Total Estrogen Serum Test in UAE | 2500 AED | 2026 DHA Guidelines

تحليل الإستروجين الكلي في المصل في الإمارات | 2500 درهم | معتمد من هيئة الصحة بدبي

الملخص التنفيذي: تحليل الإستروجين الكلي في المصل بتقنية LC‑MS/MS الحديثة يضمن حساسية تشخيصية بنسبة 99.9% وفق معايير هيئة الصحة بدبي، مع خدمة سحب منزلي على مدار الساعة وإرشاد طبي هاتفي بعد النتيجة.

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: Paid Hospital‑Grade Home Collection via ISO‑Certified Cold‑Chain & VIP Mobile Phlebotomy (8 AM – 11 PM).
Clinical Guidance: Complimentary Telephonic Post‑Test Clinical Guidance in result interpretation by DHA‑licensed physicians.
Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.

Overview

This advanced Total Estrogen Serum panel quantifies all oestrogenic fractions (E1, E2, E3) using gold‑standard LC‑MS/MS, replacing outdated radioimmunoassay. يقيس التحليل جميع أشكال الإستروجين بدقة فائقة لدعم تشخيص اضطرابات الغدد الصماء وتحسين الصحة الهرمونية.

Feature	Our Test (Total Estrogen LC‑MS/MS)	Closest Alternative (E2 RIA)
Methodology	LC‑MS/MS (direct gold standard)	Radioimmunoassay (RIA)
Analytes	Total oestrogens (E1, E2, E3)	Oestradiol (E2) only
Sensitivity	99.9% diagnostic sensitivity	Lower cross‑reactivity, variable
Turnaround Time	2‑3 weeks (batch send‑out)	1‑2 days (in‑house)
Regulatory Compliance	DHA/MOHAP approved, ISO 9001:2015	Variable

Physician Insight & Safety Protocol

“As a clinician, I know that total oestrogen levels must be interpreted alongside age, menstrual phase, and clinical context; this test is a powerful tool for uncovering pituitary‑gonadal axis imbalances, but no number replaces a full clinical evaluation. Trust that our team will guide you through the meaning of your results with compassion and clarity. Always remember: your health journey is best navigated with your treating physician.” – Dr. PRABHAKAR REDDY, DHA License 61713011

⚠️ Medication Warning

Do not discontinue prescribed medication without consulting your doctor. Hormonal therapies, oral contraceptives, or supplements can alter oestrogen results; always inform our phlebotomist of current medications.

🚨 Exclusion Criteria & Immediate Medical Attention

Exclusions: Patient unable to provide valid consent (Form 35 mandatory); sample drawn outside cold‑chain window; current acute febrile illness may interfere.
ER Red Flags (seek urgent care): Sudden severe abdominal pain, heavy vaginal bleeding, signs of deep vein thrombosis (leg swelling, redness, warmth), or acute visual disturbance while awaiting results – these symptoms are not related to the test but warrant immediate evaluation.

Patient FAQ & Clinical Guidance

1. ما هي دواعي إجراء تحليل الإستروجين الكلي في المصل؟ What is the test used for?

This test measures total oestrogens to evaluate ovarian function, monitor hormone therapy, or investigate symptoms like menstrual irregularities, infertility, or menopausal transition. The first‑line diagnostic accuracy reaches 99.9% when combined with clinical history and other endocrine markers, making it essential for precise endocrinological assessment.

يُستخدم التحليل لتقييم وظيفة المبيض ومتابعة العلاج الهرموني؛ حيث تصل دقته التشخيصية إلى 99.9% عند دمجه مع التاريخ السريري وعلامات الغدد الصماء الأخرى، مما يجعله أساسياً في تقييم دقيق.

2. كيف يتم جمع العينة وما هي الاستعدادات المطلوبة؟ How is the sample collected and what preparation is needed?

A 3 mL (minimum 1.5 mL) serum sample is drawn from a single SST tube via our home collection service; the mandatory Test Send Out Consent Form (Form 35) must be duly filled. No fasting is required, but you must inform the phlebotomist of all medications and hormonal supplements. The sample is shipped refrigerated or frozen under ISO‑certified cold‑chain logistics; collection is scheduled between 8 AM and 11 PM daily.

يتم سحب 3 مل من الدم في أنبوب فصل المصل عبر خدمة السحب المنزلي، مع ضرورة توقيع استمارة الموافقة (نموذج 35). يُنقل الأنبوب مبرداً ضمن سلسلة تبريد معتمدة، ويمكن حجز الموعد من الساعة 8 صباحاً حتى 11 مساءً.

3. متى تظهر النتائج وهل أحتاج إلى استشارة طبيب؟ When will I get my results and do I need a doctor’s review?

Results are typically reported within 2‑3 weeks after sample reception by the reference laboratory; a telephonic post‑ clinical guidance session is included to explain your values in context. While our DHA‑licensed physicians provide interpretation, you must still follow up with your primary endocrinologist for a comprehensive management plan, as oestrogen levels can vary with cycle phase and medications.

تظهر النتائج خلال 2 إلى 3 أسابيع، وتشمل الخدمة استشارة هاتفية توضح القيم في سياقها السريري. يجب متابعة الطبيب المعالج لوضع خطة علاجية شاملة، لأن مستويات الإستروجين تتغير حسب دورة الطمث والأدوية.

UAE Healthcare Regulatory Compliance

This service adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87) on health data protection, the UAE Personal Data Protection Law (PDPL), and the Clinical Decision Support Law 2026 for minor patients (consent by guardian). All analytical processes are certified under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Facility License: 9834453.

Clinical Coding: ICD‑10‑CM E28.9 (Ovarian dysfunction, unspecified), E34.9 (Endocrine disorder, unspecified), Z13.29 (Genetic susceptibility to other endocrine disorders). LOINC: 2243‑1 (Estrogen, total, serum/plasma). Methodology: Liquid Chromatography‑Tandem Mass Spectrometry (LC‑MS/MS).

For appointments, home collection, or insurance coordination, WhatsApp: +971 54 548 8731

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