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Test Price

700 AED

โœ… Home Collection Available

Influenza A (H1N1) pdm09 (Swine Flu) & Human RNase P RNA Detection Test | 700 AED | DHA Licensed | DNA Labs UAE

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
  • Premium Logistics: VIP Mobile Home Collection with Temperature-Controlled Cold-Chain Transport โ€” Available daily from 8 AM to 11 PM.
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
  • Turnaround: Preliminary result by phone within 24 hours; official DHA-compliant PDF report within 36 hours.

Test Overview & Methodology

The Influenza A (H1N1) pdm09 RNA Detection Test is a multiplex real-time PCR assay that simultaneously identifies the pandemic swine flu viral RNA and the human RNase P internal control from a single nasopharyngeal swab. This gold-standard molecular test provides definitive diagnosis and epidemiological surveillance for respiratory season evaluation in the UAE.

The assay targets conserved regions of the hemagglutinin (HA) and matrix (M) genes of the H1N1 pdm09 strain, ensuring high specificity against seasonal influenza subtypes. The co-amplification of the human RNase P gene confirms specimen adequacy and extraction integrity, eliminating false negatives due to poor sample collection or degradation.

Feature Our Test (RT-qPCR + RNase P Control) Closest Alternative (Rapid Antigen Test)
Precision / Methodology Real-Time PCR (RT-qPCR) with dual-target detection and RNase P internal control Lateral flow immunoassay (antigen detection)
Diagnostic Sensitivity โ‰ฅ99.9% (95% CI: 98.5โ€“100%) 50โ€“70% (limited by viral load and timing)
Turnaround Time 24 hours (phone), 36 hours (email report) 15โ€“30 minutes
Sample Type Nasopharyngeal swab / aspirate (deep nasal and throat) Nasal swab (anterior nares)
Regulatory Compliance DHA/MOHAP licensed, ISO 9001:2015, UAE PDPL, Federal Law No. 2 of 2019 May lack full molecular certification

Physician Insight & Safety Protocols

โ€œPCR results for H1N1 pdm09 must always be correlated with the patientโ€™s clinical history, symptom onset timeline, and known exposure risk. A negative result does not exclude infection if swabbing occurred within the first 24 hours of symptom appearance due to potentially low viral shedding. Use this molecular assay as one component of a comprehensive clinical evaluation including physical examination and chest imaging when indicated.โ€

โ€” Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132

Advisory โ€“ Medication Continuation

Continue all prescribed antiviral or symptomatic medications unless explicitly advised otherwise by your treating physician. Abrupt discontinuation of therapy may compromise clinical recovery.

Safety Exclusion Criteria & Emergency Red Flags

Home collection should not proceed if any of the following are present:

  • Recent nasal trauma, epistaxis, or sinonasal surgery (within 2 weeks)
  • Untreated coagulopathy or severe thrombocytopenia (platelet count < 50,000/ยตL)
  • Severe respiratory distress with SpOโ‚‚ < 92% on room air
  • Altered mental status, confusion, or inability to provide informed consent

Emergency Red Flags โ€“ Dial 998 immediately if experiencing:

  • Bluish discoloration of lips or face (central cyanosis)
  • Severe shortness of breath or gasping at rest
  • Sudden loss of consciousness or new-onset seizures

Patient FAQ & Clinical Guidance

1. What is the accuracy of the H1N1 pdm09 PCR test offered by DNA Labs UAE?

This clinically validated real-time PCR assay delivers 99.9% diagnostic sensitivity and 99.8% specificity for detecting Influenza A H1N1 pdm09 viral RNA when a properly collected nasopharyngeal swab is used. The inclusion of the human RNase P internal control ensures that inadequate specimens are flagged, virtually eliminating false negatives caused by poor sampling quality.

2. When will I receive my test results after sample collection?

Preliminary positive or negative results are communicated by phone within 24 hours of sample receipt at our ISO-accredited laboratory. The official DHA-compliant PDF report, suitable for insurance claims and employer records, is dispatched to your registered email within 36 hours.

3. Is home collection for a nasopharyngeal swab safe and authorized in the UAE?

Yes. Our DHA-licensed healthcare professionals follow ISO-certified cold-chain transport protocols and stringent infection control measures including N95 masking, hand hygiene, and single-use PPE. Home collection for nasopharyngeal swabbing is as safe and clinically reliable as a hospital outpatient visit and is fully authorized under DHA regulations.

UAE Regulatory & Data Privacy Adherence

Your data is protected under UAE law. DNA Labs UAE complies 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. All clinical test results, patient identifiers, and genomic data are encrypted at rest and in transit, accessed only by authorized personnel on a strict need-to-know basis, and never shared with third parties without explicit patient consent. Our DHA-licensed facility undergoes annual audits to maintain full regulatory alignment with UAE data protection standards.

Clinical safety and patient consent are governed under Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring that every step of the diagnostic pathway โ€” from specimen collection to result delivery โ€” meets the highest standards of medical accountability.

Clinical & Logistical Metadata

Test Name Influenza A (H1N1) pdm09 (Swine Flu) & Human RNase P RNA Detection Test
Price (AED) 700 AED
Turnaround Time 24 hours (preliminary phone result) / 36 hours (official PDF report)
Sample Type / Matrix Nasopharyngeal swab (deep nasal and throat) โ€” Home collection is available daily from 8 AM to 11 PM via VIP Mobile Collection with Temperature-Controlled Cold-Chain Transport.
Methodology Used Real-Time PCR (RT-qPCR) with dual-target detection of H1N1 pdm09 HA/M genes and human RNase P internal control
ICD-10-CM Code J09.X2 (Influenza due to identified novel influenza A virus with other respiratory manifestations)
LOINC Code 55466-5 (Influenza virus A H1N1 RNA [Presence] in Respiratory specimen by NAA with probe detection)
DHA Facility License & Laboratory Address DHA Facility License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE โ€” DNA Labs UAE

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ุงู„ุชุญู‚ู‚ ู…ู† ุงู„ุชุบุทูŠุฉ ุงู„ุชุฃู…ูŠู†ูŠุฉ

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ุชูˆู‚ู ุนู† ุงู„ุชุฎู…ูŠู†. ุฃุฑุณู„ ุตูˆุฑุฉ ู…ู† ุจุทุงู‚ุฉ ุงู„ุชุฃู…ูŠู† ูˆูˆุตูุฉ ุงู„ุทุจูŠุจ ุฅู„ู‰ ูุฑูŠู‚ ุงู„ุชุญู‚ู‚ ุงู„ู…ุนุชู…ุฏ ู…ู† ู‡ูŠุฆุฉ ุงู„ุตุญุฉ ุจุฏุจูŠ ุนุจุฑ ุงู„ูˆุงุชุณุงุจ. ุงุญุตู„ ุนู„ู‰ ุชุญุฏูŠุซ ุงู„ุญุงู„ุฉ ููŠ ุฏู‚ุงุฆู‚.

โœ… DHA Certified โœ… ISO 15189 โœ… HIPAA Compliant

Available in Arabic, English, Hindi & Urdu

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ISMS 27001:2022

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ISO Accredited

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HIPAA

All reports reviewed by DHA-Certified physicians