Test Price
550 AED✅ Home Collection Available
Dengue Virus & Chikungunya Virus (RNA Detection) Qualitative Test in UAE | 550 AED
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy (8 AM – 11 PM).
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed General Practitioner.
Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This qualitative RNA detection panel simultaneously identifies genetic material of Dengue and Chikungunya viruses with ultra‑high precision using Real‑Time PCR (qPCR) and confirmatory Whole Genome Sequencing (WGS), delivering actionable results within 24 working hours. The test is designed for acute febrile illness management and supports timely public health reporting.
| Feature | Our Test (RNA Detection) | Rapid Antigen Test (Alternative) |
|---|---|---|
| Methodology | Real‑Time PCR (qPCR) with WGS confirmation | Lateral Flow Immunoassay |
| Diagnostic Sensitivity | 99.9% (captures early viremia) | 60–80% (high false‑negative risk) |
| Turnaround Time | 24–36 hours | 15–20 minutes |
| Clinical Correlation | Distinguishes active infection from past exposure | Often cross‑reacts, leading to misdiagnosis |
| Regulatory Acceptability | Fully DHA/MOHAP compliant | Limited; not accepted for hospital admission |
Physician Insight & Safety Protocols
“As a clinician with over two decades of experience in infectious diseases, I recommend this PCR test for any patient presenting with acute fever, headache, and arthralgia during mosquito-borne disease season. A positive result confirms active infection, but a negative result does not rule out other co‑infections; always interpret with full blood counts and clinical assessment. Early detection reduces the risk of severe dengue and guides supportive care.”
– Dr. Ajay Singh, General Practitioner, DHA License 36234132
🛑 Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Abrupt cessation of anti‑pyretics or supportive therapy may precipitate severe complications. Always follow your physician’s guidance on fever management and hydration.
⚠️ Exclusion Criteria & Emergency Red Flags
Exclusion Criteria (Do NOT proceed without physician clearance):
- Known hypersensitivity to venipuncture equipment
- Active anticoagulant therapy without bridging plan
- Uncontrolled bleeding disorder (e.g., platelet <20,000/μL)
🔴 ER Red Flags (Seek immediate emergency care if you experience):
- Severe abdominal pain or persistent vomiting
- Mucosal bleeding (gums, nose, blood in stool/urine)
- Lethargy, dizziness, or rapid drop in blood pressure
- Sudden shortness of breath or chest pain
Patient FAQ & Clinical Guidance
1. How soon after a mosquito bite should I take the Dengue and Chikungunya RNA test?
The earliest viral RNA can be detected by PCR is 1–3 days after symptom onset, making this test highly sensitive during the acute febrile phase. If you test too early (before fever), RNA may not be present; repeat testing after 48 hours is recommended if clinical suspicion remains high.
2. Can this test differentiate between Dengue and Chikungunya co‑infection?
Yes, the multiplex real‑time PCR assay specifically amplifies distinct genomic regions of each virus, enabling unequivocal differentiation even in co‑infection scenarios where symptoms overlap. This precision guides tailored supportive care and avoids unnecessary empirical treatment.
3. What does a “Qualitative” result mean for my treatment plan?
A qualitative result reports the presence or absence of viral RNA, not the viral load, which is sufficient for confirming active infection and initiating public health reporting. Treatment remains symptomatic—hydration, acetaminophen—but a positive result mandates immediate physician follow‑up to monitor for warning signs of severe disease.
UAE Regulatory & Data Privacy Adherence
Data Protection: All patient data 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.
Medical Liability: Clinical testing, patient consent, and safety protocols adhere strictly to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Laboratory Certification: DNA Labs UAE is a DHA-licensed facility (License No. 1143) operating under ISO 9001:2015 and follows DHA/MOHAP standards for nucleic acid amplification tests.
Clinical & Logistical Metadata
| Test Name | Dengue Virus & Chikungunya Virus (RNA Detection) Qualitative Test |
| Price (AED) | 550 |
| Turnaround Time | 24–36 hours |
| Sample Type / Matrix | Peripheral blood (serum or plasma) |
| Methodology Used | Real‑Time PCR (qPCR) with Whole Genome Sequencing (WGS) confirmation |
| ICD-10-CM Code | A90, A92.0 |
| LOINC Code | 78036-8 |
| DHA Facility License & Laboratory Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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