专用分叉支架与药物洗脱支架治疗冠状动脉分叉病变:一项系统回顾和荟萃分析

Christopher E Uy, Ahmed Alsunbuli, V. Maravilla
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引用次数: 0

摘要

冠状动脉分叉病变(CBL)占所有冠状动脉病变的五分之一,并且没有最佳的治疗方法。(1)进行了多项试验,以研究不同的治疗方式,如药物洗脱支架,生物可吸收支架,(3)本系统综述旨在比较DBS与DES的临床结果,但不包括裸金属支架和生物可吸收支架。(4)方法按照PRISMA指南,(5)进行系统的数据检索,包括EMBASE、PUBMED、MEDLINE、CINAHL、Cochrane数据库、TRIP数据库和clinicaltrials.gov。纳入标准为2015年至2018年间发表的前瞻性双组随机试验,仅比较DBS和DES,报告的临床结果包括心源性死亡、心肌梗死、靶病变血管重建和支架血栓形成。采用Cochrane偏倚风险评估工具RoB1进行偏倚风险评估。(6)两位审稿人使用Microsoft Excel 365 ProPlus独立提取数据。meta分析采用限制性最大似然法比较临床结果的相对危险度(RR),(7)通过Jamovi平台使用MAJOR R pack,报告对数相对危险度(Log RR)。(8,9)结果6项比较DBS和DES的试验(共涉及1914例患者)符合纳入标准。大多数研究在欧洲进行,参与者年龄为DBS: 65.56, DES: 65.18 (p值= 0.52)。男性DBS: 74.9% DES: 77.5% (p值= 0.44),有吸烟史的DBS: 28% DES: 27.36% (p值=0.70)。出现急性冠脉综合征的患者占所有参与者的五分之一(p值= 0.74)。每组参与者中约70%患有高血压,约25%患有糖尿病和吸烟。三分之一的参与者既往有心肌梗死(表1)。除一项研究(Genereux等- 9个月)外,所有研究均报告了12个月的临床结果。(10)DBS组中只有1例心脏性死亡,而DES组中有6例心脏性死亡。对MACE(图1)、心肌梗死(MI)、支架血栓形成(ST)和靶病变血运重建(TLR)进行meta分析。DBS组的主要不良心脏事件(MACE)为13.3%,DES组为12.4%,RR为1.078 (Log RR = 0.07, p值= 0.612)(图1和表2)。其他测量结果显示两组均无优势。结论冠状动脉分叉病变支架置入术1年临床效果比较;专用分叉支架与药物洗脱支架在MACE、CD、MI、TLR和st方面无统计学差异
本文章由计算机程序翻译,如有差异,请以英文原文为准。
44 Dedicated bifurcation stents versus drug eluting stents in coronary bifurcation lesions: a systemic review and meta-analysis
Introduction Coronary bifurcation lesions (CBL) constitute a fifth of all coronary lesions and have no optimal method for treatment.(1) Multiple trials were conducted to investigate different modalities of treatment such as drug eluting stents, bioresorbable scaffolds, and dedicated bifurcation stents.(2) There are limited data discussing the clinical outcomes of these trials as most tend to report procedural outcomes.(3) This systematic review aimed to compare clinical outcomes of DBS compared to DES, while excluding bare metal stents and bioresorbable scaffolds.(4) Methods Following the PRISMA guidelines,(5) a systematic data search was conducted including EMBASE, PUBMED, MEDLINE, CINAHL, Cochrane database, TRIP database, and clinicaltrials.gov. Inclusion criteria were for prospective two-arm randomised trials published between the years from 2015 to 2018 comparing DBS and DES exclusively and reported clinical outcomes including cardiac death, myocardial infarction, target lesion revascularisation, and stent thrombosis. Risk of bias was assessed using Cochrane risk of bias assessment tool RoB1.(6) Two reviewers extracted data independently using Microsoft Excel 365 ProPlus. Meta-analysis is performed by restricted maximum-likelihood method comparing relative risks (RR) of clinical outcomes,(7) using MAJOR R pack through Jamovi platform and reported in logarithmic relative risk (Log RR).(8, 9) Results Six trials comparing DBS and DES involving 1914 patients met the inclusion criteria. Most of the studies were conducted in Europe, participants’ ages were DBS: 65.56, DES: 65.18 (p-value = 0.52). Participants of male gender were DBS: 74.9% DES: 77.5% (p-value = 0.44) and patients with smoking history were DBS: 28%, DES: 27.36% (p-value=0.70). Patients who presented with acute coronary syndrome were a fifth of all participants (p-value = 0.74). Around 70% of each arm participants had hypertension, and around 25% suffer from diabetes, as well as smoking. A third of participants had previous myocardial infarction (Table-1). Clinical outcomes were reported for 12 months in all study but one (Genereux et al. – 9 months).(10) There was only one cardiac death in the DBS arm compared to six cardiac deaths in the DES arm. A meta-analysis was performed for MACE (Figure-1), myocardial infarction (MI), stent thrombosis (ST), and target lesion revascularisation (TLR). Major adverse cardiac events (MACE) were 13.3% for DBS and 12.4% for DES with a RR of 1.078 (Log RR = 0.07, p-value = 0.612) (Figure-1 & Table-2). Other measured outcomes showed no superiority for either arms. Conclusion When comparing the one-year clinical outcomes for coronary bifurcation lesions stenting; there was no statistically significant difference between dedicated bifurcation stents and drug eluting stents regarding MACE, CD, MI, TLR, and ST. Conflict of Interest None
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