Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12615
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dc.contributor.authorHaines, Kimberley Jen
dc.contributor.authorDenehy, Lindaen
dc.contributor.authorSkinner, Elizabeth Hen
dc.contributor.authorWarrillow, Stephen Jen
dc.contributor.authorBerney, Susan Cen
dc.date.accessioned2015-05-16T02:19:57Z
dc.date.available2015-05-16T02:19:57Z
dc.date.issued2015-05-01en
dc.identifier.citationCritical Care Medicine; 43(5): 1112-20en
dc.identifier.govdoc25654174en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12615en
dc.description.abstractThe objective of the review was to evaluate and synthesize the prevalence, risk factors, and trajectory of psychosocial morbidity in informal caregivers of critical care survivors.A systematic search of MEDLINE, PsychInfo, PubMed, CINAHL, Cochrane Library, Scopus, PILOTS, EMBASE, and Physiotherapy Evidence Database was undertaken between January and February 2014.Citations were screened independently by two reviewers for studies that investigated psychosocial outcomes (depression, anxiety, stress, posttraumatic stress disorder, burden, activity restriction, and health-related quality of life) for informal caregivers of critical care survivors (mechanically ventilated for 48 hr or more).Data on study outcomes were extracted into a standardized form and quality assessed by two independent reviewers using the Newcastle-Ottawa Scale, the Physiotherapy Evidence Database, and the National Health and Medical Research Council Hierarchy of Evidence guide. Preferred Reporting Items for Systematic Reviews guidelines were followed.Fourteen studies of 1,491 caregivers were included. Depressive symptoms were the most commonly reported outcome with a prevalence of 75.5% during critical care and 22.8-29% at 1-year follow-up. Risk factors for depressive symptoms in caregivers included female gender and younger age. The greatest period of risk for all outcomes was during the patient's critical care admission although psychological symptoms improved over time. The overall quality of the studies was low.Depressive symptoms were the most prevalent in informal caregivers of survivors of intensive care who were ventilated for more than 48 hours and persist at 1 year with a prevalence of 22.8-29.0%, which is comparable with caregivers of patients with dementia. Screening for caregiver risks could be performed during the ICU admission where intervention can be implemented and then evaluated. Further high-quality studies are needed to quantify anxiety, stress, caregiver burden, and posttraumatic stress disorder outcomes in informal caregivers of long-stay patients surviving ICU.en
dc.language.isoenen
dc.titlePsychosocial outcomes in informal caregivers of the critically ill: a systematic review.en
dc.typeJournal Articleen
dc.identifier.journaltitleCritical Care Medicineen
dc.identifier.affiliationDepartment of Physiotherapy, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Physiotherapy, Western Centre for Health Research and Education, Western Health, St Albans, Victoria, Australiaen
dc.identifier.affiliationDepartment of Physiotherapy, Melbourne School of Health Sciences, The University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.doi10.1097/CCM.0000000000000865en
dc.description.pages1112-20en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25654174en
dc.type.austinJournal Articleen
local.name.researcherBerney, Susan C
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptClinical Education-
crisitem.author.deptIntensive Care-
crisitem.author.deptPhysiotherapy-
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