Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25536
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dc.contributor.authorTu, Jacky-
dc.contributor.authorGowdie, Peter-
dc.contributor.authorCassar, Julian-
dc.contributor.authorCraig, Simon-
dc.date2020-12-30-
dc.date.accessioned2021-01-04T23:56:32Z-
dc.date.available2021-01-04T23:56:32Z-
dc.date.issued2020-12-30-
dc.identifier.citationBMJ Open 2020; 10(12): e038088en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25536-
dc.description.abstractSeptic arthritis is an uncommon but potentially significant diagnosis to be considered when a child presents to the emergency department (ED) with non-traumatic limp. Our objective was to determine the diagnostic accuracy of clinical findings (history and examination) and investigation results (pathology tests and imaging) for the diagnosis of septic arthritis among children presenting with acute non-traumatic limp to the ED. Systematic review of the literature published between 1966 and June 2019 on MEDLINE and EMBASE databases. Studies were included if they evaluated children presenting with lower limb complaints and evaluated diagnostic performance of items from history, physical examination, laboratory testing or radiological examination. Data were independently extracted by two authors, and quality assessment was performed using the Quality Assessment Tool for Diagnostic Accuracy Studies 2 tool. 18 studies were identified, and included 2672 children (560 with a final diagnosis of septic arthritis). There was substantial heterogeneity in inclusion criteria, study setting, definitions of specific variables and the gold standard used to confirm septic arthritis. Clinical and investigation findings were reported using varying definitions and cut-offs, and applied to differing study populations. Spectrum bias and poor-to-moderate study design quality limit their applicability to the ED setting.Single studies suggest that the presence of joint tenderness (n=189; positive likelihood ratio 11.4 (95% CI 5.9 to 22.0); negative likelihood ratio 0.2 (95% CI 0.0 to 1.2)) and joint effusion on ultrasound (n=127; positive likelihood ratio 8.4 (95% CI 4.1 to 17.1); negative likelihood ratio 0.2 (95% CI 0.1 to 0.3)) appear to be useful. Two promising clinical risk prediction tools were identified, however, their performance was notably lower when tested in external validation studies. Differentiating children with septic arthritis from non-emergent disorders of non-traumatic limp remains a key diagnostic challenge for emergency physicians. There is a need for prospectively derived and validated ED-based clinical risk prediction tools.en
dc.language.isoeng
dc.subjectpaediatric A&E and ambulatory careen
dc.subjectpaediatric infectious disease & immunisationen
dc.subjectpaediatric orthopaedicsen
dc.titleTest characteristics of history, examination and investigations in the evaluation for septic arthritis in the child presenting with acute non-traumatic limp. A systematic review.en
dc.typeJournal Articleen
dc.identifier.journaltitleBMJ Openen
dc.identifier.affiliationSchool of Clinical Sciences at Monash Health, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Paediatrics, School of Clinical Sciences, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationPediatric Emergency Department, Monash Medical Centre, Emergency Service, Monash Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationEmergency Research, Murdoch Children's Research Institute, Parkville, Victoria, Australiaen
dc.identifier.affiliationMonash Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationAustin Healthen
dc.identifier.affiliationDepartment of Paediatrics and Department of Paediatric Rheumatology, Monash Children's Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Paediatrics, School of Clinical Sciences, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1136/bmjopen-2020-038088en
dc.type.contentTexten
dc.identifier.orcid0000-0003-2594-1643en
dc.identifier.pubmedid33380476
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
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