Test Price
850 AED✅ Home Collection Available
Respiratory Panel 6 Test in UAE | 850 AED | Molecular Diagnostic
Executive Summary & Core Metrics
Comprehensive molecular detection of six major respiratory pathogens with rapid turnaround, ensuring accurate diagnosis and targeted therapy.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing with Whole Genome Sequencing confirmation.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by a licensed General Practitioner.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- Turnaround: Results within 48 hours of sample collection.
Test Overview & Methodology
The Respiratory Panel 6 Test delivers comprehensive molecular detection of six core respiratory pathogens — influenza A, influenza B, respiratory syncytial virus (RSV), SARS‑CoV‑2, adenovirus, and parainfluenza — with rapid turnaround and genomic precision. By combining multiplex real‑time PCR with confirmatory Whole Genome Sequencing, it provides unmatched sensitivity and specificity tailored to UAE clinical needs. This assay is designed to guide targeted antimicrobial therapy, reduce unnecessary antibiotic use, and support infection control decisions in both outpatient and hospital settings.
| Feature | DNA Labs UAE Respiratory Panel 6 | Conventional Multiplex PCR |
|---|---|---|
| Precision | 99.9% sensitivity & specificity (qPCR + WGS confirmation) | ~95–97% sensitivity; no genomic confirmation |
| Methodology | Multiplex Real-Time PCR with Whole Genome Sequencing | Conventional multiplex end-point PCR, gel confirmation |
| Turnaround Time | Results within 48 h (Mon/Wed/Fri → Tue/Thu/Sat) | Often 72+ hours; limited batch processing |
| Pathogen Coverage | 6 targets incl. SARS-CoV-2, RSV, Influenza A/B, Adenovirus, Parainfluenza | Typically 3–4 targets; no SARS-CoV-2 inclusion |
Physician Insight & Safety Protocols
“As a general practitioner managing respiratory infections daily, I value tests that deliver rapid, definitive pathogen identification. The Respiratory Panel 6 with genomic confirmation allows me to prescribe precisely, avoid unnecessary antibiotics, and reassure patients. However, no test replaces a thorough clinical assessment — please share your results with your treating physician for a complete care plan tailored to your history.”
— Dr. Ajay Singh, General Practitioner | DHA Registration ID: 36234132
Advisory & Precautions
⚠️ Do not discontinue prescribed medication without consulting your doctor. This test is a diagnostic aid; treatment decisions must be made by a licensed physician based on the full clinical context.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Active nasal trauma, severe coagulopathy, recent nasal/sinus surgery, tracheostomy, or inability to provide an adequate swab/sputum/BAL specimen. Bronchoalveolar lavage must be performed in a clinically supervised setting.
- Seek Emergency Care If You Experience: Severe shortness of breath, cyanosis (blue lips/face), chest pain, confusion, or sudden worsening of symptoms. Do not wait for test results if you have these red flags.
Patient FAQ & Clinical Guidance
1. What pathogens does the Respiratory Panel 6 test detect?
The Respiratory Panel 6 test detects six core respiratory pathogens: influenza A, influenza B, respiratory syncytial virus (RSV), SARS‑CoV‑2, adenovirus, and parainfluenza. All targets are identified with genomic precision using multiplex real-time PCR and confirmed by Whole Genome Sequencing, ensuring accurate differentiation between viral species.
2. How should I prepare for the test?
No special preparation is required. A trained phlebotomist will collect a nasal swab or sputum sample following standard infection control protocols. For bronchoalveolar lavage, the procedure is performed in a hospital setting under clinical supervision. Please inform the phlebotomist if you have any nasal trauma, recent surgery, or bleeding disorders.
3. When will I receive my results?
Results are typically reported within 48 hours after sample collection. Samples collected Monday, Wednesday, or Friday by 9:00 AM yield reports on Tuesday, Thursday, or Saturday respectively. Results are delivered electronically via secure patient portal and SMS notification.
4. Can I take this test if I have taken antibiotics or antivirals?
Yes, the test can still be performed. However, prior antimicrobial therapy may reduce viral load and potentially affect sensitivity. Please inform your physician about any medications you are taking before the test so the results can be interpreted accurately.
5. Is home collection available for this test?
Yes, VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection is available daily from 8 AM to 11 PM across Dubai and the Northern Emirates. A certified phlebotomist will visit your home or office to collect the nasal swab or sputum sample. Bronchoalveolar lavage is excluded from home collection and must be performed in a hospital.
UAE Regulatory & Data Privacy Adherence
- Data Protection: All patient data is processed in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Your health information is encrypted, access-controlled, and used solely for diagnostic purposes with your explicit consent.
- Patient Safety & Consent: Clinical testing safety and informed consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring that all diagnostic procedures are performed with the highest standard of care and respect for patient autonomy.
- Accreditation: DNA Labs UAE operates under DHA Facility License Number 1143 and maintains ISO accreditation for all molecular diagnostic processes.
Clinical & Logistical Metadata
| Test Name | Respiratory Panel 6 Test |
| Price (AED) | 850 AED |
| Turnaround Time | 48 hours (Mon/Wed/Fri collection → Tue/Thu/Sat results) |
| Sample Type / Matrix | Nasal Swab, Sputum, or Bronchoalveolar Lavage (BAL) |
| Methodology Used | Multiplex Real-Time PCR with Whole Genome Sequencing Confirmation |
| ICD-10-CM Code | J06.9 (Acute upper respiratory infection, unspecified) |
| LOINC Code | 80563-1 (Respiratory pathogens DNA and RNA panel) |
| DHA Facility License & Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE |
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