首页> 外文期刊>Catheterization and cardiovascular interventions: Official journal of the Society for Cardiac Angiography & Interventions >Poly (l-lactic acid) bioresorbable scaffolds versus metallic drug-eluting stents for the treatment of coronary artery disease: A meta-analysis of 11 randomized trials
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Poly (l-lactic acid) bioresorbable scaffolds versus metallic drug-eluting stents for the treatment of coronary artery disease: A meta-analysis of 11 randomized trials

机译:聚(L-乳酸)生物可吸收支架与金属药物洗脱支架用于治疗冠状动脉疾病:11种随机试验的META分析

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Background Bioresorbable vascular scaffolds (BVS) have been proposed for overcoming the long-term limitations of permanent metallic stents, while theoretically warranting similar advantages in plaque stabilization and anti-restenotic drug delivery in the early postrevascularization phase. However, increased rates of malapposition, restenosis, or thrombosis have emerged from initial trials with BVS, that were nevertheless underpowered for the evaluation of the real outcome benefits of these coronary devices. The recent completion of newer randomized clinical trials paves the way to the present meta-analysis, aiming at the comparison of Poly (l-Lactic acid) BVS (PLLA-BVS) versus metallic drug-eluting stents (DES) in the treatment of coronary stenoses. Methods Literature and main scientific session abstracts were searched for randomized clinical trials (RCTs) comparing drug-eluting BVS versus metallic DES for the treatment of coronary artery disease (CAD). The primary efficacy endpoint was mortality, secondary endpoints were cardiovascular death, myocardial infarction, target lesion revascularization (TLR), stent thrombosis and the composite of device-oriented target lesion failure (TLF). Results We included 11 randomized trials, for a total population of 10,707 patients, 54.5% treated with BVS. The major indication for PCI was stable CAD, whereas acute coronary syndrome represented 30% of the patients. At a mean follow-up of 2.64 years (1-5 years), mortality occurred in 2.71% of the patients, with no difference according to the type of implanted stent (OR[95%CI] = 0.94 [0.74, 1.20], p = .62). No interaction was observed according to patients' risk profile or the rate of diabetes and ACS. However, a significant increase in myocardial infarction, stent thrombosis, TLR and TLF was observed with BVS as compared to DES. Conclusions The present meta-analysis provides the most updated data on the use of PLLA-BVS for the treatment of CAD. We documented a poorer performance of these new coronary devices, as compared to new generation metallic DES, being associated with an increased rate of recurrent cardiovascular events. However, such ischemic complications did not impact on mortality, with a comparable survival independently from the type of stent.
机译:背景生物可吸收血管支架(BVS)已被提出用于克服永久性金属支架的长期局限性,同时在理论上保证在血管重建早期的斑块稳定和抗再狭窄药物输送方面具有类似的优势。然而,在BVS的初步试验中,出现了更多的对位不良、再狭窄或血栓形成的发生率,但在评估这些冠状动脉装置的实际结果益处方面,这些研究还不够充分。最近完成的新的随机临床试验为目前的荟萃分析铺平了道路,旨在比较聚(l-乳酸)BVS(PLLA-BVS)和金属药物洗脱支架(DES)在治疗冠状动脉狭窄中的作用。方法检索文献和主要科学会议摘要,比较药物洗脱BVS和金属DES治疗冠心病(CAD)的随机临床试验(RCT)。主要疗效终点是死亡率,次要终点是心血管死亡、心肌梗死、靶病变血运重建(TLR)、支架血栓形成和器械导向靶病变衰竭(TLF)的复合物。结果我们包括11项随机试验,共10707名患者,54.5%接受BVS治疗。PCI的主要适应症是稳定的CAD,而急性冠脉综合征占患者的30%。在平均随访2.64年(1-5年)时,2.71%的患者发生死亡率,根据植入支架的类型没有差异(或[95%CI]=0.94[0.74,1.20],p=0.62)。根据患者的风险状况或糖尿病和ACS的发病率,未观察到相互作用。然而,与DES相比,BVS组心肌梗死、支架血栓形成、TLR和TLF显著增加。结论本荟萃分析提供了PLLA-BVS治疗冠心病的最新数据。我们证明,与新一代金属DES相比,这些新型冠状动脉装置的性能较差,与心血管事件复发率增加有关。然而,这种缺血性并发症对死亡率没有影响,与支架类型无关的存活率具有可比性。

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