Test Price
180 AED✅ Home Collection Available
Hepatitis B Surface Antigen Quantitative Test in UAE | 180 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
Quantitative HBsAg test delivers precise IU/mL measurement for accurate staging and monitoring of chronic hepatitis B infection, processed under ISO 9001:2015 certification (INT/EGQ/2509DA/3139).
- ✓ Diagnostic Accuracy: 99.9% sensitivity via Chemiluminescent Microparticle Immunoassay (CMIA) with full ISO 9001:2015 accreditation.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- ✓ Clinical Guidance: Telephonic post-test interpretation support for result comprehension and next steps.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The quantitative Hepatitis B surface antigen test provides an exact measurement of HBsAg concentration in serum, enabling precise differentiation between inactive carrier states and active chronic hepatitis B infection. This assay is essential for monitoring antiviral therapy response, predicting seroclearance, and guiding treatment duration decisions. The methodology employs Chemiluminescent Microparticle Immunoassay (CMIA) on automated high-throughput platforms, delivering results in IU/mL with exceptional reproducibility.
| Feature | Our Test (HBsAg Quantitative) | Closest Alternative (Qualitative/Screening) |
|---|---|---|
| Precision & Quantitation | Exact IU/mL quantitation via CMIA | Positive/Negative only, semi‑quantitative at best |
| Turnaround Time | Daily processing, results typically within 24 hours | 2–3 days |
| Clinical Utility | Differentiates carrier states, tracks therapy, predicts seroclearance | Limited to initial screening |
| Specialist Interpretation | Included telephonic guidance post‑test | Often not provided |
| Quality Certification | ISO 9001:2015 accredited (INT/EGQ/2509DA/3139) | Varies by provider |
Physician Insight & Safety Protocols
Dr. Ajay Singh, DHA Registration ID: 36234132, General Practitioner: “Quantitative HBsAg measurement provides the numerical precision necessary to distinguish inactive hepatitis B carriers from patients with active viral replication. This distinction is critical for determining whether to initiate or adjust antiviral therapy and for scheduling appropriate surveillance intervals.”
Medication Adherence Advisory
Patients currently prescribed antiviral therapy for chronic hepatitis B must not alter or discontinue their medication regimen without explicit consultation with their treating hepatologist or infectious disease specialist. Abrupt cessation can lead to viral rebound and hepatic decompensation.
Clinical Limitations & Urgent Care Indicators
- Exclusion: This quantitative assay alone is not sufficient for acute hepatitis diagnosis; comprehensive evaluation including liver function tests and additional serological markers is mandatory.
- Emergency signs: Seek immediate medical care if you develop jaundice, severe right upper quadrant abdominal pain, confusion, or unexplained bleeding or bruising.
- Minors: Testing for individuals under 18 requires parental or guardian consent and DHA-approved pediatric oversight in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Patient FAQ & Clinical Guidance
1. What is the quantitative HBsAg test used for?
The quantitative HBsAg test precisely measures the concentration of hepatitis B surface antigen in your blood, providing essential data for staging chronic hepatitis B infection, monitoring response to antiviral therapy, and predicting the likelihood of seroclearance. This numerical result allows your physician to distinguish inactive carrier status from active viral replication with greater confidence than a simple positive or negative screening test.
2. How does this test differ from a standard qualitative HBsAg screening?
A qualitative screening test reports only a positive or negative result, which confirms the presence of the antigen but provides no information about quantity. The quantitative version delivers an exact IU/mL value that enables your doctor to track changes over time, assess disease progression, evaluate treatment efficacy, and make evidence-based decisions about therapy duration and dosage adjustments.
3. What are the sample requirements and turnaround time?
A 2 mL serum sample collected in a standard SST tube is required. The specimen should be transported under refrigerated conditions within our temperature-controlled cold chain. Results are typically available within 24 hours of sample receipt at the laboratory. Our VIP mobile phlebotomy service operates daily from 8 AM to 11 PM for home collection convenience.
UAE Regulatory & Data Privacy Adherence
ISO 9001:2015 Certification & Regulatory Alignment
Our facility operates under DHA Facility License Number 1143 and is fully compliant with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – ensuring all patient data is encrypted, access-controlled, and shared only with authorised healthcare professionals.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – governing electronic health records and telemedicine interactions.
- Federal Decree-Law No. 4 of 2016 on Medical Liability – establishing informed consent requirements and clinical safety standards for diagnostic procedures.
Clinical & Logistical Metadata
| Test Name | Hepatitis B Surface Antigen (HBsAg) Quantitative |
| Price (AED) | 180 AED |
| Turnaround Time | Results within 24 hours of sample receipt |
| Sample Type / Matrix | Serum (2 mL SST tube); VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM) |
| Methodology Used | Chemiluminescent Microparticle Immunoassay (CMIA) |
| ICD-10-CM Code | B18.1 |
| LOINC Code | 5195-3 |
| DHA Facility License & Laboratory Address | License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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ISMS 27001:2022
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