Drug-Eluting Stents versus Bare Metal Stents Prior to Noncardiac Surgery

被引:9
作者
Bangalore, Sripal [1 ]
Silbaugh, Treacy S. [2 ]
Normand, Sharon-Lise T. [2 ,3 ]
Lovett, Ann F. [2 ]
Welt, Frederick G. P. [2 ,4 ]
Resnic, Frederic S. [2 ,5 ]
机构
[1] NYU, Sch Med, New York, NY 10016 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Boston, MA 02115 USA
[5] Lahey Clin Fdn, Boston, MA USA
关键词
bare metal stents; drug-eluting stents; noncardiac surgery; CORONARY STENTS; CARDIAC EVENTS; ANTIPLATELET THERAPY; PROPENSITY SCORE; RISK; THROMBOSIS; DISCONTINUATION; COMPLICATIONS; INCREASE; OUTCOMES;
D O I
10.1002/ccd.25617
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe safety of drug-eluting stents (DES) vs. bare metal stents (BMS) in the perioperative setting, a heightened state of inflammation and thrombosis is not well defined. MethodsAll adults undergoing noncardiac surgical (NCS) procedures within 1 year following percutaneous coronary intervention (PCI) in Massachusetts between April 1, 2004, and September 30, 2007, were identified from an administrative claims database. Patients were divided into those who received BMS vs. DES at index PCI. Primary net clinical outcome was death, myocardial infarction (MI) or bleeding within 30 days of NCS. Primary clinical outcome was 30-day death or MI. ResultsAmong 8,415 (22% BMS) patients that satisfied our inclusion criteria, 1,838 BMS patients were matched with 3,565 DES patients with similar propensity scores. In the DES cohort, the 30-day primary net clinical outcome rate was lower with longer time from PCI to NCS (P=0.02) with lowest rates if NCS was performed after 90 days from PCI (event rate 8.57, 7.53, 5.21, and 5.75% for 1-30, 31-90, 91-180, and 181-365 days from PCI to NCS). However, in the BMS cohort, the event rate was uniformly high regardless of the time from PCI to NCS (P=0.60) (event rate 8.20, 6.56, 8.05, and 8.82% for 1-30, 31-90, 91-180, and 181-365 days from PCI to NCS). There was no significant difference between DES and the BMS group for 30-day primary net clinical outcome (6.64 vs. 7.89%; P=0.10), but there was a 26% lower odds of primary clinical outcome (OR=0.74, 95% CI 0.58-0.94) with DES when compared with BMS, driven mainly by differences in event rates when NCS was performed >90 days post PCI. ConclusionDES implantation was not associated with higher adverse events after NCS. Moreover, the incidence of adverse events following NCS was lower when NCS was performed >90 days post-DES implantation suggesting that it may not be necessary to wait until 12 months post PCI with DES before NCS. (c) 2014 Wiley Periodicals, Inc.
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收藏
页码:533 / 541
页数:9
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