischemic symptoms1,2,3,9. Based on these findings, the diagnostic criteria for MINS were established using postoperative cardiac troponin concentrations above the 99th-percentile URL4. However, for the preoperative period, cardiac troponin concentrations below this limit have generally been defined as normal without accurately evaluating the associated risk. According to our results, uniformly applying this threshold for perioperative cardiac troponin may also lead to a misinterpretation. These findings are in line with studies of other biomarkers showing associations between the baseline measurements within the normal range and adverse outcomes in stable patients12,13,14.

Another issue to be discussed is the generalizability of the 99th-percentile URL and whether a preoperative cardiac troponin threshold other than the 99th-percentile URL is needed to “rule in” or “rule out” patients at risk. As mentioned above, the 99th-percentile URL was previously well validated to rule out myocardial infarction18, and was also adopted for perioperative evaluations. Based on clinical relevance shown in previous studies3,4,5,20, the Fourth Universal Definition of Myocardial Infarction also recommended using the 99th-percentile URL of any assay to define myocardial injury, but at the same time it specifically highlighted myocardial injury as discrete from myocardial infarction5. Moreover, some investigators recently argued that a lower cut-off should be applied even for ruling out acute myocardial infarction21. In addition, the 99th-percentile URLs provided by immunoassay manufacturers are derived from a limited number of apparently healthy individuals22, and several factors such as age, sex, kidney and heart function, and the presence of inflammation that are known to affect troponin level are not considered17,23. Therefore, clinical application of the same limit to surgical patients requires closer scrutiny, because surgical patients are likely to show discrete characteristics from the reference population.

A mechanism for the increased mortality in the mild elevation group can be inferred from our additional analysis involving the occurrence of MINS. The incidence of MINS, as well as peak postoperative troponin concentration, was greater in the mild elevation group, and the increased mortality of the mild elevation group was mostly driven by the patients who were diagnosed with MINS. Furthermore, the increased risk of mortality was more notable in patients diagnosed with MINS regardless of preoperative cardiac troponin level. These findings provide a clue that the development of MINS still plays a key role for mortatlity, and the patients with cardiac troponin above the LOD were more likely to develop MINS. However, the mild elevation group consistently showed increased mortality in patients without MINS, and in patients with MINS, the prognosis did not seem to differ according to mild elevation of preoperative hs-cTn. These findings have clinical implications for extending the use of hs-cTn in perioperative risk management. The current guidelines aimed at preventing or detecting MINS, and the treatments are also focused on postoperative cardiac troponin concentrations24,25, because secondary prevention with cardiovascular drugs was shown to be beneficial and cost-effective4,6,7,26. However, previous evidences also indicated incremental increase of mortality according to preoperative cardiac troponin elevation8, and supported the assessment of both pre- and postoperative in cardiac troponin9,10. As an extension of these studies, our results indicate preventive measures should be considered for patients with preoperative cardiac troponin below the 99th-percentile URL.

In further analyses, the mild elevation group was divided into two groups according to the median preoperative hs-cTn concentration. Because only the patients with troponin concentrations above the median value consistently had increased mortality after propensity score matching, we estimated the threshold preoperative hs-cTn I concentration where the risk for mortality significantly increased. Although mortality significantly differed according to the estimated threshold in this study, the clinical relevance of this threshold needs further evaluation after inclusion of patients with hs-cTn over the 99th-percentile URL.

Our results have the following limitations. First, as a single-center retrospective study, our results may have been affected by confounding factors. Despite rigorous adjustments in the multivariate and propensity-score-matched analyses and sensitivity analysis, it is possible the result were impacted by unmeasured variables related to postoperative morbidities or oxygen/supply demand mismatch. Second, perioperative hs-cTn measurement was not included as a routine practice at our institution, and it could also have been measured at the discretion of attending clinician despite the institutional indication. And also, cardiac troponin was generally measured in patients with risk or ischemic symptom, so the median duration from the surgery to the peak cardiac troponin level was longer in the mild elevation group. Consequently, the results of the current study may have been biased. Moreover, postoperative serum troponin measurements were available for only about half of the patients, and the patients without postoperative measurements were considered not to have MINS. Although those patients were likely to be asymptomatic with lower cardiac risk, the results might have been biased, and further studies with a detailed protocol for cardiac troponin measurement are needed. Despite these limitations, this is the first study on the association between hs-cTn above the lowest LOD but below the 99th-percentile URL and 30-day mortality using a robust propensity score matching. Our results provide evidence that clinicians should be cautious when interpreting serum hs-cTn concentrations below the 99th-percentile URL as “normal” in the preoperative risk assessment for noncardiac surgery patients.

Methods

Study population and data curation

This study was approved by the Institutional Review Board of the Samsung Medical Center, Seoul, Korea (SMC 2019-08-048) on 12th July 2019 and was conducted according to the principles of the Declaration of Helsinki. The requirement for individual informed consent was waived by the Institutional Review Board of the Samsung Medical Center considering the minimal risk to the patients. From January 2010 to April 2019, all consecutive adult patients who underwent noncardiac surgery with serum hs-cTn I concentrations below the 99th-percentile URL during their preoperative evaluation at our institution were enrolled. All data in this study were curated using “Clinical Data Warehouse Darwin-C.” It is an electronic system built for investigators to search and retrieve de-identified medical records from the institutional archive system containing clinical data from more than 4 million patients, including data from more than 2 million surgeries, 900 million laboratory findings, and 200 million prescriptions. In this system, mortalities outside of our institution were consistently updated and validated against the National Population Registry of the Korea National Statistical Office using a unique personal identification number when available. The patients were divided into two groups according to preoperative hs-cTn I concentration: (1) the LOD group (having [hs-cTn I] < 6 ng/L) and (2) the mild elevation group (having [hs-cTn I] < 40 ng/L).

Study outcomes and definitions

The primary outcome was 30-day mortality, and in-hospital mortality was also compared between the two study groups. The peak hs-cTn I concentration within 30 days after surgery was compared in patients with available postoperative hs-cTn I measurements. Since preoperative hs-cTn level of our study population was below the 99th-percentile URL, postoperative hs-cTn I elevation above the URL within 30 days was all regarded as MINS, and patients without elevated postoperative hs-cTn I were regarded as not having been diagnosed with MINS. The baseline characteristics were derived from the preoperative evaluation sheets of the patients’ electronic medical records. Surgical risk was stratified according to the 2014 European Society of Cardiology/Anesthesiology (ESC/ESA) guidelines24.

Preoperative evaluation and Hs-cTn I measurement

Preoperative evaluation at our institution starts at the outpatient department and includes routine blood tests, plain chest film and echocardiography within the 30 days prior to the surgery. If necessary, further evaluations are made in a multidisciplinary manner at the anesthesiologist’s discretion.

Perioperative hs-cTn I was recommended for the patients with moderate- to severe cardiovascular risk or for those undergoing intermediate- to high-risk surgery according to the guidelines24, but it was also measured at the discretion or request of an attending clinician in patients with mild risk. An automated analyzer (Advia Centaur XP, Siemens Healthcare Diagnostics, Erlangen, Germany) was used throughout the entire study period to assess the results of the highly sensitive immunoassay. The lowest LOD was 6 ng/L, and the 99th-percentile URL of 40 ng/L was provided by the manufacturer.

Statistical analyses

Baseline characteristics were presented as numbers and percentages for categorical variables and as the mean ± standard deviation or median with IQR for continuous variables. We used parametric or non-parametric tests as appropriate to compare differences in baseline characteristics in the preliminary analyses. Kaplan–Meier survival curves were constructed and compared with the log-rank test. Variables for the multivariate Cox regression model were selected based on a standardized mean difference larger than 10%. To further reduce selection bias while maintaining a balance between the confounding variables of the two groups, we used propensity score matching on preoperative variables. An appropriate balance between the groups with an absolute SMD of less than 10% for all pre-and intraoperative variables suggested successful propensity matching. In the propensity-score-matched population, we computed HR and 95% CI for outcomes using a multivariate Cox regression model with adjustments for intraoperative variables. The sensitivity analysis for the primary outcome was conducted by estimating the potential impact of unmeasured confounders, and the power of the study regarding the sample size was calculated using Spearman's rank correlation27,28.

We also calculated a threshold of preoperative hs-cTn I concentration associated with 30-day mortality using a modified Mazumdar approach29. We selected covariates for multiple logistic regression using a stepwise Akaike information criterion method, and chose an initial threshold to maximize the log-likelihood of the estimated multiple model. For the sensitivity analysis of the calculated threshold, split sample generation was repeated 500 times to obtain the distribution of thresholds and HRs. Based on the results of the Cox proportional hazards model, we also determined the attributable fraction for each variable that was independently associated with 30-day mortality30. This is a measure that represents the proportional reduction in mortality within a population that would occur if the variable was causal and the incidence of the variable was reduced to none. All statistical analyses were performed with R 4.0.0 (Vienna, Austria; https://www.R-project.org/). All tests were two-tailed, and a p < 0.05 was considered statistically significant.

Conclusions

In patients undergoing noncardiac surgery, preoperative hs-cTn I concentrations above the lowest LOD but below the 99th-percentile URL were significantly associated with 30-day mortality. A larger registry-based or cohort study is needed to confirm this finding.