Test Price
200 AED✅ Home Collection Available
Syphilis Serology Test in UAE | 200 AED | DHA Licensed
Executive Summary & Core Metrics
Executive Summary
- 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing, delivering reliable screening for Treponema pallidum infection.
- VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM for safe, discreet specimen pickup.
- Telephonic Post-Test Clinical Guidance on result interpretation, supporting informed health decisions.
- Insurance Direct Billing Verification via WhatsApp at +971 54 548 8731 within minutes.
Test Overview & Methodology
The Syphilis Serology Test employs a modern chemiluminescent microparticle immunoassay (CMIA) that detects IgG and IgM antibodies against Treponema pallidum with high sensitivity, facilitating diagnosis of syphilis at any stage. This automated method provides quantitative results and significantly reduces false-positive rates commonly seen with traditional non-treponemal tests.
| Feature | Our Test (CMIA) | Traditional RPR / VDRL |
|---|---|---|
| Precision | Treponemal-specific Ab; sensitivity >99.5% | Non-treponemal; prone to biological false positives |
| Methodology | Automated CMIA, quantitative results | Manual flocculation; subjective reading |
| Speed | Next-day report after sample receipt | Often 24–48 hours plus confirmation steps |
Physician Insight & Safety Protocols
“A reactive syphilis serology result is an important screening indicator, but it must always be interpreted alongside clinical symptoms and confirmatory testing such as the TPPA. Please share your results with your treating physician to determine the appropriate stage-specific treatment and to rule out latent infection.”
— Dr. Ajay Singh, General Practitioner (DHA Registration ID: 36234132)
Advisory Guidance
- Medication Caution: Do not discontinue or modify prescribed antibiotics without consulting your physician. Self-adjustment may mask symptoms or contribute to antimicrobial resistance.
- Guardian Consent for Minors: In compliance with UAE Federal Decree-Law No. 4 of 2016 on Medical Liability, patients under 18 require mandatory guardian consent and presence during sample collection.
Exclusion Criteria & Emergency Red Flags
- Do Not Proceed at Home If: You have an active fever (>38.5 °C), severe cellulitis at the venipuncture site, or a known severe latex allergy (tourniquet). Notify our team to reschedule or arrange a hospital visit.
- Seek Emergency Care After Collection If: You develop difficulty breathing, facial or throat swelling, sudden vision loss, or a severe headache with neck stiffness — these may signal neurosyphilis exacerbation requiring urgent evaluation.
Patient FAQ & Clinical Guidance
1. How accurate is this syphilis serology test compared to older methods?
Our CMIA-based assay detects Treponema pallidum antibodies with over 99.5% diagnostic sensitivity and specificity, significantly reducing false-positive rates common with non-treponemal tests like RPR. The automated immunoassay provides a numeric index value that helps differentiate early infection from past treated disease when correlated with clinical history.
2. Do I need to fast before the blood draw for syphilis serology?
Fasting is not required for this analysis; the sample can be drawn at any time and is not affected by food or drink. However, please inform the phlebotomist of any antibiotics you are currently taking, as they may influence antibody timing. Sample collection follows cold-chain protocols to ensure result accuracy.
3. When will I receive my report and how is it interpreted?
Your report will be available the next day if the sample reaches our lab by 6 pm Sunday, and it includes a clear “reactive” or “non-reactive” result along with a numeric index value. A reactive result requires confirmatory treponemal testing (e.g., TPPA) and clinical staging by your primary care doctor. Our post-test telephonic guidance will walk you through the next steps and can arrange a specialist referral.
UAE Regulatory & Data Privacy Adherence
Data Protection & Clinical Compliance Framework
All syphilis serology results and personal health data are processed 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 follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Reports are delivered via encrypted channels. No data is shared with third parties without explicit written consent.
ISO 9001:2015 Accredited Facility | Cert: INT/EGQ/2509DA/3139
Clinical & Logistical Metadata
| Test Name | Syphilis Serology (CMIA) |
| Price (AED) | 200 |
| Turnaround Time | Next day (sample received by 6 pm) |
| Sample Type / Matrix | Serum or plasma (peripheral whole blood) |
| Methodology Used | Chemiluminescent Microparticle Immunoassay (CMIA) |
| ICD-10-CM Code | Z11.3 |
| LOINC Code | 24113-3 |
| DHA Facility License & Address | License: 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians