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Rotavirus Antigen Test -
Detects rotavirus antigen to diagnose diarrhea, causing dehydration or fever
Synonym Rotavirus Test
Test Code VIRT26040044
Test Type Virology
Pre-Test Condition No special
Report Availability 1–2 D(s)
# Test(s) 1
Test details Sample Report
Rotavirus Antigen Test Sample Report Cowin-PathLab
Synonym Rotavirus Test
Test Code VIRT26040044
Test Category Rotavirus Infection
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 1–2 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 2 H(s)
Stability @ 2-8 deg. C 24 H(s)
Stability @ Frozen Not frozen
# Test(s) 1
Processing Method Immunoassay
Overview: Rotavirus Antigen Test
Introduction: The Rotavirus Antigen Test detects rotavirus antigen to diagnose diarrhea, causing dehydration or fever. Aligned with 2023 IDSA guidelines, it uses immunoassays for high specificity, supporting infection screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in virology for patients with suspected rotavirus infection.
Other Names: Rotavirus Assay, Stool Rotavirus Test.
FDA Status: Laboratory-developed test (LDT), meeting virology standards for diagnostic accuracy.
Historical Milestone: Rotavirus testing began in the 1970s with diarrhea research. Immunoassay methods improved in the 2000s, enhancing diagnostic precision.
Purpose: Detects rotavirus antigen to diagnose diarrhea, guides treatment, and evaluates patients with dehydration or fever.
Test Parameters: 1. Rotavirus Antigen
Pretest Condition: No fasting required. Collect stool. Report history of diarrhea, dehydration, or fever.
Specimen: Stool (sterile container, 5-10 gm). Transport in a biohazard container.
Sample Stability at Room Temperature: 2 hours
Sample Stability at Refrigeration: 24 hours
Sample Stability at Frozen: Not frozen
Medical History: Document diarrhea, dehydration, or history of viral infections. Include current medications, especially anti-diarrheals.
Consent: Written consent required, detailing the tests purpose, rotavirus infection implications, and risks of sample collection.
Procedural Considerations: Uses enzyme-linked immunosorbent assay (ELISA) to detect rotavirus antigen. Results are available in 1-2 days, supporting clinical decisions. Performed in laboratories, often for rotavirus diagnosis.
Factors Affecting Result Accuracy: Improper sample collection or storage can affect results. Early or late testing may yield false negatives.
Clinical Significance: Positive rotavirus antigen confirms infection, guiding rehydration therapy. Negative results may require PCR testing.
Specialist Consultation: Consult an infectious disease specialist or pediatrician for result interpretation and treatment planning.
Additional Supporting Tests: Rotavirus PCR, electrolyte panel, or clinical evaluation to confirm rotavirus diagnosis.
Test Limitations: Non-specific for certain viral diarrheas; clinical correlation is needed. Sample quality affects sensitivity.
References: IDSA Rotavirus Guidelines, 2023; Clinical Infectious Diseases, Bernstein DI, 2022.

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