Utility of bedside leucocyte esterase testing to rule out septic arthritis.

dc.contributor.authorKnapper, Thomas
dc.contributor.authorMurphy, Richard J
dc.contributor.authorRocos, Brett
dc.contributor.authorFagg, James
dc.contributor.authorMurray, Nick
dc.contributor.authorWhitehouse, Michael Richard
dc.date.accessioned2024-01-10T16:22:17Z
dc.date.available2024-01-10T16:22:17Z
dc.date.issued2021-09
dc.description.abstract<h4>Introduction</h4>Suspected septic arthritis is a common presentation to EDs. The underlying diagnosis is often non-infective pathology. Differentiating between aetiologies is difficult. A bedside test with high negative predictive value (NPV) may allow safe discharge of patients, reduce the time in the ED, hospital admission and associated costs. This study aims to evaluate the NPV of bedside leucocyte esterase (LE) in the assessment of these patients.<h4>Methods</h4>A prospective multicentre observational study of ED adult patients referred to orthopaedics with suspected native joint septic arthritis between October 2015 and April 2016. At three hospital sites in the Bristol region, the results of the LE test exposed to aspirated synovial fluid were recorded along with Gram stain, culture, haematinics and length of stay. A positive LE test was considered 2+ or 3+ leucocytes based on the test strip colour. Data were analysed to establish sensitivity, specificity, NPV and positive predictive value (PPV) against the gold standard 48-hour culture. We determined the potential number of inpatient bed-days that might be avoided using this bedside test.<h4>Results</h4>Eighty patients underwent joint aspiration. Five cases had positive 48-hour culture. All (5/5) infected cases showed ≥2+ LE, sensitivity of 100% (95% CI 47.8% to 100%) while the Gram stain was positive in only one case (sensitivity 20%, 95% CI 0.51% to 71.6%). Twenty-three LE were read negative or 1+, all with negative 48-hour culture results, resulting in an NPV of 100% (95% CI 82.1% to 1.00%) for a negative LE test. Specificity of a positive LE test was 30.7% (95% CI 20.5% to 42.45%) with PPV of 8.77% (95% CI 7.64% to 10.1%). It was calculated that 57 orthopaedic bed-days could have potentially been saved by immediately discharging those with a negative LE test.<h4>Conclusions</h4>LE point-of-care testing for suspected septic arthritis of native joints has a high NPV. Implementation of LE may facilitate more rapid discharge of patients with negative results. This test has the potential to reduce diagnostic uncertainty and costs to the healthcare system.
dc.identifieremermed-2020-209842
dc.identifier.issn1472-0205
dc.identifier.issn1472-0213
dc.identifier.urihttps://hdl.handle.net/10161/29703
dc.languageeng
dc.publisherBMJ
dc.relation.ispartofEmergency medicine journal : EMJ
dc.relation.isversionof10.1136/emermed-2020-209842
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0
dc.subjectHumans
dc.subjectArthritis, Infectious
dc.subjectCarboxylic Ester Hydrolases
dc.subjectHospitalization
dc.subjectSensitivity and Specificity
dc.subjectProspective Studies
dc.subjectPredictive Value of Tests
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectEmergency Service, Hospital
dc.subjectEngland
dc.subjectFemale
dc.subjectMale
dc.subjectBiomarkers
dc.subjectPoint-of-Care Testing
dc.titleUtility of bedside leucocyte esterase testing to rule out septic arthritis.
dc.typeJournal article
duke.contributor.idRocos, Brett|1241189
duke.contributor.orcidRocos, Brett|0000-0002-0808-5585
pubs.begin-page707
pubs.end-page710
pubs.issue9
pubs.organisational-groupDuke
pubs.organisational-groupSchool of Medicine
pubs.organisational-groupClinical Science Departments
pubs.organisational-groupOrthopaedic Surgery
pubs.organisational-groupNeurosurgery
pubs.publication-statusPublished
pubs.volume38

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