Respiratory Panel 5 Test
Short Name: Respiratory Panel 6
Also known as: Respiratory Pathogen Panel 6, Respiratory Viral and Bacterial Panel, Multiplex PCR Respiratory Panel 6
Respiratory Panel 5 Test test available at DNA Labs India for ₹4,500. Uses Real Time PCR on Throat / Nasal swab, Sputum, or Bronchoalveolar lavage fluid samples. Results in Samples are accepted on Monday, Wednesday, and Friday by 9 am. Reports are delivered on Tuesday, Thursday, and Saturday, typically within 24-48 hours after sample collection.. 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 the Respiratory Panel 6 Test is to identify the presence of common viral and bacterial pathogens responsible for respiratory tract infections. The detection of specific organisms such as Influenza A/B, RSV, hMPV, Adenovirus, and Bordetella pertussis helps clinicians differentiate between viral and bacterial etiologies, guide antiviral or antibiotic therapy, reduce unnecessary testing, and implement appropriate infection control measures. This panel is especially useful in patients with persistent fever, cough, or difficulty in breathing, and in vulnerable populations such as children, elderly, and immunocompromised individuals.
- Test Code
- 3593
- Price
- ₹4,500
- Sample Type
- Throat / Nasal swab, Sputum, or Bronchoalveolar lavage fluid
- Result Time
- Samples are accepted on Monday, Wednesday, and Friday by 9 am. Reports are delivered on Tuesday, Thursday, and Saturday, typically within 24-48 hours after sample collection.
- Fasting Required
- No
- Method
- Real Time PCR
Sample Collection
No special preparation is required. Fasting is not necessary. If the patient is using antiviral or antibiotic medication, the healthcare provider should be informed as it may affect the test results.
Method: Swab collection or expectoration / BAL
Laboratory Analysis
For swab collection, a healthcare professional will gently insert a sterile swab into the throat or nasal passage. For sputum, you will be asked to cough deeply to produce mucus from the lungs into a sterile container. Bronchoalveolar lavage fluid is collected by a physician during a bronchoscopy procedure in a clinical setting.
Report Delivery
You can resume normal activities immediately. There are no restrictions after sample collection. Minor throat irritation is possible after a throat swab but resolves quickly.
Timeline: Samples are accepted on Monday, Wednesday, and Friday by 9 am. Reports are delivered on Tuesday, Thursday, and Saturday, typically within 24-48 hours after sample collection.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Respiratory Panel 6 Test is to identify the presence of common viral and bacterial pathogens responsible for respiratory tract infections. The detection of specific organisms such as Influenza A/B, RSV, hMPV, Adenovirus, and Bordetella pertussis helps clinicians differentiate between viral and bacterial etiologies, guide antiviral or antibiotic therapy, reduce unnecessary testing, and implement appropriate infection control measures. This panel is especially useful in patients with persistent fever, cough, or difficulty in breathing, and in vulnerable populations such as children, elderly, and immunocompromised individuals.
How to Prepare
- Use only the provided sterile collection swab or container
- For sputum sample, collect early morning preferably before food
- Do not add any preservative to the sample
- Seal the container securely to avoid leakage
- Label the sample container with patient name and identification details
- Transport the sample to the laboratory as per instructions
Doctor's Notes
Reviewed by Dr Kothari Ramesh Shantilal — MBBS, MD (Microbiology) · Reg. No. 27670
"Early identification of respiratory pathogens through multiplex PCR enables targeted therapy, reduces unnecessary antibiotic use, and improves clinical outcomes in both community and hospital-acquired respiratory infections."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Mislabeled or unlabeled sample
- Sample in incorrect transport medium
- Sample not reaching laboratory within specified stability period
- Inadequate sample volume or quantity
- Leaked or damaged container
Understanding Your Results
Detection indicates influenza A infection; antiviral therapy may be considered.
Detection indicates influenza B infection; clinical management as appropriate.
Detection indicates RSV infection especially common in children and elderly.
Detection suggests hMPV-associated respiratory tract infection.
Detection indicates adenovirus infection, which can cause various respiratory symptoms.
Detection supports diagnosis of whooping cough; prompt antibiotics are recommended.
If you or your child experience any symptoms of respiratory infection — especially persistent fever, prolonged cough, difficulty in breathing, or signs of wheezing — it is important to consult a doctor and undergo testing. Early medical attention is crucial in high-risk patients such as infants, older adults, pregnant women, and those with weakened immunity. If you have already received the test and your result is positive, contact your healthcare provider for appropriate treatment and advice.
Limitations
- ⚠Detection is limited to the six pathogens included in this panel
- ⚠A negative result does not rule out infection by other respiratory pathogens
- ⚠This test is not intended to determine antimicrobial susceptibility
- ⚠Results should be interpreted in conjunction with clinical symptoms and other diagnostic findings
Risks & Considerations
- ●Minor transient discomfort during throat/nasal swab
- ●Possible gag reflex when collecting throat swab
- ●No significant risk from sputum collection
- ●Bronchoalveolar lavage is performed under medical supervision with minimal risk
Interfering Factors
- ●Recent use of antiviral or antibiotic therapy may reduce pathogen load and cause false negatives
- ●Improper sample collection or insufficient clinical material
- ●Contamination of sample with blood or mucus
- ●Delay in transportation leading to degradation of nucleic acids
- ●Cross-reactivity in rare cases due to organism genetic variability
Compare With Similar Tests
| Test | Respiratory Panel 5 Test | Respiratory Panel 5 Test | Rapid Influenza Antigen Test | Sputum Culture & Sensitivity |
|---|---|---|---|---|
| Comparison | Respiratory Panel 5 Test |
Frequently Asked Questions
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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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