Test Price
750 AEDโ Home Collection Available
Epstein-Barr Virus (EBV) VCA IgG & IgM Antibody Test in UAE | 750 AED
Executive Summary & Core Metrics
- Diagnostic Accuracy: 99.9% clinical sensitivity with >98% specificity using automated CLIA-enhanced ELISA platform, exceeding standard ELISA performance.
- ISO-Certified Logistics: VIP mobile phlebotomy with temperature-controlled cold-chain transport (ISO 9001:2015 certified, certificate INT/EGQ/2509DA/3139).
- Post-Test Teleconsultation: Complimentary phone consultation with a licensed physician for personalized result interpretation and clinical guidance.
- Insurance Direct Billing: Verification and processing available via WhatsApp at +971 54 548 8731.
- Rapid Turnaround: Same-day reporting for samples received by 9 AM Saturday, enabling faster clinical decisions.
Test Overview & Methodology
The Epstein-Barr Virus (EBV) VCA IgG & IgM antibody test is a high-precision serological panel that identifies antibodies directed against the viral capsid antigen, enabling clinicians to differentiate acute primary infection from past exposure or reactivation. This assay employs automated chemiluminescent immunoassay (CLIA) technology on the latest generation analytical platform, delivering standardized, reproducible results with minimal manual variability.
| Parameter | CLIA-Enhanced Platform | Standard ELISA Alternative |
|---|---|---|
| Diagnostic Precision | 99.9% sensitivity, >98% specificity | Often <95% sensitivity, manual titer interpretation |
| Methodology | Automated chemiluminescent immunoassay (CLIA) โ rapid, standardized | Manual enzyme immunoassay โ variable signal, labour-intensive |
| Turnaround Time | Same-day reporting (sample by 9 AM Saturday) | Typically 48โ72 hours |
| Sample Requirement | 2 mL serum (1 mL min.), SST; refrigerated/frozen transport | Similar volume, often without cold-chain guarantee |
Physician Insight & Safety Protocols
โThe EBV VCA IgG/IgM serology profile is a cornerstone for diagnosing acute infectious mononucleosis when correlated with fever, pharyngitis, and cervical lymphadenopathy. I advise clinicians to interpret these results alongside EBNA and heterophile antibody testing to fully differentiate primary infection, past exposure, or reactivation. Patients should never alter or stop prescribed medications without consulting their treating physician. Early and accurate laboratory confirmation supports tailored management and helps reduce the risk of complications such as splenic rupture or neurological involvement.โ
โ Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Advisory Protocol for Medication Safety
Important Medication Advisory:
Do not discontinue, adjust, or initiate any antiviral, immunosuppressive, or prescription therapy based solely on these laboratory results. All treatment decisions must be made by your qualified healthcare provider following a comprehensive clinical evaluation.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Active haemolysis, blood transfusion within the preceding three months, high-dose immunosuppressive therapy, or acute severe systemic illness that may impair antibody synthesis.
- Emergency Red Flags (seek immediate medical attention): Severe sore throat with difficulty swallowing saliva or breathing; sudden left upper quadrant abdominal pain, lightheadedness, or pallor (suggesting possible splenic rupture); new-onset confusion, stiff neck, seizures, or focal neurological deficits.
Patient FAQ & Clinical Guidance
1. What does a positive EBV VCA IgM with negative IgG indicate?
This serological pattern signals acute primary Epstein-Barr virus infection, typically appearing within the first two to four weeks of illness. When accompanied by clinical features such as fever, pharyngitis, and lymphadenopathy, it confirms the diagnosis of infectious mononucleosis. A follow-up IgG test after several weeks will usually show seroconversion to IgG positivity, confirming past resolved infection.
2. Is fasting required before the blood draw, and how is the sample collected?
No fasting, dietary restrictions, or special preparation is necessary. A simple venous blood sample (2 mL serum, SST tube) is collected by our trained phlebotomist. The VIP mobile phlebotomy service uses a temperature-controlled cold-chain transport system to preserve sample integrity from your home to our ISO-accredited laboratory in Dubai Healthcare City.
3. Can this test distinguish between mononucleosis and chronic fatigue syndrome?
Elevated VCA IgG alone without IgM indicates past infection and is not diagnostic of active mononucleosis. Such a pattern may be observed in post-viral fatigue states, including chronic fatigue syndrome. However, chronic fatigue syndrome is a diagnosis of exclusion that requires comprehensive clinical assessment and additional laboratory markers such as EBNA and early antigen testing, along with the exclusion of other organic and psychiatric causes.
UAE Regulatory & Data Privacy Adherence
All laboratory testing, data handling, and reporting procedures at DNA Labs UAE comply fully with the UAE Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL), ensuring that your personal health information is collected, stored, and transmitted under strict privacy safeguards. Additionally, we adhere to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, which governs the secure management of electronic health records and telemedicine services. Clinical safety and patient consent protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability, guaranteeing that every step of the diagnostic pathway respects your rights and well-being.
Clinical & Logistical Metadata
| Test Name | Epstein-Barr Virus (EBV) VCA IgG & IgM Antibody Test |
| Price (AED) | 750 |
| Turnaround Time | Same-day reporting (sample by 9 AM Saturday) |
| Sample Type / Matrix | Serum (2 mL, SST tube; refrigerated or frozen transport) |
| Methodology Used | Automated Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | B27.90 (Infectious mononucleosis, unspecified) |
| LOINC Code | 16703-7 (EBV VCA IgG Ab [Units/volume] in Serum) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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