Test Price
600 AED✅ Home Collection Available
Placental Growth Factor (PlGF) Test in UAE | 600 AED | DHA Licensed
Executive Summary & Core Metrics
Test: Placental Growth Factor (PlGF) — Serum Biomarker for Pre‑eclampsia Risk Evaluation
Price: 600 AED (includes VIP home phlebotomy, cold‑chain logistics, and digital report)
Turnaround Time: Same‑day results when sample collected by 9 AM (Tue / Thu / Sat)
Methodology: Electrochemiluminescence Immunoassay (ECLIA) — 99.9% diagnostic sensitivity at ISO 9001:2015 certified laboratory
Collection: VIP Mobile Phlebotomy with temperature‑controlled cold‑chain home collection (Available daily from 8 AM to 11 PM)
Clinical Support: Complimentary telephonic guidance by our DHA‑registered General Practitioner; direct insurance billing verification via WhatsApp +971 54 548 8731
DHA Facility License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE
Test Overview & Methodology
Placental Growth Factor (PlGF) is a key biomarker for evaluating placental function and predicting pre‑eclampsia, a serious pregnancy complication. Our advanced ECLIA‑based test delivers precise quantification from a single serum sample, empowering clinicians to make timely, evidence‑based decisions. The assay is calibrated against international reference standards and validated for clinical use in pregnant women presenting with hypertensive disorders or other risk factors for placental insufficiency.
| Feature | Our PlGF Test (DHA Licensed) | Closest Alternative (Generic CLIA) |
|---|---|---|
| Method | Electrochemiluminescence Immunoassay (ECLIA) | Chemiluminescent Immunoassay (CLIA), lower signal‑to‑noise ratio |
| Diagnostic Sensitivity | 99.9% at ISO 9001:2015 certified lab | Typically 95–97% |
| Turnaround Time | Same‑day (if sample collected by 9 AM on Tue/Thu/Sat) | 24–48 hours, often on‑site draw required |
| Specimen Type | Serum (single peripheral venipuncture) | Serum or plasma, variable collection protocols |
Physician Insight & Safety Protocols
“Placental Growth Factor testing is a valuable screening tool for assessing placental function and identifying patients at elevated risk for pre‑eclampsia. As a General Practitioner, I emphasize that PlGF results must be interpreted alongside clinical signs—blood pressure, proteinuria, and maternal symptoms—and should always be reviewed by the managing obstetric specialist. This test supports early, risk‑stratified care but does not replace comprehensive prenatal monitoring.”
— Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
Advisory: Medication & Clinical Oversight
Important Clinical Guidance
- Do not discontinue or alter any prescribed antihypertensive or obstetric medication without consulting your treating physician.
- PlGF results should be used adjunctively with blood pressure monitoring and urine protein assessment for complete pre‑eclampsia evaluation.
- Always share your complete obstetric history and current medications with the phlebotomist and reporting clinician.
Exclusion Criteria & Red Flags
When to Seek Emergency Care Immediately
- This test is not a substitute for emergency obstetric evaluation or hospital admission.
- Seek emergency care without delay if you experience: sudden severe headache, visual disturbances (blurring, flashing lights), epigastric or right‑upper‑quadrant pain, rapid swelling of the face or hands, shortness of breath, or decreased fetal movement.
- PlGF values alone cannot rule out acute placental abruption or evolving eclampsia; clinical judgment remains paramount.
- Not intended for patient self‑interpretation; all results must be discussed with a licensed healthcare provider.
Patient FAQ & Clinical Guidance
1. What is the purpose of the Placental Growth Factor test in the UAE?
PlGF testing accurately assesses placental health and predicts pre‑eclampsia risk in pregnant women, guiding timely interventions. With a single blood draw collected at your home by our DHA‑certified phlebotomists, results are delivered on the same day, enabling your obstetric provider to make informed decisions regarding your pregnancy management. The test is performed at our ISO 9001:2015 certified laboratory using ECLIA technology for maximum precision.
2. How should I prepare for the PlGF blood test?
No fasting or special preparation is needed. Simply schedule your VIP home collection on Tuesday, Thursday, or Saturday before 9 AM. Our team arrives with a pre‑cooled transport kit to maintain sample integrity from vein to lab. You may continue your normal diet and daily activities. Inform the phlebotomist of any current medications or supplements you are taking.
3. What do abnormal PlGF results indicate during pregnancy?
Low PlGF levels may signal placental dysfunction and heightened risk of pre‑eclampsia, warranting closer surveillance by your obstetrician. High or normal levels generally reflect healthy placental development, but clinical correlation with blood pressure, urinary protein, and maternal symptoms is essential. An abnormal result does not confirm a diagnosis—it is a risk indicator that prompts further evaluation. Always discuss your PlGF report with your treating physician for personalized care planning.
4. Can I get the PlGF test done if I am already diagnosed with pre‑eclampsia?
Yes. The PlGF test can be used for risk stratification and monitoring in patients with established hypertensive disorders of pregnancy. However, it should never delay emergency treatment for severe pre‑eclampsia or eclampsia. If you have symptoms such as severe headache, visual changes, or epigastric pain, seek immediate medical attention regardless of PlGF results.
UAE Regulatory & Data Privacy Adherence
Your health data is protected under the UAE’s legal framework for medical confidentiality and data security. DNA Labs UAE strictly complies with all applicable federal laws:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) — governing the collection, processing, and storage of personal data, including health information.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields — regulating health data exchange, telemedicine, and electronic medical records.
- Federal Decree-Law No. 4 of 2016 on Medical Liability — ensuring patient safety, informed consent, and clinical accountability for all diagnostic procedures.
All PlGF results are transmitted via encrypted channels, stored on UAE‑based secure servers, and accessible only to your designated healthcare provider. Your consent is obtained prior to sample collection and data processing in accordance with DHA regulatory standards.
Clinical & Logistical Metadata
| Test Name | Placental Growth Factor (PlGF), Serum |
| Price (AED) | 600 |
| Turnaround Time | Same‑day (sample collected by 9 AM Tue/Thu/Sat) |
| Sample Type / Matrix | Serum (peripheral venous blood) |
| Methodology Used | Electrochemiluminescence Immunoassay (ECLIA) |
| ICD-10-CM Code | O14.9, Z36.8 |
| LOINC Code | 33940-4 |
| DHA Facility License & Address | License No. 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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