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A clinical decision rule to rule out bloodstream infection in the emergency department: retrospective multicentric observational cohort study
  1. Jonathan Pehlivan1,
  2. Delphine Douillet2,3,
  3. Riou Jérémie4,5,
  4. Clément Perraud2,
  5. Alexandre Niset6,
  6. Matthieu Eveillard7,
  7. Rachel Chenouard7,
  8. Rafael Mahieu8,9
  1. 1 Service de maladies infectieuses et tropicales, Centre hospitalier universitaire d'Angers, Centre Hospitalier Universitaire d'Angers, Angers, France
  2. 2 Emergency Department, Angers University Hospital, CHU Angers, Angers, France
  3. 3 UMR MitoVasc CNRS 6015—INSERM 1083, University of Angers, Angers, France
  4. 4 Micro et Nano médecines translationnelles, MINT, UMR INSERM 1066, UMR CNRS 6021, University of Angers, Angers, France
  5. 5 Methodology and Biostatistics Department, Delegation to Clinical Research and Innovation, Angers University Hospital, CHU Angers, Angers, France
  6. 6 Emergency Department, Cliniques Universitaires Saint-Luc, Université catholique de Louvain, Hopital à Bruxelles—Cliniques universitaires Saint-Luc, Bruxelles, Belgium
  7. 7 Laboratoire de Bactériologie, Institut de Biologie en Santé—PBH, CHU Angers, Angers, France
  8. 8 Service de maladies infectieuses et tropicales, Centre hospitalier universitaire d'Angers, CHU Angers Maladies infectieuses et tropicales, Angers, France
  9. 9 Faculty of Medicine, Université de Nantes, Inserm, CRCINA, SFR ICAT, University of Angers, Angers, France
  1. Correspondence to Dr Rafael Mahieu, Service de maladies infectieuses et tropicales, Centre hospitalier universitaire d'Angers, 4 rue Larrey, 49100 Angers, France, CHU Angers Maladies infectieuses et tropicales, Angers 49100, France; rafael.mahieu{at}gmail.com

Abstract

Background We aimed to identify patients at low risk of bloodstream infection (BSI) in the ED.

Methods We derived and validated a prediction model to rule out BSI in the ED without the need for laboratory testing by determining variables associated with a positive blood culture (BC) and assigned points according to regression coefficients. This retrospective study included adult patients suspected of having BSI (defined by at least one BC collection) from two European ED between 1 January 2017 and 31 December 2019. The primary end point was the BSI rate in the validation cohort for patients with a negative Bacteremia Rule Out Criteria (BAROC) score. The effect of adding laboratory variables to the model was evaluated as a second step in a two-step diagnostic strategy.

Results We analysed 2580 patients with a mean age of 64 years±21, of whom 46.1% were women. The derived BAROC score comprises 12 categorical clinical variables. In the validation cohort, it safely ruled out BSI without BCs in 9% (58/648) of patients with a sensitivity of 100% (95% CI 95% to 100%), a specificity of 10% (95% CI 8% to 13%) and a negative predictive value of 100% (95% CI 94% to 100%). Adding laboratory variables (creatinine ≥177 µmol/L (2.0 mg/dL), platelet count ≤150 000/mm3 and neutrophil count ≥12 000/mm3) to the model, ruled out BSI in 10.2% (58/570) of remaining patients who had been positive on the BAROC score. The BAROC score with laboratory results had a sensitivity of 100% (95% CI 94% to 100%), specificity of 11% (95% CI 9% to 14%) and negative predictive value of 100% (95% CI 94 to 100%). In the validation cohort, there was no evidence of a difference in discrimination between the area under the receiver operating characteristic for BAROC score with versus without laboratory testing (p=0.6).

Conclusion The BAROC score safely identified patients at low risk of BSI and may reduce BC collection in the ED without the need for laboratory testing.

  • emergency department
  • clinical medicine
  • diagnostic tests
  • infections

Data availability statement

Data are available on reasonable request.

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Data availability statement

Data are available on reasonable request.

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Footnotes

  • Handling editor Kirsty Challen

  • Contributors RM, JP, ME, RC and DD designed and supervised the study. JP, CP and AN supervised the study in their respective centres and included a large number of patients. RJ and RM performed statistical analysis. RM and JP drafted the manuscript and all authors contributed substantially to its revision. RM is responsible for all data and is the guarantor.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.