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TRIPLE MARKER - SECOND TRIMESTER(TRIPLE MARKER SECOND TRIMESTER 14-22 WEEK)

TRIPLE MARKER – SECOND TRIMESTER(TRIPLE MARKER SECOND TRIMESTER 14-22 WEEK)

Original price was: ₹3,058.00.Current price is: ₹2,700.00.

The Triple Marker test is a second-trimester prenatal screening test performed between the 14th and 22nd week of pregnancy (ideally 15-20 weeks) to assess the risk of neural tube defects and chromosomal abnormalities, such as Down syndrome and Trisomy 18, in the fetus. It measures levels of three substances in the mother’s blood: Alpha-fetoprotein (AFP), Human chorionic gonadotropin (HCG), and Estriol (uE3). The results, combined with the mother’s age and ultrasound data, are used to calculate the risk for these conditions. A high-risk result indicates the need for further, more invasive, diagnostic tests to confirm the findings. 

What the Test Measures

The test analyzes three substances in the mother’s blood: 

Why It’s Performed
  • Risk Assessment: To determine the probability of certain genetic and developmental issues. 
  • Screening for:
    • Down Syndrome (Trisomy 21) 
    • Edward’s Syndrome (Trisomy 18) 
    • Open Neural Tube Defects 
When It’s Performed
  • Window: Between 14 and 22 weeks of pregnancy. 
  • Ideal Timing: The optimal period for a combined risk assessment is between 15 and 20 weeks. 
What to Expect
  1. Blood Sample: A blood sample is collected from the mother. 
  2. Risk Calculation: The results are combined with factors like maternal age, weight, and ethnicity to provide a risk assessment. 
  3. Further Steps:
    • Low-risk result: Provides reassurance that the baby is unlikely to have these conditions. 
    • High-risk result: Does not mean the baby has the condition but signifies the need for a more definitive test, such as an amniocentesis. 
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SKU: TRIPLE Category:

Description

Method: CLIA
Comment:
Price: 3058.00
Report: Sample Mon through Sat by 9 am; Report Same day
Usage: Triple Screen test is used for Prenatal Screening of Down Syndrome (Trisomy 21), Edward’s Syndrome (Trisomy 18) and Open Neural Tube Defects. The approximate detection rate with this test is 55–65% with a false positive rate of 5%.
Doctor Specialty: Gynecologist
Disease: Prenatal Diagnosis
Components: *AFP *Beta HCG *Free Estriol *Risk Evaluation
Courier Charges: 0.00
Home Collection: Available
Department:
Pre Test Information: Provide maternal Date of birth (dd/mm/yy); LMP or Ultrasound; IVF, Number of Fetuses (Single/ Twins); Diabetic status and Body Weight in Kg, Smoking & Previous history of Trisomy 21 pregnancy. Duly filled Maternal Serum Screen requisition form (Form 11) is mandatory. Valid between 14-22 weeks gestation (Ideal 15-20 weeks).

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