Five Viruses. One Swab. Results in 24 Hours.
The five questions you actually ask in respiratory virus season — SARS-CoV-2, Flu A, Flu B, RSV A, RSV B — answered in one run.
Outpatient respiratory season is a stream of patients who all look the same at the front desk: cough, fever, congestion. The clinical question is binary per pathogen — antiviral, isolation, return to work — but the differential is five-deep.
One nasopharyngeal swab, one multiplex PCR run, all five high-impact respiratory viruses resolved in 24–48 hours. No stacking of rapid antigen, send-out flu PCR, and a separate RSV order.
The clinical weight behind this panel.
Industry statistics from public-health bodies and peer-reviewed literature — context for why this testing matters.
Same-day PCR keeps that window open.
Figures reflect publicly reported epidemiology and clinical literature for context only. They are not performance claims for the Chaseville Labs assay. See individual citations from the U.S. Centers for Disease Control and Prevention, World Health Organization, National Institutes of Health, and peer-reviewed journals.
Conditions, syndromes & infections covered.
The clinical scenarios where this panel is the right call — built around the differential your providers are actually working through.
Seasonal Respiratory Viruses
3Confirmatory PCR for symptomatic patients during respiratory virus season.
The classic flu — fever, body aches, cough, fatigue, often severe in elderly and pediatric patients.
Leading cause of hospitalization in infants and a major driver of pneumonia in elderly adults.
Triage Decisions
2The patient at the front desk who could have any of five things — resolved in one swab.
Flu + COVID, COVID + RSV, and other dual infections that worsen outcomes.
5 targets, resolved from a single specimen.
Each organism below is reported individually as Detected, Not Detected, or Inconclusive — grouped here by pathogen class for clinical scanability.
Viral
5 targetsCulture was built for a different century.
Multiplex real-time PCR resolves what culture and rapid antigen miss — fastidious organisms, polymicrobial infections, viruses, and resistance markers — from a single specimen.
Culture & rapid antigen
- 3–5 daysPatient empirically treated before any answer arrives
- Misses fastidious & viral organismsNo growth ≠ no infection
- Single-organism biasPolymicrobial infections under-reported
- No resistance dataSusceptibilities arrive a day later, if at all
- Specimen-quality dependentPre-treated patients culture negative
Respiratory on Bio-Rad CFX384
- 24–48 hoursMost reports back the next clinical day
- 5 targets, one runBacterial, viral, fungal, and parasitic in a single multiplex
- Detects what culture can'tFastidious organisms, viruses, and polymicrobial infections, all reported individually
- Validated LDTCLIA-certified, internally controlled, per-target Detected / Not Detected reporting
Per-target results, with clinical context.
Every analyte is reported individually as Detected, Not Detected, or Inconclusive. What a Detected result means clinically depends on which category the target falls into:
Rapid differentiation of SARS-CoV-2, influenza A/B, and RSV directs antiviral eligibility (oseltamivir, nirmatrelvir, RSV mAb prophylaxis), isolation, and cohorting decisions in the first visit.