首页> 美国卫生研究院文献>British Medical Journal >Bare metal stents durable polymer drug eluting stents and biodegradable polymer drug eluting stents for coronary artery disease: mixed treatment comparison meta-analysis
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Bare metal stents durable polymer drug eluting stents and biodegradable polymer drug eluting stents for coronary artery disease: mixed treatment comparison meta-analysis

机译:用于冠状动脉疾病的裸金属支架耐用的聚合物药物洗脱支架和可生物降解的聚合物药物洗脱支架:混合治疗比较荟萃分析

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摘要

>Objective To compare the efficacy and safety of biodegradable polymer drug eluting stents with those of bare metal stents and durable polymer drug eluting stents.>Design Mixed treatment comparison meta-analysis of 258 544 patient years of follow-up from randomized trials.>Data sources and study selection PubMed, Embase, and Central were searched for randomized trials comparing any of the Food and Drug Administration approved durable polymer drug eluting stents (sirolimus eluting, paclitaxel eluting, cobalt chromium everolimus eluting, platinum chromium everolimus eluting, zotarolimus eluting-Endeavor, and zotarolimus eluting-Resolute) or biodegradable polymer drug eluting stents, with each other or against bare metal stents.>Outcomes Long term efficacy (target vessel revascularization, target lesion revascularization) and safety (death, myocardial infarction, stent thrombosis). Landmark analysis at more than one year was evaluated to assess the potential late benefit of biodegradable polymer drug eluting stents.>Results From 126 randomized trials and 258 544 patient years of follow-up, for long term efficacy (target vessel revascularization), biodegradable polymer drug eluting stents were superior to paclitaxel eluting stents (rate ratio 0.66, 95% credibility interval 0.57 to 0.78) and zotarolimus eluting stent-Endeavor (0.69, 0.56 to 0.84) but not to newer generation durable polymer drug eluting stents (for example: 1.03, 0.89 to 1.21 versus cobalt chromium everolimus eluting stents). Similarly, biodegradable polymer drug eluting stents were superior to paclitaxel eluting stents (rate ratio 0.61, 0.37 to 0.89) but inferior to cobalt chromium everolimus eluting stents (2.04, 1.27 to 3.35) for long term safety (definite stent thrombosis). In the landmark analysis after one year, biodegradable polymer drug eluting stents were superior to sirolimus eluting stents for definite stent thrombosis (rate ratio 0.29, 0.10 to 0.82) but were associated with increased mortality compared with cobalt chromium everolimus eluting stents (1.52, 1.02 to 2.22). Overall, among all stent types, the newer generation durable polymer drug eluting stents (zotarolimus eluting stent-Resolute, cobalt chromium everolimus eluting stents, and platinum chromium everolimus eluting stents) were the most efficacious (lowest target vessel revascularization rate) stents, and cobalt chromium everolimus eluting stents were the safest with significant reductions in definite stent thrombosis (rate ratio 0.35, 0.21 to 0.53), myocardial infarction (0.65, 0.55 to 0.75), and death (0.72, 0.58 to 0.90) compared with bare metal stents.>Conclusions Biodegradable polymer drug eluting stents are superior to first generation durable polymer drug eluting stents but not to newer generation durable polymer stents in reducing target vessel revascularization. Newer generation durable polymer stents, and especially cobalt chromium everolimus eluting stents, have the best combination of efficacy and safety. The utility of biodegradable polymer stents in the context of excellent clinical outcomes with newer generation durable polymer stents needs to be proven.
机译:>目的比较可生物降解的聚合物药物洗脱支架与裸金属支架和耐用的聚合物药物洗脱支架的疗效和安全性。>设计 258 treatment544混合治疗比较荟萃分析>数据来源和研究选择,对PubMed,Embase和Central进行了随机对照研究,比较了美国食品药品管理局批准的任何耐用的聚合物药物洗脱支架(西罗莫司洗脱) ,紫杉醇洗脱,钴铬依维莫司洗脱,铂铬依维莫司洗脱,佐他莫司洗脱-Endeavor和佐他莫司洗脱-牢固)或可生物降解的聚合物药物洗脱支架彼此结合或相对于裸金属支架。>结果术语疗效(靶血管血运重建,靶病变血运重建)和安全性(死亡,心肌梗塞,支架血栓形成)。 >结果来自126个随机试验和258 544病人年的随访,以评估长期疗效(目标),对超过一年的里程碑式分析进行了评估,以评估可生物降解聚合物药物洗脱支架的潜在后期获益。血管血运重建),可生物降解的聚合物药物洗脱支架优于紫杉醇洗脱支架(比率为0.66,95%可信区间为0.57至0.78)和佐他莫司洗脱支架-Endeavor(0.69,0.56至0.84),但不优于新一代的耐用聚合物药物洗脱支架(例如:相对于钴铬依维莫司洗脱支架的1.03、0.89至1.21)。同样,可生物降解的聚合物药物洗脱支架在长期安全性(明确的支架血栓形成)方面优于紫杉醇洗脱支架(比率0.61,0.37至0.89),但次于钴铬依维莫司洗脱支架(2.04,1.27至3.35)。在一年后的里程碑式分析中,在确定性支架血栓形成方面,可生物降解的聚合物药物洗脱支架优于西罗莫司洗脱支架(比率0.29,0.10至0.82),但与钴铬依维莫司洗脱支架相比(1.52,1.02至1.02)具有更高的死亡率。 2.22)。总体而言,在所有类型的支架中,新一代耐用型聚合物药物洗脱支架(左唑佐莫司洗脱支架-Resolute,钴铬依维莫司洗脱支架和铂铬依维莫司洗脱支架)是最有效的(目标血管血运重建率最低),而钴铬依维莫司洗脱支架最安全,与裸金属支架相比,明确的支架血栓形成(比率0.35,0.21至0.53),心肌梗塞(0.65,0.55至0.75)和死亡(0.72,0.58至0.90)显着降低。 strong>结论可生物降解的聚合物药物洗脱支架在减少目标血管血运重建方面优于第一代耐用聚合物药物洗脱支架,但不优于新一代耐用聚合物聚合物洗脱支架。新一代耐用聚合物支架,尤其是钴铬依维莫司洗脱钴支架,具有疗效和安全性的最佳组合。需要证明生物可降解聚合物支架在具有新一代耐用聚合物支架的优异临床效果的背景下的实用性。

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