Armazones vasculares bioabsorbibles en la práctica habitualresultados a largo plazo
- Ricardo Mori Junco 1
- Luis Furuya-Kanamori 2
- Pablo Salinas Sanguino 1
- L. Nombela Franco 1
- Pilar Jiménez-Quevedo 1
- Hernán D. Mejía Rentería 1
- Nieves Gonzalo 1
- Javier Escaned 1
- María J. Pérez Vizcayno 1
- Antonio Fernández-Ortiz 1
- Carlos Macaya Miguel 1
- Iván Javier Núñez Gil 1
- 1 Cardiología Intervencionista, Instituto Cardiovascular, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Hospital Clínico San Carlos, Madrid, España
- 2 Research School of Population Health, Australian National University, Canberra, Australia
ISSN: 2604-7276, 2604-7306
Año de publicación: 2020
Volumen: 2
Número: 3
Páginas: 168-174
Tipo: Artículo
Otras publicaciones en: REC: Interventional Cardiology
Resumen
Introducción y objetivos: Las publicaciones sugieren que los armazones vasculares bioabsorbibles (AVB) conllevan un exceso de complicaciones trombóticas. Se describen los resultados en la vida real y a largo plazo de una serie de pacientes a los que se implantó un AVB Absorb (Abbott Vascular, EE.UU.). Métodos: Se analizaron 213 pacientes consecutivos que recibieron al menos un AVB entre mayo de 2012 y diciembre de 2016. El objetivo principal del estudio fue la incidencia de fracaso del vaso diana, un evento compuesto que incluye infarto de miocardio, revascularización del vaso diana y muerte cardiaca. Resultados: El 75% de los pacientes eran varones (edad media, 61,4 años). La causa más común de ingreso fue el infarto sin elevación del ST (53,52%). La mediana de seguimiento fue de 44 meses [28 meses]. La incidencia del evento primario fue del 6,57% durante los primeros 24 meses y del 7,98% al final del seguimiento. Respecto al dispositivo, hubo 6 casos (2,81%) de trombosis (definitiva, probable o posible) y 10 casos (4,69%) de reestenosis. Los pacientes con antecedentes de diabetes mellitus (HR = 1,72; IC95%, 1,01-2,95; p = 0,05) o con anticoagulación oral crónica (HR = 5,71; IC95%, 1,12-28,94; p = 0,04) tuvieron mayor riesgo de fracaso del vaso diana. Conclusiones: En esta serie de pacientes, la incidencia de fracaso del vaso diana fue comparable a la descrita previamente en ensayos clínicos aleatorizados. Los eventos adversos fueron más frecuentes en los primeros 2 años de seguimiento y en presencia de mayor comorbilidad cardiovascular.
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