Test Price
650 AED✅ Home Collection Available
Parvovirus B19 Antibody IgM Test in Dubai | 650 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Certified ELISA (ISO 9001:2015).
- 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 for result interpretation by a DHA-licensed General Practitioner.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Parvovirus B19 IgM antibody test detects recent or acute infection with human parvovirus B19. It is essential for diagnosing erythema infectiosum (fifth disease) in children, transient aplastic crisis in patients with hemolytic disorders, and evaluating fetal risk in pregnant women. The assay uses enzyme-linked immunosorbent assay (ELISA) technology with high specificity and sensitivity.
| Feature | Our Test (ISO Certified) | Closest Alternative |
|---|---|---|
| Methodology | ELISA / EIA (Enzyme Immunoassay) – high specificity | Outsourced ELISA, variable sensitivity |
| Turnaround Time | Next-day report (sample received by Thu 6 PM) | 2–3 working days |
| Home Collection | Included, certified cold-chain logistics | Often limited or not available |
| Clinical Support | Post-test tele‑guidance by DHA-licensed General Practitioner | Basic report without interpretation |
Physician Insight & Safety Protocols
"IgM positivity strongly indicates recent parvovirus B19 infection, but false positives from rheumatoid factor or cross-reactivity require clinical correlation with symptoms such as rash, arthralgia, or aplastic crisis. This test should not be used alone for fetal risk assessment; IgG avidity or PCR may be necessary. Always interpret results in the full clinical context." – Dr. Ajay Singh, General Practitioner (DHA ID: 36234132)
Advisory: Medication Safety
⚠️ Important: Do not discontinue any prescribed medication without consulting your physician. Always inform your healthcare provider about all medications you are taking before the test.
Exclusion Criteria & ER Red Flags
- Patients with known hypersensitivity to phlebotomy materials.
- Individuals unable to provide informed consent without legal guardian.
- Known severe anemia – monitor for vasovagal syncope during collection.
- Seek emergency care immediately if: sudden severe joint pain, worsening anemia signs (pallor, shortness of breath, dizziness), or unexplained fever and rash.
Patient FAQ & Clinical Guidance
1. When is the Parvovirus B19 IgM test recommended?
This test is recommended when a patient presents with acute febrile illness, arthralgia, or a “slapped cheek” rash suggestive of recent parvovirus B19 infection. It is also ordered for pregnant women with exposure to fifth disease and for immunocompromised patients with unexplained anemia.
2. How long does it take to get results?
Results are available the next day if the sample is received by 6 PM Thursday. This rapid turnaround time supports timely clinical decisions, especially for high-risk patients such as pregnant women or those with hemolytic disorders.
3. Is this test safe during pregnancy?
Yes, the blood draw itself is safe. However, a positive IgM result in pregnancy requires immediate fetal monitoring and consultation with a maternal-fetal medicine specialist. False positives are rare but possible, so follow-up testing (IgG avidity or PCR) is recommended.
UAE Regulatory & Data Privacy Adherence
Trust & Compliance
All patient data is handled in strict 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. Clinical testing and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. Our facility is DHA licensed (License 1143) and ISO 9001:2015 certified.
Clinical & Logistical Metadata
| Test Name | Parvovirus B19 Antibody IgM Test |
| Price (AED) | 650 AED |
| Turnaround Time | Next-day report (sample received by Thu 6 PM) |
| Sample Type / Matrix | Serum or plasma (VIP Mobile Phlebotomy available daily 8 AM–11 PM) |
| Methodology Used | ELISA / EIA (Enzyme Immunoassay) |
| ICD-10-CM Code | B08.3 (Erythema infectiosum [fifth disease]) |
| LOINC Code | 22313-2 (Parvovirus B19 IgM Ab [Units/volume] in Serum) |
| DHA Facility License & Laboratory Address | License 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