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Heart ; 104(12): 1006-1013, 2018 06.
Artigo em Inglês | MEDLINE | ID: mdl-29269379

RESUMO

OBJECTIVE: Chronic heart failure with reduced ejection fraction (HF-REF) represents a major public health issue and is associated with considerable morbidity and mortality. We evaluated the cost-effectiveness of sacubitril/valsartan (formerly LCZ696) compared with an ACE inhibitor (ACEI) (enalapril) in the treatment of HF-REF from the perspective of healthcare providers in the UK, Denmark and Colombia. METHODS: A cost-utility analysis was performed based on data from a multinational, Phase III randomised controlled trial. A decision-analytic model was developed based on a series of regression models, which extrapolated health-related quality of life, hospitalisation rates and survival over a lifetime horizon. The primary outcome was the incremental cost-effectiveness ratio (ICER). RESULTS: In the UK, the cost per quality-adjusted life-year (QALY) gained for sacubitril/valsartan (using cardiovascular mortality) was £17 100 (€20 400) versus enalapril. In Denmark, the ICER for sacubitril/valsartan was Kr 174 000 (€22 600). In Colombia, the ICER was COP$39.5 million (€11 200) per QALY gained. Deterministic sensitivity analysis showed that results were most sensitive to the extrapolation of mortality, duration of treatment effect and time horizon, but were robust to other structural changes, with most scenarios associated with ICERs below the willingness-to-pay threshold for all three country settings. Probabilistic sensitivity analysis suggested the probability that sacubitril/valsartan was cost-effective at conventional willingness-to-pay thresholds was 68%-94% in the UK, 84% in Denmark and 95% in Colombia. CONCLUSIONS: Our analysis suggests that, in all three countries, sacubitril/valsartan is likely to be cost-effective compared with an ACEI (the current standard of care) in patients with HF-REF.


Assuntos
Aminobutiratos/economia , Aminobutiratos/uso terapêutico , Fármacos Cardiovasculares/economia , Fármacos Cardiovasculares/uso terapêutico , Custos de Medicamentos , Insuficiência Cardíaca/tratamento farmacológico , Insuficiência Cardíaca/economia , Volume Sistólico/efeitos dos fármacos , Tetrazóis/economia , Tetrazóis/uso terapêutico , Função Ventricular Esquerda/efeitos dos fármacos , Aminobutiratos/efeitos adversos , Compostos de Bifenilo , Fármacos Cardiovasculares/efeitos adversos , Doença Crônica , Ensaios Clínicos Fase III como Assunto , Colômbia , Análise Custo-Benefício , Dinamarca , Combinação de Medicamentos , Insuficiência Cardíaca/diagnóstico , Insuficiência Cardíaca/fisiopatologia , Humanos , Anos de Vida Ajustados por Qualidade de Vida , Ensaios Clínicos Controlados Aleatórios como Assunto , Recuperação de Função Fisiológica , Tetrazóis/efeitos adversos , Fatores de Tempo , Resultado do Tratamento , Reino Unido , Valsartana
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