Elevated troponin T and C-reactive protein predict impaired outcome for 4 years in patients with refractory unstable angina, and troponin T predicts benefit of treatment with abciximab in combination with PTCA

被引:42
作者
Lenderink, T [1 ]
Boersma, E
Heeschen, C
Vahanian, A
de Boer, MJ
Umans, V
van den Brand, MJBM
Hamm, CW
Simoons, ML
机构
[1] Erasmus MC, Thoraxctr, Dept Cardiol, Rotterdam, Netherlands
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[3] Kerckhoff Heart Ctr, Bad Nauheim, Germany
[4] Tenon Hosp, Paris, France
[5] Hosp Weezenlanden, Zwolle, Netherlands
[6] Med Ctr Alkmaar, Alkmaar, Netherlands
关键词
glycoprotein IIb/IIIa receptor antagonist; unstable angina pectoris; troponin T; C-reactive protein; long-term follow-up;
D O I
10.1016/S0195-668X(02)00322-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Treatment with the glycoprotein IIb/IIIa receptor antagonist abciximab before and during coronary intervention in refractory unstable angina improves early outcome. We collected 4-year follow-up data to assess whether this benefit is sustained. Additionally, we investigated the predictive value of baseline troponin T and CRP for long-term cardiovascular events. Methods and Results Of 1265 patients enrolled in the CAPTURE trial follow-up was available in 94% of the patients alive after 6 months (median 48 months). Survival was similar in both groups. Both elevated troponin T and CRP were associated with impaired outcome, independently of other established risk factors, but with a different time course. Elevated troponin was associated with increased procedure related risk, and elevated CRP with increased risk for subsequent events. Lower rates of the composite end-point of death or myocardial infarction with abciximab vs. placebo were sustained during long-term follow up: 15.7% vs 17.2% at 4 years (P = ns), particularly in patients with elevated troponin T: 16.9% with abciximab vs 28.4% with placebo: P = 0.015. Elevated CRP was not associated with specific benefit of abciximab. Conclusion Troponin T, as a marker of thrombosis and CRP as a marker of inflammation are independent predictors of impaired outcome at 4 years follow-up. The initial benefit from abciximab with regard to death and myocardial infarction was preserved at 4 years. No specific benefit with abciximab was observed for patients with elevated CRP, suggesting that a chronic inflammatory process is not affected by abciximab. In contrast the benefit of treatment in patients with elevated troponin T implies that the acute thrombotic process in refractory unstable angina is treated effectively. (C) 2002 The European Society of Cardiology., Published by Elsevier Science Ltd. All rights reserved.
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页码:77 / 85
页数:9
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