Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/35461
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dc.contributor.authorKhan, Nasim Ahmeden_US
dc.contributor.authorSpencer, Horace Jacken_US
dc.contributor.authorNikiphorou, Elenaen_US
dc.contributor.authorNaranjo, Antonioen_US
dc.contributor.authorAlten, Riekien_US
dc.contributor.authorChirieac, Rodica M.en_US
dc.contributor.authorDrosos, Alexandros A.en_US
dc.contributor.authorGéher, Pálen_US
dc.contributor.authorInanc, Nevsunen_US
dc.contributor.authorKerzberg, Eduardoen_US
dc.contributor.authorAncuta, Codrina Mihaelaen_US
dc.contributor.authorMüller, Rüedigeren_US
dc.contributor.authorOrnbjerg, Lykkeen_US
dc.contributor.authorSokka, Tuullikien_US
dc.contributor.otherNaranjo Hernandez, Antonio
dc.contributor.otherKerzberg, Eduardo
dc.date.accessioned2018-04-20T11:05:19Z-
dc.date.available2018-04-20T11:05:19Z-
dc.date.issued2017en_US
dc.identifier.issn1462-0324en_US
dc.identifier.urihttp://hdl.handle.net/10553/35461-
dc.description.abstractObjective. To assess intercentre variability in the ACR core set measures, DAS28 based on three variables (DAS28v3) and Routine Assessment of Patient Index Data 3 in a multinational study. Methods. Seven thousand and twenty-three patients were recruited (84 centres; 30 countries) using a standard protocol in the Quantitative Standard Monitoring of Patients with RA study. Analysis of variance (ANOVA) and mixed-effect analysis of covariance models were used to model the relationship between study centre and different patient-reported and physician-reported RA activity measures. These models were built to adjust for the remaining ACR core set measure (for each ACR core set measure or each composite index), socio-demographics and medical characteristics. ANOVA and analysis of covariance models yielded similar results, and ANOVA tables were used to present variance attributable to recruiting centre. Results. The proportion of variances attributable to recruiting centre was lower for patient reported outcomes (PROs: pain, HAQ, patient global) compared with objective measures (joint counts, ESR, physician global) in all models. In the full model, variance in PROs attributable to recruiting centre ranged from 1.53% for patient global to 3.71% for HAQ compared with objective measures that ranged from 5.92% for physician global to 9.25% for ESR; and was lower for Routine Assessment of Patient Index Data 3 (2.6%) compared with DAS28v3 (11.75%). Conclusion. Intercentre variability in PROs is lower than objective measures of RA activity demonstrating that PROs may be more comparable across centres, and the need for standardization of objective measures.en_US
dc.languageengen_US
dc.relation.ispartofRheumatologyen_US
dc.sourceRheumatology[ISSN 1462-0324],v. 56 (8), p. 1395-1400en_US
dc.subject32 Ciencias médicasen_US
dc.subject.otherRheumatoid arthritisen_US
dc.subject.otherDisease activity assessmenten_US
dc.subject.otherPatient reported outcomesen_US
dc.subject.otherIntercentre varianceen_US
dc.titleIntercentre variance in patient reported outcomes is lower than objective rheumatoid arthritis activity measures: a cross-sectional studyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1093/rheumatology/kex076
dc.identifier.scopus85028346045
dc.identifier.isi000406150400021
dcterms.isPartOfRheumatology
dcterms.sourceRheumatology[ISSN 1462-0324],v. 56 (8), p. 1395-1400
dc.contributor.authorscopusid36728286700
dc.contributor.authorscopusid7201921775
dc.contributor.authorscopusid35784968200
dc.contributor.authorscopusid7003297397
dc.contributor.authorscopusid6701509139
dc.contributor.authorscopusid34876356000
dc.contributor.authorscopusid7005958732
dc.contributor.authorscopusid6602177088
dc.contributor.authorscopusid55904805400
dc.contributor.authorscopusid6602898497
dc.contributor.authorscopusid34876157600
dc.contributor.authorscopusid7404247065
dc.contributor.authorscopusid24069275900
dc.contributor.authorscopusid7005197367
dc.identifier.eissn1462-0332-
dc.description.lastpage1400-
dc.identifier.issue8-
dc.description.firstpage1395-
dc.relation.volume56-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000406150400021-
dc.contributor.daisngid1059011
dc.contributor.daisngid123769
dc.contributor.daisngid225250
dc.contributor.daisngid550893
dc.contributor.daisngid24190230
dc.contributor.daisngid728192
dc.contributor.daisngid34572
dc.contributor.daisngid383065
dc.contributor.daisngid220838
dc.contributor.daisngid961251
dc.contributor.daisngid381835
dc.contributor.daisngid4480418
dc.contributor.daisngid1179999
dc.contributor.daisngid14975993
dc.identifier.investigatorRIDE-7910-2010
dc.identifier.investigatorRIDNo ID
dc.contributor.wosstandardWOS:Khan, NA
dc.contributor.wosstandardWOS:Spencer, HJ
dc.contributor.wosstandardWOS:Nikiphorou, E
dc.contributor.wosstandardWOS:Naranjo, A
dc.contributor.wosstandardWOS:Alten, R
dc.contributor.wosstandardWOS:Chirieac, RM
dc.contributor.wosstandardWOS:Drosos, AA
dc.contributor.wosstandardWOS:Geher, P
dc.contributor.wosstandardWOS:Inanc, N
dc.contributor.wosstandardWOS:Kerzberg, E
dc.contributor.wosstandardWOS:Ancuta, CM
dc.contributor.wosstandardWOS:Muller, R
dc.contributor.wosstandardWOS:Ornbjerg, L
dc.contributor.wosstandardWOS:Sokka, T
dc.date.coverdateAgosto 2017
dc.identifier.ulpgces
dc.description.sjr2,344
dc.description.jcr5,245
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Grupo de investigaciones infecciosas, nutricionales e inflamatorias en pacientes hospitalarios / Study Group on infectious, nutritional and inflammatory diseases in hospitalized patients-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-2013-6664-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameNaranjo Hernández, Antonio-
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