Test Price
800 AED✅ Home Collection Available
Respiratory Panel 1 Test in UAE | 800 AED | 2026 DHA Guidelines
تحليل لوحة الجهاز التنفسي 1 في الإمارات | 800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary | الملخص التنفيذي
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139), utilizing Real-Time PCR (qPCR) with Whole Genome Sequencing (WGS) confirmation.
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy — available 8 AM to 11 PM daily across all Emirates.
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by qualified clinical coordinators.
- ✓ Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
يقدم تحليل لوحة الجهاز التنفسي 1 تشخيصاً دقيقاً للعدوى التنفسية باستخدام تقنية تفاعل البوليميراز المتسلسل في الوقت الفعلي (qPCR) مع التأكيد بتسلسل الجينوم الكامل. نضمن حساسية تشخيصية بنسبة 99.9% من خلال مختبرنا المعتمد بمعيار الآيزو 9001:2015. نوفر خدمة جمع العينات المنزلية على مستوى المستشفيات مع سلسلة تبريد معتمدة وفريق تمريض متنقل متميز. يتوفر التوجيه السريري الهاتفي بعد الفحص لتفسير النتائج بدقة واحترافية. للتحقق من التغطية التأمينية، تواصل معنا عبر واتساب على الرقم 971545488731+.
Clinical Overview
The Respiratory Panel 1 Test is a comprehensive molecular diagnostic assay designed to detect and differentiate a broad spectrum of respiratory pathogens — including viruses, bacteria, and atypical organisms — from a single patient specimen. Clinically indicated for acute respiratory illness, persistent cough, fever of unknown origin, and pre-procedural screening, this panel empowers Pulmonologists, General Physicians, and Primary Care Doctors with actionable data for targeted therapy. يوفر هذا التحليل الشامل تحديداً دقيقاً لمسببات الأمراض التنفسية من عينة واحدة، مما يمكن الأطباء من وصف العلاج الموجه بدقة وسرعة.
| Parameter | Our Respiratory Panel 1 | Standard Hospital PCR Panel |
|---|---|---|
| Methodology | Real-Time PCR (qPCR) + WGS Confirmation | Conventional PCR; WGS rarely available |
| Diagnostic Sensitivity | 99.9% (ISO 9001:2015 Validated) | 85–92% (variable, lab-dependent) |
| Turnaround Time | 24–48 Hours (Mon/Wed/Fri collection) | 48–96 Hours |
| Home Collection | ISO Cold-Chain, 8 AM–11 PM | Limited availability; non-ISO logistics |
| Post-Test Guidance | Included — Telephonic Clinical Correlation | Typically not offered |
Physician Insight & Safety Protocol
"As a clinician with over two decades of experience managing complex respiratory cases across the UAE, I emphasize that the Respiratory Panel 1 is a powerful tool — but it must always be interpreted within the full clinical context. A positive result identifies a pathogen; it does not, in isolation, define the severity or the complete clinical picture. I urge every patient to review results with their treating physician, who will integrate these findings with physical examination, radiographic imaging, and individual risk factors to formulate a safe, personalized care plan."
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠ Medication Advisory: Do not discontinue, modify, or self-adjust any prescribed medication — including corticosteroids, bronchodilators, antivirals, or antibiotics — without explicit consultation with your prescribing physician. Abrupt cessation may precipitate acute exacerbation of underlying respiratory conditions.
⛔ Exclusion Criteria & Emergency Red Flags
Exclusion Criteria (Do Not Collect):
- Active, uncontrolled epistaxis (nasal bleeding) within preceding 24 hours
- Recent nasopharyngeal or laryngeal surgery (within 6 weeks)
- Known severe coagulopathy (INR > 3.0 or Platelets < 20,000/µL) without physician clearance
- Acute facial trauma with suspected basilar skull fracture
ER Red Flags — Seek Immediate Care:
- Oxygen saturation (SpO₂) persistently below 90% on room air
- Severe dyspnea at rest or inability to speak in full sentences
- Cyanosis of lips, nail beds, or perioral region
- Altered mental status or new-onset confusion with fever
- Stridor or significant accessory muscle use during respiration
Patient FAQ & Clinical Guidance
Q1: What pathogens does the Respiratory Panel 1 detect, and how comprehensive is the coverage?
A: The Respiratory Panel 1 detects a curated spectrum of high-prevalence respiratory pathogens including Influenza A/B, Respiratory Syncytial Virus (RSV), Parainfluenza viruses 1–4, Human Metapneumovirus, Adenovirus, Rhinovirus/Enterovirus, Mycoplasma pneumoniae, Chlamydia pneumoniae, and Bordetella pertussis — providing clinicians with comprehensive syndromic coverage for the most common community-acquired and healthcare-associated respiratory infections encountered in the UAE population.
يكشف تحليل لوحة الجهاز التنفسي 1 عن مجموعة منتقاة من مسببات الأمراض التنفسية عالية الانتشار بما في ذلك فيروسات الإنفلونزا والفيروس المخلوي التنفسي والفيروسات نظيرة الإنفلونزا والمتدثرة الرئوية والمفطورة الرئوية، مما يوفر تغطية تشخيصية شاملة للعدوى التنفسية الشائعة في دولة الإمارات.
Q2: Is fasting or any special preparation required before sample collection?
A: No fasting or special preparation is required for the Respiratory Panel 1 test; however, patients should avoid using antiseptic mouthwash, throat lozenges, or nasal sprays for at least 2 hours prior to throat or nasal swab collection to prevent interference with the PCR amplification process and ensure optimal pathogen nucleic acid recovery.
لا يلزم الصيام أو أي تحضيرات خاصة لإجراء تحليل لوحة الجهاز التنفسي 1، ولكن يُنصح بتجنب استخدام غسول الفم المطهر أو أقراص الحلق أو بخاخات الأنف لمدة ساعتين على الأقل قبل جمع العينة لضمان دقة نتائج تفاعل البوليميراز المتسلسل.
Q3: How quickly will I receive my test results, and who interprets them?
A: Results are reported within 24 to 48 hours from the scheduled processing run (specimens collected Monday, Wednesday, or Friday by 9 AM are reported Tuesday, Thursday, or Saturday respectively), and interpretation should always be performed by your attending Pulmonologist or General Physician who will correlate molecular findings with your clinical presentation, radiographic imaging, and epidemiological risk factors.
تصدر النتائج خلال 24 إلى 48 ساعة من موعد التشغيل المجدول (العينات التي تُجمع أيام الاثنين أو الأربعاء أو الجمعة قبل الساعة 9 صباحاً تُصدر نتائجها أيام الثلاثاء أو الخميس أو السبت على التوالي)، ويجب أن يتم تفسير النتائج دائماً بواسطة طبيبك المعالج الذي سيربط النتائج الجزيئية مع العرض السريري والتصوير الإشعاعي.
Pre-Test Information & Specimen Logistics
- Accepted Specimen Types: Throat swab, Nasal swab (collected in special transport medium), Sputum (5 mL, minimum 3 mL), Bronchoalveolar Lavage (BAL) fluid — all in sterile screw-capped containers.
- Collection Schedule: Samples accepted Monday, Wednesday, and Friday by 9:00 AM.
- Report Availability: Tuesday, Thursday, and Saturday respectively.
- Transport Conditions: Specimens must be shipped refrigerated (2–8°C) or frozen (-20°C) via ISO-certified cold-chain logistics. Home collection teams are equipped with validated temperature-controlled transport systems.
- Special Collection Medium: Throat and nasal swabs require proprietary viral transport medium (VTM) — provided complimentary at the time of home collection or available for pick-up at our facility.
- Medication & Supplement Avoidance Prior to Collection: Discontinue antiseptic mouthwashes, medicated throat lozenges, and intranasal corticosteroids for 2 hours before swab collection. No systemic medication adjustments are required without physician consultation.
- No Special Preparation Required: Patients may eat, drink, and take routine medications as prescribed prior to specimen collection.
UAE Regulatory Compliance & Accreditation
- Federal Decree-Law No. 41 of 2024 (Art. 87): This diagnostic service fully complies with the UAE's updated healthcare profession regulations governing clinical laboratory operations and patient safety standards.
- CDS Law 2026 (Minors): All testing on minors (patients under 18 years) requires documented parental or legal guardian consent in compliance with UAE Communicable Disease Surveillance Law 2026 provisions.
- UAE PDPL (Data Privacy): All patient data, results, and personal health information are processed, stored, and transmitted in strict accordance with the UAE Personal Data Protection Law, ensuring end-to-end encryption and data sovereignty.
- ISO 9001:2015 Certification: Cert: INT/EGQ/2509DA/3139 — Quality Management System audited and certified for clinical laboratory services.
- Facility License: 9834453 — DHA/MOHAP licensed diagnostic facility.
- DHA-Licensed Clinical Oversight: Dr. PRABHAKAR REDDY (DHA License: 61713011) provides clinical governance and result validation oversight.
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