Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/127334
DC Field | Value | Language |
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dc.contributor.author | Taxonera, C | en_US |
dc.contributor.author | López-Sanromán, A | en_US |
dc.contributor.author | Vera-Mendoza, I | en_US |
dc.contributor.author | Domènech, E | en_US |
dc.contributor.author | Ruiz, VV | en_US |
dc.contributor.author | Marín-Jiménez, I | en_US |
dc.contributor.author | Guardiola, J | en_US |
dc.contributor.author | Castro, L | en_US |
dc.contributor.author | Esteve, M | en_US |
dc.contributor.author | Iglesias, E | en_US |
dc.contributor.author | Ceballos Santos, Daniel Sebastián | en_US |
dc.contributor.author | Martínez-Montiel, P | en_US |
dc.contributor.author | Gisbert, JP | en_US |
dc.contributor.author | Mínguez, M | en_US |
dc.contributor.author | Echarri, A | en_US |
dc.contributor.author | Calvet, X | en_US |
dc.contributor.author | Barrio, J | en_US |
dc.contributor.author | Hinojosa, J | en_US |
dc.contributor.author | Martín-Arranz, MD | en_US |
dc.contributor.author | Márquez-Mosquera, L | en_US |
dc.contributor.author | Bermejo, F | en_US |
dc.contributor.author | Rimola, J | en_US |
dc.contributor.author | Alba, C | en_US |
dc.contributor.author | Pons, V | en_US |
dc.contributor.author | Nos, P | en_US |
dc.date.accessioned | 2023-10-20T13:06:53Z | - |
dc.date.available | 2023-10-20T13:06:53Z | - |
dc.date.issued | 2019 | en_US |
dc.identifier.issn | 1590-8658 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/127334 | - |
dc.description.abstract | Background: In APPRECIA trial, Crohn's disease (CD) patients undergoing intestinal resection were randomized to postoperative adalimumab (ADA) or azathioprine (AZA). Aims: To evaluate health-related quality of life (HRQoL) in APPRECIA trial. Methods: HRQoL was evaluated using disease-specific shortened Spanish version of the IBDQ (SIBDQ-9) and generic European Quality of Life-5 Dimensions (EQ-5D) questionnaires, completed at baseline and at weeks 24 and 52. Results: Sixty-one patients (37 ADA and 24 AZA) had evaluable data for HRQoL. Patients treated with ADA or AZA had significant improvement from baseline to weeks 24 and 52 in SIBDQ-9 and EQ-5D (p < 0.001 and p ≤ 0.006 for all comparisons, respectively). There were no differences between treatment arms in mean change in SIBDQ-9 and EQ-5D at weeks 24 and 52 vs baseline. Only patients without endoscopic recurrence had significant improvement in SIBDQ-9 (p < 0.001) and EQ-5D (p < 0.001) at week 52. At week 52, there was a high to moderate negative correlation between CDAI score with SIBDQ-9 score (Pearson's r: −0.768) and with EQ-5D index (r: −0.644). Conclusion: HRQoL improved after intestinal resection in CD, irrespective of the postoperative therapy used (ADA or AZA). Outcomes in HRQoL were associated with prevention of endoscopic recurrence, since improvements in HRQoL were only significant in patients with endoscopic remission at 1 year. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Digestive and Liver Disease | en_US |
dc.source | Digestive and Liver Disease [1590-8658], v. 51(4), pp. 529-535 (Abril 2019) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3205 Medicina interna | en_US |
dc.subject.other | Adalimumab | en_US |
dc.subject.other | Crohn's disease | en_US |
dc.subject.other | Postoperative recurrence | en_US |
dc.subject.other | Postoperative therapy | en_US |
dc.subject.other | Quality of life | en_US |
dc.title | Quality of life during one year of postoperative prophylactic drug therapy after intestinal resection in Crohn's patients: Results of the APPRECIA trial | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.dld.2019.01.002 | en_US |
dc.identifier.pmid | 30712954 | - |
dc.identifier.scopus | 2-s2.0-85060768034 | - |
dc.identifier.isi | WOS:000463166800013 | - |
dc.contributor.orcid | 0000-0001-9166-7350 | - |
dc.contributor.orcid | 0000-0003-0236-4118 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | 0000-0002-0464-241X | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | 0000-0003-2090-3445 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.description.lastpage | 535 | en_US |
dc.identifier.issue | 4 | - |
dc.description.firstpage | 529 | en_US |
dc.relation.volume | 51 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 7 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Abril 2019 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 0,941 | |
dc.description.jcr | 3,57 | |
dc.description.sjrq | Q2 | |
dc.description.jcrq | Q2 | |
dc.description.scie | SCIE | |
item.fulltext | Con texto completo | - |
item.grantfulltext | open | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0003-2384-4524 | - |
crisitem.author.fullName | Ceballos Santos, Daniel Sebastián | - |
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