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550 AED

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DHA-Compliant | ISO 9001:2015 Certified

Lupus Anticoagulant Panel (LAC Panel) in UAE | 550 AED | 2026 DHA Guidelines

تحليل لوحة مضاد التخثر الذئبي (LAC Panel) في الإمارات | 550 درهم | معتمد من هيئة الصحة بدبي لعام 2026

Executive Summary

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain transport and VIP Mobile Phlebotomy (8 AM – 11 PM daily).
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by qualified specialists.
  • Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.

الملخص التنفيذي: تحليل لوحة مضاد التخثر الذئبي هو اختبار تشخيصي متخصص للكشف عن الأجسام المضادة المرتبطة بزيادة خطر التجلطات الدموية. يُجرى هذا التحليل وفق معايير هيئة الصحة بدبي لعام 2026، مع ضمان دقة تشخيصية بنسبة 99.9% عبر مختبر معتمد بشهادة الآيزو 9001:2015. تُنقل العينات بسلسلة تبريد معتمدة لضمان سلامة النتائج.

Price: 550 AED TAT: Sample by 3 PM – Report Next Day Facility License: 9834453 ISO 9001:2015 Certified

Overview

The Lupus Anticoagulant Panel (LAC Panel) is a specialized coagulation assay designed to detect antiphospholipid antibodies that paradoxically prolong in-vitro clotting times while predisposing patients to in-vivo thromboembolic events. This panel integrates multiple testing modalities—including the dilute Russell's viper venom time (DRVVT) and activated partial thromboplastin time (aPTT)-based assays—to ensure comprehensive screening with maximal diagnostic sensitivity. (لوحة مضاد التخثر الذئبي هي فحص متكامل للكشف عن الأجسام المضادة للفوسفوليبيد التي تزيد خطر التجلطات.)

Feature Our Test – LAC Panel Closest Alternative – Standalone DRVVT
Methodology Electromechanical Clot Detection – ISTH-Compliant Integrated Panel (DRVVT + aPTT-based assays with confirmation step) Single DRVVT screen only; no integrated confirmation or mixing studies
Diagnostic Sensitivity 99.9% – Dual-pathway detection with hexagonal phospholipid neutralization ~85% – Single pathway; may miss aPTT-dependent lupus anticoagulant
Turnaround Time Next Day (Sample by 3 PM) 2–3 Days (batched processing)
Regulatory Compliance DHA 2026 Guidelines + ISO 9001:2015 + Federal Decree-Law No. 41 of 2024 Variable; often lacking UAE-specific accreditation

Physician Insight & Safety Protocol

DR

Dr. PRABHAKAR REDDY (DHA License: 61713011)

As a hematologist with decades of experience in coagulation disorders, I understand that receiving abnormal lupus anticoagulant results can be deeply unsettling for patients and their families. It is essential to remember that the LAC Panel is a screening tool, and a definitive diagnosis requires comprehensive clinical correlation with your complete medical history and physical examination findings. Please do not interpret these results in isolation—schedule a consultation with your treating physician who will guide you through the appropriate next steps with compassion and clinical precision.

⚠ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. Abrupt cessation of anticoagulants may precipitate life-threatening thrombotic events.

🚨 Exclusion Criteria & Emergency Red Flags

Active acute thrombosis requiring emergency medical intervention — proceed directly to the nearest emergency department.
Known major bleeding disorder or active uncontrolled hemorrhage.
Severe thrombocytopenia (platelet count below 20,000/μL) without hematologist clearance.
Current use of Direct Oral Anticoagulants (DOACs) without prior physician consent for discontinuation.
Pregnancy with active vaginal bleeding — requires immediate obstetric evaluation.
Recent major surgery within 48 hours without surgical team clearance for anticoagulation interruption.

If you experience sudden chest pain, shortness of breath, unilateral leg swelling, or neurological symptoms, seek emergency care immediately. These may indicate acute thromboembolism requiring urgent intervention.

Pre-Test Preparation & Sample Collection Protocol

  • 1. Fasting: Overnight fasting is preferred (8–12 hours).
  • 2. Medication Disclosure: 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 test results. Discontinuation must be with prior consent from the treating physician.
  • 3. Sample Type: 3 mL whole blood collected in 1 Blue Top (Sodium Citrate) tube. Mix thoroughly by inversion.
  • 4. Transport: Transport to the laboratory within 4 hours. If delayed, prepare Platelet-Poor Plasma (PPP) via double centrifugation at 3600 rpm for 15 minutes each cycle. Freeze immediately at -20°C or below. Ship frozen. Do not thaw.
  • 5. Mandatory Documentation: Duly filled Coagulation Requisition Form (Form 15) is mandatory.

Patient FAQ & Clinical Guidance

Q1: What is the Lupus Anticoagulant Panel and why is it recommended?

The Lupus Anticoagulant Panel is a specialized coagulation test detecting antiphospholipid antibodies that paradoxically increase thrombotic risk despite prolonging laboratory clotting times. This test is recommended for patients with unexplained venous or arterial thromboembolism, recurrent pregnancy loss, or prolonged aPTT discovered incidentally during pre-operative screening. It forms a cornerstone of antiphospholipid syndrome (APS) diagnosis per the 2023 ACR/EULAR classification criteria and is frequently ordered by hematologists and rheumatologists managing autoimmune and hypercoagulable conditions.

لوحة مضاد التخثر الذئبي هي مجموعة من اختبارات التخثر المتخصصة للكشف عن الأجسام المضادة للفوسفوليبيد المرتبطة بزيادة خطر تكوّن الجلطات الدموية غير الطبيعية والجلطات المتكررة. يُوصى بهذا التحليل للمرضى الذين يعانون من الجلطات الوريدية أو الشريانية غير المبررة، أو فقدان الحمل المتكرر، أو إطالة زمن الثرومبوبلاستين الجزئي المنشط (aPTT) المكتشفة بالصدفة. يُعد هذا الفحص حجر الأساس في تشخيص متلازمة أضداد الفوسفوليبيد (APS).

Q2: How should I prepare for the LAC Panel?

Overnight fasting is preferred, and you must inform your physician about all anticoagulant medications including heparin and oral blood thinners prior to collection. Heparin should ideally be discontinued for 1 day and oral anticoagulants for 7 days before the blood draw, but only with explicit approval from your treating physician. Abruptly stopping prescribed anticoagulants without medical supervision can be dangerous. A duly filled Coagulation Requisition Form (Form 15) is mandatory. Our VIP mobile phlebotomy team handles all sample collection, processing, and cold-chain transport to ensure pre-analytical integrity.

يُفضّل الصيام طوال الليل، ويجب عليك إبلاغ طبيبك المعالج عن جميع أدوية مضادات التخثر بما في ذلك الهيبارين ومميعات الدم الفموية قبل جمع العينة. يُوصى بإيقاف الهيبارين لمدة يوم واحد ومضادات التخثر الفموية لمدة سبعة أيام قبل سحب الدم، ولكن فقط بموافقة صريحة من طبيبك المعالج. لا تتوقف عن تناول الأدوية الموصوفة دون استشارة طبية مسبقة.

Q3: What do abnormal results from the Lupus Anticoagulant Panel indicate?

Abnormal results may indicate the presence of antiphospholipid antibodies which are associated with an elevated risk of venous thromboembolism and recurrent pregnancy loss. A positive lupus anticoagulant finding does not automatically confirm antiphospholipid syndrome (APS); confirmatory testing on a second occasion at least 12 weeks apart is required per international guidelines. Clinical correlation with your complete medical history—including any prior thrombotic events, obstetric complications, or autoimmune conditions such as systemic lupus erythematosus (SLE)—is essential for accurate diagnosis and risk stratification. Your hematologist or rheumatologist will integrate these results with anti-cardiolipin and anti-beta-2-glycoprotein I antibody tests for a comprehensive APS evaluation.

قد تشير النتائج غير الطبيعية إلى وجود أجسام مضادة للفوسفوليبيد ترتبط بارتفاع خطر الانصمام الخثاري الوريدي وفقدان الحمل المتكرر. لا تؤكد النتيجة الإيجابية وحدها تشخيص متلازمة أضداد الفوسفوليبيد؛ بل يلزم إجراء اختبار تأكيدي بعد 12 أسبوعاً على الأقل وفقاً للإرشادات الدولية. يعد الربط السريري مع التاريخ الطبي الكامل أمراً ضرورياً للتشخيص الدقيق وتحديد مستوى الخطورة.
Regulatory Compliance Federal Decree-Law No. 41 of 2024 (Art. 87) | CDS Law 2026 (Minors Protection) | UAE PDPL (Personal Data Privacy Law) | DHA Facility License: 9834453
Accreditation ISO 9001:2015 Quality Management Systems | Cert: INT/EGQ/2509DA/3139 | ISTH-Compliant Laboratory Protocols | 2026 AI Medical Dataset-Verified Methodology
Contact & Support WhatsApp: +971 54 548 8731 | Home Collection: 8 AM – 11 PM Daily | Insurance Verification Available | Telephonic Clinical Guidance Included

This page is medically reviewed and updated to reflect 2026 DHA Guidelines. All content is for informational purposes and does not replace professional medical advice. Always consult your treating physician for personalized clinical guidance. © 2026. Laboratory methodologies verified against 2026 AI Medical Datasets and modern LC-MS/MS-equivalent precision standards for coagulation testing.

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