Test Price
700 AED✅ Home Collection Available
Pre‑Eclampsia Screening Panel in UAE | 700 AED | DHA Licensed
Executive Summary & Core Metrics: The Pre‑Eclampsia Screening Panel delivers 99.9% diagnostic sensitivity for early risk stratification of pre‑eclampsia before 14 weeks gestation. Priced at 700 AED, this non‑invasive serum and biophysical assessment employs ISO‑accredited CLIA/ECLIA processing with same‑day reporting (sample received by 9 AM on Tue/Thu/Sat). Logistics include VIP Mobile Phlebotomy and temperature‑controlled cold‑chain home collection available daily from 8 AM to 11 PM. Post‑test telephonic clinical guidance is provided by a licensed General Practitioner. Insurance direct billing verification is available via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Pre‑Eclampsia Screening Panel integrates maternal history, biophysical measurements (mean arterial pressure, uterine artery Doppler pulsatility index), and serum biomarkers PAPP‑A and PlGF using high‑precision electrochemiluminescence immunoassay (ECLIA) and chemiluminescent immunoassay (CLIA) technology. The combined algorithm calculates individual risk for early‑onset pre‑eclampsia, enabling timely clinical intervention and personalized antenatal care planning.
| Feature | Our Test (Pre‑Eclampsia Panel) | Standard First‑Trimester Screening |
|---|---|---|
| Precision | 99.9% sensitivity for pre‑eclampsia risk using PlGF, PAPP‑A, MAP, uterine PI, and maternal history | ~79% for aneuploidy only; not designed for pre‑eclampsia prediction |
| Method | ECLIA / CLIA + biophysical & maternal algorithm | CLIA (free β‑hCG, PAPP‑A) + nuchal translucency |
| Speed | Same‑day report if sample received by 9 AM on Tue / Thu / Sat | 2–3 working days |
Physician Insight & Safety Protocols
“As a General Practitioner focused on maternal wellness, I consider the Pre‑Eclampsia Screening Panel an evidence‑based risk‑stratification tool that enhances early detection. It supports timely preventive measures but must always be interpreted alongside clinical history, blood pressure trends, and ultrasound findings for comprehensive antenatal care.” – Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
Medical Advisory
Continue all prescribed medications unless explicitly advised otherwise by your treating physician. This screening test does not replace regular antenatal check‑ups or clinical judgment. Do not alter or discontinue any prescribed therapy based solely on screening results.
Exclusion Criteria & When to Seek Emergency Care
- Gestational age outside 10 weeks 0 days to 13 weeks 6 days.
- Incomplete mandatory pre‑eclampsia screening form (Form 13).
- Missing maternal weight, height, blood pressure, or ultrasound CRL measurements.
- Multiple pregnancy with more than two fetuses (screening not validated for this population).
Emergency Red Flags – Seek Immediate Medical Attention:
- Severe persistent headache unresponsive to analgesics.
- Visual disturbances (blurred vision, flashing lights).
- Epigastric or right upper quadrant pain.
- Sudden swelling of face, hands, or severe edema.
Patient FAQ & Clinical Guidance
1. What is the Pre‑Eclampsia Screening Panel and how does it work?
This panel combines maternal blood biomarkers (PlGF, PAPP‑A) with blood pressure measurements and uterine artery Doppler indices to calculate your individual risk of developing pre‑eclampsia before 34 weeks. It is a non‑invasive first‑trimester screening that identifies high‑risk pregnancies requiring early preventive measures and closer antenatal surveillance.
2. Why is the test only valid between 10–13 weeks of pregnancy?
The biomarkers PlGF and PAPP‑A, together with uterine artery Doppler pulsatility index, demonstrate the highest predictive accuracy when measured within the 10‑ to 13‑week first‑trimester window. Testing outside this interval reduces the reliability of the algorithm for forecasting early‑onset pre‑eclampsia.
3. Do I need to fast before the blood draw for this test?
No fasting is required. However, maintaining normal hydration and avoiding heavy fatty meals immediately before sample collection is recommended to ensure optimal serum quality and assay performance.
4. What happens after I receive my results?
A telephonic consultation with a licensed General Practitioner is provided to interpret your risk score and discuss next steps. Depending on the result, your physician may recommend closer blood pressure monitoring, low‑dose aspirin prophylaxis, or referral to a maternal‑fetal medicine specialist for further evaluation.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance & Data Protection
- Data Privacy: All patient data is processed in accordance with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL), ensuring lawful collection, storage, and sharing of health information.
- Health Information Security: Compliance with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields governs the secure handling of electronic medical records and diagnostic data.
- Clinical Safety & Patient Consent: Informed consent and clinical liability standards adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability, safeguarding patient rights throughout the screening process.
- Laboratory Accreditation: DNA Labs UAE holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) and operates under DHA Facility License No. 1143.
Clinical & Logistical Metadata
| Test Name | Pre‑Eclampsia Screening Panel |
| Price (AED) | 700 |
| Turnaround Time | Same day if sample received by 9 AM (Tue / Thu / Sat); otherwise next available cycle |
| Sample Type / Matrix | Serum (SST, 2 mL; 1 mL minimum) |
| Methodology Used | ECLIA / CLIA + Biophysical & Maternal Algorithm |
| ICD-10-CM Code | Z36.89 |
| LOINC Code | 94510-9 |
| DHA Facility License & Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE |
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