Bacterial Pneumonia Multiplex RNA Detection Panel in UAE | 1700 AED

Executive Summary & Core Metrics

Executive Summary

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Laboratory 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

This state-of-the-art multiplex real-time PCR panel rapidly detects and differentiates RNA from Bordetella pertussis, Legionella pneumophila, and Klebsiella pneumoniae in respiratory specimens, enabling clinicians to initiate pathogen-specific therapy within 48 hours.

Feature	Our Test (Multiplex PCR + WGS)	Alternative (Standard Culture)
Method	Multiplex qPCR + Whole Genome Sequencing (confirmatory)	Bacterial culture on agar plates
Turnaround Time	Email report within 48 hours; phone alert at 36 hours	3–5 days (delayed for fastidious organisms)
Sensitivity & Specificity	>99.9% sensitivity, near 100% specificity	50–60% sensitivity, risk of contamination
Detection Range	Differentiates all three pathogens + provides resistance gene insights	Often fails to grow Legionella, requires special media

Physician Insight & Safety Protocols

"This multiplex panel provides a clear molecular snapshot of the causative pathogen, allowing for timely and targeted antimicrobial therapy. While the test is highly accurate, clinical correlation remains essential. Always discuss results with your treating physician."

— Dr. Ajay Singh, General Practitioner, DHA License 36234132

Important Advisory

Do not discontinue or adjust any prescribed medication, especially antibiotics, antivirals, or inhalers, without consulting your doctor. This test is for diagnosis, not to replace clinical judgment.

Exclusion Criteria & Emergency Red Flags

Exclusion: Recent vaccination with live attenuated Bordetella pertussis vaccine (within 4 weeks) may cause false-positive RNA detection; inform your doctor.
Exclusion: Inability to provide a deep sputum or BAL sample (non-invasive swabs may be used but discuss with lab).
Red Flag - Seek Immediate Emergency Care if: You experience severe shortness of breath, bluish discoloration of lips/face, confusion, high fever >40°C (104°F), or coughing up significant blood.
Red Flag: Rapidly worsening chest pain or pressure combined with difficulty breathing.

Patient FAQ & Clinical Guidance

1. What does a positive Bordetella result mean?

A positive Bordetella result indicates pertussis infection requiring immediate antibiotic therapy and isolation. Consult your doctor for appropriate treatment.

2. How should I prepare for nasopharyngeal swab collection?

No special preparation needed; avoid eating, drinking, or brushing teeth 30 minutes before collection. The sample will be taken at the hospital by trained medical staff.

3. Is this test available for children in the UAE?

Yes, with parental consent as per UAE regulations. Pediatric sample collection is available in the hospital setting.

4. How long does it take to get results?

Results are typically available within 48 hours via email, with a preliminary phone alert at 36 hours for critical findings.

5. Can this test detect antibiotic resistance?

Yes, the confirmatory whole genome sequencing component can provide insights into resistance genes, aiding in treatment planning.

UAE Regulatory & Data Privacy Adherence

Data Protection & Legal Compliance

This test and its associated data handling comply with UAE 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. Clinical safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Laboratory accreditation: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	Bacterial Pneumonia Multiplex RNA Detection Panel (Bordetella, Legionella, Klebsiella)
Price (AED)	1,700 AED
Turnaround Time	48 hours (preliminary alert at 36 hours)
Sample Type / Matrix	Respiratory specimen (nasopharyngeal swab, sputum, or bronchoalveolar lavage)
Methodology Used	Multiplex real-time PCR + Confirmatory Whole Genome Sequencing
ICD-10-CM Code	J15.9 (Unspecified bacterial pneumonia), J15.0 (Klebsiella pneumoniae), A37.9 (Pertussis, unspecified), A48.1 (Legionnaires' disease)
LOINC Code	54081-2 (Infectious disease panel - Respiratory by NAA with probe detection)
DHA Facility License & Laboratory Address	License No. 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE \| DNA Labs UAE