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Test Price

4,500 AED

โœ… Home Collection Available

Von Willebrand Disease (VWD) Panel in UAE | 4,500 AED | DHA Licensed | DNA Labs UAE

Executive Summary & Core Metrics

Diagnostic Accuracy: 99.9% sensitivity for von Willebrand factor activity and antigen detection via ISO 9001:2015 certified 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: Post-test telephonic consultation with a DHA-licensed general practitioner for result interpretation and follow-up recommendations.

Insurance Support: Direct billing verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Von Willebrand Disease (VWD) Panel is a comprehensive coagulation assessment that quantifies von Willebrand factor (VWF) activity via ristocetin cofactor, VWF antigen, and factor VIII clotting activity. The panel employs advanced chemiluminescent immunoassay (CLIA) and electromechanical clot detection to deliver a complete diagnostic profile within a single blood draw.

Feature DNA Labs UAE VWD Panel Standard Alternative Lab
Diagnostic Precision 99.9% Sensitivity, ISO-Certified Variable Sensitivity, Non-Specialized Methods
Methodology CLIA, Electromechanical Clot Detection, Calculated Parameters ELISA-Based Immunoassay Only
Turnaround Time Same Day by 6 PM (Sample Received by 11 AM) 3โ€“5 Working Days
Home Collection ISO Cold-Chain, 8 AM โ€“ 11 PM Daily Limited or Unavailable

Physician Insight & Safety Protocols

โ€œThe VWD Panel is a cornerstone for accurate diagnosis of von Willebrand disease, yet it must always be interpreted alongside thorough clinical history, bleeding assessment tools, and family studies. Borderline values demand repeat testing and potential genetic consultation. Our team ensures every result is reviewed with care.โ€ โ€“ Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Medication Advisory

Do not discontinue prescribed anticoagulants, antiplatelet drugs, or heparin without explicit consent from your treating physician. Pre-test discontinuation of heparin for 24 hours and oral anticoagulants for 7 days must only be performed under direct medical supervision. Always consult your doctor before making any medication changes.

Exclusion Criteria & Emergency Red Flags

  • Active bleeding, recent major surgery, or significant trauma within the past 2 weeks.
  • Known hypersensitivity to ristocetin, bovine, or porcine proteins.
  • Inability to maintain cold-chain integrity โ€” samples must remain frozen and must not be thawed.
  • If severe spontaneous bruising, sudden chest pain, or shortness of breath occurs after collection, seek emergency medical care immediately.

Patient FAQ & Clinical Guidance

1. What exactly does the Von Willebrand Disease Panel measure?

The panel quantifies von Willebrand factor activity (ristocetin cofactor), VWF antigen, and factor VIII clotting activity, delivering a complete diagnostic profile within 8 hours of sample receipt. This enables your physician to differentiate VWD subtypes and guide appropriate management.

2. How should I prepare for the blood collection?

Overnight fasting is preferred but not mandatory. A fully completed Coagulation Requisition Form (Form 15) is required, and you must obtain explicit physician consent before temporarily stopping any anticoagulant therapy. Our mobile phlebotomist will confirm all details upon arrival.

3. My results came back abnormal โ€” what are the next steps?

An abnormal result should be reviewed by a hematologist. Our post-test telephonic consultation includes a specialist interpretation and personalized guidance on repeat testing or genetic evaluation. We coordinate directly with your referring physician to ensure continuity of care.

4. Is home collection available for this test?

Yes. Our ISO-certified cold-chain mobile phlebotomy service is available daily from 8 AM to 11 PM. A trained phlebotomist will collect the sample at your home or office, ensuring proper handling and temperature control throughout transport to our laboratory.

UAE Regulatory & Data Privacy Adherence

Data Protection & Compliance: All personal health data is processed in strict 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 safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Our laboratory holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) and operates under DHA Facility License No. 1143.

Clinical & Logistical Metadata

Test Name Von Willebrand Disease (VWD) Panel
Price (AED) 4,500
Turnaround Time Same Day by 6 PM (Sample Received by 11 AM)
Sample Type / Matrix Blood (Plasma) โ€“ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM โ€“ 11 PM)
Methodology Used Chemiluminescent Immunoassay (CLIA), Electromechanical Clot Detection, Calculated Parameters
ICD-10-CM Code D68.0
LOINC Code 58332-7
DHA Facility License & Laboratory Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE โ€“ DNA Labs UAE

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All reports reviewed by DHA-Certified physicians