This study is aimed at evaluating 1-year clinical outcomes and their predictors in patients with unprotected left main coronary artery (ULMCA)-related acute myocardial infarction (AMI). In total 248 patients diagnosed with AMI involving the ULMCA as the culprit vessel and registered in the Korean Acute Myocardial Infarction database were enrolled in this study. Patients were divided according to the absence (shock−, n = 206) or presence (shock+, n = 42) of cardiogenic shock at initial presentation. Independent risk factors of in-hospital cardiac death associated with ULMCA-related AMI were elucidated by multivariate regression analysis. In-hospital mortality rates were 8.7% in the shock− group and 47.6% in the shock+ group (p = 0.001). During 1-year follow-up after discharge, major adverse cardiac events developed in 16.3% of patients in the shock− group and 18.2% of patients in the shock+ group (p = 0.828); cardiac death, MI, and ischemia-driven target vessel revascularization were similar between the 2 groups at 1 year. On multivariate analysis, initial shock presentation (odds ratio 8.9, confidence interval 4.1 to 19.2, p = 0.004) and left ventricular ejection fraction <30% (odds ratio 7.6, confidence interval 2.7 to 21.1, p = 0.001) were independent risk factors of in-hospital cardiac death associated with ULMCA-related AMI. In conclusion, almost 1/2 of patients with ULMCA-related AMI presenting with cardiogenic shock had a fatal in-hospital outcome compared to <10% of those without cardiogenic shock; however, clinical outcomes after survival of the in-hospital period were not different between these groups.
Acute myocardial infarction (AMI) related to an unprotected left main coronary artery (ULMCA) often leads to pump failure, refractory arrhythmia, and sudden cardiac death; however, its incidence is rare, with only 0.8% of patients who undergo primary percutaneous coronary intervention (PCI) developing this condition. Current guidelines recommend coronary artery bypass grafting to treat the ULMCA lesion. However, these guidelines do not assist with the treatment of ULMCA-related AMI, which often presents with hemodynamic instability requiring prompt restoration of blood flow to the coronary artery. Also, there are insufficient data on ULMCA-related AMI. The aim of this study was to evaluate clinical outcomes and their predictors of ULMCA-related AMI.
Methods
The Korean Acute Myocardial Infarction Registry (KAMIR) is a prospective, observational, multicenter registry to reflect real-world practice for Korean patients with AMI. Fifty highly experienced hospitals in primary PCI participated and registered online consecutive patients with AMI. The ethics committee of each hospital approved the study protocol. From November 2005 to June 2008, 11,872 patients with AMI were registered in the KAMIR database. Of these, 248 patients with AMI of the ULMCA as the culprit vessel were enrolled in this study. These patients were divided in 2 groups according to the absence (shock−, n = 206) or presence (shock+, n = 42) of shock at initial presentation.
PCI was performed using standard techniques. All patients received aspirin 325 mg orally and a loading dose of clopidogrel 300 mg before coronary angiography or after PCI for emergency cases. After PCI patients were routinely treated with aspirin 100 mg/day, clopidogrel 75 mg/day, and/or cilostazol 200 mg/day at the operator’s discretion. Patients were advised to maintain lifelong aspirin therapy. Duration of clopidogrel therapy was left to the operator’s discretion depending on the complexity of the lesion and procedure.
Study outcome was a composite of major adverse cardiac events including cardiac death, MI, and ischemia-driven target vessel revascularization for 1 year. Stent thrombosis was also evaluated. Cardiogenic shock was defined as sustained hypotension with systolic blood pressure <90 mm Hg for ≥30 minutes. MI was defined as typical ischemic chest pain and/or ST-segment and/or T-wave abnormalities with an increased creatine kinase-MB level ≥2 times reference values without any new pathologic Q waves. ST-segment elevation MI was defined as electrocardiographic findings of ST-segment elevation of ≥2 mm in 2 contiguous precordial leads or >1 mm in 2 limb leads or presumably new-onset left bundle branch block. All other electrocardiographic patterns including ST-segment depression or T-wave inversion, were diagnosed as non–ST-segment elevation MI. Ischemia-driven target vessel revascularization was defined as emergency or elective coronary artery bypass grafting or repeat PCI in the target vessel for chest pain or a positive test result for ischemia (exercise stress test, stress echocardiogram, 24-hour Holter monitor, evidence of ST-segment depression or increase in >1 lead on echocardiogram at rest, or radionuclide study showing a reversible defect). Stent thrombosis was defined as previously described by the Academic Research Consortium. Cumulative rates of event-free survival and major adverse cardiac events were analyzed over a 1-year follow-up.
All results in this study are expressed as mean ± SD or number (percentage). Comparisons of categorical variables were performed using chi-square test. Student’s t test was used to compare continuous variables. Multiple logistic regression analysis was performed to determine independent predictors of in-hospital mortality associated with AMI of the ULMCA. The following variables were tested: use of intra-aortic balloon pump, initial ST-segment elevation MI, Thrombolysis In Myocardial Infarction score before the procedure, initial shock at presentation, left ventricular ejection fraction <30%, and diabetes mellitus. Major adverse cardiac event-free survival distributions were estimated according to Kaplan–Meier methods. Log-rank test was used to compare major adverse cardiac event-free survival between the 2 groups. A p value <0.05 was considered statistically significant. Data were analyzed using SPSS 12.0 for Windows (SPSS, Inc., Chicago, Illinois).
Results
Baseline characteristics between the 2 groups were found to be similar ( Table 1 ). However, the number of patients with ST-segment elevation MI was larger in the shock+ than in the shock− group (12.1% vs 80.9%, respectively, p = 0.001); however, all patients without ST-segment elevation were acutely ill. Table 2 presents angiographic and procedural results. Most lesions were type B2/C (75.7% in shock− group vs 76.2% in shock+ group, p = 0.543). Thrombolysis In Myocardial Infarction score before the procedure was higher in the shock− than in the shock+ group (1.9 ± 1.1 vs 1.2 ± 1.1, respectively, p = 0.001), however, Thrombolysis In Myocardial Infarction score after the procedure was not different between the 2 groups (2.8 ± 0.5 in shock− group vs 2.8 ± 0.4 in shock+ group, p = 0.582). PCI was performed in 134 patients in the shock− group (65%) and in 36 patients in the shock+ group (85.7%). Drug-eluting stenting was used in 126 patients in the shock− group and in 34 patients in the shock+ group (94.0% vs 94.4%, p = 0.476). Mean stent length and diameter did not differ between the 2 groups ( Table 2 ). Treatment in hospital is presented in Table 3 . Conservative treatment by medical therapy was performed in 24.7% of patients in the shock− group and in 11.9% of patients in the shock+ group (p = 0.137). Thrombolytics were given in 3.8% of patients in the shock− group and in 9.5% of patients in the shock+ group (p = 0.134). Revascularization by PCI and/or coronary artery bypass grafting was performed in 75.3% of patients in the shock− group and in 88.1% of patients in the shock+ group. Overall in-hospital mortality was 14.9% (38 of 248), which was broken down as 8.7% in the shock− group and 47.6% in the shock+ group (p = 0.001). By multivariate analysis, initial shock at presentation (odds ratio 8.9, 95% confidence interval 4.1 to 19.2, p = 0.004) and left ventricular ejection fraction <30% (odds ratio 7.6, 95% confidence interval 2.7 to 21.1, p = 0.001) were independent risk factors for in-hospital mortality associated with ULMCA-related AMI. Use of medical therapy or revascularization was associated with a statistically similar in-hospital mortality (19.6% in medical therapy vs 14.1% in revascularization, p = 0.308).
Variables | Cardiogenic Shock | p Value | |
---|---|---|---|
No | Yes | ||
(n = 206) | (n = 42) | ||
Age (years) | 65 ± 13 | 66 ± 12 | 0.607 |
Men | 140 (67.9%) | 35 (83.3%) | 0.057 |
Diabetes mellitus | 78 (37.9%) | 16 (38.1%) | 0.986 |
Hypertension | 109 (52.9%) | 20 (47.6%) | 0.531 |
Current smoking | 66 (32.0%) | 15 (35.7%) | 0.688 |
Diagnosis | 0.001 | ||
ST-segment elevation myocardial infarction | 25 (12.1%) | 34 (80.9%) | |
Non–ST-segment elevation myocardial infarction | 81 (87.9%) | 8 (19.1%) | |
Creatinine (mg/dl) | 1.3 ± 1.4 | 1.7 ± 1.5 | 0.199 |
Peak creatine kinase-MB (mg/dl) | 99 ± 180 | 254 ± 267 | 0.001 |
Peak troponin I (ng/dl) | 47 ± 148 | 63 ± 82 | 0.543 |
Low-density lipoprotein (mg/dl) | 117 ± 43 | 99 ± 37 | 0.020 |
Variables | Cardiogenic Shock | p Value | |
---|---|---|---|
No | Yes | ||
(n = 206) | (n = 42) | ||
Type of disease* | 0.543 | ||
A | 11 (5.4%) | 2 (4.8%) | |
B1 | 39 (18.9%) | 8 (19.0%) | |
B2 | 80 (38.8%) | 18 (42.9%) | |
C | 76 (36.9%) | 14 (33.3%) | |
3-Vessel disease | 39 (18.9%) | 6 (14.3%) | 0.463 |
Thrombolysis In Myocardial Infarction score | |||
Before | 1.9 ± 1.1 | 1.2 ± 1.1 | 0.001 |
After | 2.8 ± 0.5 | 2.8 ± 0.4 | 0.582 |
Used stent | |||
Length (mm) | 21.7 ± 6.7 | 21.9 ± 6.1 | 0.858 |
Diameter (mm) | 3.4 ± 0.4 | 3.3 ± 0.3 | 0.289 |
Intra-aortic balloon pump | 25 (12.1%) | 29 (69%) | 0.001 |
Variables | Cardiogenic Shock | p Value | |
---|---|---|---|
No | Yes | ||
(n = 206) | (n = 42) | ||
Conservative treatment | 51 (24.7%) | 5 (11.9%) | 0.137 |
Use of thrombolytics | 8 (3.8%) | 4 (9.5%) | 0.134 |
Revascularization | 155 (75.3%) | 37 (88.1%) | |
Percutaneous coronary intervention | 134 (65.0%) | 36 (85.7%) | 0.476 |
Bare-metal stent | 8 (6.0%) | 2 (5.6%) | |
Drug-eluting stent | 126 (94.0%) | 34 (64.4%) | |
Coronary artery bypass grafting | 26 (12.3%) | 2 (4.5%) | 0.133 |
In-hospital mortality | 18 (8.7%) | 20 (47.6%) | 0.001 |