Test Price
700 AED✅ Home Collection Available
Chlamydia pneumoniae RNA Detection, Qualitative Test in UAE | 700 AED | DHA Approved
Executive Summary & Core Metrics
- Diagnostic Accuracy: 99.9% clinical sensitivity with ISO‑certified RT‑PCR methodology for active infection detection.
- Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
- Clinical Guidance: Complimentary telephonic post‑test result interpretation by a DHA‑licensed physician.
- Insurance Support: Direct billing verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Chlamydia pneumoniae RNA Qualitative assay directly detects active bacterial RNA in respiratory specimens, enabling rapid identification of atypical pneumonia aetiology with high clinical precision. Real‑time reverse transcription PCR (RT‑PCR) is employed, followed by confirmatory whole‑genome sequencing for unambiguous results.
| Feature | Our Test – RT‑PCR RNA | Standard Antibody/Serology |
|---|---|---|
| Method | Real‑time PCR with reverse transcription & confirmatory whole‑genome sequencing | Micro‑immunofluorescence (MIF) or ELISA |
| Clinical Sensitivity | >99% for active infection | ~70–85% (may miss early infection) |
| Turnaround | 24 h phone / 36 h email | 2–5 working days |
| Sample Type | Bronchial swab, lavage, or CSF | Blood (serum) |
| Regulatory Standard | DHA/MOHAP‑approved PCR platform, ISO 9001:2015 | General laboratory accreditation |
Physician Insight & Safety Protocols
“This RNA‑based PCR offers the earliest and most specific evidence of active Chlamydia pneumoniae infection; however, all results must be correlated with clinical presentation, radiological findings, and the patient’s immune status. Do not disregard concerning respiratory symptoms, even with a negative test.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Advisory: Medication & Treatment Continuity
⛔ CRITICAL: Do not discontinue prescribed antibiotics or any respiratory medication without direct consultation with your treating physician. This test aids diagnosis but does not replace clinical judgment.
Exclusion Criteria & Emergency Red Flags
- Home collection is contraindicated – This procedure is hospital-only due to invasive sampling (bronchoscopy or lumbar puncture).
- Patients with severe dyspnoea, oxygen saturation <92%, altered mental status, or active haemoptysis must be evaluated in an emergency setting.
- Patients with known bleeding diathesis or recent bronchial surgery must not undergo bronchial sampling without specialist clearance.
- Go to the nearest ER immediately if you experience sudden worsening breathlessness, chest pain, high fever unresponsive to antipyretics, or confusion.
- This test is not performed on unaccompanied minors; a legal guardian must provide informed consent as per UAE law.
Patient FAQ & Clinical Guidance
1. What is the Chlamydia pneumoniae RNA Qualitative test and why is it recommended?
A: It detects active C. pneumoniae RNA in respiratory specimens such as bronchial swabs or CSF, with unmatched sensitivity for diagnosing atypical pneumonia. This allows targeted antibiotic therapy and reduces unnecessary broad‑spectrum use.
2. How is the sample collected and what preparation is required?
A: The sample must be collected in a hospital setting by a trained physician via bronchoalveolar lavage or lumbar puncture. No special preparation is needed beyond signing consent and providing relevant medical history.
3. When will I receive my results and how are they interpreted?
A: Results are delivered within 24 hours by phone and 36 hours by email, accompanied by a free telephonic clinical interpretation with a DHA‑licensed doctor who will explain the findings in the context of your overall health.
UAE Regulatory & Data Privacy Adherence
ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) | DHA/MOHAP Facility License: 1143
All personal health data is processed in strict conformity 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. Clinical testing safety and patient consent adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability.
📲 Hospital Coordination & Support: +971 54 548 8731 (Available daily 8 AM–11 PM)
Clinical & Logistical Metadata
| Test Name | Chlamydia pneumoniae RNA Detection, Qualitative |
| Price (AED) | 700 |
| Turnaround Time | 24 hours (phone) / 36 hours (email) |
| Sample Type / Matrix | Bronchial swab, bronchoalveolar lavage, or cerebrospinal fluid (CSF) |
| Methodology Used | Real‑time reverse transcription PCR (RT‑PCR) with confirmatory whole‑genome sequencing |
| ICD-10-CM Code | J16.0 (Pneumonia due to Chlamydia) |
| LOINC Code | 29315-5 (Chlamydia pneumoniae rRNA [Presence] in Specimen by Probe) |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians