Literature DB >> 25641533

Predictors and impact of target vessel revascularization after stent implantation for acute ST-segment elevation myocardial infarction: lessons from HORIZONS-AMI.

Sorin J Brener1, Konstanze Ertelt2, Roxana Mehran3, Philippe Genereux2, Ke Xu2, Bernhard Witzenbichler4, Bruce R Brodie5, Giulio Guagliumi6, Gregg W Stone7.   

Abstract

BACKGROUND: Target vessel revascularization (TVR) may compromise the benefits of primary percutaneous coronary intervention in ST-segment elevation myocardial infarction (STEMI) We set out to identify the predictors and examine the impact of TVR after STEMI in patients receiving a coronary stent.
METHODS: In HORIZONS-AMI, 3,602 patients with STEMI were randomized to bivalirudin versus heparin and a glycoprotein IIb/IIIa inhibitor. Stents were implanted in 3,202 patients (2,982 were randomized to bare-metal stents versus paclitaxel-eluting stents, and 220 received nonrandomized stents).
RESULTS: Target vessel revascularization occurred in 219 patients (6.9%) at 1 year and in 437 patients (14.4%) at 3 years. Target vessel revascularization was ischemia-driven in 418 cases (95.7%). Target vessel revascularization was due to restenosis in 219 patients (50.1%), definite stent thrombosis in 124 (28.4%), and disease progression in 94 (21.5%). Independent predictors of TVR were more extensive coronary artery disease, smaller vessel size, longer lesion length and the number of stents implanted, post-percutaneous coronary intervention diameter stenosis, symptom onset to balloon time, treatment with bare-metal stents rather than paclitaxel-eluting stents, and scheduled angiographic follow-up. Target vessel revascularization was an independent predictor of subsequent myocardial infarction (hazard ratio [HR] 5.25, P < .0001), ST (HR 5.98, P < .0001), and major bleeding (HR 5.25, P < .0001) but not mortality (HR 0.88, P = .61).
CONCLUSIONS: In HORIZONS-AMI, TVR within 3 years after stent implantation was performed in ~1 of every 7 patients and was associated with more extensive coronary disease, more complex procedures, and bare metal stents. Target vessel revascularization was often due to stent thrombosis and disease progression as well as restenosis and was strongly associated with adverse outcomes but not mortality.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25641533     DOI: 10.1016/j.ahj.2014.11.005

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  4 in total

1.  Triglyceride to high-density lipoprotein cholesterol ratio as a risk factor of repeat revascularization among patients with acute coronary syndrome after first-time percutaneous coronary intervention.

Authors:  Ya-Min Su; Rui Zhang; Rong-Feng Xu; Hong-Lei Wang; Hai-Hua Geng; Min Pan; Yang-Yang Qu; Wen-Jie Zuo; Zhen-Jun Ji; Gen-Shan Ma
Journal:  J Thorac Dis       Date:  2019-12       Impact factor: 2.895

2.  Association between RDW and stent thrombosis in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention.

Authors:  Abdullah Tunçez; Mehmet Serkan Çetin; Elif Hande Özcan Çetin; Samet Yilmaz; Ahmet Korkmaz; Fatih Mehmet Uçar
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.889

3.  Atherogenic index of plasma for non-diabetic, coronary artery disease patients after percutaneous coronary intervention: a prospective study of the long-term outcomes in China.

Authors:  Yitian Zheng; Chen Li; Jie Yang; Samuel Seery; Yu Qi; Wenyao Wang; Kuo Zhang; Chunli Shao; Yi-Da Tang
Journal:  Cardiovasc Diabetol       Date:  2022-02-22       Impact factor: 9.951

4.  Elevated HsCRP in Chronic Obstructive Pulmonary Disease: A Prospective Study of Long-Term Outcomes After Percutaneous Coronary Intervention.

Authors:  Yitian Zheng; Yu Qi; Samuel Seery; Jie Yang; Chen Li; Wenyao Wang; Jun Gao; Xiangbin Meng; Chunli Shao; Yi-Da Tang
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2022-10-07
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.