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Test Price

950 AED

✅ Home Collection Available

Parvovirus B19 Antibodies Panel IgG & IgM Test in UAE

Executive Summary & Core Metrics

Accuracy Guarantee:

99.9% Diagnostic Sensitivity via ISO Accredited Processing.

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.

Insurance:

Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Parvovirus B19 Antibodies Panel measures IgG and IgM via Enzyme-Linked Immunosorbent Assay (ELISA), differentiating past immunity from acute infection. This test is critical in pregnancy, haematological disorders, and diagnosis of Fifth disease.

Feature Our Test (ELISA/EIA) Rapid Lateral Flow
Methodology Enzyme Immunoassay (ISO 9001:2015) Qualitative immunochromatography
Precision High quantitative sensitivity & specificity Moderate; may miss early infection
Turnaround Time Next-day report (sample by Thu 6 pm) Same-day (point-of-care)
Clinical Use Definitive immunity/acute diagnosis Screening only; confirmation required

Physician Insight & Safety Protocols

“Dr. Ajay Singh (DHA License: 36234132) emphasizes that Parvovirus B19 serology results must be interpreted in conjunction with clinical symptoms and patient history. In pregnant women and immunocompromised patients, timely clinical correlation is essential to prevent complications such as fetal hydrops or aplastic crisis. Always consult your treating physician before making any changes to medication.”

Advisory

Serology results should not be used as the sole criterion for clinical decisions. A negative result does not completely rule out infection if the patient is in the early window period. If symptoms persist, repeat testing may be warranted. Do not discontinue or alter prescribed medications without consulting your doctor.

Exclusion Criteria & ER Red Flags

  • Acute haemolysis or recent blood transfusion may alter antibody levels.
  • Do not take this test as the sole criterion for clinical decisions without prior medical evaluation.
  • Seek immediate emergency care if you experience: severe joint pain, persistent high fever, sudden pallor, fainting, or rapid heart rate – they may indicate an aplastic crisis.

Patient FAQ & Clinical Guidance

1. What does the Parvovirus B19 IgG and IgM test detect?

The test detects past or recent infection by measuring IgG (long-term immunity) and IgM (acute phase) antibodies, distinguishing immunity status. Positive IgG with negative IgM indicates past exposure, while IgM positivity suggests recent infection that may require further monitoring, especially during pregnancy.

2. Is fasting or special preparation required before sample collection?

No fasting or special preparation is needed. Our cold-chain home collection team handles sample preservation professionally. You need only provide a 2 mL serum sample, which is transported refrigerated to maintain antibody stability before analysis.

3. Can this test rule out infection in a pregnant woman with known exposure?

A negative IgM and negative IgG result suggests no current or past infection, but retesting after 2–3 weeks may be warranted. Serology should be interpreted alongside ultrasound and clinical examination to exclude fetal infection risk. Consult your obstetrician immediately if exposure is suspected during pregnancy.

UAE Regulatory & Data Privacy Adherence

Data Protection & Compliance

All patient data is handled in strict 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. Our facility holds DHA License No. 1143 and operates under the corporate brand DNA Labs UAE. Patient consent and data security are paramount. No clinical data is shared without prior authorization.

Clinical & Logistical Metadata

Test Name Parvovirus B19 Antibodies Panel (IgG & IgM)
Price (AED) 950
Turnaround Time Next day (sample received by 6 PM Thu)
Sample Type / Matrix Serum (2 mL)
Methodology Used Enzyme-Linked Immunosorbent Assay (ELISA/EIA)
ICD-10-CM Code B08.3
LOINC Code 95709-2
DHA Facility License & Laboratory Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE

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