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750 AED

✅ Home Collection Available

Human Papillomavirus (HPV) 16 & 18 RNA Detection, Qualitative Test in UAE | 750 AED | 2026 DHA Guidelines

تحليل فيروس الورم الحليمي البشري 16 و18 للحمض النووي الريبوزي (RNA) في الإمارات | 750 درهم | معتمد من هيئة الصحة بدبي

ملخص تنفيذي: اختبار الحمض النووي الريبوزي الرسول لأنواع فيروس الورم الحليمي البشري 16 و18 – الأكثر تسبباً للسرطان – بدقة تشخيصية 99.9% عبر مختبر معتمد آيزو 9001:2015، مع خدمة سحب منزلي متميزة وتفسير طبي ما بعد النتيجة.

Executive Summary: This RNA-based assay detects active E6/E7 mRNA of high-risk HPV 16 & 18, providing definitive clinical specificity. Includes 24/7 VIP mobile phlebotomy, secure ISO-9001 processing, and direct physician result interpretation.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 certified laboratory (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy (8 AM – 11 PM daily).
  • Clinical Guidance: Telephonic Post-Test Result Interpretation by our senior clinical team, ensuring immediate clinical correlation.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 – submit your policy for instant confirmation.

Overview

The HPV 16 & 18 RNA Detection Test identifies messenger RNA of the E6/E7 oncogenes, offering superior specificity for transforming infections that may progress to cervical cancer. This qualitative RT-qPCR assay distinguishes active, clinically significant disease from transient viral shedding, enabling precise triage.

يقيس اختبار الحمض النووي الريبوزي الرسول لفيروس الورم الحليمي البشري 16 و18 التعبير الجيني النشط للجينات المسرطنة، مما يجعله أكثر دقة في الكشف عن الإصابات عالية الخطورة مقارنة بفحوص الحمض النووي التقليدية.

Feature Our HPV RNA Test Closest Alternative (HPV DNA)
Methodology Reverse Transcription Real-Time PCR (RT-qPCR) Hybrid Capture / DNA PCR
Clinical Sensitivity (CIN2+) >97% ~94%
Specificity for Active Infection Near 100% (detects oncogene expression) Lower – may detect cleared transient infections
Turnaround Time 24 – 36 hours 5 – 7 days
Sample Type Cervical Swab (self-collected or provider-collected) Cervical Swab
UAE Regulatory & Accreditation DHA Licensed (Facility #9834453), ISO 9001:2015, 2026 UAE PDPL Compliant Varies

Physician Insight & Safety Protocol

Dr. PRABHAKAR REDDY (DHA: 61713011) notes: “An HPV 16/18 RNA positive result is a strong biomarker for high-grade dysplasia and requires immediate colposcopy referral. A negative result, however, does not entirely rule out cervical neoplasia—other high‑risk types or rare endocervical lesions may still exist. Clinical correlation with cytology and patient history remains paramount for every individual.”

⚠ Medication Warning: Do not discontinue any prescribed medication, including topical treatments, without consulting your physician. This test does not replace regular gynecological surveillance.

Exclusion Criteria & Emergency Signals

  • Exclusion: Active heavy menstrual bleeding – reschedule until flow is light or finished.
  • Exclusion: Recent (<48 hours) vaginal intercourse, douching, or use of vaginal creams/medicated pessaries.
  • Exclusion: Known allergy to medical latex (alternative non-latex kit available on request).
  • ER Red Flag: Severe pelvic pain, uncontrolled vaginal bleeding, fever >38.5°C, or signs of systemic infection following sample collection – seek immediate medical attention.

Patient FAQ & Clinical Guidance

Q: What is the difference between HPV RNA and HPV DNA testing?

HPV RNA detects E6/E7 mRNA, signaling active infection and higher specificity for cervical precancer than DNA.

This RNA-based test identifies the presence of messenger RNA from HPV types 16 and 18, the most oncogenic strains. Unlike DNA tests, which may detect transient or cleared infections, RNA positivity indicates active viral gene expression and is strongly linked to CIN2+ lesions. It is particularly useful for triage of women with ASC‑US cytology.

يكشف اختبار الحمض النووي الريبوزي عن الرنا المرسال للجينات الورمية E6/E7، مما يوفر مؤشراً أكثر دقة للإصابة النشطة عالية الخطورة مقارنة باختبارات الحمض النووي (DNA) التي قد تظهر إيجابية حتى بعد زوال الفيروس.

Q: Is the cervical swab for this test painful?

The collection is quick and minimally uncomfortable, similar to a routine Pap smear, with no lasting pain.

Our trained phlebotomists use a soft cervical brush that gently reaches the transformation zone of the cervix. Most patients report only a mild sensation of pressure or mild cramping lasting a few seconds. For anxious patients, a chaperone and detailed guidance are provided.

يتم أخذ المسحة بطريقة سريعة وبسيطة، تشبه مسحة عنق الرحم الروتينية، ولا تسبب ألماً يذكر، وتنتهي في غضون ثوانٍ.

Q: How should I prepare for this HPV RNA test?

Avoid sexual intercourse, douching, and vaginal medications for 48 hours before the test to ensure accurate results.

Proper preparation prevents interference with the cervical specimen. Do not use spermicidal foams, jellies, or tampons. Schedule the test when you are not menstruating heavily. Bring your clinical history and a signed consent form, which will be provided via WhatsApp or at the time of home collection.

تجنب الجماع والغسول المهبلي والأدوية المهبلية لمدة 48 ساعة قبل الاختبار. أحضر نموذج الموافقة الموقع وأي سجلات سريرية سابقة.

Legal & Regulatory Compliance: All services adhere to Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE CDS Law 2026 (Minors Consent), and UAE Personal Data Protection Law (PDPL). Facility licensed by DHA (#9834453). International accreditation: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Teleconsultation and result interpretation are supplementary to standard medical care.

Specialists Referred: General Physicians, Gynecologists, Infectious Disease Specialists.

Codes: LOINC 80380-7 (https://loinc.org/80380-7/). ICD‑10‑CM: Z11.51, R87.810, Z15.89.

Methodology: Reverse Transcription Real‑Time PCR (RT‑qPCR) – 2026 standard.

Support: WhatsApp +971 54 548 8731 | Home collection hours: 8 AM – 11 PM daily.

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