Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5439
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWynne, Rochelleen
dc.contributor.authorRendell, Georgiaen
dc.contributor.authorSorrell, Julie Louiseen
dc.contributor.authorMcTier, Laurenen
dc.date.accessioned2023-12-05T02:59:56Z-
dc.date.available2023-12-05T02:59:56Z-
dc.date.issued2023-07-01-
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/5439-
dc.description.abstractLower life expectancy, higher rates of chronic disease, and poorer uptake of health services are common in remote patient populations. Patients with poor health literacy (HL) are less likely to attend appointments, adhere to medications, and have higher rates of chronic illness. Evidence underpinning the relationship between HL and inequity in remote critical care populations is sparse. Objectives: The primary study aim was to explore a multidimensional HL profile of patients requiring critical care in a remote area health service. Secondary aims were to explore HL in subgroups of the sample and to explore associations between HL and emergency department representation and discharge against medical advice. Methods: This was a cross-sectional study of consecutive eligible patients admitted to the Mount Isa hospital intensive care unit. The Health Literacy Questionnaire was administered in a semistructured interview. Results: In a 5-month period, there were 141 patient admissions to the five-bed intensive care unit, 67 patients (47.5%) met inclusion criteria and were not discharged prior to recruitment, and 37 (26.2%) agreed to participate. Participants felt understood and supported by healthcare providers, had sufficient information to manage their health, proactively engaged with healthcare providers, and had strong social supports. More challenging was their capacity to advocate on their own behalf, to explore and appraise information and to navigate healthcare systems. Patients who represented to the emergency department (n ¼ 8, 21.6%) felt more empowered to seek healthcare advice. Of the 11 patients that discharged against medical advice, only one participated in the study. Conclusion: Trends in the data showed that Aboriginal and Torres Strait Islander participants were marginally less likely to be information explorers and to understand all written information. Findings provide guidance for the development of interventions to progress a reduction in health disparities experienced by this population.en
dc.language.isoenen
dc.relation.ispartofAustralian critical careen
dc.subjectHealth literacy, Critical care, Patient participation, Indigenous Australians, Remote area health serviceen
dc.titleHealth literacy of critical care patients in a remote area health service: A cross-sectional surveyen
dc.typeArticleen
dc.identifier.doihttps://doi.org/10.1016/j.aucc.2022.08.007-
dc.rights.holderJulie Sorrellen
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
Appears in Sites:North West HHS Publications
Queensland Health Publications
Files in This Item:
File Description SizeFormat 
Health literacy of critical care patients in a remote area health service.pdfHealth literacy of critical care patients in a remote area health service.pdf307.56 kBAdobe PDFThumbnail
View/Open
Show simple item record

Page view(s)

96
checked on May 8, 2025

Download(s)

230
checked on May 8, 2025

Google ScholarTM

Check

Altmetric


Items in DORA are protected by copyright, with all rights reserved, unless otherwise indicated.