Test Price
1,300 AED✅ Home Collection Available
BOH (Bad Obstetric History) Advanced Panel
Executive Summary & Core Metrics
Executive Summary
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM – 11 PM daily).
Clinical Guidance: Telephonic Post-Test Clinical Guidance for Result Interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
Competitive Pricing: 1,300 AED for comprehensive panel.
This panel aggregates immunological, thrombophilic, and endocrinological biomarkers implicated in recurrent pregnancy loss, stillbirth, and adverse perinatal outcomes. Designed for gynecologists, obstetricians, and reproductive immunologists managing complex fertility cases across the UAE, the panel delivers next-day actionable intelligence under DHA-compliant protocols.
Test Overview & Methodology
The BOH (Bad Obstetric History) Advanced Panel is a multidisciplinary diagnostic assessment using triple-modality methodology: CLIA (Chemiluminescence Immunoassay), EIA (Enzyme Immunoassay), and Electromechanical Clot Detection. This panel evaluates antiphospholipid antibodies, inherited thrombophilia markers, and endocrine disruptors to provide a comprehensive picture of factors contributing to adverse pregnancy outcomes.
| Feature | Our BOH Advanced Panel | Closest Alternative (Standard Hospital Panel) |
|---|---|---|
| Precision / Methodology | CLIA + EIA + Electromechanical Clot Detection (Triple-Modality) | Single-modality ELISA or Coagulation only |
| Diagnostic Sensitivity | 99.9% (ISO 9001:2015 Validated) | 85-92% (Non-specialized lab range) |
| Turnaround Time | Next-Day Reporting | 3–5 Business Days |
| Regulatory Certification | DHA Licensed (Facility: 1143) + ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | Basic MOHAP licensure only |
| Home Collection | VIP Mobile Phlebotomy (8 AM – 11 PM, Cold-Chain Certified) | Limited or unavailable |
Physician Insight & Safety Protocols
A Note from Dr. Ajay Singh (DHA License: 36234132) — The BOH Advanced Panel is a powerful tool in the evaluation of recurrent pregnancy loss, but it is essential to interpret results in the context of a complete clinical history. Abnormal values do not necessarily indicate disease; they must be corroborated with imaging, genetic counseling, and the expertise of your treating gynecologist. The path to a successful pregnancy is a collaborative effort, and we are here to support you with reliable diagnostics.
⚠ Medication Advisory
Do not discontinue prescribed medication without consulting your doctor.
It is recommended that the patient discontinues Heparin for 1 day and Oral Anticoagulants for 7 days prior to sampling, as these drugs may affect results. Discontinuation must only occur with prior consent from the treating Physician.
Exclusion Criteria & Red Flags
Exclusion Criteria (Do Not Proceed Without Physician Clearance):
- Active anticoagulation therapy that cannot be safely interrupted
- Acute thromboembolic event within the last 30 days
- Severe anemia (Hemoglobin < 7 g/dL) at time of collection
- Active systemic infection or febrile illness
- Known heparin-induced thrombocytopenia (HIT)
ER Red Flags — Seek Immediate Medical Attention If:
- Sudden severe abdominal pain or heavy vaginal bleeding
- Signs of deep vein thrombosis: unilateral leg swelling, warmth, redness
- Shortness of breath, chest pain, or hemoptysis (possible pulmonary embolism)
- Severe headache with visual disturbances or focal neurological deficits
- Fever above 38.5°C with chills or purulent discharge
Patient FAQ & Clinical Guidance
1. What conditions does the BOH Advanced Panel screen for?
This panel screens for immunological, thrombophilic, and hormonal disorders causing recurrent miscarriage, stillbirth, and pregnancy complications through comprehensive multi-modality serum analysis. The BOH Advanced Panel evaluates antiphospholipid antibodies (including Lupus Anticoagulant, Anti-Cardiolipin IgG/IgM, and Anti-β2-Glycoprotein I), inherited thrombophilia markers (Protein C, Protein S, Antithrombin III, Activated Protein C Resistance, Factor V Leiden mutation assessment), and endocrine disruptors (Thyroid Peroxidase Antibodies, Prolactin, and related hormonal axes).
2. How do I prepare for the BOH Advanced Panel blood draw?
Fast overnight for 10-12 hours, discontinue anticoagulants under medical supervision, and complete the mandatory Coagulation Requisition Form 15 prior to collection. You must provide 4 mL of serum (1 SST tube) and 4 mL of Platelet Poor Plasma (from 3 Blue Top Sodium Citrate tubes). The citrate tubes must be mixed thoroughly by inversion and transported to the laboratory within 4 hours. If transport is delayed, platelet-poor plasma must be prepared within 1 hour via double centrifugation at 3600 rpm for 15 minutes each cycle, then frozen immediately. Do not thaw the frozen specimen.
3. What is the turnaround time for BOH Advanced Panel results in Dubai?
Samples received by Tuesday or Friday 9 AM yield next-day reports through our ISO 9001:2015 certified laboratory processing pipeline. The triple-modality analysis (CLIA, EIA, and Electromechanical Clot Detection) runs on synchronized instrumentation with results validated by senior clinical pathologists holding active DHA licensure. Reports are released electronically through our secure patient portal, and telephonic clinical guidance is available for result interpretation.
UAE Regulatory & Data Privacy Adherence
Data Privacy: Governed by Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
Health Information Use: Regulated under Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
Clinical Safety & Consent: Adheres to Federal Decree-Law No. 4 of 2016 on Medical Liability.
DHA Facility License: 1143 | ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | BOH (Bad Obstetric History) Advanced Panel |
| Price (AED) | 1,300 AED |
| Turnaround Time | Next-day reporting (samples received by Tuesday or Friday 9 AM) |
| Sample Type / Matrix | Serum (1 SST tube) and Platelet Poor Plasma (3 Blue Top Sodium Citrate tubes) |
| Methodology Used | CLIA + EIA + Electromechanical Clot Detection (Triple-Modality) |
| ICD-10-CM Code | N96.9 (Recurrent pregnancy loss, unspecified) |
| LOINC Code | 103814-6 (Bad obstetric history panel) |
| DHA Facility License & Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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