Test Price
320 AED✅ Home Collection Available
Estradiol Ultrasensitive Test in UAE | 320 AED | 2026 DHA Guidelines
تحليل الإستراديول فائق الحساسية في الإمارات | 320 درهم | إرشادات هيئة الصحة بدبي لعام 2026
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
ملخص تنفيذي: دقة تشخيصية 99.9% عبر معالجة معتمدة من ISO. خدمة سحب منزلي بمستوى المستشفيات مع سلسلة تبريد وفريق تمريض متنقل. استشارة هاتفية بعد الفحص لتفسير النتائج. التحقق المباشر من تغطية التأمين عبر واتساب.
For patients under 18 years, valid guardian consent is required per UAE Child Digital Safety Law 2026. All personal and medical data is protected under UAE PDPL. Laboratory services comply with Federal Decree-Law No. 41 of 2024, Article 87 and hold ISO 9001:2015 Certification (INT/EGQ/2509DA/3139). Facility License: 9834453.
Comprehensive Overview of Estradiol Ultrasensitive Testing
The Estradiol Ultrasensitive Test provides the most accurate measurement of 17-beta-estradiol, the principal female sex hormone, employing Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) to reach picogram-level sensitivity. This technique eliminates cross-reactivity seen in older immunoassays, rendering it essential for evaluating menopause, pediatric endocrinology, male hypogonadism, sports endocrinology, and anti-aging therapies.
The test uses only 2 mL serum from a plain red-top tube (no additive); SST gel barrier tubes are strictly prohibited. Specimens are shipped refrigerated or frozen to maintain stability. Results are reported within 2–3 working days depending on collection day (Sample Mon/Thu by 9 am, Report Wed/Sat).
| Parameter | Our LC-MS/MS Test | Standard Immunoassay (EIA) |
|---|---|---|
| Technology | LC-MS/MS (Tandem Mass Spectrometry) | Enzyme Immunoassay |
| Sensitivity | Picogram/mL – detects trace levels | Nanogram/mL – unreliable at low ends |
| Turnaround | Wed / Sat (based on collection day) | 3–5 business days, variable |
| Clinical Relevance | Gold‑standard for menopause, pediatric, anti‑aging & sports endocrinology | Adequate only for routine screening |
Pre‑test Information & Sample Logistics
Patient Preparation: No special preparation such as fasting is required. However, inform our mobile phlebotomist that a red-top serum tube (no additive) must be used. Never use SST gel barrier tubes – they introduce interference that degrades ultrasensitive measurement.
Sample Handling: 2 mL (1 mL min.) serum. Specimens must be kept refrigerated or frozen during transport; our home collection team follows ISO-certified cold‑chain protocols.
Physician Insight & Safety Protocol
“I interpret estradiol results with full attention to the patient's clinical picture, including menstrual cycle phase, age, and concurrent medications; a single value does not define a diagnosis. Anomalies may signal polycystic ovary syndrome, ovarian failure, or pituitary disorders and warrant a thorough endocrine workup. Please never stop or adjust your prescribed medication without direct consultation with your doctor.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠️ Medical Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & When to Seek Emergency Care
- This test is not appropriate within 48 hours of receiving radioiodine contrast or certain hormone interventions; acute febrile illness may alter results. Inform our clinical team if you have any acute condition.
- ER Red Flags: If you experience severe lower abdominal pain, heavy abnormal vaginal bleeding, sudden vision loss, or signs of deep vein thrombosis (leg swelling/pain) after starting/adjusting estrogen therapy, seek immediate medical attention.
Patient FAQ & Clinical Guidance
1. What exactly does an ultrasensitive estradiol test measure, and why is the ultrasensitive method important?
Snippet: This test precisely quantifies estradiol, the primary female sex hormone, in blood using mass spectrometry with detection limits down to picogram levels. The ultra‑high sensitivity is critical for accurately measuring low estrogen concentrations in men, postmenopausal women, and children, where standard assays fail. Elevated or suppressed values guide fertility treatments, hormone replacement monitoring, and evaluate gonadal function.
يقيس هذا الفحص بدقة هرمون الإستراديول، الهرمون الأنثوي الرئيسي، في الدم باستخدام مطياف الكتلة بحدود كشف تصل إلى مستويات البيكوغرام. الحساسية الفائقة ضرورية لدقة القياس عند الرجال والنساء بعد سن اليأس والأطفال حيث تفشل المقايسات التقليدية. تستخدم النتائج لتوجيه علاجات الخصوبة، ومراقبة العلاج الهرموني التعويضي، وتقييم وظيفة الغدد التناسلية.
2. How should I prepare for the blood draw, and are there any restrictions?
Snippet: No fasting or special preparation is needed; simply inform your phlebotomist to use a red-top tube without gel barrier. For healthcare providers: do not use SST gel separator tubes, as they introduce interference. The sample must be transported under refrigeration to guarantee stability. Our home collection team adheres to cold‑chain protocols.
لا يحتاج المريض إلى صيام أو تحضير خاص؛ كل ما عليه إبلاغ أخصائي سحب الدم باستخدام أنبوب أحمر بدون مادة هلامية. يمنع استخدام أنابيب الفصل الهلامية لأنها تسبب تداخلاً. يجب نقل العينة مبردة لضمان الاستقرار. يلتزم فريق السحب المنزلي ببروتوكولات سلسلة التبريد.
3. When will I receive my results, and how are they clinically interpreted?
Snippet: Results are typically available within 2–3 working days; a teleconsultation will explain the values in clinical context. The report includes age‑ and sex‑specific reference ranges, along with a brief interpretive comment by the laboratory. In the UAE, interpretation must be correlated with symptoms and imaging by a DHA‑licensed physician.
تتوفر النتائج عادةً خلال 2-3 أيام عمل؛ وستشرح استشارة هاتفية القيم في السياق السريري. يتضمن التقرير نطاقات مرجعية حسب العمر والجنس مع تعليق تفسيري من المختبر. في الإمارات، يجب ربط النتائج بالأعراض والتصوير الطبي بواسطة طبيب مرخص من هيئة الصحة.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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