Test Price
1,700 AEDโ Home Collection Available
Bas-Congo Virus & Heartland Virus Multiplex Detection, Differentiation, and Viral Load (Quantitative PCR/Whole Genome Sequencing) in UAE | 1700 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139) using dual methodology: Real-Time PCR (qPCR) and Whole Genome Sequencing (WGS).
- Sample Collection: Hospital Extraction Only โ Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by a DHA-licensed physician (Dr. Lina Osama Zaki Quteineh, DHA: 9294403).
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This multiplex molecular test simultaneously detects and quantifies Bas-Congo virus (BASV) and Heartland virus (HRTV) using quantitative real-time PCR and confirmatory whole genome sequencing. It provides precise differentiation and viral load measurement from blood or CSF, critical for managing acute febrile illnesses with haemorrhagic or cardiac manifestations in the UAE. The dual methodology ensures both rapid screening through qPCR and definitive confirmation with WGS, achieving a limit of detection of 10 copies/mL for each virus.
Test Comparison
| Feature | Our Test (Bas-Congo & Heartland Multiplex) | Closest Alternative (Singleplex PCR) |
|---|---|---|
| Precision | qPCR + WGS, LOD 10 copies/mL, Differentiation | qPCR only, single virus, no confirmatory sequencing |
| Methodology | Real-Time PCR with Whole Genome Sequencing | Real-Time PCR without sequencing |
| Turnaround Time | 48 hours (email), 36 hours (phone) | 72 โ 96 hours |
Physician Insight & Safety Protocols
Clinical Note from Dr. Lina Osama Zaki Quteineh (DHA: 9294403):
โBas-Congo and Heartland viruses are rare but serious tick-borne pathogens; this multiplex assay with viral load quantitation empowers accurate diagnosis and risk stratification, particularly in patients with unexplained fever and thrombocytopenia or myocarditis. Always interpret results alongside clinical presentation and epidemiological history. Do not delay supportive care while awaiting results.โ
Exclusion Criteria & ER Red Flags
- Exclusion: Active bleeding diathesis or hemodynamic instability precluding phlebotomy.
- Exclusion: Inability to provide informed consent (consent form mandatory per Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Red Flag: If you experience sudden high fever, severe headache, mucocutaneous bleeding, chest pain, or confusion, seek emergency medical attention immediately.
Patient FAQ & Clinical Guidance
1. How is this test different from a standard PCR test?
This multiplex panel detects both Bas-Congo and Heartland viruses simultaneously with viral load quantification and confirmatory whole genome sequencing, providing comprehensive diagnostic clarity that singleplex PCR cannot achieve. Standard PCR typically targets one pathogen and lacks the confirmatory sequencing step.
2. When should I consider this test?
Consider testing if you present with sudden onset fever, thrombocytopenia, or unexplained cardiac symptoms following a tick bite or travel to endemic regions, enabling rapid pathogen identification and targeted care. Early differentiation between these viruses is critical for appropriate management.
3. What are the risks associated with sample collection?
Sample collection is performed exclusively within accredited hospital facilities by DHA-licensed professionals, using strict aseptic technique to eliminate infection risks. For CSF collection, the procedure is done under sterile conditions in a clinical setting, ensuring patient safety and sample integrity.
UAE Regulatory & Data Privacy Adherence
Data Protection & Compliance: This service operates under the 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. All patient data is encrypted and processed in accordance with UAE health data security standards. Clinical consent is governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. The facility is licensed by DHA (License No: 1143) and holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Bas-Congo Virus & Heartland Virus Multiplex Detection, Differentiation, and Viral Load (Quantitative PCR/Whole Genome Sequencing) |
| Price (AED) | 1,700 |
| Turnaround Time | 48 hours (email), 36 hours (phone) |
| Sample Type / Matrix | Hospital Extraction Only โ Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. Specimens include whole blood (3 mL in EDTA tube), serum/plasma (gold-top or green-top), or CSF (1 mL sterile). |
| Methodology Used | Quantitative Real-Time PCR (qPCR) with confirmatory Whole Genome Sequencing (WGS) |
| ICD-10-CM Code | A98.8, A93.8, Z20.828 |
| LOINC Code | 88118-9 |
| DHA Facility License & Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians