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ABSTRACT
Bioresorbable vascular scaffold (BRS) is an innovative device that provides structural support and drug release to prevent early recoil or restenosis, and then degrades into nontoxic compounds to avoid late complications related with metallic drug-eluting stents (DESs). BRS has several putative advantages. However, recent randomized trials and registry studies raised clinical concerns about the safety and efficacy of first generation BRS. In addition, the general guidance for the optimal practice with BRS has not been suggested due to limited long-term clinical data in Korea. To address the safety and efficacy of BRS, we reviewed the clinical evidence of BRS implantation, and suggested the appropriate criteria for patient and lesion selection, scaffold implantation technique, and management.
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Texto completo: 1 Índice: WPRIM Assunto principal: Trombose / Stents / Doença das Coronárias / Stents Farmacológicos / Liberação Controlada de Fármacos / Coreia (Geográfico) Tipo de estudo: Clinical_trials / Guideline Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Korean Circulation Journal Ano de publicação: 2017 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Trombose / Stents / Doença das Coronárias / Stents Farmacológicos / Liberação Controlada de Fármacos / Coreia (Geográfico) Tipo de estudo: Clinical_trials / Guideline Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Korean Circulation Journal Ano de publicação: 2017 Tipo de documento: Article