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dc.contributorElsevieres_CL
dc.contributor.authorLavados, Pablo M. [Chile.Universidad del Desarrollo]es_CL
dc.contributor.authorMar, Javier [España. Hospital Alto Deba. Unidad de Manejo Clínico]es_CL
dc.contributor.authorComas, Merce [España. Hospital del Mar. Instituto de Investigaciones Medicas]es_CL
dc.date.accessioned2018-09-07T14:11:42Z
dc.date.available2018-09-07T14:11:42Z
dc.date.issued2016es_CL
dc.identifier.citationHoffmeister, L., Lavados, P. M., Mar, J., Comas, M., Arrospide, A., & Castells, X. (2016). Minimum intravenous thrombolysis utilization rates in acute ischemic stroke to achieve population effects on disability: A discrete-event simulation model. Journal of the neurological sciences, 365, 59-64.es_CL
dc.identifier.issnISSN 0022-510Xes_CL
dc.identifier.issnESSN 1878-5883es_CL
dc.identifier.urihttps://ac.els-cdn.com/S0022510X16301885/1-s2.0-S0022510X16301885-main.pdf?_tid=f168c461-ae13-4267-9196-0892732c87ef&acdnat=1535993567_c691bd1130a326eeec82fbbb599ed286es_CL
dc.identifier.urihttp://dx.doi.org/10.1016/j.jns.2016.04.005es_CL
dc.identifier.urihttp://repositorio.umayor.cl/xmlui/handle/sibum/2733
dc.description.abstractBackground: The only pharmacological treatment with proven cost-effectiveness in reducing acute ischemic stroke (AIS) associated disability is intravenous thrombolysis with recombinant tissue plasminogen activator but it's utilization rate is still low in most of the world. We estimated the minimum thrombolysis utilization rate needed to decrease the prevalence of stroke-related disability at a population level by using a discrete event simulation model. Methods: The model included efficacy according to time to treatment up to 4.5 h, and four scenarios for the utilization of intravenous thrombolysis in eligible patients with AIS: a) 2%; b) 12% c) 25% and d) 40%. We calculated the prevalence of AIS related disability in each scenario, using population based data. The simulation was performed from 2002 to 2017 using the ARENA software. Results: A 2% utilization rate yielded a prevalence of disability of 359.1 per 100,000. Increasing thrombolysis to 12% avoided 779 disabled patients. If the utilization rate was increased to 25%, 1783 disabled patients would be avoided. The maximum scenario of 40% decreased disability to 335.7 per 100,000, avoiding 17% of AIS-related disability. Conclusion: The current utilization rate of intravenous thrombolysis of 2% has minimal population impact. Increasing the rate of utilization to more than 12% is the minimum to have a significant population effect on disability and should be a public policy aim.es_CL
dc.description.sponsorshipEste trabajo fue financiado por: Grant Fondo Nacional de Investigación en Salud (FONIS SA 10I20030), Comisión Nacional de Investigación Científica y Tecnológica de Chile (CONICYT).es_CL
dc.format.extentARTÍCULO ORIGINALes_CL
dc.language.isoenes_CL
dc.publisherCIENCIASes_CL
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chilees_CL
dc.subjectNEUROLOGÍAes_CL
dc.titleMinimum intravenous thrombolysis utilization rates in acute ischemic stroke to achieve population effects on disability: A discrete-event simulation modeles_CL
dc.typeArtículo o Paperes_CL
umayor.indizadorCOTes_CL
umayor.politicas.sherpa/romeoLicencia color: VERDE C/R (Se puede archivar el pre-print y el post-print o versión de editor/PDF, el autor no puede archivar la versión del editor/PDF)--Pre-print del autor: el autor puede archivar la versión pre-print (ie la versión previa a la revisión por pares) Post-print del autor: el autor puede archivar la versión post-print (ie la versión final posterior a la revisión por pares) Versión de editor/PDF: el autor no puede archivar la versión del editor/PDF. Condiciones generales: Authors pre-print on any website, including arXiv and RePEC, Author's post-print on author's personal website immediately, Author's post-print on open access repository after an embargo period of between 12 months and 48 months, Permitted deposit due to Funding Body, Institutional and Governmental policy or mandate, may be required to comply with embargo periods of 12 months to 48 months, Author's post-print may be used to update arXiv and RepEC, La versión de editor/PDF no puede utilizarse, Debe enlazar a la versión de editor con DOI, Author's post-print must be released with a Creative Commons Attribution Non-Commercial No Derivatives License// Disponible en: http://www.sherpa.ac.uk/romeo/issn/0022-510X/es/es_CL
umayor.indexadoWOSes_CL
umayor.indexadoSCOPUSes_CL
dc.identifier.doi10.1016/j.jns.2016.04.005es_CL]
umayor.indicadores.wos-(cuartil)Q3es_CL
umayor.indicadores.scopus-(scimago-sjr)sin informaciónes_CL


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