Utility of bedside leucocyte esterase testing to rule out septic arthritis.
Adult
Aged
Aged, 80 and over
Arthritis, Infectious
/ diagnosis
Biomarkers
/ analysis
Carboxylic Ester Hydrolases
/ analysis
Emergency Service, Hospital
England
Female
Hospitalization
Humans
Male
Middle Aged
Point-of-Care Testing
Predictive Value of Tests
Prospective Studies
Sensitivity and Specificity
cost effectiveness
diagnosis
infection
musculo-skeletal
non traumatic problems
soft tissue infection
Journal
Emergency medicine journal : EMJ
ISSN: 1472-0213
Titre abrégé: Emerg Med J
Pays: England
ID NLM: 100963089
Informations de publication
Date de publication:
Sep 2021
Sep 2021
Historique:
received:
01
05
2020
revised:
14
01
2021
accepted:
11
02
2021
pubmed:
12
3
2021
medline:
21
9
2021
entrez:
11
3
2021
Statut:
ppublish
Résumé
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. 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. 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. 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.
Identifiants
pubmed: 33692113
pii: emermed-2020-209842
doi: 10.1136/emermed-2020-209842
doi:
Substances chimiques
Biomarkers
0
leukocyte esterase
EC 3.1.-
Carboxylic Ester Hydrolases
EC 3.1.1.-
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
707-710Informations de copyright
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.