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  3. Unselected Use of Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent Versus Durable Polymer Everolimus-Eluting Stent for Coronary Revascularization.
 

Unselected Use of Ultrathin Strut Biodegradable Polymer Sirolimus-Eluting Stent Versus Durable Polymer Everolimus-Eluting Stent for Coronary Revascularization.

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BORIS DOI
10.7892/boris.121283
Publisher DOI
10.1161/CIRCINTERVENTIONS.118.006741
PubMed ID
30354590
Description
BACKGROUND

Biodegradable polymer sirolimus-eluting stents (BP-SESs) have been reported to be noninferior compared with durable polymer everolimus-eluting stents (DP-EES) in a randomized clinical trial. We sought to compare the efficacy and safety of an ultrathin strut BP-SES with a DP-EES in an all-comers population.

METHODS AND RESULTS

Among 7640 consecutive patients who underwent percutaneous coronary intervention between March 2011 and June 2015, 4638 patients were exclusively treated with BP-SES (N=1896; 3137 lesions) or DP-EES (N=2742; 4468 lesions). After propensity score matching within strata of clinical indications, the final study population consisted of 2902 matched patients (BP-SES 2406 lesions and DP-EES 2368 lesions). The primary device-oriented composite end point (DOCE) included cardiac death, target vessel myocardial infarction, and target lesion revascularization at 1 year. BP-SES (6.9%) was noninferior to DP-EES (8.0%) with respect to device-oriented composite end point (hazard ratio [HR], 0.85; 95% CI, 0.65-1.11; P for noninferiority <0.001; P for superiority=0.24). No differences in cardiac death (BP-SES, 2.3% versus DP-EES, 3.0%; HR, 0.76; 95% CI, 0.49-1.20; P=0.25), myocardial infarction (BP-SES, 4.6% versus DP-EES, 4.6%; HR, 1.00; 95% CI, 0.71-1.40; P=0.99), or target lesion revascularization (BP-SES, 2.8% versus DP-EES, 2.5%; HR, 1.11; 95% CI, 0.71-1.74; P=0.65) were observed. The rate of periprocedural myocardial infarction was comparable between the 2 groups (2.1% versus 2.2%; HR, 0.97; 95% CI, 0.59-1.58; P=0.89). The rate of definite stent thrombosis was similarly low throughout 1 year (BP-SES, 0.8% versus DP-EES, 0.8%; HR, 1.00; 95% CI, 0.45-2.22; P=1.00).

CONCLUSIONS

In a consecutively enrolled percutaneous coronary intervention population reflecting routine clinical practice, BP-SES was noninferior to DP-EES for device-oriented composite end point at 1 year.

CLINICAL TRIAL REGISTRATION

URL: https://www.clinicaltrials.gov . Unique identifier: NCT02241291.
Date of Publication
2018-09
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
300 Social sciences, sociology & anthropology > 360 Social problems & social services
Keyword(s)
coronary artery disease drug-eluting stents stents thrombosis
Language(s)
en
Contributor(s)
Yamaji, Kyohei
Universitätsklinik für Kardiologie
Zanchin, Thomas
Zanchin, Christian
Universitätsklinik für Kardiologie
Stortecky, Stefan
Universitätsklinik für Kardiologie
Koskinas, Konstantinos
Universitätsklinik für Kardiologie
Hunziker Munsch, Lukas Christoph
Universitätsklinik für Kardiologie
Praz, Fabien Daniel
Universitätsklinik für Kardiologie
Blöchlinger, Stefan
Universitätsklinik für Kardiologie
Moro, Christina
Moschovitis, Aris
Universitätsklinik für Kardiologie
Seiler, Christian
Universitätsklinik für Kardiologie
Valgimigli, Marco
Universitätsklinik für Kardiologie
Billinger, Michael
Universitätsklinik für Kardiologie
Pilgrim, Thomas
Universitätsklinik für Kardiologie
Heg, Dierik Hansorcid-logo
Clinical Trials Unit Bern (CTU)
Institut für Sozial- und Präventivmedizin (ISPM)
Windecker, Stephan
Universitätsklinik für Kardiologie
Räber, Lorenz
Universitätsklinik für Kardiologie
Additional Credits
Universitätsklinik für Kardiologie
Clinical Trials Unit Bern (CTU)
Series
Circulation: Cardiovascular interventions
Publisher
Lippincott Williams & Wilkins
ISSN
1941-7632
Access(Rights)
restricted
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