Test Price
1,800 AED✅ Home Collection Available
Q Fever (Coxiella burnetii) Antibodies IgG & IgM Test | 1800 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
Gold-Standard Serology for Q Fever Diagnosis
The Q Fever (Coxiella burnetii) Antibodies IgG & IgM Test is the definitive serological assay employing Immunofluorescence Assay (IFA) – the WHO reference standard – to detect acute and chronic Q fever with 99.9% diagnostic sensitivity. Processed under ISO 9001:2015 accreditation (Cert: INT/EGQ/2509DA/3139).
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (daily 8 AM – 11 PM).
- Clinical Guidance: Post-test telephonic interpretation by DHA-licensed physicians.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Q Fever (Coxiella burnetii) Antibodies IgG & IgM Test uses Immunofluorescence Assay (IFA) to differentiate phase-specific antibodies. Phase II IgM indicates acute infection (titer ≥1:50), while elevated Phase I IgG (titer ≥1:800) suggests chronic Q fever. This level of resolution is critical for guiding therapy in culture-negative endocarditis, hepatitis, and persistent febrile illness.
| Feature | Our Test (IFA) | Alternative (ELISA) |
|---|---|---|
| Precision | Phase I & II IgG/IgM discrimination – highest specificity | Total antibody, less phase resolution |
| Methodology | Immunofluorescence Assay (WHO reference standard) | Enzyme Immunoassay |
| Turnaround | Batch processing: sample by 7th, report in 2–3 weeks | Often faster but less clinically validated for phase discrimination |
| Clinical Utility | Guides therapy for acute vs. chronic Q fever | Screening only, confirm with IFA |
Physician Insight & Safety Protocols
“Q fever serology requires careful correlation with clinical presentation — unexplained pyrexia, culture-negative endocarditis, or granulomatous hepatitis. Phase-specific IFA provides the diagnostic precision needed to distinguish acute from chronic infection. A negative result in early illness does not rule out Q fever; repeat serology in 2–4 weeks is recommended. Never modify antibiotic therapy without consulting your physician.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Medication Advisory
Do not discontinue or alter any prescribed medication — including antibiotics or anticoagulants — without explicit discussion with your treating clinician. This diagnostic test is intended to inform clinical decision-making and does not replace ongoing medical management.
Safety Exclusion Criteria & ER Red Flags
- Do not proceed with blood draw if you have a severe bleeding disorder or are on high-dose anticoagulants without prior medical clearance.
- If you experience sudden high fever, severe headache, confusion, or chest pain, seek emergency care immediately — do not wait for test results.
- This test requires a Duly filled Test Send Out Consent Form (Form 35) — mandatory for sample shipment and regulatory compliance.
- Sample stability: collect in SST tube; ship refrigerated (2–8°C) or frozen to maintain antibody integrity during transport.
Patient FAQ & Clinical Guidance
1. What is the purpose of Q Fever IgG and IgM testing?
It distinguishes acute infection (IgM Phase II titer ≥1:50) from chronic Q fever (IgG Phase I titer ≥1:800), guiding targeted antibiotic therapy and long-term monitoring. The IFA method provides the phase-specific resolution necessary for accurate staging.
2. How should I prepare for the blood draw?
No fasting is required. You must sign the Test Send Out Consent Form (Form 35) prior to collection. Ensure the sample is transported under refrigerated conditions (2–8°C) to preserve antibody stability. Our VIP Mobile Phlebotomy service handles all logistics.
3. When will I receive my results and how are they interpreted?
Samples are processed in monthly batches; if your sample is received by the 7th of the month, results are delivered within 2–3 weeks. Your physician will interpret the Phase I and Phase II titers in the context of your clinical presentation. Repeat testing at 2–4 weeks may be recommended if early infection is suspected.
4. Can I have the sample collected at home?
Yes, home collection is available daily from 8 AM to 11 PM via our VIP Mobile Phlebotomy service with temperature-controlled cold-chain transport. This service is ideal for patients who prefer the convenience and safety of collection in their own residence.
UAE Regulatory & Data Privacy Adherence
Data Protection & Healthcare Compliance
Your personal health information is protected under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and managed in accordance with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All clinical testing and patient safety protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. DNA Labs UAE operates under DHA Facility License Number 1143 and maintains ISO 9001:2015 certification for quality management systems.
- Results are delivered via secure, encrypted channels to ensure confidentiality.
- Data access is restricted to authorized clinical personnel only.
- All sample handling and shipping comply with UAE health information technology standards.
Clinical & Logistical Metadata
| Test Name | Q Fever (Coxiella burnetii) Antibodies IgG & IgM Test |
| Price (AED) | 1,800 AED |
| Turnaround Time | 2–3 weeks (batch processing; samples received by 7th of month) |
| Sample Type / Matrix | Serum (SST tube) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available |
| Methodology Used | Immunofluorescence Assay (IFA) – WHO reference standard |
| ICD-10-CM Code | A78 (Q fever) |
| LOINC Code | 16328-2 (Coxiella burnetii Ab.IgG [Titer] in Serum) / 16329-0 (Coxiella burnetii Ab.IgM [Titer] in Serum) |
| 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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