Paclitaxel-eluting stents versus paclitaxel-coated balloons in coronary artery disease: a meta-analysis of randomized controlled trials

B. G. de Liyis, Made Dhiyo Wiweka Aryaweda, Luh Oliva Saraswati Suastika
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Abstract

The efficacy of drug-coated balloons (DCB) versus drug-eluting stents (DES) for coronary artery disease (CAD) remains inconclusive. Despite paclitaxel's common use in both DES and DCB, there is a lack of meta-analyses comparing paclitaxel-eluting stents (PES) and paclitaxel-coated balloons (PCB). This meta-analysis aims to evaluate and compare DES and DCB outcomes using paclitaxel. A Systematic literature search in Medline and Cochrane databases yielded six randomized controlled trials with 951 patients (1:1 ratio). Primary endpoints were mortality, target lesion vascularization (TLV), myocardial infarction (MI), target vessel revascularization (TVR), and major adverse cardiovascular events (MACEs). Secondary endpoints included in-device binary stenosis, in-segment binary stenosis, late luminal loss (LLL), post minimal lumen diameter (MLD), and post diameter stenosis. Within the study populations, the incidence of previous MI was significantly lower in the PES group compared to the PCB group (26.70% vs. 39.22%, OR:0.56, 95%CI:0.41–0.76, p=0.0002).  The meta-analysis results showed that mortality (OR:1.57, 95%CI:0.67-3.66, p=0.29), TLV (OR:0.74, 95%CI:0.37-1.48, p=0.39), MI (OR:1.76, 95%CI:0.79-3.88, p=0.16), TVR (OR:0.76, 95%CI:0.51-1.12, p=0.16), and MACEs (OR:1.11, 95%CI:0.48-2.58, p=0.81) did not exhibit significant differences between PES and PCB group in CAD. Furthermore, in stent or in balloon binary stenosis (OR:0.80, 95%CI:0.34-1.87, p=0.60), in segment binary stenosis (OR:1.16, 95%CI:0.48-2.80, p=0.74), LLL (MD:0.03, 95%CI:-0.11 to 0.17, p=0.65), post MLD (MD:0.04, 95%CI:-0.23 to 0.30, p=0.77), and post diameter stenosis (MD:-5.48, 95%CI:-13.88 to 2.92, p=0.20) were similar in both groups. Our comprehensive analysis concludes that both PES and PCB manifest comparable effectiveness and safety in the management of CAD.
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紫杉醇洗脱支架与紫杉醇涂层球囊治疗冠心病:随机对照试验的荟萃分析
药物涂层球囊(DCB)与药物洗脱支架(DES)对冠状动脉疾病(CAD)的疗效仍无定论。尽管紫杉醇常用于药物洗脱支架(DES)和药物涂层球囊(DCB),但缺乏比较紫杉醇洗脱支架(PES)和紫杉醇涂层球囊(PCB)的荟萃分析。本荟萃分析旨在评估和比较使用紫杉醇的 DES 和 DCB 的疗效。通过在 Medline 和 Cochrane 数据库中进行系统文献检索,得出了六项随机对照试验,共 951 名患者(1:1 的比例)。主要终点包括死亡率、靶病变血管化(TLV)、心肌梗死(MI)、靶血管血运重建(TVR)和主要不良心血管事件(MACE)。次要终点包括器内二元狭窄、段内二元狭窄、晚期管腔损失(LLL)、最小管腔后直径(MLD)和直径后狭窄。在研究人群中,PES 组既往心肌梗死的发生率明显低于 PCB 组(26.70% 对 39.22%,OR:0.56,95%CI:0.41-0.76,P=0.0002)。 荟萃分析结果显示,死亡率(OR:1.57,95%CI:0.67-3.66,P=0.29)、TLV(OR:0.74,95%CI:0.37-1.48,P=0.39)、MI(OR:1.76,95%CI:0.79-3.88,P=0.16)、TVR(OR:0.76,95%CI:0.51-1.12,p=0.16)和MACEs(OR:1.11,95%CI:0.48-2.58,p=0.81)在PES组和PCB组的CAD之间没有表现出显著差异。此外,在支架或球囊二元狭窄(OR:0.80,95%CI:0.34-1.87,p=0.60)、节段二元狭窄(OR:1.16,95%CI:0.48-2.80,p=0.74)、LLL(MD:0.03,95%CI:-0.11至0.17,p=0.65)、MLD后(MD:0.04,95%CI:-0.23至0.30,p=0.77)和直径狭窄后(MD:-5.48,95%CI:-13.88至2.92,p=0.20)在两组中相似。我们的综合分析得出结论,PES 和 PCB 在治疗 CAD 方面的有效性和安全性相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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