Test Price
750 AED✅ Home Collection Available
Mycoplasma Pneumonia (RNA Detection) Qualitative Test in UAE – 750 AED
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity via ISO Accredited Processing
VIP Home Collection Service (Throat Swab) – Daily 8 AM – 11 PM
Telephonic Post-Test Clinical Guidance by DHA-Licensed Specialist
Direct Insurance Billing Verification via WhatsApp +971 54 548 8731
The Mycoplasma Pneumonia (RNA Detection) Qualitative Test uses real‑time PCR (qPCR) to directly detect ribosomal RNA of Mycoplasma pneumoniae in respiratory specimens, providing results within 24 hours by phone and 36 hours via email. This molecular assay replaces slower culture and serology, enabling early targeted therapy and reducing unnecessary antibiotic use. The test is performed at DNA Labs UAE, a DHA‑licensed facility (License No. 1143) compliant 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.
Test Overview & Methodology
The test targets highly conserved 16S ribosomal RNA sequences, achieving a limit of detection below 10 copies per reaction. It can identify acute infection even in samples with low pathogen burden, outperforming culture (sensitivity 40–80%) and serology (which may be negative in early stages). The assay is performed on respiratory specimens including throat swab, sputum, or bronchoalveolar lavage (BAL). Home collection is available for throat swab and sputum; BAL requires hospital extraction.
| Feature | Our Test (Real‑Time PCR) | Standard Culture/Serology |
|---|---|---|
| Analytical Sensitivity | 99.9% (detects <10 copies/reaction) | 40–80% (slow growth, cross‑reactivity) |
| Turnaround Time | 24 hours (phone) / 36 hours (email) | 5–14 days |
| Method | Real‑Time PCR (qPCR) | Culture, CF, or EIA IgM/IgG |
| Clinical Utility | Direct pathogen detection from throat swab, sputum, BAL | Often retrospective; IgM may be negative early |
Physician Insight & Safety Protocols
“As a general practitioner, I see the profound impact of rapid RNA detection in guiding timely macrolide or doxycycline therapy for Mycoplasma pneumonia. Even a 24‑hour delay can prevent deterioration in children and young adults. This test, when combined with clinical evaluation, changes management decisively.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Clinical Advisory
⚠ Medication Warning:
Do not discontinue any prescribed antibiotic or medication without consulting your treating physician. A positive RNA result confirms the need for targeted antibiotics, but empirical therapy should only be adjusted under medical supervision.
Patient Exclusion Criteria
- Exclusion Criteria: Active bleeding diathesis (BAL sample), severe hypoxemia precluding safe bronchoscopy, inability to provide informed consent.
- ER Red Flags: Sudden worsening shortness of breath, cyanosis, confusion, or high fever unresponsive to antipyretics — seek emergency care immediately.
- Minors: All testing for patients under 18 requires parental consent as per Federal Decree-Law No. 4 of 2016 on Medical Liability and UAE Minor Protection regulations.
- Pre‑Test: Sign the consent document and provide recent clinical history. Fasting is not required for throat swab or sputum collection.
Patient FAQ & Clinical Guidance
1. What is the Mycoplasma Pneumonia RNA Detection test, and how does it differ from a standard culture?
The real‑time PCR RNA test directly identifies Mycoplasma pneumoniae genetic material in your respiratory sample within 24 hours, unlike culture which may take weeks. It detects active infection even in low‑burden samples.
2. How is the sample collected, and is the home collection service suitable for me?
A trained phlebotomist will gently swab the back of your throat or collect a small amount of sputum; the procedure is quick and minimally uncomfortable. Home collection is available daily from 8 AM to 11 PM across all Emirates.
3. Why should I choose this over antibody blood tests or X‑ray alone?
RNA detection confirms active infection within hours, enabling precise antibiotic selection and avoiding unnecessary empiric therapy based solely on X‑ray shadows. It is the gold standard for early diagnosis.
4. How quickly will I receive my results?
Results are reported within 24 hours by telephone and 36 hours by email. Urgent results can be expedited upon request.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance
DNA Labs UAE operates under DHA Facility License No. 1143. All clinical data is processed in strict adherence to 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. Patient consent and clinical safety follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | Mycoplasma Pneumonia (RNA Detection) Qualitative Test |
| Price (AED) | 750 |
| Turnaround Time | 24–36 hours |
| Sample Type / Matrix | Respiratory specimen (throat swab, sputum, bronchoalveolar lavage); home collection available for throat swab and sputum |
| Methodology Used | Real‑Time PCR (qPCR) targeting 16S ribosomal RNA |
| ICD-10-CM Code | J15.7 (Pneumonia due to Mycoplasma pneumoniae) |
| LOINC Code | 59078-8 (Mycoplasma pneumoniae RNA [Presence] in Specimen by NAA with probe detection) |
| DHA Facility License & Laboratory Address | DHA License: 1143 | DNA Labs UAE, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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