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Test Price

700 AED

✅ Home Collection Available

Bordetella pertussis (RNA Detection) Qualitative Test in UAE | 700 AED | DHA Licensed

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Laboratory Processing.
Premium Logistics: VIP Home Collection Service & Temperature-Controlled Cold-Chain Logistics for Nasopharyngeal Swab.
Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance for Result Interpretation & Next Steps.
Insurance: Swift Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

Bordetella pertussis RNA detection qualitative test utilises Real-Time PCR to rapidly identify the genetic material of the whooping cough bacterium, enabling early diagnosis and outbreak control in the UAE. The assay specifically targets ribosomal RNA sequences unique to Bordetella pertussis, providing superior sensitivity in the acute phase of infection.

Feature Our Test (RNA Detection) Culture / Serology (Closest Alternative)
MethodologyReal-Time PCR (qPCR) + optional WGS confirmationBacterial culture / ELISA serology
Analytical Sensitivity>99% (low detection limit)40–70% (slow growth, cross‑reactivity)
Turnaround Time36 hours (phone) / 48 hours (email)5–10 days
Clinical UtilityEarly detection, outbreak management, antibiotic guidanceRetrospective confirmation only

Physician Insight & Safety Protocols

“As a general practitioner, I see many patients suffering from persistent cough illness. This RNA‑based test provides near‑certainty within hours, allowing us to initiate targeted antibiotics, protect close contacts, and avoid unnecessary hospital isolation. Always confirm treatment decisions with the full clinical presentation.”

— Dr. Ajay Singh, General Practitioner | DHA Registration ID: 36234132

Important Medication Advisory

⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your doctor. Antibiotic therapy for pertussis must be managed by a licensed physician.

Exclusion Criteria & Emergency Red Flags

  • Not suitable for patients with active severe epistaxis or untreated coagulopathy that contraindicates nasopharyngeal swabbing.
  • Individuals unable to cooperate with swab collection (e.g., acute respiratory distress without stabilisation).
  • Seek emergency care immediately if you experience: cyanosis (blue lips), apnoea pauses, severe breathing difficulty, or lethargy in an infant.

Patient FAQ & Clinical Guidance

1. What exactly does the Bordetella pertussis RNA qualitative test detect, and why is it preferred?

This molecular test rapidly identifies Bordetella pertussis RNA with high sensitivity to confirm whooping cough infection and guide early antibiotic therapy. It significantly outperforms culture and serology in the first two weeks of illness.

2. How is the sample collected, and will it be uncomfortable?

A trained healthcare professional gently inserts a soft swab into the back of your nose or throat; the procedure takes seconds and causes only momentary mild discomfort. No blood draw is required.

3. When will I receive my results, and what do the reports mean?

Results are delivered within 36 hours by phone and 48 hours by email; a positive RNA report indicates active pertussis infection requiring immediate medical follow‑up for antibiotic treatment and contact prophylaxis.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance

  • Data security and patient privacy are protected under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
  • Clinical safety and patient consent for testing procedures follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
  • Health information systems and telemedicine practices comply with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.

All clinical decisions must be based on a complete evaluation by a licensed physician. This service is provided by DNA Labs UAE, an ISO 9001:2015 certified facility.

Clinical & Logistical Metadata

Test Name Bordetella pertussis RNA Detection, Qualitative
Price (AED) 700 AED
Turnaround Time 36 hours (phone) / 48 hours (email)
Sample Type / Matrix Nasopharyngeal swab or throat swab
Methodology Used Real-Time PCR (qPCR) targeting ribosomal RNA
ICD-10-CM Code A37.0
LOINC Code 34076-4
DHA Facility License & Laboratory Address DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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