Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/123922
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dc.contributor.authorPérez Ruiz, Fernando-
dc.contributor.authorSanchez-Piedra, Carlos A.-
dc.contributor.authorSánchez Costa, Jesús T.-
dc.contributor.authorAndrés, Mariano-
dc.contributor.authorDíaz-Torné, César-
dc.contributor.authorJimenez-Palop, Mercerdes-
dc.contributor.authorDe Miguel, Eugenio-
dc.contributor.authorMoragues, Carmen-
dc.contributor.authorSivera, Francisca-
dc.date.accessioned2018-07-25T09:48:39Z-
dc.date.available2018-07-25T09:48:39Z-
dc.date.issued2018-06-01-
dc.identifier.urihttp://hdl.handle.net/2445/123922-
dc.description.abstractThe objective of the study was to evaluate changes regarding main European League Against Rheumatism (EULAR) recommendations on diagnosis and treatment of gout compared to a previous assessment. The GEMA-2 (Gout Evaluation and MAnagement) is a transversal assessment of practice for gout by rheumatologists. Main outcome variables were improvement of the previous GEMA assessment regarding the rate of crystal-proven diagnosis and that reaching therapeutic serum urate target below 6 mg/dl at last visit. Other management variables (prophylaxis, treatment of flares, lifestyle change advice) were also evaluated along with general characteristics. The sample was powered to include at least 483 patients for up to 50% change. Data on management of 506 patients were retrieved from 38 out of 41 rheumatology units that participated in the previous GEMA audit. Crystal-proved diagnosis rate increased from 26% to 32% (31% improvement) and was higher in gout-dedicated practices; ultrasonography contributed to diagnosis in less than 1% of cases. Therapeutic serum urate at last visit improved from 41% to 64% of all patients (66% of patients on urate-lowering medications), in any case over 50% improvement from the previous assessment. The use of any urate-lowering medication available was not prescribed as per label dosing in patients who failed to achieve target serum urate. Clinical inertia to increase doses of either allopurinol or febuxostat was still present in clinical practice. Over 50% improvement in targeting therapeutic serum urate has been observed, but clinical inertia is still present. Diagnosis is still mostly clinically based, ultrasonography not being commonly contributive. Menarini Espaa.-
dc.format.extent11 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1007/s40744-017-0091-1-
dc.relation.ispartofRheumatology And Therapy, 2018, vol. 5, Issue 1, P. 243-253-
dc.relation.urihttps://doi.org/10.1007/s40744-017-0091-1-
dc.rightscc by (c) Fernando Perez Rui et al., 2018-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationReumatologia-
dc.subject.classificationEuropa-
dc.subject.classificationTerapèutica-
dc.subject.otherRheumatology-
dc.subject.otherEurope-
dc.subject.otherTherapeutics-
dc.titleImprovement In Diagnosis And Treat-to-target Management Of Hyperuricemia In Gout: Results From The Gema-2 Transversal Study On Practice-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2018-07-24T11:38:49Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid29204859-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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