Test Price
180 AED✅ Home Collection Available
TORCH Panel Avidity IgG Test in Dubai | 180 AED | DHA Licensed & PDPL Compliant
Executive Summary & Core Metrics
Precise Differentiation of Recent vs. Past TORCH Infection for Informed Pregnancy Management
Diagnostic Accuracy: 99.9% sensitivity via ISO 9001:2015 accredited Enzyme Immunoassay (ELISA) with avidity indexing.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection, available daily 8 AM – 11 PM.
Clinical Guidance: Complimentary telephonic consultation with a DHA‑licensed physician for result interpretation.
Insurance Verification: Direct billing check via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The TORCH Panel Avidity IgG Test employs Enzyme Immunoassay (ELISA) technology to measure the binding strength (avidity index) of IgG antibodies targeting TORCH pathogens — Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus types 1 and 2. By calculating the avidity ratio, clinicians can accurately distinguish recent infections (low avidity, typically <3–4 months) from past or remote infections (high avidity). This distinction is critical for pregnancy planning, fertility work‑up, and immune status assessment, helping to avoid unnecessary interventions while ensuring timely obstetric follow‑up when indicated.
| Feature | Our Avidity Panel | Standard TORCH IgG Serology |
|---|---|---|
| Methodology | Enzyme Immunoassay (ELISA) with Avidity Index calculation | ELISA without avidity measurement |
| Clinically Relevant Metrics | Avidity ratio (low/high) paired with quantitative IgG | Qualitative IgG positive/negative only |
| Turnaround Time | Same Day (Mon/Wed/Fri by 9 AM cut‑off) | 2–3 business days |
| Pregnancy Risk Stratification | Precise infection dating for informed decision‑making | Cannot determine infection timing |
Physician Insight & Safety Protocols
“Avidity testing adds a critical layer of temporal precision to routine TORCH screening. A high avidity index reliably indicates an infection that occurred more than three to four months prior, which often provides reassurance during early pregnancy. Conversely, a low avidity result signals a more recent infection that warrants prompt obstetric evaluation. Always correlate laboratory data with the full clinical picture — no single test replaces comprehensive medical assessment.” — Dr. Ajay Singh, General Practitioner (DHA Registration ID: 36234132)
Clinical Advisory: Medication Continuity & Follow‑up
Do not alter or discontinue any prescribed treatment regimen based solely on avidity test results. All findings must be reviewed by your treating physician within the context of your full medical history, current symptoms, and physical examination. A single laboratory value should never replace ongoing clinical supervision.
Exclusion Criteria & Red‑Flag Symptoms
- Blood draw is contraindicated if the phlebotomist identifies an active infection at the puncture site or if the patient presents with an acute febrile illness requiring immediate hospital care.
- If you experience sudden high fever, severe headache with visual changes, extensive rash, or lymphadenopathy, proceed directly to the nearest Emergency Department without delay.
- This avidity panel is not a substitute for urgent diagnostic evaluation in symptomatic pregnant women; emergent obstetric consultation must take precedence.
Patient FAQ & Clinical Guidance
1. What does the TORCH Panel Avidity IgG test measure?
This test measures the strength of IgG antibody binding against TORCH pathogens to differentiate recent infections (low avidity index) from past infections (high avidity index, typically >3–4 months). The avidity ratio is calculated using ELISA, allowing your doctor to precisely date the infection and make informed decisions about pregnancy management, fertility treatment, and immune surveillance — reducing unnecessary interventions while ensuring appropriate follow‑up.
2. How should I prepare, and when can I expect my results?
No special preparation is required. Our certified home collection team will obtain a single blood sample using temperature‑controlled cold‑chain transport to maintain specimen integrity. Samples received by 9 AM on Monday, Wednesday, or Friday are processed the same day, and your report is released after rigorous quality control checks, enabling rapid clinical decision‑making without unnecessary delays.
3. Can I order this test during pregnancy without a doctor’s referral?
Yes, the avidity panel can be ordered directly for proactive pregnancy planning or fertility assessment without a mandatory physician referral. However, every result includes a complimentary telephonic consultation with a DHA‑licensed physician to ensure safe, accurate interpretation and to recommend any necessary follow‑up steps tailored to your individual health profile.
4. Is home collection safe and available for this test?
Absolutely. Because the TORCH Avidity Panel requires only a standard peripheral blood draw (serum/plasma), our VIP Mobile Phlebotomy service is fully available from 8 AM to 11 PM daily. All samples are transported under strict cold‑chain conditions and processed in our ISO 9001:2015 accredited laboratory, ensuring both safety and diagnostic accuracy.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License Number 1143 and adheres to the highest standards of data protection and clinical safety. All patient information is handled in 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 testing procedures and patient consent protocols follow Federal Decree‑Law No. 4 of 2016 on Medical Liability. Our laboratory is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139), and all services meet DHA and MOHAP standards. For home collection scheduling or insurance verification, please contact us via WhatsApp at +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | TORCH Panel Avidity IgG |
| Price (AED) | 180 |
| Turnaround Time | Same Day (Mon/Wed/Fri by 9 AM cut‑off) |
| Sample Type / Matrix | Serum (peripheral venipuncture) – VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily 8 AM – 11 PM |
| Methodology Used | Enzyme Immunoassay (ELISA) with Avidity Index calculation |
| ICD-10-CM Code | Z11.59, Z36.88 |
| LOINC Code | 24318-7 |
| 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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