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dc.contributor.authorGillespie, Iain A.es_ES
dc.contributor.authorFloege, Jürgenes_ES
dc.contributor.authorGioni, Ioannaes_ES
dc.contributor.authorDrüeke, Tilman B.es_ES
dc.contributor.authorMartín de Francisco Hernández, Ángel Luis es_ES
dc.contributor.authorAnker, Stefan D.es_ES
dc.contributor.authorKubo, Yumies_ES
dc.contributor.authorWheeler, David C.es_ES
dc.contributor.authorFroissart, Marces_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-05-30T15:15:56Z
dc.date.available2023-05-30T15:15:56Z
dc.date.issued2014es_ES
dc.identifier.issn1099-1557es_ES
dc.identifier.issn1053-8569es_ES
dc.identifier.urihttps://hdl.handle.net/10902/29155
dc.description.abstractPurpose: The generalisability of randomised controlled trials (RCTs) may be limited by restrictive entry criteria or by their experimental nature. Observational research can provide complementary findings but is prone to bias. Employing propensity score matching, to reduce such bias, we compared the real-life effect of cinacalcet use on all-cause mortality (ACM) with findings from the Evaluation of Cinacalcet Therapy to Lower Cardiovascular Events (EVOLVE) RCT in chronic haemodialysis patients. Methods: Incident adult haemodialysis patients receiving cinacalcet, recruited in a prospective observational cohort from 2007-2009 (AROii; n = 10,488), were matched to non-exposed patients regardless of future exposure status. The effect of treatment crossover was investigated with inverse probability of censoring weighted and lag-censored analyses. EVOLVE ACM data were analysed largely as described for the primary composite endpoint. Results: AROii patients receiving cinacalcet (n = 532) were matched to 1790 non-exposed patients. The treatment effect of cinacalcet on ACM in the main AROii analysis (hazard ratio 1.03 [95% confidence interval (CI) 0.78-1.35]) was closer to the null than for the Intention to Treat (ITT) analysis of EVOLVE (0.94 [95%CI 0.85-1.04]). Adjusting for non-persistence by 0- and 6-month lag-censoring and by inverse probability of censoring weight, the hazard ratios in AROii (0.76 [95%CI 0.51-1.15], 0.84 [95%CI 0.60-1.18] and 0.79 [95%CI 0.56-1.11], respectively) were comparable with those of EVOLVE (0.82 [95%CI 0.67-1.01], 0.83 [95%CI 0.73-0.96] and 0.87 [95%CI 0.71-1.06], respectively). Conclusions: Correcting for treatment crossover, we observed results in the 'real-life' setting of the AROii observational cohort that closely mirrored the results of the EVOLVE RCT. Persistence-corrected analyses revealed a trend towards reduced ACM in haemodialysis patients receiving cinacalcet therapy.es_ES
dc.description.sponsorshipFunding: DWreports having received research funding from Abbott,Genzyme and AstraZeneca and honoraria from Amgen,Abbott, Fresenius, Janssen, Otsuka, Shire and Vifor.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourcePharmacoepidemiology and Drug Safety, 2014, 24, 738-747es_ES
dc.subject.otherBiases_ES
dc.subject.otherCinacalcetes_ES
dc.subject.otherHaemodialysises_ES
dc.subject.otherMortalityes_ES
dc.subject.otherPersistencees_ES
dc.subject.otherPharmacoepidemiologyes_ES
dc.titlePropensity score matching and persistence correction to reduce bias incomparative effectiveness: the effect of cinacalcet use on all-causemortalityes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1002/pds.3789es_ES
dc.type.versionacceptedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 International