Test Price
1,000 AED✅ Home Collection Available
Crimean-Congo Hemorrhagic Fever CCHF Viral Load Quantitative PCR Test in Dubai
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing (Cert: INT/EGQ/2509DA/3139).
- Collection Protocol: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety due to the inclusion of cerebrospinal fluid specimen requirements.
- Clinical Guidance: Telephonic post‑test clinical guidance for result interpretation by DHA‑licensed physicians.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731 before appointment.
Test Overview & Methodology
The CCHF Viral Load Quantitative Test precisely measures the level of Crimean‑Congo Hemorrhagic Fever virus RNA in blood, serum, plasma, or cerebrospinal fluid using Real‑Time PCR combined with Whole Genome Sequencing (WGS). This dual‑methodology approach ensures early detection, viral strain typing, and therapeutic monitoring for high‑risk patients.
| Feature | Our CCHF Viral Load Test | Standard PCR Alternative |
|---|---|---|
| Methodology | Real-Time PCR qPCR + WGS confirmation | Conventional RT‑PCR only |
| Analytical Sensitivity | 99.9% LoD 10 copies per mL | ~95% LoD 100 copies per mL |
| Turnaround Time | Phone 36 hours – Email 4th working day | 5 to 7 working days |
| Price AED | 1000 | 1500 to 2000 |
| Collection Setting | Hospital Only | Variable |
Physician Insight & Safety Protocols
As a DHA-licensed general practitioner, I recommend the quantitative CCHF viral load assay for any patient presenting with acute febrile illness following tick exposure or contact with livestock in endemic regions. The PCR result must always be correlated with complete blood count, coagulation profile, and liver enzymes. Early viral load quantification informs ribavirin therapy decisions and helps predict disease severity. A negative result within the first five days of symptom onset should prompt repeat testing if clinical suspicion remains high.
— Dr. Ajay Singh, DHA License: 36234132, General Practitioner
Advisory Information for Referring Physicians
Clinical Notice
Do not discontinue any prescribed antiviral, anticoagulant, or supportive medication without consulting the treating physician. This test is a diagnostic aid and must be interpreted alongside comprehensive clinical assessment. All suspected CCHF cases are immediately notifiable to the UAE Ministry of Health and Prevention under federal communicable disease surveillance protocols.
Patient Safety Exclusion Criteria & Emergency Red Flags
- Active uncontrolled bleeding such as melena or hematemesis – seek immediate emergency care before any laboratory visit.
- Known severe thrombocytopenia with platelets below 20000 per microliter or coagulopathy – phlebotomy decision must be made by supervising physician.
- History of anaphylaxis to latex or antiseptics used in venipuncture – inform the hospital collection team in advance.
- Red flags include sudden high fever above 39 degrees Celsius, ecchymoses, confusion, or uncontrolled epistaxis – proceed to nearest UAE hospital emergency department.
- This test is not a substitute for acute medical evaluation; CCHF requires urgent infectious disease consultation and isolation precautions.
Patient FAQ & Clinical Guidance
1. What exactly does the CCHF viral load quantitative test detect?
This test quantifies the number of Crimean‑Congo Hemorrhagic Fever virus RNA copies per millilitre of blood or cerebrospinal fluid using real‑time PCR technology. The result is reported as copies per mL and provides a direct measure of viral replication activity in the body.
2. Why would my doctor order this test instead of a routine viral panel?
Clinicians use this specialised assay when there is high clinical suspicion of CCHF after tick exposure, contact with livestock, travel to endemic regions, or occupational exposure in healthcare or agricultural settings. Routine viral panels do not detect CCHF virus and lack the quantitative precision needed for therapeutic monitoring.
3. What is the preparation required before giving the sample?
No fasting is mandatory. You must sign a consent form and provide complete clinical history including any anticoagulant use, recent travel, tick bites, and occupational exposures. The sample collection will take place inside a designated hospital isolation room or dedicated phlebotomy bay under strict infection control protocols.
4. How long does it take to receive results and how are they delivered?
Preliminary results are available by phone within 36 hours of sample receipt at the laboratory. The official detailed report including whole genome sequencing analysis is delivered by email on the fourth working day. Reports include viral load quantification, genotype information, and interpretive comments from the reporting physician.
5. Can I collect the sample at home through mobile phlebotomy?
No. Because this test may require cerebrospinal fluid collection and involves a Biosafety Level 3 pathogen, sample collection is restricted to accredited hospital facilities only. This policy ensures patient safety, proper specimen handling, and compliance with UAE infection control regulations.
UAE Regulatory & Data Privacy Adherence
Data Protection & Healthcare Compliance
All patient data associated with the CCHF Viral Load Quantitative Test is processed in full 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. Laboratory practices adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient consent, clinical safety, and chain-of-custody documentation for all biological specimens.
Clinical & Logistical Metadata
| Test Name | Crimean-Congo Hemorrhagic Fever CCHF Viral Load Quantitative PCR with Whole Genome Sequencing |
| Price AED | 1000 |
| Turnaround Time | Phone 36 hours – Email 4th working day |
| Sample Type / Matrix | Blood serum plasma or cerebrospinal fluid CSF – Hospital Extraction Only |
| Methodology Used | Real-Time PCR qPCR followed by Whole Genome Sequencing WGS confirmation |
| ICD-10-CM Code | A98.0 |
| LOINC Code | 101387-5 |
| 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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