Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36300
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dc.contributor.authorBell S.en
dc.contributor.authorCronin O.en
dc.contributor.authorYang L.en
dc.contributor.authorSpizzo P.en
dc.contributor.authorFehily S.en
dc.contributor.authorHair C.en
dc.date.accessioned2021-05-14T12:18:31Zen
dc.date.available2021-05-14T12:18:31Zen
dc.date.copyright2019en
dc.date.created20191003en
dc.date.issued2019-10-03-
dc.date.issued2019-10-03en
dc.identifier.citationJournal of Gastroenterology and Hepatology. Conference: Gastroenterological Society of Australia, GESA Australian Gastroenterology Week, AGW "The Universe Within". Adelaide, SA Australia. 34 (Supplement 2) (pp 120), 2019. Date of Publication: September 2019.en
dc.identifier.issn0815-9319en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36300en
dc.description.abstractBackground and Aim: Anxiety, depression, and disability are common in patients with inflammatory bowel disease (IBD). The aim of this study was to assess the underlying disability, anxiety, and depression in a combined IBD cohort. Secondary aims were to analyze the clinical predictors of anxiety and depression; assess the correlation between the Hospital Anxiety and Depression Scale (HADS) with the IBD Disability Index (IBD-DI); and assess the change in anxiety and depression with a repeat HADS questionnaire. Method(s): This prospective observational study included patients with IBD from two tertiary referral centers. Baseline characteristics were recorded for all patients. Disability, anxiety, and depression were measured using the IBD-DI and HADS questionnaires. HADS and a subjective measure of disease control were repeated after 1 year. Result(s): A total of 150 patients were included in this study, of whom 61 had ulcerative colitis (UC) and 89 had Crohn's disease (CD). The prevalences of disability, anxiety, and depression were 71%, 41%, and 23%, respectively. Anxiety was associated with disability and depression (P = 0.003 and P < 0.001, respectively). Depression was associated with disability, anxiety, and active disease (P = 0.003, P < 0.001, and P = 0.003, respectively). Disability was associated with depression, anxiety, and active disease (P = 0.003, P < 0.001, and P < 0.001, respectively). Anxiety, depression, and psychological distress were all associated with disability (P < 0.001). Disability was associated with active disease (P = 0.004). There was less psychological distress on follow-up after 1 year (P = 0.009), but overall prevalences of anxiety and depression remained similar. Conclusion(s): Disability is associated with active IBD. In addition to traditional measures of disease control, measurement of disability, depression, and anxiety through objective measures would allow for an improved global assessment of disease, to better identify those patients needing more support from the IBD multidisciplinary team.en
dc.languageenen
dc.languageEnglishen
dc.publisherACT Publishing Group Liminteden
dc.titleAnxiety, depression, and disability in patients with inflammatory bowel disease.en
dc.typeConference Abstracten
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/jgh.14801en
dc.publisher.placeNetherlandsen
local.date.conferencestart20190908en
dc.identifier.source629456969en
dc.identifier.institution(Cronin, Yang) St Vincent's Hospital, Australia (Fehily) Alfred Hospital, Australia (Bell) Monash Medical Centre, Melbourne, Australia (Hair) University Hospital, Geelong, VIC, Australia (Spizzo) Flinders Medical Center, Adelaide, SA, Australiaen
dc.description.addressO. Cronin, St Vincent's Hospital, Australiaen
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend20190910en
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeConference Abstract-
crisitem.author.deptGastroenterology and Hepatology-
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