Syphilis Comprehensive Panel Test in UAE | 550 AED | DHA Licensed

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance for results interpretation by a DHA-licensed physician.
Insurance: Direct Billing Verification & Pre-Approval via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Syphilis Comprehensive Panel combines highly sensitive treponemal (TPHA, FTA‑ABS) and non‑treponemal (VDRL) serological assays to detect all stages of syphilis infection, ensuring accurate screening, staging, and post‑treatment monitoring. This panel utilises a 3 mL venous blood sample collected into a serum separator tube (SST) and processed under ISO‑certified conditions for maximum reliability.

Feature	Our Syphilis Panel	Closest Alternative (Standalone VDRL)
Precision	Treponemal + Non‑treponemal confirmation (99.9% sensitivity)	Non‑treponemal only; risk of false positives/negatives
Methodology	VDRL, TPHA, FTA‑ABS (ISO‑certified lab)	Charcoal flocculation (VDRL) alone
Turnaround Time	Same‑day report (sample collected by 9 AM on Tue/Thu/Sat)	Often 24–48 hours
UAE Compliance	Full DHA & Federal Decree‑Law No. 4 of 2016 adherence	May not include all statutory reporting requirements
Home Collection	Yes – cold‑chain, 8 AM‑11 PM, DHA‑licensed phlebotomist	Often unavailable

Physician Insight & Safety Protocols

Dr. Ajay Singh (DHA Registration ID: 36234132), General Practitioner

“Syphilis remains a significant public health concern in the region, and accurate serological staging is critical for effective treatment. This comprehensive panel eliminates the guesswork by combining treponemal and non‑treponemal assays in a single workflow. Patients should be aware that a negative result during the early window period does not rule out infection; clinical correlation and repeat testing after 4–6 weeks are advised when suspicion persists.”

Medication Advisory

Do not discontinue prescribed antibiotic therapy without consulting your treating physician. Completing the full course of treatment is essential to prevent disease progression and complications.

Exclusion Criteria & Emergency Red Flags

Exclusion: This panel is not suitable for blood donor screening without explicit informed consent; parental consent is mandatory for individuals under 18 years.
Exclusion: Do not use as a standalone test for neurosyphilis – dedicated CSF analysis is required.
Emergency Red Flags: Sudden severe headache, vision loss, hearing impairment, chest pain, or new neurological deficits – seek immediate emergency care.
Emergency Red Flags: Severe allergic reaction (difficulty breathing, swelling) after blood draw – call 998.

Patient FAQ & Clinical Guidance

1. What does the Syphilis Comprehensive Panel detect?

The panel detects antibodies to Treponema pallidum using non‑treponemal (VDRL) and treponemal (TPHA, FTA‑ABS) serological assays, enabling precise diagnosis and staging of syphilis infection from primary to tertiary stages.

2. How is the sample collected for this test?

A 3 mL venous blood sample is drawn into a serum separator tube (SST) using standard phlebotomy technique. The sample is transported under refrigerated or frozen conditions via temperature‑controlled cold‑chain logistics to preserve analyte stability.

3. Is any preparation required before the test?

No special preparation is necessary; you may eat and drink normally. Please inform the phlebotomist of any medications, especially antibiotics, and ideally schedule the blood draw before starting or changing antibiotic therapy.

4. When will I receive my results?

Results are delivered the same day if the sample is collected before 9 AM on Tuesday, Thursday, or Saturday. For samples collected outside these windows, results are available within 24 hours.

5. Can I get a home collection for this test?

Yes. VIP Mobile Phlebotomy with Temperature‑Controlled Cold‑Chain Home Collection is available daily from 8 AM to 11 PM. A DHA‑licensed phlebotomist will collect the sample at your residence or office.

UAE Regulatory & Data Privacy Adherence

This diagnostic service operates in full compliance with UAE federal health data and privacy regulations. All patient data is processed and stored in accordance 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 procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory holds DHA Facility License No. 1143 and ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	Syphilis Comprehensive Panel
Price (AED)	550
Turnaround Time	Same-day report (sample collected by 9 AM on Tue/Thu/Sat)
Sample Type / Matrix	3 mL venous blood in SST (Serum Separator Tube)
Methodology Used	VDRL, TPHA, FTA‑ABS
ICD-10-CM Code	A53.9, A51.9, A52.9
LOINC Code	17785-9
DHA Facility License & Address	License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE