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dc.contributor.authorWalshe, Margaret
dc.contributor.authorDuncan, Sallyanne
dc.contributor.authorMcGaughey, Jennifer
dc.contributor.authorFallis, Richard
dc.contributor.authorMcAuley, Daniel F.
dc.contributor.authorWalshe, Margaret
dc.contributor.authorBlackwood, Bronagh
dc.date.accessioned2020-02-11T16:53:03Z
dc.date.available2020-02-11T16:53:03Z
dc.date.issued2019
dc.date.submitted2019en
dc.identifier.citationDuncan, S., McGaughey, J., Fallis, R., McAuley, D.F., Walshe, M. & Blackwood, B., Interventions for oropharyngeal dysphagia in acute and critical care: A protocol for a systematic review and meta analysis, Systematic Reviews, 283, 8, 2019, 1 - 8en
dc.identifier.otherY
dc.description.abstractBackground: Oropharyngeal dysphagia or swallowing difficulties are common in acute care and critical care, affecting 47% of hospitalised frail elderly, 50% of acute stroke patients and approximately 62% of critically ill patients who have been intubated and mechanically ventilated for prolonged periods. Complications of dysphagia include aspiration leading to chest infection and pneumonia, malnutrition, increased length of hospital stay and re-admission to hospital. To date, most dysphagia interventions in acute care have been tested with acute stroke populations. While intervention studies in critical care have been emerging since 2015, they are limited and so there is much to learn about the type, the delivery and the intensity of treatments in this setting to inform future clinical trials. The aim of this systematic review is to summarise the evidence regarding the relationship between dysphagia interventions and clinically important patient outcomes in acute and critical care settings. Methods: We will search MEDLINE, EMBASE, CENTRAL, Web of Science, CINAHL and clinical trial registries from inception to the present. We will include studies conducted with adults in acute care settings such as acute hospital wards or units or intensive care units and critical care settings. Studies will be restricted to randomised controlled trials and quasi-randomised controlled trials comparing a new dysphagia intervention with usual care or another intervention. The main outcomes that will be collected include length of time taken to return to oral intake, change in incidence of aspiration and pneumonia, nutritional status, length of hospital stay and quality of life. Key intervention components such as delivery, intensity, acceptability, fidelity and adverse events associated with such interventions will be collected to inform future clinical trials. Two independent reviewers will assess articles for eligibility, data extraction and quality appraisal. A meta-analysis will be conducted as appropriate. Discussion: No systematic review has attempted to summarise the evidence for oropharyngeal dysphagia interventions in acute and critical care. Results of the proposed systematic review will inform practice and the design of future clinical trials. Systematic review registration: PROSPERO CRD 42018116849 (http://www.crd.york.ac.uk/PROSPERO/)en
dc.format.extent1en
dc.format.extent8en
dc.language.isoenen
dc.relation.ispartofseriesSystematic Reviews;
dc.relation.ispartofseries283;
dc.relation.ispartofseries8;
dc.rightsYen
dc.subjectDysphagiaen
dc.subjectDeglutition disordersen
dc.subjectAcute careen
dc.subjectAcute hospitalen
dc.subjectCritical careen
dc.subjectIntensive careen
dc.subjectSwallow interventionsen
dc.titleInterventions for oropharyngeal dysphagia in acute and critical care: A protocol for a systematic review and meta analysisen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/walshema
dc.identifier.rssinternalid207800
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDTagDYSPHAGIAen
dc.subject.darat_impairmentChronic Health Conditionen
dc.subject.darat_impairmentOtheren
dc.status.accessibleNen
dc.contributor.sponsorNational Health and Medical Research Councilen
dc.identifier.urihttps://systematicreviewsjournal.biomedcentral.com/articles/10.1186/s13643-019-1196-0
dc.identifier.urihttp://hdl.handle.net/2262/91503


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