RESUMO
DISCLOSURES: No outside funding supported this commentary. The authors have nothing to disclose.
Assuntos
Doenças Cardiovasculares/tratamento farmacológico , Análise Custo-Benefício/normas , Ácido Eicosapentaenoico/análogos & derivados , Hemorragia/epidemiologia , Rivaroxabana/efeitos adversos , Fatores Etários , Aspirina/administração & dosagem , Aspirina/efeitos adversos , Aspirina/economia , Doenças Cardiovasculares/economia , Doenças Cardiovasculares/mortalidade , Relação Dose-Resposta a Droga , Custos de Medicamentos/estatística & dados numéricos , Quimioterapia Combinada/efeitos adversos , Quimioterapia Combinada/economia , Quimioterapia Combinada/métodos , Revisão de Uso de Medicamentos , Término Precoce de Ensaios Clínicos , Ácido Eicosapentaenoico/administração & dosagem , Ácido Eicosapentaenoico/efeitos adversos , Ácido Eicosapentaenoico/economia , Hemorragia/induzido quimicamente , Hemorragia/economia , Humanos , Medicare/economia , Medicare/estatística & dados numéricos , Modelos Econômicos , Ensaios Clínicos Controlados Aleatórios como Assunto/normas , Projetos de Pesquisa/normas , Fatores de Risco , Rivaroxabana/administração & dosagem , Rivaroxabana/economia , Fatores de Tempo , Resultado do Tratamento , Estados UnidosRESUMO
DISCLOSURES: Funding for this summary was contributed by Arnold Ventures, Commonwealth Fund, California Health Care Foundation, National Institute for Health Care Management (NIHCM), New England States Consortium Systems Organization, Blue Cross Blue Shield of Massachusetts, Harvard Pilgrim Health Care, Kaiser Foundation Health Plan, and Partners HealthCare to the Institute for Clinical and Economic Review (ICER), an independent organization that evaluates the evidence on the value of health care interventions. ICER's annual policy summit is supported by dues from Aetna, America's Health Insurance Plans, Anthem, Allergan, Alnylam, AstraZeneca, Biogen, Blue Shield of CA, Cambia Health Services, CVS, Editas, Express Scripts, Genentech/Roche, GlaxoSmithKline, Harvard Pilgrim, Health Care Service Corporation, Health Partners, Johnson & Johnson (Janssen), Kaiser Permanente, LEO Pharma, Mallinckrodt, Merck, Novartis, National Pharmaceutical Council, Premera, Prime Therapeutics, Regeneron, Sanofi, Spark Therapeutics, and United Healthcare. Pearson is employed by ICER; Synnott was employed by ICER at the time of this report. Ollendorf, Campbell, and McQueen received grants from ICER for work on this review. Ollendorf also reports advisory board, consulting, and other fees from Sarepta Therapeutics, DBV Technologies, EMD Serono, Gerson Lehman Group, The CEA Registry Sponsors, Autolus, Analysis Group, Amgen, AbbVie, Cytokinetics, Aspen Institute/University of Southern California, and University of Colorado, unrelated to this review.
Assuntos
Aspirina/administração & dosagem , Doenças Cardiovasculares/tratamento farmacológico , Análise Custo-Benefício , Ácido Eicosapentaenoico/análogos & derivados , Rivaroxabana/administração & dosagem , Aspirina/efeitos adversos , Aspirina/economia , Doenças Cardiovasculares/economia , Doenças Cardiovasculares/mortalidade , Relação Dose-Resposta a Droga , Custos de Medicamentos , Quimioterapia Combinada/efeitos adversos , Quimioterapia Combinada/economia , Quimioterapia Combinada/métodos , Ácido Eicosapentaenoico/administração & dosagem , Ácido Eicosapentaenoico/efeitos adversos , Ácido Eicosapentaenoico/economia , Hemorragia/induzido quimicamente , Hemorragia/economia , Hemorragia/epidemiologia , Humanos , Modelos Econômicos , Ensaios Clínicos Controlados Aleatórios como Assunto , Rivaroxabana/efeitos adversos , Rivaroxabana/economia , Fatores de Tempo , Resultado do TratamentoRESUMO
OBJECTIVES: To examine the cost-effectiveness of a triglyceride lowering medication-icosapent ethyl added on to statin from Australian healthcare system perspective. METHODS: A Markov-model was developed using data from the pivotal trial of icosapent ethyl in a secondary prevention population. Probabilities of CVD events were derived and extrapolated from the published Kaplan-Meier curve using a valid algorithm. Management cost of CVD, health-related quality of life, and background non-CVD mortality were extracted from publicly available sources. Acquisition cost of icosapent ethyl from the United States was used in the current analysis. Australian patients with histories of CVD were modelled for a 25â¯year time horizon and costs and benefits were discounted. Sensitivity analyses (SA) were undertaken. Value of perfect information (VPI) was quantified. RESULTS: Treatment with icosapent ethyl was associated with both higher costs and benefits (i.e. quality-adjusted life year [QALY] and life year [LY]), resulting in an incremental cost-effectiveness ratio (ICER) of AUD59,036/QALY or AUD54,358/LY. Using the often quoted willingness-to-pay (WTP)/QALY of AUD50,000/QALY, icosapent ethyl was not considered cost-effective. SA showed that time horizon, drug cost, and discount rate were the key drivers of the ICER. Total monetary VPI for icosapent ethyl was over AUD15 million over 5â¯years. CONCLUSIONS: Patients with established CVD in whom level of triglycerides is high would benefit from the treatment using icosapent ethyl, however, it is not a cost-effective from an Australian healthcare system perspective. The government may consider subsidising this medication given the clinical need but at a discounted acquisition cost.
Assuntos
Doenças Cardiovasculares/prevenção & controle , Análise Custo-Benefício , Ácido Eicosapentaenoico/análogos & derivados , Hipertrigliceridemia/tratamento farmacológico , Reguladores do Metabolismo de Lipídeos/economia , Reguladores do Metabolismo de Lipídeos/uso terapêutico , Austrália , Doenças Cardiovasculares/etiologia , Atenção à Saúde , Ácido Eicosapentaenoico/economia , Ácido Eicosapentaenoico/uso terapêutico , Ácidos Graxos Ômega-3/economia , Feminino , Humanos , Hipertrigliceridemia/complicações , Masculino , Pessoa de Meia-IdadeRESUMO
The U.S. military may consider exploring the inclusion of the long-chain omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), in the diets of active duty military personnel. To be successful, certain challenges must be overcome including determining appropriate dosage, ensuring cost efficiency, and optimizing stability. To increase EPA and DHA intake, the military should consider using one of three strategies, including mandates or recommendations on omega-3 supplement usage, contracts to purchase commercially available foods for distribution in the food supply chain, or direct addition of EPA and DHA into currently consumed foods. This review presents the challenges and strategies and provides potential suggestions to the military to increase the likelihood of success.