Safety and efficacy of a cardiovascular polypill in people at high and very high risk without a previous cardiovascular event: the international VULCANO randomised clinical trial
Mostaza, J.M.; Suárez-Fernández, C.; Cosín-Sales, J.; Gómez-Huelgas, R.; Brotons, C.; Araujo, F.P.; Borrayo, G.; Ruiz, E.; Pérez, P.; Espinosa, J.; Sobrino, J.; Pose Reino, Antonio; Arroyo Díaz, J.A.; García Vallejo, O.; Cubo Romano, M.P.; Jansen Chaparro, S.; Cabezón Mariscal, J.; Rico Corral, M.A.; Abellán Alemán, J.; Orozco Beltrán, D.; Escobar Jimenez, L.; Valdivieso Felices, P.; Pedro-Botet Montoya, J.C.; Masana Marín, L.; Guijarro, C.; Díaz Rodríguez, Á.; Díaz Díaz, José Luis; De la Peña Fernández, A.; Coloma Bazán, E.; Cuenca Acevedo, R.; Civeira, F.; Castellano Vázquez, J.M.; Mostaza Prieto, J.M.; Suárez Tembra, M.; Alfonso Megido, J.; Castiella Herrero, J.; Tamarit, J.J.; Martínez-Hervás Alonso, M.Á.; Carrasco Franco, F.J.; Álvarez Sala, L.; Calderón Sandubete, E.; Rovira Daudi, E.; Bonilla Rovira, F.; Murcia Zaragoza, J.M.; Cuixart Costa, L.; Bianchi Llave, J.L.; Álvarez Sánchez, C.; Marqués Da Silva, P.; Cunha, V.; Santos, C.; Araujo, F.; Moura, J.; Rosas Peralta, M.

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Fecha de publicación
2022Título de revista
BMC Cardiovascular Disorders
Tipo de contenido
Article
Resumen
Background: Cardiovascular (CV) polypills are a useful baseline treatment to prevent CV diseases by combining different drug classes in a single pill to simultaneously target more than one risk factor. The aim of the present trial was to determine whether the treatment with the CNIC-polypill was at least non-inferior to usual care in terms of low-density lipoprotein cholesterol (LDL-c) and systolic BP (SBP) values in subjects at high or very high risk without a previous CV event. Methods: The VULCANO was an international, multicentre open-label trial involving 492 participants recruited from hospital clinics or primary care centres. Patients were randomised to the CNIC-polypill -containing aspirin, atorvastatin, and ramipril- or usual care. The primary outcome was the comparison of the mean change in LDL-c and SBP values after 16 weeks of treatment between treatment groups. Results: The upper confidence limit of the mean change in LDL-c between treatments was below the prespecified margin (10 mg/dL) and above zero, and non-inferiority and superiority of the CNIC-polypill (p = 0.0001) was reached. There were no significant differences in SBP between groups. However, the upper confidence limit crossed the prespecified non-inferiority margin of 3 mm Hg. Significant differences favoured the CNIC-polypill in reducing total cholesterol (p = 0.0004) and non-high-density lipoprotein cholesterol levels (p = 0.0017). There were no reports of major bleeding episodes. The frequency of non-serious gastrointestinal disorders was more frequent in the CNIC-polypill arm. Conclusion: The switch from conventional treatment to the CNIC-polypill approach was safe and appears a reasonable strategy to control risk factors and prevent CVD. Trial registration This trial was registered in the EU Clinical Trials Register (EudraCT) the 20th February 2017 (register number 2016-004015-13; https://www.clinicaltrialsregister.eu/ctr-search/search?query=2016-004015-13).
