(Circulation. 2006;114:I-448 I-453.)
© 2006 American Heart Association, Inc.
Surgery for Coronary Artery Disease |
From the Department of Thoracic and Cardiovascular Surgery, West-German Heart Center Essen (M.T., P.M., G.M., M.K., K.T., H.J.), Institute for Medical Informatics, Biometry, and Epidemiology (M.N.), Department of Clinical Chemistry (K.M.), Department of Cardiology, West-German Heart Center Essen (R.E.), University Hospital Essen, Essen, Germany.
Correspondence to Matthias Thielmann, MD, Department of Thoracic and Cardiovascular Surgery, West-German Heart Center Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122 Essen, Germany. E-mail matthias.thielmann{at}uni-essen.de
| Abstract |
|---|
|
|
|---|
Methods and Results A possible correlation between preoperative cTnI and in-hospital mortality and major adverse cardiac events (MACE) was investigated in 57 patients with ST-elevation AMI (STEMI) in group 1 and 197 with Non-ST-elevation AMI (NSTEMI) in group 2, who were operated within 24 hours after onset of symptoms. Primary study end point was all-cause in-hospital mortality. Secondary end points were low cardiac output syndrome (LCOS) and hospital course. CTnI levels on admission were higher in group 1 compared with group 2 (7.1±1.8 versus 1.4±1.8 ng/mL; P<0.001). Overall in-hospital mortality was higher in group 1 compared with group 2 (14.3 versus 4.1%; odds ratio [OR], 3.9, 95% confidence interval [CI], 1.3 to 12.3; P<0.01). LCOS occurred in 16/57 (28.1%), and 18/197 (9.1%) patients, respectively (OR, 3.9, 95% CI, 1.7 to 8.8; P<0.001). Postoperative ventilation time, intensive care, and hospital stay were significantly longer in group 1 versus group 2. Multivariate logistic regression analyses revealed preoperative cTnI as the strongest independent predictor for in-hospital mortality (P<0.001) and MACE (P<0.001) in all AMI patients, regardless whether ST-elevation was included as an additional risk factor or not.
Conclusions Preoperative cTnI measurement before emergency CABG appears as a powerful and independent determinant of in-hospital mortality and MACE in acute STEMI and NSTEMI.
Key Words: coronary artery bypass grafting acute coronary syndromes troponin I risk stratification
| Introduction |
|---|
|
|
|---|
The present study therefore focused on the clinical significance of a single preoperative cTnI serum level before CABG and its predictive value for major adverse cardiac events (MACE) and in-hospital mortality in patients with acute STEMI or NSTEMI.
| Methods |
|---|
|
|
|---|
Study End Points and Definitions
Primary end points of the study were in-hospital mortality, defined as death from any cause within 30 days after CABG surgery or during the same time period of hospitalization, as well as postoperative MACE during the period of hospitalization including low cardiac output syndrome (LCOS), which was supposed with a postoperative cardiac index below 2.0 L/min/m2 or with a systolic arterial pressure below 90mmHg despite high-dose inotropic support (IV dopamine
8 µg/kg/min or dobutamine
6 µg/kg/min or epinephrine >0.1 µg/kg/min or norepinephrine >0.1 µg/kg/min), cardiopulmonary resuscitation (CPR), and new-onset ventricular arrhythmia.
Patient Selection
Patients were enrolled into the present study, if they underwent an isolated emergency CABG procedure and a preoperative cTnI serum level had been obtained within 12 hours before surgery. Patients were classified into STEMI or NSTEMI, depending on whether they had ST-elevations on admission ECG or not. An acute STEMI was supposed to be present on admission with (1) ST-segment elevations in two contiguous leads (
0.1 mV in lead I, II, III, aVF, aVL, V4V6 or
0.2 mV in leads V1V3) (2) with a positive cTnI level and (3) new onset of chest pain or accelerating chest pain within the previous 24 hours occurring at rest or with minimal exertion. An acute NSTEMI was supposed to be present on admission with (1) no ST-segment elevations on the ECG, (2) a positive cTnI level, and(3) new onset of chest pain or accelerating chest pain within the previous 24 hours. Patients were excluded from the study, if any of the following preoperative criteria were present: (1) new onset left bundle-branch block, (2) reoperations, (3) any concomitant heart surgery besides CABG, (4) any concomitant AMI complications. The study was approved by the Institutional Review Board and all patients gave their informed consent.
Surgical Management
Standard cardiopulmonary bypass (CPB) technique was used with ascending aortic and two-stage venous cannulation. During CPB, moderate hemodilution (hematocrit 20% to 25%) with mild systemic hypothermia (>32°C) was maintained. Myocardial protection was achieved using antegrade and optional retrograde crystalloid cardioplegic arrest and additional topical cooling. Patients were postoperatively monitored with respect to arterial pressure, pulmonary pressure, and central venous pressure.
Troponin I Measurement
Venous blood samples were drawn from each patient preoperatively before surgery. CTnI was measured using a specific two-side immunoassay (Dimension Flex, Dade Behring GmbH, Marburg, Germany). The detection range for cTnI was 0.04 to 40 ng/mL, requiring further dilutions if necessary. The assays reference interval was 0.00 to 0.05 ng/mL. A cTnI value above 0.1 ng/mL was considered as abnormal.
Statistical Analysis
Continuous variables are reported as mean± SD or as medians and interquartile range. Categorical variables are reported as number and percentages. An exact Pearsons
2 test was used in the univariate analysis of categorical data and a Mann-Whitney U test in univariate analysis of continuous data. Univariate and multivariate logistic regression analyses were performed to identify preoperative independent predictors for in-hospital mortality and MACE. All preoperative predictor variables that were identified as significant at a two-tailed nominal probability value of less than 0.10 in univariate regression analyses were then entered into a multivariate logistic regression analysis model. The interaction between ST-elevation and preoperative cTnI value was included into this multivariate model, if its probability value was less than 0.10. Receiver operating characteristic (ROC) curve analyses were applied to determine optimal cut-off values of cTnI for in-hospital mortality and to evaluate the predictive power of cTnI in comparison to the logistic EuroSCORE. A probability value less than 0.05 was considered to indicate statistical significance. All statistical analyses were performed using the SPSS software (SPSS Inc., Chicago, IL, USA) and logistic regression analyses were performed using the SAS System®, version 8 (SAS Institute Inc., Cary, USA).
Statement of Responsibility
The authors had full access to the data and take full responsibility for its integrity. All authors have read and agree to the manuscript as written.
| Results |
|---|
|
|
|---|
|
|
Postoperative Outcome
Postoperative in-hospital outcome, like postoperative ventilation time, as well as ICU- and hospital stay were significantly longer in STEMI compared with NSTEMI patients (Table 2). According to the primary study end points, STEMI patients had significantly higher all-cause in-hospital mortality, and MACE occurred more often compared with NSTEMI patients (Figure 1). Comparing the preoperative cTnI levels with postoperative survival status, a significant difference within the STEMI as well as within the NSTEMI patients could be observed between survivors and non-survivors (Figure 2).
|
|
To evaluate preoperative predictors of in-hospital death for the entire AMI study population (STEMI and NSTEMI), a logistic regression analysis model was constructed. Several univariate factors like age, female sex, renal disease, failed PCI, LVEF, unstable angina, preoperative Killip class, ST-segment elevation, CK, as well as preoperative cTnI levels were significantly associated with in-hospital death. After adjustment using a multivariate logistic regression analysis model, only LVEF and the preoperative cTnI level were significantly predictive for in-hospital death. Analyzing the predictors for MACE, univariate factors were age, COPD, unstable angina, preoperative Killip class, as well as the preoperative cTnI level. Independent multivariate factors predicting in-hospital MACE were then unstable angina, as well as the preoperative cTnI level (Table 3).
|
After separation of the entire AMI study population into those with STEMI and NSTEMI, again, multivariate logistic regression analyses revealed preoperative cTnI as the strongest independent predictor for in-hospital death (OR, 1.22, 95% CI, 1.03 to 1.41; P<0.02) and MACE (OR, 1.29, 95% CI, 1.09 to 1.58; P=0.002) in STEMI, as well as the strongest independent predictor for in-hospital death (OR, 1.08, 95% CI 1.02 to 1.09, P<0.001) and MACE (OR, 1.11, 95% CI, 1.03 to 1.12; P<0.001) in NSTEMI patients.
The discriminative power of the preoperative cTnI levels for in-hospital mortality using the ROC curve analyses yielded an area under curve (AUC) of 0.77±0.07 for the entire AMI study population (STEMI+NSTEMI), 0.79±0.02 for STEMI, and 0.72±0.08 for NSTEMI. In contrast, ROC analyses of the EuroSCORE in the same patient cohort revealed a significantly lower predictive power with an AUC of 0.70±0.06 for all STEMI+NSTEMI patients (P=0.03), 0.74±0.02 for STEMI (P=0.04), and 0.69±0.08 for NSTEMI (P=0.01; Table 4).
|
| Discussion |
|---|
|
|
|---|
Elevated markers of myocardial cell necrosis, most notably cardiac troponins (T and I), have been shown to be associated with adverse outcome and increased mortality rates in patients with acute STEMI,11,12 but also minor elevations of cardiac troponins among patients with NSTEMI were demonstrated to go along with a higher risk of death and reinfarction.3,18 More pronounced by elevated serum levels of cardiac troponins on admission, indicating a more extensive myocardial injury, have been unequivocally demonstrated to predict a worse clinical outcome and a more complicated course following primary PCI for acute STEMI.11,12 Patients with acute coronary syndromes and elevated cTnI levels on admission were found to have a lower reperfusion rate, a lower success rate for primary PCI, but a higher risk for in-hospital death and congestive heart failure, and a higher incidence of long-term cardiac mortality and overall cardiac events.9,12 In the setting of cardiac surgery, both, preoperative cTnI was described as predictive for patient outcome in elective CABG patients,19 and postoperative cTnI was reported to be highly predictive in cardiac surgical and/or CABG patients5,14 to 16. Whether postoperative cTnI is likewise capable to predict outcome in AMI patients undergoing emergency CABG has not been answered so far and should be evaluated in the future.
The addition of a highly sensitive biomarker, such as cardiac troponins, indicating myocardial cellular necrosis at the time of determination may well enrich the battery of preoperative risk stratification models for patients undergoing CABG surgery. As shown by the results of the present study, the extent of preoperative cTnI elevation indicates the degree of myocardial cellular injury and thus, the patient surgical risk before emergency CABG.
Limitations
Our study encompasses the experience at a single tertiary care medical center; therefore, the generalizability of our findings may not extend to all of the clinical centers performing CABG surgery. CTnI serum levels depend on many variables, including first of all the type of cTnI immunoassay test kit and additionally several differences in the preoperative management and treatment of AMI patients may result in different preoperative cTnI serum levels. Furthermore, the prognostic ability of our multivariate regression risk model has not been tested in a validation cohort. Finally, only the in-hospital (short-term) outcome is reported in the present study, whether a pre-CABG cTnI level also predicts mortality and MACE in the long-term is as yet uncertain.
Conclusions
The present study is the first suggesting that preoperative cTnI measurement can serve as an incremental variable of risk for in-hospital mortality and MACE in AMI patients with STEMI or NSTEMI. With rising preoperative serum levels of cardiac troponin I, the risk of mortality and MACE increases. Therefore, preoperative cTnI measurement as the most sensitive and specific biomarker for myocardial injury may provide important prognostic information and thus, should be taken into consideration for preoperative risk stratification to decide about the appropriate timing of surgical intervention in those patients.
Whether, after elevated preoperative cTnI level has been shown, certain preoperative management strategies (eg, IABP, timing to surgery, preoperative anticoagulation regime, etc.) may have a beneficial impact on patient outcome remains uncertain and has to be elucidated in further studies.
| Acknowledgments |
|---|
None.
| Footnotes |
|---|
| References |
|---|
|
|
|---|
2. Alpert JS, Thygesen K, Antman E, Bassand JP. Myocardial infarction redefined - a consensus document of The Joint European Society of Cardiology/American College of Cardiology Committee for the redefinition of myocardial infarction. J Am Coll Cardiol. 2000; 36: 959969.
3. Antman EM, Tanasijevic MJ, Thompson B, Schactman M, McCabe CH, Cannon CP, Fischer GA, Fung AY, Thompson C, Wybenga D, Braunwald E. Cardiac-specific troponin I levels to predict the risk of mortality in patients with acute coronary syndromes. N Engl J Med. 1996; 335: 13421349.
4. Newby LK, Christenson RH, Ohman EM, Armstrong PW, Thompson TD, Lee KL, Hamm CW, Katus HA, Cianciolo C, Granger CB, Topol EJ, Califf RM. Value of serial troponin T measures for early and late risk stratification in patients with acute coronary syndromes. Circulation. 1998; 98: 18531859.
5. Lehrke S, Steen H, Sievers HH, Peters H, Opitz A, Muller-Bardorff M, Wiegand UKH, Katus HA, Giannitsis E. Cardiac troponin T for prediction of short- and long-term morbidity and mortality after elective open heart surgery. Clin Chem. 2004; 50: 15601570.
6. Kim LJ, Martinez EA, Faraday N, Dorman T, Fleisher LA, Perler BA, Williams GM, Chan D, Pronovost PJ. Cardiac troponin I predicts short-term mortality in vascular surgery patients. Circulation. 2002; 106: 23662371.
7. Greenson N, Macoviak J, Krishnaswamy P, Morrisey R, James C, Clopton P, Fitzgerald R, Maisel A. Usefulness of cardiac troponin I in patients undergoing open heart surgery. Am Heart J. 2001; 141: 447455.[CrossRef][Medline] [Order article via Infotrieve]
8. Hamm CW, Giannitsis E, Katus HA. Cardiac troponin elevations in patients without acute coronary syndrome. Circulation. 2002; 106: 28712872.
9. Giannitsis E, Lehrke S, Wiegand UKH, Kurowski V, Muller-Bardorff M, Weidtmann B, Richardt G, Katus HA. Risk stratification in patients with inferior acute myocardial infarction treated by percutaneous coronary interventions: the role of admission troponin T. Circulation. 2000; 102: 20382044.
10. Heidenreich PA, Alloggiamento T, Melsop K, McDonald KM, Go AS, Hlatky MA. The prognostic value of troponin in patients with non-ST elevation acute coronary syndromes: a meta-analysis. J Am Coll Cardiol. 2001; 38: 478485.
11. Matetzky S, Sharir T, Domingo M, Noc M, Chyu K-Y, Kaul S, Eigler N, Shah PK, Cercek B. Elevated troponin I level on admission is associated with adverse outcome of primary angioplasty in acute myocardial infarction. Circulation. 2000; 102: 16111616.
12. Giannitsis E, Muller-Bardorff M, Lehrke S, Wiegand U, Tolg R, Weidtmann B, Hartmann F, Richardt G, Katus HA. Admission troponin T level predicts clinical outcomes. TIMI flow, and myocardial tissue perfusion after primary percutaneous intervention for acute ST-segment elevation myocardial infarction Circulation. 2001; 104: 630635.
13. Herrmann J, Haude M, Lerman A, Schulz R, Volbracht L, Ge J, Schmermund A, Wieneke H, von Birgelen C, Eggebrecht H, Baumgart D, Heusch G, Erbel R. Abnormal coronary flow velocity reserve after coronary intervention is associated with cardiac marker elevation. Circulation. 2001; 103: 23392345.
14. Thielmann M, Massoudy P, Schmermund A, Neuhauser M, Marggraf G, Kamler K, Herold U, Aleksic I, Mann K, Haude M, Heusch G, Erbel R, Jakob H. Diagnostic discrimination between graft-related and non-graft-related perioperative myocardial infarction with cardiac troponin I after coronary artery bypass surgery. Eur Heart J. 2005; 26: 24402447.
15. Fellahi J-L, Gue X, Richomme X, Monnier E, Guillon L, Riou B. Short- and long-term prognostic value of postoperative cardiac troponin I concentration in patients undergoing coronary artery bypass grafting. Anesthesiology. 2003; 99: 270274.[CrossRef][Medline] [Order article via Infotrieve]
16. Carrier M, Pellerin M, Perrault LP, Solymoss BC, Pelletier LC. Troponin I levels in patients with myocardial infarction after coronary artery bypass grafting. Ann Thorac Surg. 2000; 69: 435440.
17. Nashef SAM, Roques F, Michel P, Gauducheau E, Lemeshow S, Salamon R. European system for cardiac operative risk evaluation (EuroSCORE). Eur J Cardio-Thorac Surg. 1999; 16: 913.
18. Thielmann M, Massoudy P, Neuhauser M, Knipp S, Kamler M, Piotrowski J, Mann K, Jakob H. Prognostic value of preoperative cardiac troponin I in patients with non-ST-segment elevation acute coronary syndromes undergoing coronary artery bypass surgery. Chest. 2005; 128: 35263536.
19. Carrier M, Pelletier LC, Martineau R, Pellerin M, Solymoss BC. In elective coronary artery bypass grafting, preoperative troponin T level predicts the risk of myocardial infarction. J Thorac Cardiovasc Surg. 1998; 115: 13281334.
This article has been cited by other articles:
![]() |
A. A. Mohammed, A. K. Agnihotri, R. R.J. van Kimmenade, A. Martinez-Rumayor, S. M. Green, R. Quiroz, and J. L. Januzzi Jr Prospective, Comprehensive Assessment of Cardiac Troponin T Testing After Coronary Artery Bypass Graft Surgery Circulation, September 8, 2009; 120(10): 843 - 850. [Abstract] [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2006 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |