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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, José M; Suárez-Fernández, Carmen; Cosín-Sales, Juan; Gómez-Huelgas, Ricardo; Brotons, Carlos; Araujo, Francisco Pestana; Borrayo, Gabriela; Ruiz, Emilio.
Afiliação
  • Mostaza JM; Internal Medicine Service, Hospital Carlos III, Madrid, Spain. josemaria.mostaza@salud.madrid.org.
  • Suárez-Fernández C; Internal Medicine Department Hospital de la Princesa, Madrid, Spain.
  • Cosín-Sales J; Fundación Investigación Biomédica del Hospital de la Princesa, Madrid, Spain.
  • Gómez-Huelgas R; Universidad Autónoma de Madrid (UAM), Madrid, Spain.
  • Brotons C; Cardiology Service, Hospital Arnau de Vilanova, Valencia, Spain.
  • Araujo FP; Medicine Department, Facultad de Ciencias de la Salud, Universidad UCH-CEU, Alfara del Patriarca, Valencia, Spain.
  • Borrayo G; Internal Medicine Department, Regional University Hospital of Málaga, Malaga, Spain.
  • Ruiz E; Biomedical Research Institute of Málaga (IBIMA), University of Málaga (UMA), Malaga, Spain.
BMC Cardiovasc Disord ; 22(1): 560, 2022 12 22.
Article em En | MEDLINE | ID: mdl-36550424
ABSTRACT

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 ).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Inibidores de Hidroximetilglutaril-CoA Redutases Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Inibidores de Hidroximetilglutaril-CoA Redutases Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article