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

dc.contributor.author

Knapper, Thomas

dc.contributor.author

Murphy, Richard J

dc.contributor.author

Rocos, Brett

dc.contributor.author

Fagg, James

dc.contributor.author

Murray, Nick

dc.contributor.author

Whitehouse, Michael Richard

dc.date.accessioned

2024-01-10T16:22:17Z

dc.date.available

2024-01-10T16:22:17Z

dc.date.issued

2021-09

dc.description.abstract

Introduction

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.

Methods

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.

Results

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.

Conclusions

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.identifier

emermed-2020-209842

dc.identifier.issn

1472-0205

dc.identifier.issn

1472-0213

dc.identifier.uri

https://hdl.handle.net/10161/29703

dc.language

eng

dc.publisher

BMJ

dc.relation.ispartof

Emergency medicine journal : EMJ

dc.relation.isversionof

10.1136/emermed-2020-209842

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

Humans

dc.subject

Arthritis, Infectious

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Carboxylic Ester Hydrolases

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Hospitalization

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Sensitivity and Specificity

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Prospective Studies

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Predictive Value of Tests

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Adult

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Aged

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Aged, 80 and over

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Middle Aged

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Emergency Service, Hospital

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England

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Female

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Male

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Biomarkers

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Point-of-Care Testing

dc.title

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

dc.type

Journal article

duke.contributor.orcid

Rocos, Brett|0000-0002-0808-5585

pubs.begin-page

707

pubs.end-page

710

pubs.issue

9

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Orthopaedic Surgery

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

38

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