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Combine screening of Pre-eclampsia & Trisomies
₹ 3,710
Combine screening of Pre-eclampsia & Trisomies
₹ 3,710
51+ booked in last 3 days

Combine screening of Pre-eclampsia & Trisomies

Also Known As :

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Report next day 05:00 pm
Fasting
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Recommended for
Recommended for female
Combine screening of Pre-eclampsia & Trisomies, Serum
₹ 3,710

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PreEclapmsia (PE) is a pregnancy condition characterized by hypertension occurring after 20 weeks of pregnancy together with proteinurea. PE if not diagnosed and treated early increases the chances of pre-term labour and related complications. Apart from USG and clinical examination, combined pre-eclampsia screening includes certain blood marker tests performed to screen the patient for the risk of PE as well as chromosomal abnormalities. The risk is assessed using a software dependent statistical analysis of risk score done using Foetal Medicine Foundation(FMF) approved assays. For better reliability of results, it is advised to carry out analysis between 11 and 13 weeks.

Written by - Dr. Shibani R, Medical Writer, Medical Affairs

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Combined screening of Preeclampsia and trisomy measures the Free beta HCG, PAPPa, PLGF and NT levels in the blood serum.

  • The test is used to screen for patients at risk of developing PreEclampsia (PE) during pregnancy.
  • The test if done early helps to prevent PE associated complications later in the pregnancy.
  • Helps the clinician to start the pregnant woman on timely treatment and ensures close monitoring throughout the pregnancy.
  • Helps to monitor cases at risk for foetal abnormalities, intrauterine growth restrictions etc.
  • Helps to detect and rule out chromosomal anomalies and trisomies.
  • Helps in the detection of neural tube defects.

  • Pregnant women at risk or suspected to have foetal anomalies should ideally undergo combined PE screening between 11 and 13 weeks of pregnancy.
  • Pregnant women with previous history of PE or adverse pregnancy outcomes.
  • Those with family history of co-morbidities like hypertension, type 1 or Type 2 diabetes mellitus, obesity, thyroid disorders, kidney disorders etc.
  • Those with an immediate family history of chromosomal abnormalities, Down’s syndrome or Edward syndrome should undergo the screening.

 

This test requires a blood sample. A tourniquet (elastic) band is placed tightly on the upper arm. The patient is then asked to make a fist. This helps in the build-up of blood filling the veins. The skin is disinfected before needle insertion and the blood sample is collected in vacutainer. The maternal clinical history, USG reports, TRF details and other details are mandatory.

 

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With 45 years of diagnostic excellence, Metropolis Healthcare has built a trusted, science led diagnostics network supported by advanced laboratory infrastructure, rigorous quality standards and deep clinical expertise.

Our capabilities span routine, specialised and super-specialised diagnostics, including molecular diagnostics, genomics, cytogenetics, oncology, neurology, nephrology, women and child health, and other advanced areas. By combining scientific expertise, technology and a strong focus on quality, we deliver precise and reliable diagnostic insights that support better-informed healthcare decisions.

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Metropolis Healthcare is one of India’s leading diagnostics companies, with 45 years of experience built on scientific expertise, quality and trust. We serve millions of patients through a growing network supported by advanced laboratory infrastructure, technology and a patient-first approach. Our comprehensive portfolio includes 4,500+ tests and profiles across routine, specialised and super-specialised diagnostics, spanning pathology, molecular diagnostics, genomics, cytogenetics, oncology, neurology, nephrology, women and child health, preventive healthcare and wellness.

With 210+ clinical laboratories and a service network of 5,000+ touchpoints reaching more than 750 towns in India, we are focused on making trusted diagnostic services more accessible while maintaining rigorous quality standards. By combining scientific excellence, advanced technology and human expertise, we deliver accurate, reliable and relevant diagnostic insights that support better-informed healthcare decisions.

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