Test Price
1,400 AED✅ Home Collection Available
Bordetella Multiplex (B. pertussis, L. pneumophila, K. pneumoniae) RNA Detection & Differentiation Qualitative Test | 1,400 AED | Dubai Healthcare City
Executive Summary & Core Metrics
Ultra-sensitive multiplex real-time PCR assay for simultaneous qualitative detection and differentiation of Bordetella pertussis (whooping cough), Legionella pneumophila (Legionnaires’ disease), and Klebsiella pneumoniae. Processed in an ISO 9001:2015 certified facility with cold‑chain logistics and post‑test telephonic guidance by a DHA‑licensed physician.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity – ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Home Collection & Temperature‑Controlled Cold‑Chain (available daily 8 AM–11 PM).
- Clinical Guidance: Telephonic post‑test interpretation by a DHA‑licensed General Practitioner.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Bordetella Multiplex RNA Qualitative Test employs real‑time reverse transcription PCR (RT‑PCR) to simultaneously detect and differentiate Bordetella pertussis, Legionella pneumophila, and Klebsiella pneumoniae from a single respiratory specimen. Designed for patients presenting with atypical or severe respiratory syndromes, the assay delivers definitive results within 36–48 hours, enabling targeted antimicrobial therapy and infection control measures. Optional whole‑genome sequencing (WGS) is available for outbreak typing.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision / Method | Multiplex Real‑Time PCR (RT‑qPCR) + optional WGS confirmation | Singleplex PCR or culture (slower, less sensitive) |
| Speed | Phone: 36 h | Email: 48 h (4th working day) | Culture: 5‑7 days; single PCR may require multiple samples |
| Coverage | 3 high‑risk pathogens in one sample | One pathogen per test; higher cumulative cost and turnaround time |
Physician Insight & Safety Protocols
“A positive result for any of these pathogens must be interpreted alongside clinical presentation, epidemiological context, and radiological findings. While the RT‑PCR assay is highly sensitive, false negatives can occur if the specimen is collected too early or after antibiotics have been started. I advise all patients to continue prescribed medications and never self‑adjust doses based solely on this panel.”
— Dr. Ajay Singh, General Practitioner, DHA License 36234132.
Medication Safety Advisory
⚠️ Medication Safety Notice
Do not discontinue prescribed antibiotics, inhalers, or immunosuppressants without consulting your treating physician. This test is designed for diagnostic differentiation only and does not replace clinical judgment or ongoing therapy.
Exclusion Criteria & Emergency Red Flags
- Not suitable for: Asymptomatic screening without clinical suspicion; self‑requested testing without a physician’s referral.
- Do not order if: Patient presents with acute respiratory distress requiring immediate resuscitation – proceed to emergency department.
- Red flags – seek emergency care immediately: Severe dyspnea, cyanosis, altered mental status, hemodynamic instability, or hemoptysis.
- Pediatric note: Minors must be accompanied by a legal guardian as per Federal Decree‑Law No. 4 of 2016 on Medical Liability; parental consent is mandatory.
Patient FAQ & Clinical Guidance
1. Is this test definitive for diagnosing whooping cough?
Answer: A positive Bordetella pertussis RNA result by RT‑PCR confirms active infection with over 99% specificity, but clinical correlation remains mandatory. Negative results do not rule out infection if collection timing was suboptimal.
2. Can I take this test if I am already on antibiotics?
Answer: Antibiotics may reduce bacterial load and increase the risk of false‑negative results. Ideally collect the specimen before starting therapy; if already on antibiotics, inform your physician for proper interpretation.
3. What sample type is required for this multiplex PCR?
Answer: The preferred specimen is a deep nasopharyngeal swab. Sputum, throat swab, bronchoalveolar lavage (BAL), or lung tissue are also validated – BAL and lung tissue require hospital collection. A respiratory sample collected from the lower airways increases diagnostic yield.
UAE Regulatory & Data Privacy Adherence
Legal Compliance & Accreditation: This test conforms to the 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. All processing is performed in an ISO 9001:2015 certified facility (Cert: INT/EGQ/2509DA/3139) under the supervision of the Dubai Health Authority. Patient data is handled in accordance with the highest privacy and security standards.
Clinical & Logistical Metadata
| Test Name | Bordetella Multiplex (B. pertussis, L. pneumophila, K. pneumoniae) RNA Detection & Differentiation Qualitative Test |
| Price (AED) | 1,400 AED |
| Turnaround Time | 36–48 hours (verbal report); written report on 4th working day |
| Sample Type / Matrix | Nasopharyngeal swab (recommended), sputum, throat swab; bronchoalveolar lavage or lung tissue (hospital collection only) |
| Methodology Used | Real-Time Reverse Transcription PCR (RT‑qPCR); optional Whole‑Genome Sequencing (WGS) for outbreak typing |
| ICD-10-CM Code | A37.0 (Whooping cough due to Bordetella pertussis), A48.1 (Legionnaires’ disease), J15.0 (Pneumonia due to Klebsiella pneumoniae) |
| LOINC Code | 94225‑6 – Bordetella pertussis + Legionella pneumophila + Klebsiella pneumoniae RNA panel |
| DHA Facility License & Laboratory Address | DHA License No. 1143 – DNA Labs UAE, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians