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Clinical Prediction Tool to Assess the Likelihood of a Positive SARS-Cov-2 (COVID-19) Polymerase Chain Reaction Test in Patients with Flu-like Symptoms.
Lara, Barbara A; Torres, Francisco; Holger, Patricia; Perales, Claudia; Basauri, Sofia; Clausdorff, Hans; Escobedo, Ernesto; Saldias, Fernando; Swadron, Stuart; Aguilera, Pablo.
  • Lara BA; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Torres F; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Holger P; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Perales C; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Basauri S; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Clausdorff H; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Escobedo E; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
  • Saldias F; Pontificia Universidad Católica de Chile, Department of Respiratory Diseases, Santiago, Chile.
  • Swadron S; Keck School of Medicine, Department of Emergency Medicine, University of Southern California, Los Angeles, California.
  • Aguilera P; Pontificia Universidad Católica de Chile, Section of Emergency Medicine, Santiago, Chile.
West J Emerg Med ; 22(3): 592-598, 2021 Mar 24.
Article in English | MEDLINE | ID: covidwho-1266877
ABSTRACT

INTRODUCTION:

The clinical presentation of coronavirus disease 2019 (COVID-19) overlaps with many other common cold and influenza viruses. Identifying patients with a higher probability of infection becomes crucial in settings with limited access to testing. We developed a prediction instrument to assess the likelihood of a positive polymerase chain reaction (PCR) test, based solely on clinical variables that can be determined within the time frame of an emergency department (ED) patient encounter.

METHODS:

We derived and prospectively validated a model to predict SARS-CoV-2 PCR positivity in patients visiting the ED with symptoms consistent with the disease.

RESULTS:

Our model was based on 617 ED visits. In the derivation cohort, the median age was 36 years, 43% were men, and 9% had a positive result. The median time to testing from the onset of initial symptoms was four days (interquartile range [IQR] 2-5 days, range 0-23 days), and 91% of all patients were discharged home. The final model based on a multivariable logistic regression included a history of close contact (adjusted odds ratio [AOR] 2.47, 95% confidence interval [CI], 1.29-4.7); fever (AOR 3.63, 95% CI, 1.931-6.85); anosmia or dysgeusia (AOR 9.7, 95% CI, 2.72-34.5); headache (AOR 1.95, 95% CI, 1.06-3.58), myalgia (AOR 2.6, 95% CI, 1.39-4.89); and dry cough (AOR 1.93, 95% CI, 1.02-3.64). The area under the curve (AUC) from the derivation cohort was 0.79 (95% CI, 0.73-0.85) and AUC 0.7 (95% CI, 0.61-0.75) in the validation cohort (N = 379).

CONCLUSION:

We developed and validated a clinical tool to predict SARS-CoV-2 PCR positivity in patients presenting to the ED to assist with patient disposition in environments where COVID-19 tests or timely results are not readily available.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Decision Support Techniques / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Female / Humans / Male Language: English Journal: West J Emerg Med Year: 2021 Document Type: Article Affiliation country: Westjem.2020.12.49200

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Decision Support Techniques / COVID-19 Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Female / Humans / Male Language: English Journal: West J Emerg Med Year: 2021 Document Type: Article Affiliation country: Westjem.2020.12.49200