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[TCT2008]三联抗血小板治疗能降低DES术后血栓、心肌梗死发生率

发布于:2008-10-16 19:28    



韩玮,医学博士,心内科主治医师,发表论文10余篇,主要从事心血管疾病介入治疗

Hanwei, attending physician in Cardiology department of the General Hospital of Chinese Armed Police Forces, doctor degree in PLA General Hospital. Be proficiency in transradial coronary artery disease interventional therapy, IVUS and Multi-slice computed tomography coronary artery imagination, published 14 articles and 3 books recent years.

 

三联抗血小板治疗能降低DES术后血栓、心肌梗死发生率

 

Triple Antiplatelet Therapy Reduced Thrombosis, MI Rates After DES

 

(北京武警总医院 韩玮 翻译)

 

DECREASE 注册研究结果显示阿司匹林、氯吡格雷和西洛他唑三联抗血小板治疗比传统的抗血小板治疗能降低DES术后的1年的支架血栓发生率和心肌梗死率。韩国Asan 医疗中心的Seong-Wook Park发表该研究1年结果,显示二联和三联抗血小板治疗严重和轻度出血没有差异。

 

在该重要研究中三联抗血小板超过一个月能降低12个月支架血栓的风险(HR=0.108; 95% CI, 0.013-0.918; P=.0415),而三联3个月或6个月则没有额外的获益。


治疗加权逆可能分析倾向性积分分析显示三联治疗能1年临床结果的MI和支架血栓发生率降低,尽管两组死亡率相似。倾向性积分配对分析累计支架血栓发生率三联抗血小板组显著低于二联抗血小板组(0.1% vs. 0.8%; log-rank P=.0192)。park说“这一结果为DES 置入三联抗血小板治疗的广泛应用提供了基础。”

 

DECREASE 是一个单中心注册研究,三联抗血小板组入选1443例,二联抗血小板组入选1656例。

 

新型抗血小板药物

 

Tufts大学医学院的Jeffrey J. Popma说即使没有TLR 的长期随访数据,我们也能肯定的对于复杂的患者三联抗血小板治疗能降低不良事件。Popma说当证实有氯吡格雷抵抗时西洛它唑就有用武之地了,氯吡格雷抵抗不能通过增加氯吡格雷的剂量来纠正,对于二联抗血小板治疗已经发生支架血栓或心肌梗死的患者也很有用,另外用于阿司匹林抵抗或高敏的患者,以及病变解剖高危的患者。

 

但要明确的是三联抗血小板治疗的患者没有充血性心力衰竭的,因此这是FDA 规定的西洛它唑的禁忌症。

 

(来源:www.tctmd.com

 

 

Triple Antiplatelet Therapy Reduced Thrombosis, MI Rates After DES       
 
Key Points:


DECREASE registry found cilostazol safe when added to aspirin and clopidogrel.

 

By TCT Daily Staff

 

Data from the DECREASE registry show that triple antiplatelet therapy adding cilostazol to aspirin and clopidogrel resulted in lower one-year rates of stent thrombosis and MI after DES implantation than standard dual antiplatelet therapy.

 

Seong-Wook Park, MD, PhD, of the Asan Medical Center in Seoul, South Korea, reported one-year clinical outcome data Tuesday, which showed no difference in major or minor bleeding rates between the triple- and dual-therapy groups.

 

In a landmark analysis, triple antiplatelet therapy for more than one month was found to reduce the 12-month risk of stent thrombosis (HR=0.108; 95% CI, 0.013-0.918; P=.0415). Triple therapy beyond three or six months had no such effect.

 

Both inverse-probability-of-treatment-weighted and propensity-score-matched data for one year clinical outcomes showed a reduction in MI risk and stent thrombosis with triple therapy, although mortality risk was similar between the two groups (see Figure). The cumulative incidence of stent thrombosis in propensity-score matched pairs was significantly lower in the triple therapy group than in the dual therapy group (0.1% vs. 0.8%; log-rank P=.0192).

"These results may provide the rationale for using triple antiplatelet therapy in a broad range of patients undergoing DES implantation," Park said.


DECREASE, a single-center registry, included 1,443 patients assigned to triple antiplatelet therapy and 1,656 assigned to standard dual therapy after DES implantation.

 

Other new agents available

 

Jeffrey J. Popma, MD, of Tufts University School of Medicine, in Boston, said that even though there is no long-term information from the registry about TLR rates, "we can certainly say that in complex patients, triple drug therapy with cilostazol has a lower event rate than with dual therapy alone."

 

Popma said that cilostazol "might be useful where clopidogrel resistance has been demonstrated in patients undergoing DES implantation, which cannot be overcome with increased clopidogrel dosing. It might also be useful in patients who have stent thrombosis or MI while on dual antiplatelet therapy, as well as in aspirin-resistant or hypersensitive patients. It may also be useful in high-risk anatomy," he said.

 

"But [clinicians] must make certain that their triple therapy patients do not have congestive heart failure, because there is an FDA-labeled contraindication for cilostazol," he said.

 

Disclosures:

 

Dr. Park reports no relevant conflicts of interest.
Dr. Popma reports having received research grants from or having served on advisory boards or speaker’s bureaus for the following: Cordis, Boston Scientific, Medtronic, Abbott-Guidant, Biosensors, Radiant, eV3, Sanofi, BMS, Pfizer.

 

(source:www.tctmd.com

 



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