Test Price
1,500 AED✅ Home Collection Available
Comprehensive Respiratory Pathogen Panel 5 in UAE | 1500 AED | DHA-Certified
Executive Summary & Core Metrics
Ultra-precise molecular screening (diagnostic sensitivity 99.9%) conducted at a DHA-licensed, ISO 9001:2015 accredited laboratory. This test simultaneously identifies five major respiratory pathogens using multiplex qPCR with confirmatory whole-genome sequencing (WGS). Hospital extraction is mandatory – sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO-Accredited Processing.
- Collection Method: Hospital extraction only – oropharyngeal/nasal swab, sputum, or bronchoalveolar lavage (BAL) under clinical supervision.
- Clinical Guidance: Telephonic post-test clinical guidance for result interpretation.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This multiplex molecular panel reliably differentiates Influenza A/B, Respiratory Syncytial Virus (RSV), SARS-CoV-2, Adenovirus, and Human Metapneumovirus using high‑sensitivity real‑time PCR (qPCR) with confirmatory whole‑genome sequencing. Turnaround time is 48–72 hours from sample receipt. The test is performed exclusively in a hospital setting to ensure specimen quality and patient safety.
| Feature | Our Test (CRP5) | Conventional Single‑Pathogen PCR |
|---|---|---|
| Methodology | Multiplex qPCR + WGS | Monoplex PCR / Rapid Antigen |
| Precision | 99.9% sensitivity; whole‑genome confirmation | Variable sensitivity; often requires culture |
| Turnaround Time | 48–72 hours (sample receipt to report) | 48 hours–5 days (batch‑dependent) |
Physician Insight & Safety Protocols
“A molecular respiratory panel provides invaluable rapid aetiological clarity, but clinical correlation remains essential – imaging, inflammatory markers, and patient history must guide final treatment decisions.”
— Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
Advisory – Medication Management
Do not discontinue any prescribed medication (e.g., inhalers, steroids, antivirals) without consulting your doctor. This test is a diagnostic aid, not a substitute for clinical judgement.
Exclusion Criteria & Safety
- Home collection is not available for this test. Sample collection is conducted strictly within an accredited hospital facility due to the invasive nature of bronchoalveolar lavage (BAL) and requirement for clinical oversight.
- If you have severe breathlessness at rest, cyanosis, or altered consciousness – proceed directly to the nearest emergency department.
- Acute haemoptysis (>2 tablespoons) or suspected epiglottitis – urgent hospital evaluation required.
- If the patient is a minor, a legal guardian must be present and valid Emirates ID provided as per UAE Personal Data Protection Law (PDPL) and Federal Law No. 2 of 2019.
Patient FAQ & Clinical Guidance
1. Which pathogens does the panel cover and why is whole‑genome sequencing added?
Our panel reliably targets Influenza A/B, RSV, SARS‑CoV‑2, Adenovirus, and Human Metapneumovirus using high‑sensitivity qPCR, with WGS providing definitive strain identification for epidemiological precision. Whole‑genome sequencing confirms ambiguous PCR signals and detects emerging variants that may escape routine primers, ensuring you receive the most clinically actionable report.
2. Why must the sample be collected in a hospital? Is there a home option?
This test requires a bronchoalveolar lavage (BAL) specimen for optimal sensitivity, which must be performed by a trained healthcare professional in a controlled hospital setting. Swab specimens may also be collected, but the invasive nature of BAL necessitates hospital extraction. Mobile phlebotomy or home collection is not available for this test to ensure patient safety and specimen integrity.
3. Is the test DHA‑certified and covered by insurance?
Yes, the test is fully authorised by the Dubai Health Authority (DHA License No. 1143) and performed at an ISO 9001:2015 certified facility. Insurance coverage is verified in real‑time via WhatsApp before sample collection. Submit your valid UAE insurance card for immediate pre‑authorisation; any copayment will be communicated in advance. All personal data is processed in compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019.
UAE Regulatory & Data Privacy Adherence
Data Protection & Compliance: This diagnostic service operates under the strict framework of UAE federal laws. Patient health information is safeguarded in accordance 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. All clinical procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory maintains ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) and is fully licensed by the Dubai Health Authority (DHA License No. 1143).
Clinical & Logistical Metadata
| Test Name | Comprehensive Respiratory Pathogen Panel 5 (CRP5) |
| Price (AED) | 1,500 AED |
| Turnaround Time | 48–72 hours from sample receipt |
| Sample Type / Matrix | Oropharyngeal/nasal swab, sputum, or bronchoalveolar lavage (BAL) – hospital extraction only |
| Methodology Used | Multiplex real‑time PCR (qPCR) + Whole‑Genome Sequencing (WGS) |
| ICD-10-CM Code | J06.9, Z20.8 |
| LOINC Code | 92856-0 |
| 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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All reports reviewed by DHA-Certified physicians