Test Price
450 AED✅ Home Collection Available
Immunophenotyping by Flow Cytometry CD41a Test in UAE | DNA Labs UAE
Executive Summary & Core Metrics
Precision Diagnostic Metrics
- Diagnostic Sensitivity: 99.9% validated through ISO‑certified multicolor flow cytometry protocols at DNA Labs UAE.
- Turnaround Time: Same‑day result availability when sample is received by 9 AM, enabling rapid clinical decision‑making.
- Logistics Excellence: VIP mobile phlebotomy and temperature‑controlled cold‑chain home collection for whole blood specimens (daily 8 AM – 11 PM).
- Clinical Oversight: Post‑test telephonic consultation with a Specialist Diagnostic Radiologist for result interpretation.
- Insurance Verification: Direct coverage confirmation via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This advanced immunophenotyping assay quantifies CD41a (platelet glycoprotein IIb) surface expression on platelets using eight‑color flow cytometry. The test is indicated for identifying platelet dysfunction in cancer‑related thrombocytopathies, primary platelet disorders such as Glanzmann thrombasthenia, and acquired anti‑GPIIb antibody syndromes. Rapid, high‑resolution analysis provides oncologists and hematologists with actionable diagnostic data within hours.
| Feature | DNA Labs UAE Precision Assay | Standard Alternative |
|---|---|---|
| Methodology | 8‑Color Immunophenotyping by Flow Cytometry | Light Transmission Aggregometry |
| Diagnostic Sensitivity | 99.9% (ISO‑Certified Processing) | Variable, often lower |
| Turnaround Time | Same Day (sample by 9 AM) | 24–48 hours |
| Price (AED) | 450 | 550 – 750 |
Physician Insight & Safety Protocols
“CD41a flow cytometry must be interpreted alongside the complete blood count, bleeding history, and current medication list. This single parameter alone should not drive definitive thrombopathy diagnoses or anticoagulant therapy modifications without a full clinical correlation.”
— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011
Medication Advisory
Maintain all prescribed medications unless explicitly directed by your treating physician. Antiplatelet agents and anticoagulants can significantly alter platelet glycoprotein expression and may confound flow cytometry results.
Exclusion Criteria & Emergency Indicators
- Exclusion Criteria: Active severe thrombocytopenia (platelet count below 20,000/µL), platelet transfusion within the preceding 7 days, or known hypersensitivity to sodium heparin used in green‑top collection tubes.
- Emergency Red Flags: New onset petechiae, unexplained mucosal bleeding, or signs suggestive of intracranial hemorrhage warrant immediate emergency department evaluation.
Patient FAQ & Clinical Guidance
1. What is the CD41a flow cytometry test used for in cancer patients?
The assay identifies platelet glycoprotein IIb abnormalities to diagnose thrombopathies associated with malignancy. It enables oncologists to differentiate immune‑mediated platelet destruction from intrinsic platelet defects, guiding decisions about transfusion support, targeted therapies, and bone marrow evaluation.
2. How is the sample collected and what precautions are necessary?
Whole blood is collected in both EDTA and sodium heparin tubes. For bone marrow aspirates, a sodium heparin tube is used exclusively. All specimens must be maintained at 18–22°C and transported immediately; refrigeration or freezing destroys CD41a epitopes and invalidates the analysis. Bone marrow collection requires a hospital‑based procedure, while whole blood can be drawn through our mobile phlebotomy service.
3. What do abnormal CD41a results indicate and how do they correlate with cancer treatment?
Reduced or absent CD41a expression suggests platelet dysfunction potentially linked to myelodysplasia, drug effects, or Glanzmann thrombasthenia. Such findings necessitate comprehensive oncological review and may influence chemotherapy selection, bleeding risk stratification, and the need for platelet transfusion support.
UAE Regulatory & Data Privacy Adherence
Legal & Privacy Compliance Framework
All clinical data handling and patient information processing strictly adhere to 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 follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Direct billing verification is available via WhatsApp at +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | Immunophenotyping by Flow Cytometry CD41a |
| Price (AED) | 450 |
| Turnaround Time | Same Day (sample received by 9 AM) |
| Sample Type / Matrix | 3 mL whole blood in Lavender Top (EDTA) + 3 mL whole blood in Green Top (Sodium Heparin) OR 2 mL bone marrow in Green Top (Sodium Heparin). Whole blood eligible for VIP mobile phlebotomy home collection; bone marrow requires hospital‑based extraction. |
| Methodology Used | 8‑Color Immunophenotyping by Flow Cytometry |
| ICD-10-CM Code | D69.1 |
| LOINC Code | 14192-0 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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