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Angiographic and clinical performance of polymer-free biolimus-eluting stent in patients with ST-segment elevation acute myocardial infarction in a metropolitan public hospital: The BESAMI MUCHO study.
Sgueglia, Gregory A; D'Errico, Fabrizio; Gioffrè, Gaetano; De Santis, Antonella; Summaria, Francesco; Piccioni, Fabiana; Gaspardone, Achille.
Afiliação
  • Sgueglia GA; Sant'Eugenio Hospital, Rome, Italy.
  • D'Errico F; Sant'Eugenio Hospital, Rome, Italy.
  • Gioffrè G; Sant'Eugenio Hospital, Rome, Italy.
  • De Santis A; Sant'Eugenio Hospital, Rome, Italy.
  • Summaria F; Sant'Eugenio Hospital, Rome, Italy.
  • Piccioni F; Sant'Eugenio Hospital, Rome, Italy.
  • Gaspardone A; Sant'Eugenio Hospital, Rome, Italy.
Catheter Cardiovasc Interv ; 91(5): 851-858, 2018 04 01.
Article em En | MEDLINE | ID: mdl-28766881
ABSTRACT

OBJECTIVES:

This study aimed at assessing the performance of a new generation polymer-free biolimus-eluting stent (BES) in real-world patients with ST-segment elevation myocardial infarction (STEMI).

BACKGROUND:

Polymers components of early-generation drug-eluting stents have been implicated in the pathogenesis of delayed arterial healing, vessel remodeling, and delayed stent thrombosis. Recently, a novel polymer-free BES has shown excellent clinical performance in clinical trial setting.

METHODS:

Overall, 175 consecutive patients (64 ± 14 years, 141 men) treated with the BioFreedom (Biosensors Europe, Morges, Switzerland) polymer-free BES because of STEMI were included in this study. The primary endpoint was the rate of major adverse cardiac events (MACE), a composite of cardiac death, recurrent myocardial infarction, and ischemia-driven target vessel revascularization at 1 year follow-up. A subgroup of patients underwent 6-month angiographic follow-up. Dual antiplatelet therapy was prescribed for 12 months after STEMI.

RESULTS:

At 1 year, the cumulative rate of MACE was 4.6%. One patient (0.6%) had an arrhythmic cardiac death and five (2.9%) had ischemia-driven target vessel revascularization, although only three (1.7%) had target lesion revascularization. Two (1.1%) patients had acute stent thrombosis yielding nonfatal myocardial infarction. In 70 patients (63 ± 14 years, 61 men), quantitative coronary angiography at 6-month follow-up revealed diameter stenosis of 24.1 ± 13.7% and minimal lumen diameter of 2.29 ± 0.56 mm, yielding a late lumen loss of 0.13 ± 0.14 mm.

CONCLUSIONS:

In real-world setting, implantation of a new-generation polymer-free BES during STEMI is associated with favorable clinical and angiographic results, pointing toward the overall efficacy and safety of the device in complex clinical scenarios.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hospitais Urbanos / Fármacos Cardiovasculares / Angiografia Coronária / Sirolimo / Stents Farmacológicos / Intervenção Coronária Percutânea / Infarto do Miocárdio com Supradesnível do Segmento ST / Hospitais Públicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hospitais Urbanos / Fármacos Cardiovasculares / Angiografia Coronária / Sirolimo / Stents Farmacológicos / Intervenção Coronária Percutânea / Infarto do Miocárdio com Supradesnível do Segmento ST / Hospitais Públicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article