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Effectiveness and safety of PCSK9 inhibitors in real-world clinical practice. An observational multicentre study. The IRIS-PCSK9I study

Authors :
Rodrigo Milán Pinilla
María Magdalena Carrillo Bailén
Marina Blanco-Ruiz
María Josefa Álvarez Soria
Belén Sánchez Rodríguez
Patricia Martínez-Sánchez
Laura Amaya-Pascasio
Roberto Valverde Moyano
Irene Pérez Ortega
María Victoria Mejías Olmedo
Pablo González Bustos
Javier Fernández Pérez
Purificación Sánchez López
Reyes de Torres Chacón
Eduardo Agüera Morales
Manuel Payán Ortiz
Luis Andrade Zumárraga
Antonio Arjona-Padillo
Alba María Castillo Fernández
Cristina Del Toro Pérez
Beatriz Hidalgo Martín
Ricardo Roa Chamorro
Source :
Atherosclerosis Plus, Vol 45, Iss, Pp 32-38 (2021)
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

Background and aims: The benefits of the PCSK9 inhibitors, alirocumab and evolocumab, in lowering LDL-cholesterol and preventing major adverse cardiac events (MACE) have been demonstrated in pivotal clinical trials. However, few studies of routine clinical practice have been conducted to analyse and compare the efficacy and safety of the two drugs. Methods: Retrospective observational study of patients treated with a PCSK9 inhibitor in five hospitals in Andalusia (southern Spain). Baseline demographic and clinical data, LDL-cholesterol levels and the occurrence of MACEs during the follow-up period were recorded. Results: A total of 141 patients were included in the study: 90 were treated with alirocumab and 51 with evolocumab. The patients’ mean age (IQR) was 58 (11) years and 58 (41%) were women. The most frequent concomitant medications were statins, 94 (66.7%), followed by antiplatelet therapy (66%) and ezetimibe (65.2%). The median (IQR) follow-up period was 18 (18) months, with 18 (24) for alirocumab and 11 (18) for evolocumab. At the six-month follow-up visit, LDL-cholesterol values had decreased to pre-treatment levels and remained significantly decreased (p

Details

Language :
English
ISSN :
26670895
Volume :
45
Database :
OpenAIRE
Journal :
Atherosclerosis Plus
Accession number :
edsair.doi.dedup.....2169b116cf8566849cf4241055ffa2d5