Getting a “high-risk” result in a double marker test can feel scary — but it’s important to understand that this is not a diagnosis, only a screening result.
At Aashakiran IVF Pvt. Ltd. – North India’s most trusted and fastest-growing IVF chain, our experts including Dr. Asmita Mahla guide couples step-by-step to understand results and choose the right next steps with confidence and clarity.
What is the Double Marker Test?
The double marker test is a first trimester screening test (11–13 weeks) that checks the risk of chromosomal abnormalities in the baby.
It measures two markers in the mother’s blood:
- Free Beta-hCG
- PAPP-A (Pregnancy-Associated Plasma Protein-A)
Combined with the NT scan (nuchal translucency ultrasound), it estimates risk for:
- Down Syndrome (Trisomy 21)
- Trisomy 18 (Edwards Syndrome)
- Trisomy 13 (Patau Syndrome)
What Does “High Risk” Mean?
A high-risk result means:
- There is a higher probability that the baby may have a chromosomal abnormality
- It does NOT confirm that the baby has a problem
👉 Example:
- Risk may be shown as 1:100 (higher risk)
- Compared to 1:1000 (lower risk)
Important: It Is NOT a Final Diagnosis
Many women with high-risk results go on to have completely healthy babies.
This test only flags risk, it does not give a confirmed answer.
What Are the Next Steps?
If your report shows “high risk”, doctors at Aashakiran IVF may recommend:
1. NIPT (Non-Invasive Prenatal Testing)
- Advanced blood test
- Highly accurate (99%+ for Down syndrome)
- Safe for mother and baby
2. Level II Ultrasound / Anomaly Scan
- Detailed scan to check baby’s structure
3. Diagnostic Tests (Confirmatory)
If needed:
- CVS (Chorionic Villus Sampling) – done around 11–13 weeks
- Amniocentesis – done after 15 weeks
These give definitive results, but are done only when necessary.
Why Do High-Risk Results Occur?
Possible reasons include:
- Maternal age (especially >35 years)
- Abnormal blood marker levels
- Increased NT thickness
- Placental factors
- Sometimes even false positives
Emotional Support Matters
A high-risk report can cause anxiety, but remember:
- You are not alone
- It is manageable with proper guidance
- Early detection helps in better decision-making and care
At Aashakiran IVF, we provide:
- Clear explanation of reports
- Genetic counselling
- Step-by-step guidance
- Emotional support for couples
Aashakiran IVF: Guiding You with Care & Clarity
We believe every report should bring understanding, not fear.
Our team ensures you get the right diagnosis, right advice, and right support at every stage of pregnancy.
📞 For appointments or pregnancy guidance: 872-8080-222
📍 Visit us at Kharar | Ludhiana | Amritsar | Bathinda
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🌐 Learn more: www.aashakiranivf.com
Aashakiran IVF – Turning uncertainty into informed decisions.




