Test Price
600 AED✅ Home Collection Available
Adenovirus Qualitative PCR Test in Dubai | 600 AED | DHA Licensed Lab
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
Clinical Guidance: Telephonic Post-Test Clinical Guidance by DHA-licensed physicians for result interpretation and next steps.
Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Physician Oversight: All results are reviewed and signed off by Dr. Ajay Singh (General Practitioner, DHA 36234132).
Test Overview & Methodology
Clinical Overview & Methodology
This qualitative Real-Time PCR (qPCR) test detects adenovirus DNA in whole blood or cerebrospinal fluid (CSF), delivering a definitive diagnosis of active adenovirus infection. It is the gold standard for early detection, especially in immunocompromised patients and severe respiratory or neurological presentations, where rapid identification directly influences clinical management and infection control. The assay targets conserved regions of the adenovirus hexon gene, ensuring high specificity across all serotypes.
| Feature | Our Adenovirus PCR | Closest Alternative (Antigen / Culture) |
|---|---|---|
| Methodology | Real-Time PCR (qPCR) | Immunofluorescence / Viral Culture |
| Turnaround Time | 2–3 working days (Sample Mon/Thu, Report Wed/Sat) | 5–14 days (culture) |
| Analytical Sensitivity | >99% (detects <10 copies/μL) | Moderate; requires viable virus |
| Clinical Utility | Early diagnosis, antiviral stewardship | Retrospective confirmation |
Physician Insight & Safety Protocols
Physician Insight
“As your General Practitioner (DHA 36234132), I emphasize that PCR timing is critical. In immunocompromised patients, a negative result does not rule out disease if the sample was collected early or late in the infection course. Always correlate symptoms, fever pattern, and immune status with lab data. The story you share with your doctor is as important as the test result.” – Dr. Ajay Singh
Pre-Analytical Safety & Sample Handling
- Sample integrity: Never freeze specimens; maintain strict cold-chain (2–8°C) during transport to preserve viral DNA.
- CSF collection: Performed only by a qualified clinician under aseptic conditions in a healthcare facility.
- Bleeding risk: Patients with coagulopathy or thrombocytopenia require extended puncture-site pressure after blood draw.
Emergency Red Flags
- Immediate ER referral: Severe headache, photophobia, altered consciousness, respiratory distress, or fever unresponsive to antipyretics.
- Medication caution: Do not discontinue any prescribed medication without direct consultation with your treating physician.
Patient FAQ & Clinical Guidance
1. What is the purpose of the Adenovirus Qualitative PCR Test?
Direct Answer: Detects adenovirus DNA in blood or CSF to confirm active infection and guide immediate antiviral management.
This molecular assay amplifies even minute quantities of adenoviral genetic material, offering a definitive “Detected” or “Not Detected” result. It is indispensable for immunocompromised individuals, transplant recipients, and patients with severe pneumonitis or meningoencephalitis, where rapid pathogen identification can alter the course of treatment and reduce transmission risk.
2. How should I prepare for sample collection?
Direct Answer: No fasting or special preparation is needed; just maintain hydration and notify us of blood-thinning medications.
Our DHA-licensed phlebotomist will collect either a blood sample from an arm vein (Lavender Top EDTA tube) using a single atraumatic puncture, or arrange for CSF collection at a partner hospital. Samples are immediately placed in verified cold-chain transport (2–8°C) to preserve viral integrity, ensuring your result is reliable and actionable.
3. When will I receive my results and how do I interpret them?
Direct Answer: Reports are issued within 2–3 working days; a positive result means adenovirus DNA was found and treatment correlation is needed.
Samples collected on Monday or Thursday before 11 AM are processed and reported by Wednesday or Saturday, respectively. A “Detected” report confirms active viral replication, which your physician will correlate with clinical symptoms and possibly order serial PCR monitoring. A “Not Detected” in the presence of strong suspicion may warrant a repeat on a new sample. Every report includes a complimentary telehealth session with our clinical team to discuss your result’s implications.
UAE Regulatory & Data Privacy Adherence
Data Privacy: All personal and medical data are 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.
Clinical Liability: Diagnostic procedures adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability, ensuring patient safety and professional accountability.
Licensing: Operated under DHA Facility License Number 1143, ISO 9001:2015 certified (INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Adenovirus Qualitative PCR (Whole Blood / CSF) |
| Price (AED) | 600 |
| Turnaround Time | 2–3 working days |
| Sample Type / Matrix | Whole Blood (EDTA) or Cerebrospinal Fluid (CSF) – CSF requires hospital collection |
| Methodology Used | Qualitative Real-Time PCR (qPCR) |
| ICD-10-CM Code | B34.0 (Adenovirus infection, unspecified) |
| LOINC Code | 20416-4 (Adenovirus DNA [Presence] in Blood by NAA with probe detection) |
| DHA Facility License & Laboratory Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – Corporate Lab: DNA Labs UAE |
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