Test Price
350 AED✅ Home Collection Available
Mycobacterium Combined Panel (TB.com) Test in UAE | 350 AED | DHA Licensed
Executive Summary & Core Metrics
📋 Core Diagnostics at a Glance
- Diagnostic Sensitivity: 99.9% using Real‑Time PCR & Whole Genome Sequencing (WGS), applicable across diverse specimen types.
- Home Collection: ISO‑certified mobile phlebotomy team with temperature‑controlled cold‑chain transport, available daily 8 AM–11 PM (except for invasive specimens requiring hospital extraction).
- Post‑Result Guidance: Teleconsultation with a licensed general practitioner to interpret findings and coordinate care.
- Insurance Direct Billing: Verify coverage instantly via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Mycobacterium Combined Panel (TB.com) is a state‑of‑the‑art molecular assay that concurrently deploys Real‑Time PCR (qPCR), Whole Genome Sequencing (WGS), and Immunochromatographic Testing (ICT) to deliver rapid, definitive diagnosis of active tuberculosis. This integrated workflow provides unparalleled sensitivity and comprehensive drug‑resistance profiling from a single specimen, enabling initiation of targeted therapy without delay.
| Feature | Our Test (TB.com Panel) | Closest Alternative (AFB Smear & Culture) |
|---|---|---|
| Diagnostic Sensitivity | 99.9% (PCR+WGS) | ~50‑80% for smear; culture takes weeks |
| Methodology | Real‑Time PCR (qPCR) + WGS + ICT | Microscopy (Ziehl‑Neelsen) & Solid/Liquid Culture |
| Turnaround Time | Interim: 14 days | Final: 6 weeks | Smear same day; culture up to 8 weeks |
| Drug Resistance Profile | Included (genotypic prediction) | Separate DST required |
Physician Insight & Safety Protocols
“The Mycobacterium Combined Panel is a powerful diagnostic tool for active tuberculosis. However, results must be interpreted in the full clinical context—including symptoms, chest imaging, and epidemiological history. A negative result does not exclude infection, particularly in immunocompromised patients. Always consult your primary care physician before making treatment decisions.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
⚠️ Advisory on Medication Continuation
Do not discontinue prescribed anti‑tubercular medication without consulting your doctor.
🛑 Safety Exclusion Criteria & ER Red Flags
Do not proceed with home collection if any of the following are present:
- Haemodynamic instability (systolic BP < 90 mmHg, tachycardia > 120 bpm).
- Active large‑volume haemoptysis requiring emergency care.
- Altered mental status or loss of consciousness within the last 24 hours.
- Children under 12 years unless accompanied by a legal guardian (per Federal Decree‑Law No. 4 of 2016 on Medical Liability).
- Inability to provide the required sample volume safely at home.
Seek immediate hospital care if you experience:
- Sudden severe shortness of breath or chest pain.
- Coughing up more than a teaspoon of bright red blood.
- High fever (>39°C) with rigors and confusion.
Patient FAQ & Clinical Guidance
1. How does the Mycobacterium Combined Panel detect tuberculosis so accurately?
By combining real‑time PCR with whole genome sequencing, the test identifies Mycobacterium tuberculosis DNA and drug‑resistance mutations in a single run, delivering results with 99.9% diagnostic sensitivity. The immunochromatographic component adds rapid antigen confirmation.
2. Can this be done from home and what samples are needed?
Our ISO‑certified mobile phlebotomist can collect sputum, blood, urine, or body fluid samples at your doorstep with full cold‑chain integrity. For invasive specimens such as CSF, bone marrow, or tissue biopsies, collection is performed strictly at an accredited hospital facility — mobile home phlebotomy is disabled for those.
3. Is insurance accepted and how long for the final report?
We provide direct insurance verification via WhatsApp prior to collection. The interim report is available in 14 days, and the final comprehensive report integrating PCR, WGS, and ICT is delivered within 6 weeks.
4. What preparation is needed before the test?
No special preparation is required. Maintain your usual medications unless specifically advised otherwise by your physician.
UAE Regulatory & Data Privacy Adherence
✅ Legal & Compliance Framework
- Data Protection: Full compliance 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.
- Medical Liability: Patient safety and consent governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability.
- Accreditation: DHA Facility License No. 1143 (Dubai Healthcare City). ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Mycobacterium Combined Panel (TB.com) |
| Price (AED) | 350 |
| Turnaround Time | Interim: 14 days, Final: 6 weeks |
| Sample Type / Matrix | Sputum, body fluids (pleural, peritoneal), CSF, urine, tissue biopsy, whole blood, bone marrow, menstrual blood |
| Methodology Used | Real‑Time PCR (qPCR) + Whole Genome Sequencing (WGS) + Immunochromatographic Test (ICT) |
| ICD‑10‑CM Code | A15.0 (confirmed pulmonary TB), Z11.1 (screening), Z20.1 (contact) |
| LOINC Code | 81380‑5 (Mycobacterium sp DNA NAA+probe) |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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التحقق من التغطية التأمينية
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ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians