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多支血管经皮冠状动脉介入治疗中药物洗脱支架、裸金属支架和混合策略在高、低重复血运重建风险患者中的长期临床结局和成本效益分析。

Long-term clinical outcomes and cost-effectiveness analysis in multivessel percutaneous coronary interventions: comparison of drug-eluting stents, bare-metal stents and a mixed approach in patients at high and low risk of repeat revascularisation.

机构信息

Ospedale S. Maria delle Croci, Ravenna, Italy.

出版信息

EuroIntervention. 2010 Apr;5(8):953-61.

Abstract

AIMS

To evaluate the long-term effectiveness and cost-efficacy of drug-eluting stents (DES) in a real world setting of multivessel percutaneous coronary intervention (PCI).

METHODS AND RESULTS

We evaluated the 2-year outcome of all multivessel PCI in de novo lesions enrolled in a prospective web-based multicentre registry from July 2003 to December 2006. Among the 2,898 eligible patients, 1,315 were treated with bare-metal stent (BMS) alone, 657 with DES alone, and 926 with both. At 2-years, use of DES was associated with a lower propensity score adjusted incidence of major adverse cardiac events (MACE), death and myocardial infarction, and target vessel revascularisation (TVR) compared with BMS but only in patients at high risk of TVR. No difference was apparent between "pure" DES and the mixed approach. The matched cost-effectiveness analysis revealed DES to be more costly and more effective with a reasonable incremental cost-efficacy ratio for any MACE avoided only in patients with a high risk of TVR and only in comparison with "pure" BMS patients.

CONCLUSIONS

In this real-world multivessel PCI registry, the use of DES and a mixed approach were associated with a 2-year reduction of adverse clinical outcomes in comparison with BMS especially in patients with a high risk of TVR. DES were cost-effective only in patients at high risk of TVR.

摘要

目的

评估药物洗脱支架(DES)在多血管经皮冠状动脉介入治疗(PCI)真实世界环境中的长期疗效和成本效益。

方法和结果

我们评估了 2003 年 7 月至 2006 年 12 月期间一项前瞻性基于网络的多中心注册研究中多血管初发型病变患者的 2 年结果。在 2898 名合格患者中,1315 名接受单纯金属裸支架(BMS)治疗,657 名接受单纯 DES 治疗,926 名接受 BMS 和 DES 联合治疗。在 2 年时,与 BMS 相比,DES 的使用与较低的主要不良心脏事件(MACE)、死亡和心肌梗死发生率以及靶血管血运重建(TVR)的倾向评分调整发生率相关,但仅在高 TVR 风险患者中。“纯”DES 与混合方法之间没有明显差异。匹配的成本效益分析显示,DES 更昂贵,但更有效,具有合理的增量成本效益比,仅在高 TVR 风险患者中,与“纯”BMS 患者相比,任何 MACE 都可避免。

结论

在这个真实世界的多血管 PCI 注册研究中,与 BMS 相比,DES 和混合方法的使用与 2 年时不良临床结局的减少相关,尤其是在高 TVR 风险患者中。DES 仅在高 TVR 风险患者中具有成本效益。

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