Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/130120
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dc.contributor.authorZozaya González, María Neboaen_US
dc.contributor.authorArrizubieta Basterrechea, Maria Iciaren_US
dc.contributor.authorBollo, Elenaen_US
dc.contributor.authorCastellví, Ivánen_US
dc.contributor.authorEspín, Jaimeen_US
dc.contributor.authorOrtego, Norbertoen_US
dc.contributor.authorPoveda-Andrés, José Luisen_US
dc.contributor.authorRodríguez Portal, José Antonioen_US
dc.contributor.authorRivero, Agustínen_US
dc.contributor.authorMarcos-Rodríguez, José Antonioen_US
dc.contributor.authorVerde, Luisen_US
dc.date.accessioned2024-05-02T15:22:02Z-
dc.date.available2024-05-02T15:22:02Z-
dc.date.issued2022en_US
dc.identifier.issn0266-4623en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/130120-
dc.description.abstractObjectives: Our aim was to assess the value of nintedanib for non-idiopathic progressive fibrosing interstitial lung disease (non-IPF PF-ILD) and systemic sclerosis-associated ILD (SSc-ILD) in the Spanish context, using a multi-criteria decision analysis (MCDA). Methods: Following an adaptation of the Evidence and Value: Impact on DEcision Making (EVIDEM) MCDA methodology, the estimated value of nintedanib was obtained by means of an additive linear model that combined individual weights (100-points distribution) of criteria with the individual scoring of nintedanib in each criterion for every indication, assigned by a multidisciplinary committee of twelve clinicians, patients, pharmacists, and decision-makers. To assess the reproducibility, an alternative weighting method was applied, as well as a re-test of weights and scores at a different moment of time. Results: The experts committee recognized nintedanib as an intervention with a positive value contribution in comparison to placebo for the treatment of non-IPF PF-ILD (0.50 0.16, on a scale from 1 to 1) and SSc-ILD (0.40 0.12), diseases which were considered as very severe and with high unmet needs. The drug was perceived as a treatment that provides an added therapeutic benefit for patients (0.06–0.07), given its proven clinical efficacy (0.05–0.06), slight improvements in patient-reported outcomes (0.01–0.02), and similar safety profile than placebo ( 0.04–0.00), which will likely be positioned as a recommended therapy in the next clinical practice guidelines updates. Conclusions: Under this increasingly used methodology, nintedanib has shown to provide a positive value estimate for non-IPF PF-ILD and SSc-ILD when compared to placebo in Spain.en_US
dc.languageengen_US
dc.relation.ispartofInternational Journal of Technology Assessment in Health Careen_US
dc.sourceInternational Journal of Technology Assessment in Health Care [ISSN 0266-4623], v. 38, n. 1, p. 1-10, (Julio 2022)en_US
dc.subject53 Ciencias económicasen_US
dc.subject531207 Sanidaden_US
dc.subject.otherInterstitial lung diseasesen_US
dc.subject.otherSystemic sclerosisen_US
dc.subject.otherPulmonary fibrosisen_US
dc.subject.otherMulti-criteria decision analysisen_US
dc.titleA multi-criteria decision analysis on the value of nintedanib for interstitial lung diseasesen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1017/S0266462322000459en_US
dc.description.lastpage10en_US
dc.identifier.issue1-
dc.description.firstpage1en_US
dc.relation.volume38en_US
dc.investigacionCiencias Sociales y Jurídicasen_US
dc.type2Artículoen_US
dc.description.numberofpages10en_US
dc.utils.revisionen_US
dc.date.coverdateJulio 2022en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-ECOen_US
dc.description.sjr0,849
dc.description.jcr3,2
dc.description.sjrqQ2
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds11,0
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR Economía de la salud y políticas públicas-
crisitem.author.orcid0000-0003-4618-6894-
crisitem.author.parentorgDepartamento de Métodos Cuantitativos en Economía y Gestión-
crisitem.author.fullNameZozaya Gonzalez,Neboa-
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