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Test Price

1,800 AED

✅ Home Collection Available

Pheochromocytoma Profile Test in Dubai | DHA Licensed Laboratory

Executive Summary & Core Metrics

  • Diagnostic Accuracy: >99.9% sensitivity and specificity for plasma and urinary metanephrines via ISO‑accredited LC‑MS/MS processing.
  • Premium Logistics: VIP mobile phlebotomy and temperature‑controlled cold‑chain home collection available daily from 8 AM to 11 PM.
  • Post‑Test Guidance: Telephonic clinical interpretation by a DHA‑licensed physician included with every result.
  • Insurance Verification: Direct billing confirmation via WhatsApp at +971 54 548 8731.

Test Overview & Methodology

The Pheochromocytoma Profile quantifies plasma free metanephrines and 24‑hour urine fractionated metanephrines, the definitive biomarker panel for detecting catecholamine‑secreting tumours arising from chromaffin cells of the adrenal medulla. Early biochemical diagnosis is critical to prevent life‑threatening hypertensive crises and guide surgical resection planning.

Feature Our Test – DHA Certified Closest Alternative
Methodology HPLC‑EC / LC‑MS/MS – Clinical Gold Standard ELISA immunoassay
Diagnostic Precision >99.9% sensitivity and specificity ~85% sensitivity
Turnaround Time 2 working days 5–7 working days
Specimen Matrix Plasma + 24‑hour urine (comprehensive dual‑matrix) Urine only (limited sensitivity)
Price (AED) 1,800 AED – insurance eligible 1,200 AED – often out‑of‑pocket
Regulatory Certification ISO 9001:2015, DHA Licensed Not specified

Physician Insight & Safety Protocols

“Metanephrine quantification must be interpreted within the full clinical context including imaging findings and blood pressure history. A single elevated value does not confirm the diagnosis; serial testing and clonidine suppression studies are sometimes warranted. Our multidisciplinary team ensures every patient receives a coordinated care pathway from biochemical detection to surgical referral.”

— Mr. Prabhakar Reddy Kalathoor | Specialist Diagnostic Radiology | DHA Registration ID: 61713011

Pre‑Collection Advisory

Strict 72‑Hour Avoidance Required

The following substances must be withheld for at least 72 hours before sample collection due to direct interference with metanephrine assays: alpha‑1 blockers, aminophylline, amphetamines, ampicillin, beta‑blockers, ephedrine, imipramine, methyldopa, buspirone, codeine, L‑Dopa, MAO inhibitors, nicotine, phenacetin, phenothiazines, theophylline, vasodilators, aspirin, PAS, alpha‑2 agonists, bromocriptine, calcium channel blockers (chronic use), clofibrate, propranolol, penicillin, reserpine, thyroxine, isoproterenol, labetalol, mandelamine, paracetamol, cimetidine, metoclopramide, and all sympathomimetic agents. Additionally avoid vigorous exercise, alcoholic beverages, caffeine, tobacco, chocolate, pepper, vanilla, and bananas.

Emergency Warning Signs

During the preparation period, seek immediate emergency care if you experience sudden severe headache, palpitations, diaphoresis, orthostatic dizziness, or chest pain — these may indicate a catecholamine surge requiring urgent medical intervention.

Exclusion Criteria & Special Populations

Pregnant patients must undergo testing only under obstetric supervision. Individuals with acute renal failure, dialysis dependence, or severe hepatic impairment may exhibit altered metanephrine clearance, requiring adjusted reference intervals. Do not discontinue prescribed antihypertensives without direct consultation with your managing physician; abrupt withdrawal can precipitate rebound hypertension or hypertensive crisis.

Patient FAQ & Clinical Guidance

1. What does the Pheochromocytoma Profile detect and why is it necessary?

The profile measures plasma free metanephrines and 24‑hour urine fractionated metanephrines — the breakdown products of adrenaline and noradrenaline. Elevated levels help confirm or exclude a pheochromocytoma, a rare but potentially fatal neuroendocrine tumour. Early detection prevents hypertensive emergencies, myocardial damage, and stroke.

2. How should I prepare for the Pheochromocytoma Profile test?

Follow the 72‑hour avoidance list provided above covering all interfering medications, stimulants, foods, and beverages. Continue essential cardiac medications only after explicit approval from your prescribing doctor. Our phlebotomist will confirm readiness before collection. Fasting is not required, but avoid caffeine and nicotine on the morning of the draw.

3. What is the cost and does insurance cover this test in the UAE?

The Pheochromocytoma Profile is priced at 1,800 AED. DNA Labs UAE offers direct insurance billing verification via WhatsApp at +971 54 548 8731. Many major UAE insurers list this test under endocrine or oncology benefits; prior approval is recommended for full coverage confirmation.

UAE Regulatory & Data Privacy Adherence

Data Protection: All patient information is processed in strict compliance 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.

Medical Liability: Clinical safety and informed consent protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability.

Certification: ISO 9001:2015 certified laboratory under certificate INT/EGQ/2509DA/3139. Full DHA facility licensing.

Clinical & Logistical Metadata

Test Name Pheochromocytoma Profile (Plasma Free Metanephrines & 24‑Hour Urine Fractionated Metanephrines)
Price (AED) 1,800 AED
Turnaround Time 2 working days
Sample Type / Matrix Plasma (EDTA) & 24‑Hour Urine (acidified) – VIP mobile phlebotomy and temperature‑controlled cold‑chain home collection available daily from 8 AM to 11 PM
Methodology Used HPLC‑EC / LC‑MS/MS (isotope dilution tandem mass spectrometry)
ICD-10-CM Code D35.00 (Benign neoplasm of adrenal gland – pheochromocytoma)
LOINC Code 32294-1 (Metanephrine [Mass/volume] in Plasma)
DHA Facility License & Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE

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