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基于真实世界证据的可生物降解聚合物与耐用聚合物药物洗脱支架的成本效益分析。

Cost-effectiveness analysis of biodegradable polymer versus durable polymer drug-eluting stents incorporating real-world evidence.

机构信息

Pharmacy and Therapeutics Office, Group Health Informatics, National Healthcare Group, Singapore, Singapore.

Department of Cardiology, National University Heart Centre, Singapore, Singapore.

出版信息

Cardiovasc Ther. 2018 Oct;36(5):e12442. doi: 10.1111/1755-5922.12442. Epub 2018 Jun 28.

DOI:10.1111/1755-5922.12442
PMID:29873191
Abstract

AIM

Compared with second-generation durable polymer drug-eluting stents (DP-DES), the cost-effectiveness of biodegradable polymer drug-eluting stents (BP-DES) remains unclear in the real-world setting. We assessed the cost-effectiveness of BP-DES in patients with coronary artery disease undergoing percutaneous coronary intervention (PCI).

METHODS

We developed a decision-analytic model to compare the cost-effectiveness of BP-DES to DP-DES over 1 year and 5 years from healthcare payer perspective. Relative treatment effects during the first year post-PCI were obtained from a real-world population analysis while clinical event risks in the subsequent 4 years were derived from a meta-analysis of published studies.

RESULTS

At 1 year, based on the clinical data analysis of 497 propensity-score matched pairs of patients, BP-DES were associated with an incremental cost-effectiveness ratio (ICER) of USD20 503 per quality-adjusted life-year (QALY) gained. At 5 years, BP-DES yielded an ICER of USD4062 per QALY gained. At the willingness-to-pay threshold of USD50 400 (one gross domestic product per capita in Singapore in 2015), BP-DES were cost-effective. Sensitivity analysis showed that the cost of stents had a significant impact on the cost-effectiveness of BP-DES. Threshold analysis demonstrated that if the cost difference between BP-DES and DP-DES exceeded USD493, BP-DES would not be cost-effective in patients with 1 year of follow-up.

CONCLUSIONS

Biodegradable polymer drug-eluting stents were cost-effective compared with DP-DES in patients with coronary artery disease at 1 year and 5 years after PCI. It is worth noting that the cost of stents had a significant impact on the findings.

摘要

目的

与第二代耐用聚合物药物洗脱支架(DP-DES)相比,可生物降解聚合物药物洗脱支架(BP-DES)在真实环境中的成本效益尚不清楚。我们评估了经皮冠状动脉介入治疗(PCI)后冠心病患者使用 BP-DES 的成本效益。

方法

我们从医疗保健支付者的角度出发,建立了一个决策分析模型,比较了 BP-DES 和 DP-DES 在 1 年和 5 年时的成本效益。PCI 后第一年的相对治疗效果来自真实人群分析,随后 4 年的临床事件风险来自已发表研究的荟萃分析。

结果

根据 497 对倾向评分匹配患者的临床数据分析,BP-DES 在 1 年内的增量成本效果比(ICER)为每获得 1 个质量调整生命年(QALY)增加 20503 美元。在 5 年内,BP-DES 每获得 1 个 QALY 的 ICER 为 4062 美元。在愿意支付的 50400 美元(2015 年新加坡人均国内生产总值)阈值下,BP-DES 具有成本效益。敏感性分析表明,支架的成本对 BP-DES 的成本效益有重大影响。阈值分析表明,如果 BP-DES 和 DP-DES 之间的成本差异超过 493 美元,BP-DES 在 1 年随访的患者中就不具有成本效益。

结论

在 PCI 后 1 年和 5 年时,与 DP-DES 相比,BP-DES 对冠心病患者具有成本效益。值得注意的是,支架的成本对结果有重大影响。

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