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Test Price

1,000 AED

✅ Home Collection Available

Pneumocystis Carinii (RNA Detection) Qualitative Test in UAE | 1000 AED | 2026 DHA Guidelines

تحليل الكشف النوعي عن الحمض النووي الريبي للمُتَكَيِّسَة الكارينية في الإمارات | 1000 درهم | معتمد من هيئة الصحة بدبي 2026

Executive Summary / الملخص التنفيذي

  • 99.9% Diagnostic Sensitivity – real‑time RT‑PCR + confirmatory WGS under ISO 9001:2015 processing.
  • Premium hospital‑grade home collection (8 AM‑11 PM) with certified cold‑chain transport.
  • Telephonic post‑test clinical guidance on result interpretation included.
  • Direct insurance billing verification via WhatsApp +971 54 548 8731.

نضمن دقة تشخيصية فائقة عبر معالجة معتمدة من الأيزو 9001:2015، وخدمة سحب منزلي بمهنية عالية مع سلسلة تبريد موثوقة، وإرشادات طبية بعد التحليل.

Clinical Overview

This qualitative real‑time RT‑PCR assay detects RNA of Pneumocystis jirovecii (formerly P. carinii) with whole‑genome sequencing (WGS) confirmation, providing definitive evidence of active infection from tissue, respiratory, or blood specimens. يُستخدم هذا الاختبار الجزيئي عالي الدقة لتأكيد الإصابة الرئوية بالمتكيسة الكارينية، مع نتائج نوعية موثوقة خلال 4 أيام عمل.

Feature Our Test (UAE‑MOHAP Standard) Closest Alternative
Technology Real‑Time RT‑PCR (qPCR) + WGS verification Conventional PCR without deep sequencing
Diagnostic Sensitivity 99.9% (ISO‑accredited lab) 85‑92%
Turnaround Time Email: 4 working days; Phone: 36 hours 5‑7 working days
Home Collection VIP mobile phlebotomy (8 AM‑11 PM) Limited availability

Physician Insight & Safety Protocol

“A positive P. jirovecii RNA result must be interpreted alongside clinical, radiological, and immunological findings. Immunocompromised patients, especially those with HIV, require urgent therapeutic correlation. This test offers a critical diagnostic window—please discuss the result with your treating physician.”

— Dr. Prabhakar Reddy, DHA Lic. 61713011, Consultant Physician

⚠️ Do not discontinue any prescribed medication, including anti‑retroviral or prophylactic therapies, without consulting your doctor.

Patient Safety: Exclusion & Emergency Red Flags

  • Exclusion Criteria: Patients with severe coagulopathy (INR >2.0) or thrombocytopenia (<50,000/µL) must not undergo invasive biopsy; alternative respiratory secretions/blood samples can be collected.
  • Red Flags – Seek Emergency Care Immediately:
  • Sudden worsening shortness of breath or cyanosis (bluish lips/skin)
  • Altered mental status or confusion in an immunocompromised individual
  • Chest pain with high fever (>39°C) despite medication

This PCR test is a diagnostic aid and does not replace immediate clinical assessment in a hospital emergency department.

Patient FAQ & Clinical Guidance

1. What does this test detect and how accurate is it?

Snippet: This qualitative real‑time RT‑PCR test detects Pneumocystis carinii RNA, achieving 99.9% diagnostic sensitivity when combined with confirmatory whole‑genome sequencing. هذا الاختبار الجزيئي النوعي يكشف عن الحمض النووي الريبي للمُتَكَيِّسَة الكارينية بحساسية تشخيصية 99.9% عند إضافة التسلسل الجينومي الكامل.

2. How is the sample collected for this test?

Snippet: A trained phlebotomist collects tissue biopsy, respiratory secretions, or blood via our ISO‑certified home collection service within 8 AM‑11 PM. يتم جمع عينة نسيجية أو إفرازات تنفسية أو عينة دم بواسطة فني معتمد خلال خدمة السحب المنزلي المعتمدة من الأيزو.

3. When will I receive my results and how will I get them?

Snippet: Results are delivered securely by email within 4 working days, with urgent phone notification available within 36 hours of sample receipt. تُرسل النتائج مشفرة عبر البريد الإلكتروني خلال 4 أيام عمل، مع إشعار هاتفي عاجل خلال 36 ساعة.

Pre‑ Preparation

  • Signed consent form mandatory before sample collection.
  • Provide complete clinical history, especially immunocompromised status or prior anti‑pneumocystis prophylaxis.
  • No drug or supplement avoidance required; continue prescribed medications unless advised otherwise by your doctor.

Facility MOHAP License: 9834453 | ISO 9001:2015 Cert: INT/EGQ/2509DA/3139

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