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Heart failure risk scores in advanced heart failure patients: insights from the LEVO-D registry.
Codina, Pau; Dobarro, David; de Juan-Bagudá, Javier; De Frutos, Fernando; Lupón, Josep; Bayes-Genis, Antoni; Gonzalez-Costello, José.
Afiliación
  • Codina P; Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
  • Dobarro D; Department of Medicine, Universitat Autonoma de Barcelona, Barcelona, Spain.
  • de Juan-Bagudá J; Hospital Álvaro Cunqueiro. Complexo Hospitalario Universitario de Vigo, Vigo, Spain.
  • De Frutos F; Department of Cardiology, University Hospital 12 de Octubre, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain.
  • Lupón J; Department of Medicine, Faculty of Biomedical and Health Science, Universidad Europea de Madrid, Madrid, Spain.
  • Bayes-Genis A; CIBERCV, Instituto de Salud Carlos III, Madrid, Spain.
  • Gonzalez-Costello J; Department of Cardiology, Hospital Universitari de Bellvitge, BIOHEART-Cardiovascular Diseases Research Group, Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
ESC Heart Fail ; 10(5): 2875-2881, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37991427
ABSTRACT

AIMS:

The prevalence of advanced heart failure (HF) is increasing due to the growing number of patients with HF and their better treatment and survival. There is a scarcity of data on the accuracy of HF web-based risk scores in this selected population. This study aimed to assess mortality prediction performance of the Meta-Analysis Global Group in Chronic HF (MAGGIC-HF) risk score and the model of the Barcelona Bio-HF Risk Calculator (BCN-Bio-HF) containing N terminal pro brain natriuretic peptide in HF patients receiving intermittent inotropic support with levosimendan as destination therapy. METHODS AND

RESULTS:

Four hundred and three advanced HF patients from 23 tertiary hospitals in Spain receiving intermittent inotropic support with levosimendan as destination therapy were included. Discrimination for all-cause mortality was compared by area under the curve (AUC) and Harrell's C-statistic at 1 year. Calibration was assessed by calibration plots comparing observed versus expected events based on estimated risk by each calculator. The included patients were predominantly men, aged 71.5 [interquartile range 64-78] years, with reduced left ventricular ejection fraction (27.5 ± 9.4%); ischaemic heart disease was the most prevalent aetiology (52.5%). Death rate at 1 year was 26.8%, while the predicted 1-year mortality by BCN-Bio-HF and MAGGIC-HF was 17.0% and 22.1%, respectively. BCN-Bio-HF AUC was 0.66 (Harrell's C-statistic 0.64), and MAGGIC-HF AUC was 0.62 (Harrell's C-statistic 0.61).

CONCLUSIONS:

The two evaluated risk scores showed suboptimal discrimination and calibration with an underestimation of risk in advanced HF patients receiving levosimendan as destination therapy. There is a need for specific scores for advanced HF.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Función Ventricular Izquierda / Insuficiencia Cardíaca Idioma: En Revista: ESC Heart Fail Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Función Ventricular Izquierda / Insuficiencia Cardíaca Idioma: En Revista: ESC Heart Fail Año: 2023 Tipo del documento: Article