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Sanjeevini Maternity & Fertility Centre

Compassionate Care for Every Step of Your Journey

From fertility treatments to safe deliveries and newborn care, our experienced team combines advanced technology with a personal touch to support you and your family at every stage.

Double & Quadruple Marker Test in Raichur | Sanjeevini Maternity & Fertility Centre
The Basics

Understanding Prenatal Marker Screening

Prenatal marker screening is a simple maternal blood test that measures specific hormone and protein levels to estimate your baby's risk of chromosomal conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and neural tube defects.

These are screening tests, not diagnostic tests — they help identify pregnancies that may benefit from further evaluation, giving you clear, timely information without any risk to your baby.

At Sanjeevini Maternity & Fertility Centre, every result is interpreted by Dr. Vasundhari M.J. and explained in simple terms, with guidance on any recommended next steps.

Simple Blood Test

A quick maternal blood draw — no risk to you or your baby.

Risk-Assessment, Not Diagnosis

Estimates probability; further tests confirm if risk is elevated.

Trimester-Specific

Double Marker in the first trimester; Quadruple Marker in the second.

Specialist-Interpreted

Results reviewed and explained clearly by our care team.

The Comparison

Double Marker vs Quadruple Marker Test

Both tests screen for chromosomal risk, but at different stages of pregnancy and using different markers.

First Trimester

Double Marker Test

Performed between 10–13 weeks of pregnancy
  • Measures two markers: free beta-hCG and PAPP-A
  • Often combined with a nuchal translucency (NT) ultrasound
  • Screens for Down syndrome and Edwards syndrome risk
  • Provides early-pregnancy reassurance or guidance
Second Trimester

Quadruple Marker Test

Performed between 15–20 weeks of pregnancy
  • Measures four markers: AFP, hCG, estriol and inhibin-A
  • Recommended for those who missed first-trimester screening
  • Screens for Down syndrome, Edwards syndrome and neural tube defects
  • Useful as a stand-alone or follow-up screening step
The Process

Your Testing & Results Journey

A simple, guided path from your blood draw to your next step in care.

1

Preparation

Your doctor confirms the right test window based on your weeks of pregnancy.

2

Sample Collection

A quick, straightforward maternal blood draw at our centre.

3

Lab Analysis

Markers are measured and combined with your clinical details to calculate risk.

4

Results & Next Steps

Your doctor explains the results and recommends any further evaluation if needed.

Meet the Team

Our Specialists

Prenatal marker screening at Sanjeevini Maternity & Fertility Centre is guided and interpreted by our experienced specialists.

VM

Dr. Vasundhari M.J.

Maternity & Fertility Specialist

Guides prenatal screening decisions and explains results clearly, ensuring every parent feels informed and supported.

AP

Dr. Apoorva

Women's Health Specialist

Supports pregnancy risk assessment and follow-up care with a patient-first, detail-oriented approach.

Common Questions

Frequently Asked Questions

Is the Double or Quadruple Marker test safe for my baby?+

Yes. Both are simple maternal blood tests with no risk to you or your baby, unlike invasive diagnostic procedures.

What's the difference between screening and diagnostic tests?+

Screening tests like these estimate risk levels. If a result shows elevated risk, your doctor may recommend a diagnostic test for confirmation.

Can I take the Quadruple Marker test if I missed the Double Marker window?+

Yes. The Quadruple Marker test is performed later in pregnancy and can be done independently if the first-trimester window was missed.

How soon will I receive my results?+

Results are typically available within a few days, after which your doctor will discuss the findings and any recommended next steps with you.

Does an abnormal result mean something is definitely wrong?+

No. An elevated-risk result simply means further evaluation is recommended — it does not confirm a diagnosis on its own.

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