Long-term clinical outcomes after drug-eluting and bare-metal stenting in Massachusetts.
Long-term clinical outcomes after drug-eluting and bare-metal stenting in Massachusetts.
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DOI:
10.1161/circulationaha.108.781377
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发表时间:
2008-10-28
期刊:
影响因子:
37.8
通讯作者:
Normand SL
中科院分区:
文献类型:
--
作者:
Mauri L;Silbaugh TS;Wolf RE;Zelevinsky K;Lovett A;Zhou Z;Resnic FS;Normand SL
Drug-eluting stents (DES) reduce the need for repeat revascularization, but their long term safety relative to bare metal stents (BMS) in general use remains uncertain. We sought to compare the clinical outcome of patients treated with DES vs. BMS. All adults undergoing percutaneous coronary intervention (PCI) with stenting between April 1, 2003 and September 30, 2004 at non-US governmental hospitals in Massachusetts were identified from a mandatory state database. Patients were classified according to stent types used from the index admission. Clinical and procedural risk factors were collected prospectively. Risk-adjusted mortality, myocardial infarction, and revascularization rate differences (DES-BMS) were estimated through propensity score matching without replacement. 11556 patients were treated with DES and 6237 treated with BMS with unadjusted 2 year mortality of 7.0% and 12.6% respectively (p<0.0001). In 5549 DES patients matched to 5549 BMS patients, 2 year risk-adjusted mortality rates were 9.8% and 12.0% (p=0.0002), myocardial infarction, 8.3% vs. 10.3% (p=0.0005), and target vessel revascularization, 11.0% vs. 16.8% (p<0.0001). DES treatment was associated with lower mortality, myocardial infarction, and target vessel revascularization compared with BMS treatment in similar patients in a matched population based study. Comprehensive follow-up in this inclusive population is warranted to identify if similar safety and efficacy remain beyond 2 years.