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Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction

BACKGROUND: Long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with ST-segment elevation myocardial infarction (STEMI) remain uncertain. OBJECTIVE: To investigate long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with S...

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Autores principales: Wang, Liping, Wang, Hongyun, Dong, Pingshuan, Li, Zhuanzhen, Wang, Yanyu, Duan, Nana, Zhao, Yuwei, Wang, Shaoxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079016/
https://www.ncbi.nlm.nih.gov/pubmed/25004414
http://dx.doi.org/10.5935/abc.20140070
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author Wang, Liping
Wang, Hongyun
Dong, Pingshuan
Li, Zhuanzhen
Wang, Yanyu
Duan, Nana
Zhao, Yuwei
Wang, Shaoxin
author_facet Wang, Liping
Wang, Hongyun
Dong, Pingshuan
Li, Zhuanzhen
Wang, Yanyu
Duan, Nana
Zhao, Yuwei
Wang, Shaoxin
author_sort Wang, Liping
collection PubMed
description BACKGROUND: Long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with ST-segment elevation myocardial infarction (STEMI) remain uncertain. OBJECTIVE: To investigate long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with ST-segment elevation myocardial infarction (STEMI). METHODS: We performed search of MEDLINE, EMBASE, the Cochrane library, and ISI Web of Science (until February 2013) for randomized trials comparing more than 12-month efficacy or safety of DES with BMS in patients with STEMI. Pooled estimate was presented with risk ratio (RR) and its 95% confidence interval (CI) using random-effects model. RESULTS: Ten trials with 7,592 participants with STEMI were included. The overall results showed that there was no significant difference in the incidence of all-cause death and definite/probable stent thrombosis between DES and BMS at long-term follow-up. Patients receiving DES implantation appeared to have a lower 1-year incidence of recurrent myocardial infarction than those receiving BMS (RR = 0.75, 95% CI 0.56 to 1.00, p= 0.05). Moreover, the risk of target vessel revascularization (TVR) after receiving DES was consistently lowered during long-term observation (all p< 0.01). In subgroup analysis, the use of everolimus-eluting stents (EES) was associated with reduced risk of stent thrombosis in STEMI patients (RR = 0.37, p=0.02). CONCLUSIONS: DES did not increase the risk of stent thrombosis in patients with STEMI compared with BMS. Moreover, the use of DES did lower long-term risk of repeat revascularization and might decrease the occurrence of reinfarction.
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spelling pubmed-40790162014-07-03 Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction Wang, Liping Wang, Hongyun Dong, Pingshuan Li, Zhuanzhen Wang, Yanyu Duan, Nana Zhao, Yuwei Wang, Shaoxin Arq Bras Cardiol Original Articles BACKGROUND: Long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with ST-segment elevation myocardial infarction (STEMI) remain uncertain. OBJECTIVE: To investigate long-term outcomes of drug-eluting stents (DES) versus bare-metal stents (BMS) in patients with ST-segment elevation myocardial infarction (STEMI). METHODS: We performed search of MEDLINE, EMBASE, the Cochrane library, and ISI Web of Science (until February 2013) for randomized trials comparing more than 12-month efficacy or safety of DES with BMS in patients with STEMI. Pooled estimate was presented with risk ratio (RR) and its 95% confidence interval (CI) using random-effects model. RESULTS: Ten trials with 7,592 participants with STEMI were included. The overall results showed that there was no significant difference in the incidence of all-cause death and definite/probable stent thrombosis between DES and BMS at long-term follow-up. Patients receiving DES implantation appeared to have a lower 1-year incidence of recurrent myocardial infarction than those receiving BMS (RR = 0.75, 95% CI 0.56 to 1.00, p= 0.05). Moreover, the risk of target vessel revascularization (TVR) after receiving DES was consistently lowered during long-term observation (all p< 0.01). In subgroup analysis, the use of everolimus-eluting stents (EES) was associated with reduced risk of stent thrombosis in STEMI patients (RR = 0.37, p=0.02). CONCLUSIONS: DES did not increase the risk of stent thrombosis in patients with STEMI compared with BMS. Moreover, the use of DES did lower long-term risk of repeat revascularization and might decrease the occurrence of reinfarction. Sociedade Brasileira de Cardiologia 2014-06 /pmc/articles/PMC4079016/ /pubmed/25004414 http://dx.doi.org/10.5935/abc.20140070 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Liping
Wang, Hongyun
Dong, Pingshuan
Li, Zhuanzhen
Wang, Yanyu
Duan, Nana
Zhao, Yuwei
Wang, Shaoxin
Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title_full Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title_fullStr Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title_full_unstemmed Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title_short Long-term Outcomes of Drug-eluting versus Bare-metal stent for ST-elevation Myocardial Infarction
title_sort long-term outcomes of drug-eluting versus bare-metal stent for st-elevation myocardial infarction
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079016/
https://www.ncbi.nlm.nih.gov/pubmed/25004414
http://dx.doi.org/10.5935/abc.20140070
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