Patients with higher-atherothrombotic risk vs. lower-atherothrombotic risk undergoing coronary intervention with newer-generation drug-eluting stents: an analysis from the randomized BIOFLOW trials

被引:3
|
作者
Hemetsberger, Rayyan [1 ]
Mankerious, Nader [2 ]
Toelg, Ralph [2 ]
Abdelghani, Mohammad [3 ,4 ]
Farhan, Serdar [5 ]
Garcia-Garica, Hector M. [6 ]
Allali, Abdelhakim [7 ]
Windecker, Stephan [8 ]
Lefevre, Thierry [9 ]
Saito, Shigeru [10 ]
Kandzari, David [11 ]
Waksman, Ron [6 ]
Richardt, Gert [2 ]
机构
[1] Med Univ Vienna, Dept Internal Med 2, Div Cardiol, Wahringer Gurtel 18-20, A-1090 Vienna, Austria
[2] Segeberger Kliniken GmbH, Heart Ctr Bad Segeberg, Bad Segeberg, Germany
[3] Al Azhar Univ, Cardiol Dept, Cairo, Egypt
[4] Univ Amsterdam, Amsterdam Univ Med Ctr, Cardiol Dept, Amsterdam, Netherlands
[5] Icahn Sch Med Mt Sinai, Zena & Michael A Wiener Cardiovasc Inst, New York, NY USA
[6] Medstar Washington Hosp Ctr, Intervent Cardiol, Washington, DC USA
[7] Univ Heart Ctr Lubeck, Med Clin 2, Lubeck, Germany
[8] Univ Hosp, Inselspital, Bern, Switzerland
[9] Hosp Prive Jaques Cartier, Massy, France
[10] Okinawa Tokushukai Shonan Kamakura Gen Hosp, Kamakura, Japan
[11] Piedmont Heart Inst, Atlanta, GA USA
关键词
BIOFLOW; Newer-generation drug-eluting stent; Orsiro; Xience; High atherothrombotic risk; CARDIOVASCULAR-DISEASES; CLOPIDOGREL; ULTRATHIN; SAFETY;
D O I
10.1007/s00392-023-02205-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Patients with atherothrombotic risk are at high hazard of ischemic events. Preventive medicine plays a major role in modifying their outcomes. Whether the choice of a BP-SES or DP-EES can contribute to the occurrence of events remains unclear. We sought to investigate the outcomes of patients with higher atherothrombotic risk (H-ATR) versus lower atherothrombotic risk (L-ATR) undergoing percutaneous coronary intervention (PCI) with either bioresorbable-polymer sirolimus-eluting stent (BP-SES) or durable-polymer everolimus-eluting stent (DP-EES).Methods Patients (n = 2361) from BIOFLOW-II,-IV, and-V randomized trials were categorized into H-ATR vs. L-ATR. L-ATR patients had = 1 and H-ATR = 2 of the following criteria: presentation in ACS, diabetes mellitus, previous myocardial infarction, previous PCI/CABG, or previous stroke. Endpoints were target lesion failure (TLF: cardiac death, target-vessel myocardial infarction [TV-MI], target lesion revascularization [TLR]) and stent thrombosis (ST) at three years.Results H-ATR patients (n = 1023) were more morbid than L-ATR patients (n = 1338). TLF rate was significantly higher in H-ATR patients as compared with L-ATR (11.6% vs. 7.0%; HR 1.67, 95% CI 1.27-2.20, p < 0.0001). With BP-SES TLF rates were numerically lower as compared with DP-EES in H-ATR (10.5% vs. 13.5%; HR 0.78, 95% CI 0.54-1.14, p = 0.20) and significantly lower in L-ATR (5.6% vs. 9.8%; HR 0.57, 95% CI 0.38-0.85, p = 0.006).Conclusion In the era of newer-generation DES, patients with H-ATR still are at hazard for ischemic events. Patients with BP-SES had lower TLF rates as compared with DP-EES, most consistent in L-ATR whereas in H-ATR patients most prob-ably secondary preventive strategies are of higher value.
引用
收藏
页码:1278 / 1287
页数:10
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