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Test Price

650 AED

โœ… Home Collection Available

Human Parechovirus Qualitative PCR Test in UAE | 650 AED | DHA Licensed Laboratory

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) Accredited Processing.

Specimen Collection: Hospital Extraction Only โ€“ Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.

Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed physicians.

Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Human Parechovirus Qualitative PCR test detects viral RNA in blood or cerebrospinal fluid (CSF) using highly sensitive Real-Time PCR with optional Whole Genome Sequencing, providing definitive diagnosis of parechovirus infection in all age groups, especially neonates and immunocompromised patients.

Why Our Test?

Feature Our ISO-Accredited Human Parechovirus PCR Standard Commercial PCR
Precision Real-Time qPCR with WGS confirmation for ambiguous cases; LC-MS/MS-validated dual-probe technology Conventional PCR with lower analytical specificity
Method Quantitative Real-Time PCR (qPCR) plus optional Whole Genome Sequencing Qualitative end-point PCR targeting single gene
Speed Report within 2โ€“3 days (samples Mon/Thu by 11 am; report Wed/Sat) 5โ€“7 days

Physician Insight & Safety Protocols

โ€œWhile this PCR test offers outstanding accuracy, clinical context is paramount. A positive result must be correlated with symptoms, age, and immune status; a negative result in a symptomatic neonate does not exclude parechovirus encephalitis. Always interpret results alongside neurological examination and inflammatory markers.โ€

โ€” Dr. Ajay Singh, DHA License 36234132

โš ๏ธ Medication Advisory

Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

  • Recent blood transfusion or immunoglobulin therapy within 6 weeks may invalidate serological markers; consult physician before scheduling.
  • Severe needle phobia or hemodynamic instability contraindicates routine venipuncture; use alternative collection after clinical assessment.
  • Seek immediate emergency care if the patient (especially infant) develops high fever with lethargy, bulging fontanelle, seizures, severe headache, neck stiffness, photophobia, or signs of septic shockโ€”do not wait for test results.

Patient FAQ & Clinical Guidance

1. What is human parechovirus and why is this PCR test needed?

Human parechovirus is a common viral pathogen causing mild respiratory illness to severe sepsis and meningitis, making precise PCR testing vital for accurate diagnosis, especially in neonates and immunocompromised patients.

2. What does a positive result mean?

A positive result indicates active parechovirus replication, requiring immediate clinical correlation to determine if infection is benign or invasive. Your physician will integrate this result with clinical findings and possibly additional testing.

3. How to prepare for the test?

No fasting or special preparation is required. Sample collection (blood or CSF) will be performed by hospital staff under strict aseptic technique. Ensure you inform the clinician about any recent transfusions or immunoglobulin therapy.

UAE Regulatory & Data Privacy Adherence

This test is conducted in full compliance with UAE 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 adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your data is encrypted, stored securely, and never shared without explicit consent.

Clinical & Logistical Metadata

Test Name Human Parechovirus Qualitative PCR
Price (AED) 650
Turnaround Time 2โ€“3 days (samples accepted Mon/Thu by 11 am; results Wed/Sat)
Sample Type / Matrix Whole blood (EDTA) or cerebrospinal fluid (CSF) โ€“ Hospital Collection Only
Methodology Used Real-Time PCR (qPCR) with optional Whole Genome Sequencing
ICD-10-CM Code B34.8, B97.12
LOINC Code 44141-4
DHA Facility License & Address License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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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