Angiotensin II (Ang II) Test in UAE | 1800 AED | DHA Licensed

Executive Summary & Core Metrics

Executive Summary

Accuracy Guarantee: 99.9 % Diagnostic Sensitivity through ISO 9001:2015 accredited laboratory processing, eliminating pre-analytic variability with strict cold‑chain EDTA plasma.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM across all Emirates – sample collected by the 7th of the month ensures batch precision.
Clinical Guidance: Telephonic post‑test clinical guidance with DHA‑licensed physicians to interpret your angiotensin II level in the context of your blood pressure profile.
Insurance & Payment: Direct Billing Verification – send your insurance card via WhatsApp at +971 54 548 8731; 1800 AED inclusive of home draw, cold‑chain transport, and test send‑out.

Test Overview & Methodology

The Angiotensin II (Ang II) test quantifies the active octapeptide of the renin‑angiotensin‑aldosterone system (RAAS) in EDTA plasma, a pivotal biomarker for classifying hypertensive disorders and guiding targeted therapy. Direct radioimmunoassay (RIA) provides single‑tube measurement without conversion distortion, offering superior precision over calculated aldosterone/renin ratios.

Feature	Our Test (Ang II)	Closest Alternative (Aldosterone/Renin Ratio)
Methodology	Direct Radioimmunoassay (RIA) – DHA/MOHAP standard	Calculated ratio from separate renin and aldosterone assays
Clinical Precision	Single‑tube EDTA plasma, no conversion distortion	Ratio may miss isolated angiotensin II dysregulation
Turnaround	Sample by 7th; report within 2‑3 weeks (batch‑processed)	Often 5‑7 days, but methodology varies

Physician Insight & Safety Protocols

“Angiotensin II serves as a direct readout of RAAS effector activity. For accurate clinical interpretation, the result must be integrated with plasma renin, aldosterone, and the patient’s hemodynamic profile. An isolated value does not replace a comprehensive cardiometabolic assessment.” – Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132.

Medication Advisory & Safety Notice

⚠️ Do not discontinue any prescribed antihypertensive, diuretic, or RAAS‑modifying drug without explicit instruction from your treating physician. Abrupt cessation can cause a hypertensive emergency.

Exclusion Criteria & Emergency Red Flags

Exclusion Criteria: Active hemolysis, EDTA tube under‑filled or clotted, sample not received refrigerated or frozen, missing Test Send Out Consent Form (Form 35).
Emergency Red Flags: Sudden severe headache, chest pain, vision changes, or fainting – seek immediate medical attention; do not rely solely on this test result.

Patient FAQ & Clinical Guidance

1. What is the purpose of the Angiotensin II test?

The angiotensin II directly measures the active RAAS peptide to differentiate low‑renin, high‑angiotensin forms of hypertension and guide renin‑angiotensin system blocker therapy.

2. How should I prepare for the blood draw?

You may be asked to fast for 8‑12 hours and to be in a seated, rested position for 15 minutes before venipuncture; certain antihypertensives may need a supervised pause.

3. What do abnormal angiotensin II results indicate?

Elevated angiotensin II can point to renovascular hypertension, malignant hypertension, or estrogen therapy effects; very low levels may accompany primary aldosteronism or salt‑sensitive hypertension.

UAE Regulatory & Data Privacy Adherence

This test is conducted in full 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. All patient data are encrypted, access‑controlled, and processed solely for diagnostic purposes. Clinical safety and patient consent follow Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring every step from sample collection to result delivery meets the highest UAE healthcare standards.

Clinical & Logistical Metadata

Test Name	Angiotensin II (Ang II) Test
Price (AED)	1800 AED
Turnaround Time	2‑3 weeks (batch‑processed; sample must be collected by the 7th of the month)
Sample Type / Matrix	EDTA Plasma
Methodology Used	Direct Radioimmunoassay (RIA)
ICD-10-CM Code	I15.0, I10
LOINC Code	2143-9
DHA Facility License & Laboratory Address	DHA Facility License No: 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE — DNA Labs UAE