What tests can be done in a pediatric ER to rule out influenza and Respiratory Syncytial Virus (RSV)?

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Last updated: December 28, 2025View editorial policy

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Diagnostic Testing for Influenza and RSV in the Pediatric Emergency Department

In a pediatric ER, use rapid molecular assays (nucleic acid amplification tests) as the first-line diagnostic test for both influenza and RSV, as these provide results in 15-30 minutes with high sensitivity (86-100%) and high specificity (>95%), far superior to rapid antigen tests which have unacceptably low sensitivity (10-70% for influenza, as low as 28% for influenza B). 1

Recommended Testing Algorithm

First-Line Testing: Rapid Molecular Assays

  • Obtain a nasopharyngeal swab or nasopharyngeal aspirate for both influenza and RSV testing, as these specimen types provide optimal sensitivity 1
  • Use rapid molecular assays (nucleic acid amplification tests) that detect influenza A, influenza B, and RSV viral RNA with results available in 15-30 minutes 1
  • Multiplex molecular assays can simultaneously detect influenza A, B, RSV, and other respiratory pathogens (adenovirus, rhinovirus, parainfluenza 1-3) in 1-2 hours with high sensitivity and specificity 1

When Rapid Molecular Testing is Unavailable

  • Direct or indirect immunofluorescence assays provide moderate sensitivity with results in 1-4 hours for both influenza and RSV 1
  • Standard RT-PCR (if rapid molecular unavailable) provides high sensitivity (86-100%) with results in 1-8 hours 1

Critical Timing Considerations

  • Collect respiratory specimens as close to illness onset as possible, ideally within the first 48 hours when viral shedding is highest and test sensitivity is optimal 1, 2
  • Do not delay antiviral treatment while waiting for test results in high-risk patients or those with severe illness 1, 2

Tests to AVOID or Use with Extreme Caution

Rapid Antigen Tests (Rapid Influenza Diagnostic Tests)

  • Rapid antigen tests have unacceptably low sensitivity (10-70% for influenza A, as low as 28% for influenza B) despite high specificity (>95%) 1, 3
  • Negative rapid antigen test results cannot rule out influenza or RSV due to high false-negative rates 1, 2
  • If rapid antigen testing is the only available option, negative results in hospitalized patients or those with high clinical suspicion should be confirmed with molecular testing (RT-PCR) 1, 2
  • Rapid antigen tests may be used to "rule in" infection when positive (high specificity 97%), but never to "rule out" when negative 1

Specimen Collection Best Practices

Optimal Specimen Types (in order of preference)

  1. Nasopharyngeal aspirate or washing - highest yield 1
  2. Nasopharyngeal swab - acceptable alternative, easier to obtain 1
  3. Throat swab combined with nasal swab - if nasopharyngeal collection not feasible 1
  4. Lower respiratory specimens (BAL fluid) - for patients with evidence of lower respiratory tract infection 1

Collection Timing

  • Collect within first 2 days of illness when sensitivity is highest (85% for RSV) 4
  • Sensitivity decreases significantly after 48 hours of symptom onset 2, 4

Additional Testing for Hospitalized or Severely Ill Children

Laboratory Studies

  • Complete blood count with differential - influenza commonly causes leukopenia and lymphopenia (lymphocyte count <1.0); thrombocytopenia occurs in 5-7% of influenza A cases 1, 5
  • Urea, creatinine, and electrolytes - assess for dehydration and renal function 1
  • Liver enzymes - elevated in 27% of influenza A cases 1
  • Blood culture - if bacterial superinfection suspected 1

Imaging and Monitoring

  • Pulse oximetry - perform in every child being assessed for admission with pneumonia or respiratory distress 1
  • Chest radiograph - only for children who are hypoxic (oxygen saturation <92%), have severe illness, or are deteriorating despite treatment 1

Common Pitfalls to Avoid

  • Never rely on negative rapid antigen tests to exclude influenza or RSV - sensitivity is too low (10-70%), especially for influenza B 1, 2, 3
  • Do not delay antiviral treatment while awaiting test results in high-risk patients (age <2 years, immunocompromised, chronic medical conditions) 1, 2
  • Do not use sputum collection in young children - unreliable except possibly in children >12 years of age 1
  • Avoid urinary pneumococcal antigen tests in children - lack both sensitivity and specificity in pediatric populations 1
  • Do not perform routine chest radiography in well-appearing children with uncomplicated respiratory illness - it does not affect clinical outcomes 1

Performance Characteristics by Age Group

RSV Testing Performance

  • Children <6 months: Optimal sensitivity 98%, specificity 96% with rapid molecular assays 6
  • Children ≥2 years: Sensitivity 87%, specificity 98% with rapid molecular assays 6
  • Overall pediatric population: Sensitivity 78.6-93%, specificity 93.9-96% for second-generation rapid tests 4, 6

Influenza Testing Performance

  • Rapid molecular assays: Sensitivity 80.6-100%, specificity 99.3% across all pediatric age groups 1, 4
  • Rapid antigen tests: Sensitivity as low as 47.7% for influenza A and 20.3% for influenza B in real-world pediatric settings 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Influenza Testing and Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Rapid assays for the diagnosis of influenza A and B viruses in patients evaluated at a large tertiary care children's hospital during two consecutive winter seasons.

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2008

Research

Evaluation of novel second-generation RSV and influenza rapid tests at the point of care.

Diagnostic microbiology and infectious disease, 2015

Guideline

Post-Influenza Ecchymosis in Infants: Diagnostic Approach

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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