Titanium-Nitride-Oxide–Coated vs Everolimus-Eluting Stents in Acute Coronary Syndrome

Author:

Bouisset Frederic12,Sia Jussi3,Mizukami Takuya14,Karjalainen Pasi P.5,Tonino Pim A. L.6,Pijls Nico H. J.6,Van der Heyden Jan7,Romppanen Hannu8,Kervinen Kari9,Airaksinen Juhani K. E.10,Lalmand Jacques11,Frambach Peter12,Roza da Costa Bruno13,Collet Carlos1,De Bruyne Bernard114,

Affiliation:

1. Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium

2. Departement of Cardiology, Toulouse University Hospital, Toulouse, France

3. Department of Cardiology, Kokkola Central Hospital, Kokkola, Finland

4. Division of Clinical Pharmacology, Department of Pharmacology, Showa University, Tokyo, Japan

5. Heart and Lung Center, Helsinki University and Helsinki University Hospital, Helsinki, Finland

6. Catharina Hospital, Eindhoven, the Netherlands

7. St Antonius Hospital, Nieuwegein, the Netherlands

8. Kuopio Heart Center, University of Kuopio, Kuopio, Finland

9. Clinical Research Center, Oulu University Hospital, Oulu, Finland

10. Turku Heart Center, University of Turku, Turku, Finland

11. CHU de Charleroi, Charleroi, Belgium

12. INCCI Luxembourg Hospital, Luxembourg City, Luxembourg

13. Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom

14. Lausanne University Center Hospital, Lausanne, Switzerland

Abstract

ImportanceTitanium-nitride-oxide (TiNO)–coated stents show faster strut coverage compared with drug-eluting stents without excessive intimal-hyperplasia observed in bare metal stents. It is important to study long-term clinical outcomes after treatment of patients with an acute coronary syndrome (ACS) by TiNO-coated stents, which are neither drug-eluting stents nor bare metal stents.ObjectiveTo compare the rate of main composite outcome of cardiac death, myocardial infarction (MI), or ischemia-driven target lesion revascularization at 5 years in patients with ACS randomized to receive either a TiNO-coated stent or a third-generation everolimus-eluting stent (EES).Design, Setting, and ParticipantsThis multicenter, randomized, controlled, open-label trial was conducted in 12 clinical sites in 5 European countries and enrolled patients from January 2014 to August 2016. Patients presenting with ACS (ST-segment elevation MI, non–ST-segment elevation MI, and unstable angina) with at least 1 de novo lesion were randomized to receive either a TiNO-coated stent or an EES. The present report analyzes the long-term follow-up for the main composite outcome and its individual components. Analysis took place between November 2022 to March 2023.Main outcomeThe primary end point was a composite of cardiac death, MI, or target lesion revascularization at 12-month follow-up.ResultsA total of 1491 patients with ACS were randomly assigned to receive either TiNO-coated stents (989 [66.3%]) or EES (502 [33.7%]). The mean (SD) age was 62.7 (10.8) years, and 363 (24.3%) were female. At 5 years, the main composite outcome events occurred in 111 patients (11.2%) in the TiNO group vs 60 patients (12%) in the EES group (hazard ratio [HR], 0.94; 95% CI, 0.69-1.28; P = .69). The rate of cardiac death was 0.9% (9 of 989) vs 3.0% (15 of 502) (HR, 0.30; 95% CI, 0.13-0.69; P = .005), the rate of MI was 4.6% (45 of 989) vs 7.0% (35 of 502) (HR, 0.64; 95% CI, 0.41-0.99; P = .049), the rate of stent thrombosis was 1.2% (12 of 989) vs 2.8% (14 of 502) (HR, 0.43; 95% CI, 0.20-0.93; P = .034), and the rate of target lesion revascularization was 7.4% (73 of 989) vs 6.4% (32 of 502) (HR, 1.16; 95% CI, 0.77-1.76; P = .47) in the TiNO-coated stent arm and in the EES arm, respectively.Conclusion and relevanceIn this study, patients with ACS had a main composite outcome that was not different 5 years after TiNO-coated stent or EES.Trial RegistrationClinicalTrials.gov Identifier: NCT02049229

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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