Hepatitis A Virus (HAV) RNA Detection Qualitative Test in UAE | 950 AED

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% clinical sensitivity via ISO‑certified real‑time PCR in a DHA‑licensed laboratory.
Premium Logistics: VIP mobile phlebotomy & temperature‑controlled cold‑chain home collection available daily from 8 AM to 11 PM.
Medical Guidance: Complimentary post‑result telephone consultation with our clinical team to ensure full comprehension of your report.
Insurance Support: Instant coverage verification via WhatsApp at +971 54 548 8731.

Test Overview & Methodology

The HAV RNA Qualitative Test detects hepatitis A virus genetic material within days of exposure, offering the earliest possible acute diagnosis before antibody seroconversion. It is the gold‑standard method for outbreak investigation, early intervention, and differential diagnosis from other hepatitis viruses.

Parameter	Our Test (HAV RNA PCR Qualitative)	Closest Alternative (HAV IgM Serology)
Methodology	Real‑Time Reverse Transcription PCR (RT‑qPCR)	ELISA / Chemiluminescence Immunoassay
Detection Window	Within 3–7 days post‑exposure	5–10 days after symptom onset (may miss early phase)
Clinical Sensitivity	99.9% (validated)	~95–98%
Turnaround Time	24–36 hours (phone) / 3rd working day (email)	2–5 working days
Use Cases	Early acute diagnosis, outbreak control, immunocompromised patients	Screening, immune status confirmation

Physician Insight & Safety Protocols

“A positive HAV RNA result confirms active viral replication and serves as the earliest marker of acute infection. Clinical correlation with symptoms, liver enzymes, and epidemiological history is essential. I always advise immediate isolation and supportive care to prevent transmission. Do not hesitate to contact your healthcare provider for guidance on next steps.”

— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Safety Advisory & Informed Consent

⚠️ Important Safety Notice

All clinical procedures adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability. Do not alter or cease any prescribed medication without consulting your doctor. Our home phlebotomy service is available only after obtaining your explicit informed consent via our digital consent platform.

Exclusion Criteria & Emergency Red Flags

Do Not Proceed With Home Collection If:

You have a known severe latex allergy (tourniquet component).
You have an uncontrolled bleeding disorder (e.g., haemophilia).
You are unable to provide informed consent.

Seek Emergency Care Immediately If You Develop:

Sudden severe abdominal pain or jaundice with confusion.
Vomiting blood or black, tarry stools.
Signs of acute liver failure (e.g., drowsiness, slurred speech).

Patient FAQ & Clinical Guidance

1. What is the clinical utility of the HAV RNA qualitative test?

The test detects hepatitis A virus RNA within days of exposure, enabling earliest possible acute diagnosis before antibody seroconversion. It is indispensable for confirming infection in the prodromal phase, guiding isolation measures, and differentiating HAV from other acute hepatitides.

2. What pre‑preparations are required?

Sign the mandatory digital consent document and provide a brief clinical history including symptom onset, recent travel, or known exposure. No fasting or medication changes are necessary unless explicitly instructed by your doctor.

3. When will I receive my results and what do they mean?

Results are delivered confidentially by phone within 24 hours and by email by the 3rd working day. A positive result indicates active HAV RNA presence, confirming acute infection and potential contagiousness; negative means no detectable RNA at the time of sampling, but clinical correlation is essential.

UAE Regulatory & Data Privacy Adherence

Your health data is protected under 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 are governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability. Our laboratory operates under DHA Facility License No. 1143 at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. All processes are ISO 9001:2015 certified and comply with DHA‑mandated quality standards.

Clinical & Logistical Metadata

Test Name	Hepatitis A Virus (HAV) RNA Qualitative Detection
Price (AED)	950
Turnaround Time	24–36 hours (phone) / 3rd working day (email)
Sample Type / Matrix	Peripheral blood (plasma/serum)
Methodology Used	Real‑Time Reverse Transcription PCR (RT‑qPCR)
ICD-10-CM Code	B15.9
LOINC Code	49275-4
DHA Facility License & Address	License No.: 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE