Relation of minor cardiac troponin I elevation to late cardiac events after uncomplicated elective successful percutaneous transluminal coronary angioplasty for angina pectoris

被引:92
作者
Bertinchant, JP
Polge, A
Ledermann, B
Genet, L
Fabbro-Peray, P
Raczka, F
Brunet, J
Poirey, S
Wittenberg, O
Pernel, I
Nigond, J
机构
[1] Univ Nimes Hosp, Dept Cardiol, F-30900 Nimes, France
[2] Univ Nimes Hosp, Dept Biochem, F-30900 Nimes, France
[3] Univ Nimes Hosp, Dept Biostat & Epidemiol, F-30900 Nimes, France
关键词
D O I
10.1016/S0002-9149(99)00191-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is little information about the relation between mild cardiac troponin I (cTn-I) increase after coronary interventions and late outcome. We therefore Focused on the long-term outcome and the clinical, morphologic, and procedural correlates of elevation of cTn-I compared with cardiac troponin T, creatine kinase (CK), CK-MB activity and mass, and myoglobin in 105 patients with successful elective percutaneous transluminal coronary angioplasty (PTCA) for stable or unstable angina. Patients with myocardial infarction and those with unstable angina who had a detectable increase in serum markers before PTCA were excluded. Markers were measured before and after the procedure and for 2 days. Patients were followed up to record recurrent angina, myocardial infarction, cardiac death, repeat PTCA, or elective coronary artery bypass graft surgery. Procedure success was achieved in all cases. Elevation in cTn-I (greater than or equal to 0.1 mu g/L) was observed in 23 of 105 patients (22%) (median peak: 0.25 mu g/L); 18% had cardiac troponin T (cTn-T) release (greater than or equal to 0.1 mu g/L, median peak (0.21); 11.4% CK-MB mass (greater than or equal to 5 mu g/L), and 7.6% myoglobin (greater than or equal to 90 mu g/L) release. Five and 2 patients had elevated CK and CK-MB activity, respectively. Fourteen of 18 patients with cTn-T elevation had a corresponding elevation in cTn-I (kappa 0.68; p = 0.001). Patients positive for cTn-I had more unstable angina (p = 0.042) and heparin before PICA (p = 0.046), and had longest total time (p = 0.004) and single inflation (p = 0.01). By multivariate logistic regression, predictors of postprocedure cTnI elevation were maximum time of each inflation (odds ratio 9.2; p = 0.0012), type B lesions (odds ratio 6.6; p = 0.013), unstable angina (p = 0.041), and age greater than or equal to 60 years (p = 0.032). Clinical follow-up was available in 103 patients (98%) (mean 19 +/- 10 months). Kaplan-Meier survival analysis showed that cTn-I elevation was not an important correlate of cardiac events (p = 0.34, by log-rank analysis). The incidence of recurrent angina, myocardial infarction, cardiac death, and repeat revascularization after 12 months was not different in patients positive or negative for cTn-I. We conclude that cTn-I elevation after successful PTCA is not associated with significantly worse late clinical outcome. levels of cTn-I allow a much higher diagnostic accuracy in detecting minor myocardial injury after PICA compared with other markers, but there is no association with periprocedural myocardial cell injury and late outcome when cTn-I and other markers are considered. (C) 1999 by Excerpta Medico, Inc.
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页码:51 / 57
页数:7
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