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Lipid-lowering therapy after acute coronary syndromes: a multinational European survey.
Tsaban, Gal; Perez, Rafael Vidal; Krychtiuk, Konstantin A; Ahrens, Ingo; Halvorsen, Sigrun; Hassager, Christian; Huber, Kurt; Schiele, Francois; Sionis, Alessandro; Claeys, Marc J.
Afiliação
  • Tsaban G; Department of Cardiology, Soroka University Medical Center.
  • Perez RV; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beersheva, Israel.
  • Krychtiuk KA; Cardiology Department, Complejo Hospitalario Universitario de A Coruña, A Coruña, Spain.
  • Ahrens I; CIBER-CV, Centro de investigación Biomédica en Red de Enfermedades Cardiovasculares, Madrid, Spain.
  • Halvorsen S; Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
  • Hassager C; Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Huber K; Department of Cardiology and Medical Intensive Care, Augustinerinnen Hospital Cologne, Academic Teaching Hospital University of Cologne, Germany and Faculty of Medicine, University of Freiburg, Germany.
  • Schiele F; Institute of Clinical Medicine, University of Oslo.
  • Sionis A; Department of Cardiology, Oslo University Hospital Ullevål, Oslo, Norway.
  • Claeys MJ; Department of Cardiology, Rigshospitalet and Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Coron Artery Dis ; 2024 Sep 12.
Article em En | MEDLINE | ID: mdl-39263716
ABSTRACT

BACKGROUND:

Recent guidelines on acute coronary syndromes (ACS) recommend initiating lipid-lowering therapy (LLT) as early as possible to obtain >50% low-density-lipoprotein cholesterol (LDL-c) reduction and an LDL-c < 1.4 mmol/l.

METHODS:

A multinational European survey study of ACS patients between 2021-2022 and acquired data on LLT and lipid levels on admission and during 1-year posthospitalization. We compared plasma lipid changes and adherence to post-ACS lipid targets across two in-hospital LLT groups high-intensity statin (HIS) monotherapy (mono-HIS) and a combination of HIS and ezetimibe (combo-HIS).

RESULTS:

Of 286 patients, 268 (94%) received in-hospital HIS and were included in the final analysis. Patients (median age 61.1 years) had a median baseline LDL-c of 3.3 mmol/l. Mono-HIS was the predominant in-hospital LLT (72.4%). In-hospital combo-HIS was administered in 27.6% of the cases. Patients from high-income countries (n = 141) were more likely to receive in-hospital combo-HIS than patients from middle-income countries [n = 127; 38.3% vs. 15.7% patients, P < 0.001). One-year post-ACS, 50 (26.5%) patients from the mono-HIS group received ezetimibe. The target of LDL-c ≤ 55 mg/dl was reached in 85 patients (31.7%), without significant difference between study groups [mono-HIS 56 (28.9%) and combo-HIS 29 (39.2%) patients, P = 0.10]. The target of >50% reduction was achieved more frequently among the combo-HIS group than in the mono-HIS group (50.0% vs. 29.9%, respectively, P = 0.002).

CONCLUSION:

LDL-c targets were achieved in less than half of the patients post-ACS, regardless of the LLT regimen. Combo-HIS was initiated in-hospital post-ACS in only 28% and was associated with greater LDL-c reduction compared to a staged approach of mono-HIS with up-titration at follow-up.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article