H9N7 & Influenza A (RNA Detection) Qualitative Test
Short Name: H9N7 & Influenza A RNA
Also known as: H9N7 PCR, Influenza A RNA Detection, Avian Influenza A (H9N7) Test
H9N7 & Influenza A (RNA Detection) Qualitative Test test available at DNA Labs India for ₹9,860. Uses Real Time PCR on Sputum; throat and nasal swabs in viral transport medium, or lung tissues, Cell Cultures etc. samples. Results in Reports are available on the 4th working day after sample collection. Email delivery within 48 hours of report generation, phone within 36 hours.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Kothari Ramesh Shantilal
Consultant Microbiologist · Reg: 27670
Last reviewed: September 7, 2026
Overview
The purpose of this test is to qualitatively detect the presence of H9N7 and Influenza A viral RNA in respiratory specimens. It aids in the diagnosis of active influenza A infection, particularly the H9N7 subtype, enabling early intervention and infection control.
- Test Code
- 6148
- CPT Code
- 87798
- ICD Code
- J10.1
- Price
- ₹9,860
- Sample Type
- Sputum; throat and nasal swabs in viral transport medium, or lung tissues, Cell Cultures etc.
- Result Time
- Reports are available on the 4th working day after sample collection. Email delivery within 48 hours of report generation, phone within 36 hours.
- Fasting Required
- No
- Method
- Real Time PCR
Sample Collection
No fasting required. Inform your physician about any medications or recent antiviral therapy. Sign the consent document and provide relevant clinical history.
Method: Nasopharyngeal/throat swab, sputum, or tissue biopsy
Laboratory Analysis
A healthcare professional will collect a nasopharyngeal or throat swab, sputum, or other respiratory sample. The procedure is quick and may cause mild discomfort.
Report Delivery
No special precautions. You can resume normal activities immediately. The sample will be transported to the laboratory for analysis.
Timeline: Reports are available on the 4th working day after sample collection. Email delivery within 48 hours of report generation, phone within 36 hours.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to qualitatively detect the presence of H9N7 and Influenza A viral RNA in respiratory specimens. It aids in the diagnosis of active influenza A infection, particularly the H9N7 subtype, enabling early intervention and infection control.
How to Prepare
- Use sterile swabs and viral transport medium
- Collect sample within 3-5 days of symptom onset
- Label the sample correctly with patient details
- Transport at 2-8°C if processed within 72 hours, otherwise freeze at -70°C
Doctor's Notes
Reviewed by Dr Kothari Ramesh Shantilal — MBBS, MD (Microbiology) · Reg. No. 27670
"Early detection of H9N7 and Influenza A is critical for timely antiviral therapy and infection control. This RT-PCR test offers high sensitivity and specificity, reducing false negatives compared to rapid antigen tests."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Unlabeled or mislabeled samples
- Inappropriate transport medium
- Samples received after prolonged delay without proper storage
- Insufficient quantity
Understanding Your Results
H9N7 RNA Detected
Positive for H9N7 influenza A infection. Clinical correlation and public health notification required.
Influenza A RNA Detected (H9N7 not specified)
Positive for Influenza A, but subtype not identified. Further testing may be needed.
Not Detected
No viral RNA detected. However, a negative result does not exclude infection; consider retesting if symptoms persist.
Consult a physician immediately if you have high fever, difficulty breathing, chest pain, or worsening symptoms. Early medical evaluation is essential for appropriate management.
Limitations
- ⚠Qualitative test does not quantify viral load
- ⚠Negative result does not rule out other respiratory infections
- ⚠May not detect other influenza subtypes (e.g., H1N1, H3N2)
- ⚠Results should be interpreted with clinical correlation
Risks & Considerations
- ●Minimal risk of bleeding or infection at collection site
- ●Slight gag reflex during throat swab
- ●No serious complications
Interfering Factors
- ●Improper sample collection or transport may cause false negatives
- ●Inhibitors in the sample (e.g., blood, mucus) can affect PCR
- ●Low viral load may not be detected in early or late stages
- ●Cross-contamination during collection or processing
Compare With Similar Tests
| Test | H9N7 & Influenza A (RNA Detection) Qualitative Test | Rapid Influenza Diagnostic Test (RIDT) | RT-PCR (this test) |
|---|---|---|---|
| Comparison | H9N7 & Influenza A (RNA Detection) Qualitative Test |
Frequently Asked Questions
What is the cost of the H9N7 & Influenza A RNA test?
How is the sample collected?
Do I need to fast before the test?
How long does it take to get results?
Is home sample collection available?
What is the difference between this test and a rapid test?
Can this test detect other influenza subtypes?
What should I do if my result is positive?
Are there any risks associated with the test?
Is the test covered by insurance?
Can I walk in without an appointment?
What is the validity of the test?
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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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