• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

药物洗脱支架时代支架内再狭窄的当代治疗及复发性支架内再狭窄的发生率。

Contemporary treatment of in-stent restenosis and the incidence of recurrent in-stent restenosis in the era of drug-eluting stents.

作者信息

Ajani Andrew E, Yan Bryan P, Clark David J, Eccleston David, Walton Anthony, Lew Robert, Meehan Adam, Brennan Angela, Reid Chris, Duffy Stephen J

机构信息

Department of Cardiology, Royal Melbourne Hospital, Melbourne, Australia.

出版信息

Heart Lung Circ. 2007 Aug;16(4):269-73. doi: 10.1016/j.hlc.2007.02.089. Epub 2007 Apr 6.

DOI:10.1016/j.hlc.2007.02.089
PMID:17419097
Abstract

BACKGROUND

Optimal treatment of in-stent restenosis (ISR) remains uncertain in the era of drug-eluting stents (DES). This study aims to determine contemporary treatment of ISR and to assess recurrent ISR rates in the era of DES.

METHODS

We examined 60 patients presenting for treatment of ISR (one lesion per patient) who were enrolled in the Melbourne Interventional Group Registry (4% of total population of 1423 patients) between April 2004 and January 2005. Twelve-month follow-up is complete for all patients.

RESULTS

The majority of ISR treated occurred in bare metal stents [BMS (n=52, 87%)] and had a focal (<10 mm) pattern of ISR (53%). In-stent restenosis of DES occurred in eight (13%) patients. The majority of ISR were treated with additional stenting with a preference for DES over BMS in almost all cases. At 12 months, one patient died of non-cardiac cause and four patients (7%) presented with recurrent ISR. The incidence of recurrent ISR in DES was 5% (n=3). No late thrombosis was reported despite only 50% of patients having >or=12 months of clopidogrel therapy.

CONCLUSIONS

Our study suggests drug-eluting stents are safe, effective and the preferred therapy for in-stent restenosis. The incidence of recurrent drug-eluting stent restenosis at 12 months is low.

摘要

背景

在药物洗脱支架(DES)时代,支架内再狭窄(ISR)的最佳治疗方法仍不明确。本研究旨在确定DES时代ISR的当代治疗方法,并评估再发ISR的发生率。

方法

我们对2004年4月至2005年1月期间纳入墨尔本介入组登记处(1423例患者总数的4%)的60例因ISR接受治疗的患者(每位患者1个病变)进行了研究。所有患者均完成了12个月的随访。

结果

接受治疗的ISR大多发生在裸金属支架[BMS(n = 52,87%)]中,且ISR呈局灶性(<10 mm)模式(53%)。8例(13%)患者发生了DES内支架再狭窄。大多数ISR通过再次置入支架进行治疗,几乎在所有情况下都更倾向于使用DES而非BMS。12个月时,1例患者死于非心脏原因,4例患者(7%)出现再发ISR。DES组再发ISR的发生率为5%(n = 3)。尽管只有50%的患者接受了≥12个月的氯吡格雷治疗,但未报告晚期血栓形成。

结论

我们的研究表明,药物洗脱支架对于支架内再狭窄是安全、有效的,且是首选治疗方法。12个月时药物洗脱支架再狭窄的发生率较低。

相似文献

1
Contemporary treatment of in-stent restenosis and the incidence of recurrent in-stent restenosis in the era of drug-eluting stents.药物洗脱支架时代支架内再狭窄的当代治疗及复发性支架内再狭窄的发生率。
Heart Lung Circ. 2007 Aug;16(4):269-73. doi: 10.1016/j.hlc.2007.02.089. Epub 2007 Apr 6.
2
Outcome differences with the use of drug-eluting stents for the treatment of in-stent restenosis of bare-metal stents versus drug-eluting stents.使用药物洗脱支架治疗裸金属支架与药物洗脱支架的支架内再狭窄的疗效差异。
Am J Cardiol. 2009 Feb 15;103(4):491-5. doi: 10.1016/j.amjcard.2008.09.107.
3
Late outcomes after drug-eluting stent implantation in "real-world" clinical practice.药物洗脱支架植入在“真实世界”临床实践中的远期疗效。
J Invasive Cardiol. 2008 Oct;20(10):493-500.
4
Clinical outcome of percutaneous treatment of in-stent restenosis with drug-eluting stents: results from the first phase of the prospective multicentre German DES.DE registry.药物洗脱支架治疗支架内再狭窄的临床结果:前瞻性多中心德国 DES.DE 注册研究第一阶段的结果。
EuroIntervention. 2011 Jun;7(2):201-8. doi: 10.4244/EIJV7I2A34.
5
Clinical presentation of patients with in-stent restenosis in the drug-eluting stent era.药物洗脱支架时代支架内再狭窄患者的临床表现
J Invasive Cardiol. 2008 Aug;20(8):401-3.
6
Predictor of subsequent target lesion revascularization in patients with drug-eluting stent restenosis undergoing percutaneous coronary intervention.药物洗脱支架再狭窄患者行经皮冠状动脉介入治疗后靶病变血运重建的预测因素。
J Cardiol. 2010 May;55(3):391-6. doi: 10.1016/j.jjcc.2010.01.003. Epub 2010 Feb 7.
7
Long-term clinical outcomes after sirolimus-eluting stent implantation for treatment of restenosis within bare-metal versus drug-eluting stents.西罗莫司洗脱支架植入治疗裸金属支架与药物洗脱支架内再狭窄后的长期临床结局。
Catheter Cardiovasc Interv. 2008 Apr 1;71(5):594-8. doi: 10.1002/ccd.21399.
8
Clinical outcome after management of unprotected left main in-stent restenosis after bare metal or drug-eluting stents.裸金属支架或药物洗脱支架内再狭窄的无保护左主干病变治疗后的临床转归。
Chin Med J (Engl). 2010 Apr 5;123(7):794-9.
9
Everolimus- and zotarolimus-eluting stents for bare metal stent in-stent restenosis treatment: a prospective study.依维莫司和佐他莫司洗脱支架治疗裸金属支架内再狭窄的前瞻性研究。
J Interv Cardiol. 2008 Oct;21(5):388-94. doi: 10.1111/j.1540-8183.2008.00381.x. Epub 2008 Aug 13.
10
Incidence and predictors of recurrent restenosis following implantation of drug-eluting stents for in-stent restenosis.药物洗脱支架植入治疗支架内再狭窄后复发性再狭窄的发生率及预测因素。
Catheter Cardiovasc Interv. 2007 Jan;69(1):104-8. doi: 10.1002/ccd.20908.

引用本文的文献

1
Small molecule agonists of integrin CD11b/CD18 do not induce global conformational changes and are significantly better than activating antibodies in reducing vascular injury.整合素CD11b/CD18的小分子激动剂不会诱导整体构象变化,并且在减轻血管损伤方面明显优于激活抗体。
Biochim Biophys Acta. 2013 Jun;1830(6):3696-710. doi: 10.1016/j.bbagen.2013.02.018. Epub 2013 Feb 26.