AI Article Synopsis

  • The study aims to assess the long-term effectiveness and cost-efficacy of drug-eluting stents (DES) in patients undergoing multivessel coronary interventions, focusing on real-world data over a 2-year period.
  • Results showed that patients using DES experienced fewer major adverse cardiac events and complications compared to those using bare-metal stents (BMS), particularly in high-risk patients, but there was no significant difference when comparing DES alone to a mixed approach.
  • The conclusion highlights that while DES are more costly, they provide better clinical outcomes and are cost-effective for high-risk patients, particularly when compared to BMS, in a real-world setting.

Article 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.

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