Test Price
650 AED✅ Home Collection Available
Listeria monocytogenes RNA Detection Qualitative Test in UAE – 650 AED
Executive Summary & Core Metrics
Executive Summary: The Listeria monocytogenes RNA Detection Qualitative Test using quantitative real-time PCR (qPCR) is the most sensitive and accurate diagnostic method for detecting active listeriosis, especially critical for pregnant women and immunocompromised patients. Our laboratory delivers ISO-certified processing with end-to-end cold chain integrity and telephonic post-test clinical consultation by DHA-licensed physicians.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Hospital Extraction Only – 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 DHA-licensed physicians.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Listeria monocytogenes RNA Detection Qualitative Test uses real-time PCR (qPCR) to directly identify active, replicating Listeria bacteria in clinical specimens. It outperforms traditional culture with 24–36 hour turnaround and near-absolute sensitivity. This highly sensitive assay detects RNA from viable bacteria, making it ideal for high-risk patient populations.
| Feature | Our Test (qPCR RNA) | Standard Culture |
|---|---|---|
| Method | Real-Time PCR (qPCR) | Bacterial Culture |
| Target | Active RNA (viable cells) | Viable but slow growth |
| Turnaround | 24–36 hours | 5–7 days |
| Sensitivity | >99% | 60–80% |
Physician Insight & Safety Protocols
From Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
This qPCR-based RNA detection test is a critical tool for early identification of active listeriosis, particularly in pregnant women and immunocompromised individuals. A negative result does not entirely exclude infection; clinical correlation with presenting symptoms remains essential. I strongly advise reviewing all laboratory findings with a qualified physician to ensure comprehensive and personalized clinical management.
Important Advisory
Do not discontinue or modify any prescribed medication without prior consultation with your treating physician. This test result should be integrated into your full clinical context for appropriate therapeutic decisions.
Safety Exclusion Criteria
- Patients with active, uncontrolled bleeding disorders.
- Individuals unable to provide informed consent, including minors without legal guardian consent as per UAE Federal Law No. 2 of 2019.
Emergency Red Flags
- Sudden high fever, severe headache, stiff neck, confusion, or muscle aches after potential Listeria exposure – seek immediate emergency care.
- Pregnant women with flu-like symptoms and a history of possible contaminated food consumption should contact their obstetrician without delay.
Patient FAQ & Clinical Guidance
1. What does a positive result mean?
A positive result indicates an active Listeria infection that requires urgent medical evaluation and treatment. This means live, replicating bacteria are present in your sample. Prompt antibiotic therapy, guided by your physician, is typically required to prevent complications such as meningitis or sepsis, especially if you are pregnant or immunocompromised.
2. How should I prepare for the sample collection?
No special preparation is needed; simply bring your medication list and a brief medical history. Ensure you have signed the consent document. The appropriate specimen (CSF, amniotic fluid, synovial fluid, serum, stool, or rectal swab) will be collected by qualified hospital staff in a sterile manner, then transported under strict cold-chain conditions to our ISO-certified laboratory for analysis.
3. How soon will I get my results?
Results are delivered within 24–36 hours from sample receipt. In urgent cases, we expedite reporting to enable rapid clinical decisions. All reports include interpretation guidance from our DHA-licensed clinical team, and you can schedule a telephonic consultation to discuss findings in detail.
4. Can I eat or drink before the test?
No dietary restrictions are required for this test. Unlike certain blood chemistry panels, qPCR-based RNA detection is not affected by food or fluid intake. Simply follow your regular routine and arrive with any relevant medical documentation.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance Framework: DNA Labs UAE operates under DHA Facility License Number 1143 and adheres to all applicable UAE federal regulations governing medical diagnostics and patient data protection.
- Data Privacy: Full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) ensuring all patient health information is securely processed, stored, and transmitted.
- Health ICT Security: Adherence to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, guaranteeing digital health data integrity and confidentiality.
- Clinical Safety & Consent: All procedures follow Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring proper patient consent protocols and clinical safety standards.
- Quality Certification: ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) for quality management systems.
Clinical & Logistical Metadata
| Test Name | Listeria monocytogenes RNA Detection Qualitative Test |
| Price (AED) | 650 AED |
| Turnaround Time | 24–36 hours from sample receipt |
| Sample Type / Matrix | CSF, Amniotic Fluid, Synovial Fluid, Serum, Stool, Rectal Swab – Hospital Extraction Only |
| Methodology Used | Real-Time PCR (qPCR) |
| ICD-10-CM Code | A32.9, A32.11, A32.12 |
| LOINC Code | 76701-3 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians