Cost-effectiveness of everolimus-eluting versus bare-metal stents in ST-segment elevation myocardial infarction: An analysis from the EXAMINATION randomized controlled trial

Autor: Salvatore Brugaletta, Matthias Schwenkglenks, Peter den Heijer, Maurizio Tespili, Andrés Iñiguez, Patrick W. Serruys, Pilar Jiménez-Quevedo, Nicolás Vázquez, Nadine Schur, Gianluca Campo, Vicente Mainar, Angel Cequier, Armando Bethencourt, Marco Valgimigli, Manel Sabaté, Antonio Serra, Zanfina Ademi
Přispěvatelé: Universitat de Barcelona, Cardiology, University of Zurich, Voskuil, Michiel, Schur, Nadine
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Genetics and Molecular Biology (all)
evaluación del desenlace del paciente
Economics
Cardiovascular Procedures
modelos de riesgos proporcionales
Cost effectiveness
Cost-Benefit Analysis
humanos
Myocardial Infarction
lcsh:Medicine
Social Sciences
costos de la atención de salud
Cardiovascular Medicine
030204 cardiovascular system & hematology
Antiplatelet Therapy
estudios de seguimiento
Vascular Medicine
Biochemistry
Geographical locations
law.invention
0302 clinical medicine
Randomized controlled trial
law
Medicine and Health Sciences
030212 general & internal medicine
Myocardial infarction
610 Medicine & health
lcsh:Science
health care economics and organizations
stents liberadores de fármacos
Coronary Artery Bypass Grafting
Multidisciplinary
Cost–benefit analysis
Pharmaceutics
Drug-Eluting Stents
General Medicine
Hematology
Health Care Costs
Cost-effectiveness analysis
Anàlisi cost-benefici
Europe
Cardiovascular Diseases
Cardiology
Stents
General Agricultural and Biological Sciences
Research Article
medicine.drug
medicine.medical_specialty
Coronary Stenting
Cost-Effectiveness Analysis
Genetics and Molecular Biology
Surgical and Invasive Medical Procedures
1100 General Agricultural and Biological Sciences
Therapeutics
NO
03 medical and health sciences
Drug Therapy
1300 General Biochemistry
Genetics and Molecular Biology

Internal medicine
medicine
Humans
European Union
Everolimus
Espanya
Follow-Up Studies
Patient Outcome Assessment
Proportional Hazards Models
ST Elevation Myocardial Infarction
Biochemistry
Genetics and Molecular Biology (all)

Agricultural and Biological Sciences (all)
Blood Coagulation
1000 Multidisciplinary
Coagulation Disorders
business.industry
Proportional hazards model
Revascularization
lcsh:R
Thrombosis
10060 Epidemiology
Biostatistics and Prevention Institute (EBPI)

medicine.disease
Terapèutica
Economic Analysis
Infart de miocardi
Spain
General Biochemistry
Stent Implantation
lcsh:Q
People and places
business
Decision analysis
Zdroj: Schur, Nadine; Brugaletta, Salvatore; Cequier, Angel; Iñiguez, Andrés; Serra, Antonio; Jiménez-Quevedo, Pilar; Mainar, Vicente; Campo, Gianluca; Tespili, Maurizio; den Heijer, Peter; Bethencourt, Armando; Vazquez, Nicolás; Valgimigli, Marco; Serruys, Patrick W; Ademi, Zanfina; Schwenkglenks, Matthias; Sabaté, Manel (2018). Cost-effectiveness of everolimus-eluting versus bare-metal stents in ST-segment elevation myocardial infarction: An analysis from the EXAMINATION randomized controlled trial. PLoS ONE, 13(8), e0201985. Public Library of Science 10.1371/journal.pone.0201985
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS ONE
PLoS One (online), 13(8):e0201985. Public Library of Science
PLoS ONE, Vol 13, Iss 8, p e0201985 (2018)
PLoS One
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
Consejo Superior de Investigaciones Científicas (CSIC)
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Dipòsit Digital de la UB
Universidad de Barcelona
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0201985
Popis: Background Use of everolimus-eluting stents (EES) has proven to be clinically effective and safe in patients with ST-segment elevation myocardial infarction but it remains unclear whether it is cost-effective compared to bare-metal stents (BMS) in the long-term. We sought to assess the cost-effectiveness of EES versus BMS based on the 5-year results of the EXAMINATION trial, from a Spanish health service perspective. Methods Decision analysis of the use of EES versus BMS was based on the patient-level clinical outcome data of the EXAMINATION trial. The analysis adopted a lifelong time horizon, assuming that long-term survival was independent of the initial treatment strategy after the end of follow-up. Life-expectancy, health-state utility scores and unit costs were extracted from published literature and publicly available sources. Non-parametric bootstrapping was combined with probabilistic sensitivity analysis to co-assess the impact of patient-level variation and parameter uncertainty. The main outcomes were total costs and quality-adjusted life-years. The incremental cost-effectiveness ratio was expressed as cost per quality-adjusted life-years gained. Costs and effects were discounted at 3%. Results The model predicted an average survival time in patients receiving EES and BMS of 10.52 and 10.38 undiscounted years, respectively. Over the life-long time horizon, the EES strategy was (sic)430 more costly than BMS ((sic) 8,305 vs. (sic)7,874), but went along with incremental gains of 0.10 quality-adjusted life-years. This resulted in an average incremental cost-effectiveness ratio over all simulations of (sic)3,948 per quality-adjusted life-years gained and was below a willingness-to-pay threshold of (sic)25,000 per quality-adjusted life-years gained in 86.9% of simulation runs. Conclusions Despite higher total costs relative to BMS, EES appeared to be a cost-effective therapy for ST-segment elevation myocardial infarction patients due to their incremental effectiveness. Predicted incremental cost-effectiveness ratios were below generally acceptable threshold values.
The EXAMINATION trial (NCT00828087) was funded by the Spanish Heart Foundation. SB has received speakers' fees from Abbott Vascular and St Jude Medical. MV has received an honorarium as a public speaker for Terumo, the Medicines Company, Medtronic, Iroko, Merck, Abbott, Ely Lilly, AstraZeneca, Cordis, Carbostent and Implantable Devices, and Bayer. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The other authors declare no competing interests.
Databáze: OpenAIRE