Test Price
1,200 AED✅ Home Collection Available
Histoplasma Quantitative PCR Test in Dubai | 1200 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
- 99.9% Analytical Sensitivity for Histoplasma capsulatum DNA via Real-Time PCR & Whole Genome Sequencing (ISO 9001:2015 Certified – Cert: INT/EGQ/2509DA/3139).
- Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
- Telephonic Post-Test Clinical Guidance by a DHA-licensed General Practitioner to interpret quantitative fungal load results.
- Direct Insurance Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Histoplasma Quantitative PCR test measures Histoplasma capsulatum DNA load with single‑copy sensitivity, enabling precise diagnosis, staging, and therapeutic monitoring of histoplasmosis. This molecular assay detects the pathogen directly from tissue biopsies, respiratory secretions, or blood, providing results within 36–48 hours.
| Feature | Our Test – Histoplasma qPCR + WGS | Closest Alternative (Culture / Antigen) |
|---|---|---|
| Precision (LoD) | ≤ 5 copies/reaction; digital-PCR converted IU/mL | ≥ 10² CFU/mL; variable sensitivity |
| Methodology | Real‑Time PCR (qPCR) + Whole Genome Sequencing confirmation | Culture (4–6 weeks) or urine antigen (false negatives) |
| Speed | Email: 48 h / Phone: 36 h | Culture: 4–6 weeks; antigen: 24–72 h but non‑quantitative |
Physician Insight & Safety Protocols
“Quantitative histoplasma PCR delivers a precise fungal DNA load that is indispensable for monitoring treatment response, especially in immunocompromised patients. However, a single positive result must always be correlated with the patient’s clinical presentation, radiographic findings, and immune status before altering therapy.”
— Dr. Ajay Singh, General Practitioner, DHA License 36234132
Medication Advisory
Do not discontinue prescribed antifungal or immunosuppressive medication without consulting your treating physician. Quantitative test trends guide treatment adjustments only under specialist supervision.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Patient refusal to sign pre-test consent document; inappropriate specimen type (e.g., superficial swabs instead of fresh tissue); active bleeding disorders contraindicating biopsy.
- ER Red Flags: Severe dyspnoea, acute respiratory distress, haemoptysis, altered mental status, or signs of disseminated intravascular coagulation – seek emergency care immediately before sample collection.
- Minors require parental consent in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Patient FAQ & Clinical Guidance
1. What does a “quantitative” histoplasma PCR result mean, and how is it used clinically?
The test measures the exact number of fungal DNA copies per milliliter of sample, enabling physicians to assess disease severity and monitor treatment response. Serial quantitative results help determine whether antifungal therapy is effective or requires adjustment.
2. Which specimens are accepted, and how must they be collected?
The test accepts fresh tissue biopsies (skin, lung, or bone marrow), bronchoalveolar lavage, and peripheral blood. All samples must be collected under sterile conditions in a hospital setting and transported via our ISO‑certified cold chain. Home phlebotomy is not available for this assay.
3. Is the test covered by insurance, and how do I verify billing?
We verify direct billing eligibility with all major UAE insurers within 15 minutes via WhatsApp. Send a photo of your insurance card to +971 54 548 8731 to confirm coverage before your hospital appointment.
UAE Regulatory & Data Privacy Adherence
Data Protection & Clinical Governance
This laboratory service operates in 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. Patient consent and clinical safety are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. All health data is encrypted during transmission and stored in secure UAE‑based servers.
Clinical & Logistical Metadata
| Test Name | Histoplasma Quantitative PCR + Whole Genome Sequencing |
| Price (AED) | 1,200 AED |
| Turnaround Time | 36–48 hours |
| Sample Type / Matrix | Hospital Extraction Only – Tissue biopsy, respiratory secretions, or blood. Collection strictly in hospital. |
| Methodology Used | Real-Time PCR (qPCR) with Whole Genome Sequencing confirmation |
| ICD-10-CM Code | B39.9 (Histoplasmosis, unspecified) |
| LOINC Code | 94712-2 (Histoplasma capsulatum DNA [Units/volume] in Specimen by NAA with probe detection) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians