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  • MyDiagnostics Non Invasive Prenatal Screening Test - NIPT/NIPS - At Home
MyDiagnostics (NABL, CAP, ISO Lab)

Non-Invasive Prenatal Screening NIPS/NIPT Test - At Home

Rs. 21,000

Rs. 12,500

(0% Discount)

NIPT Screening (Singleton)
  • Trisomy 21 (Down Syndrome) 
  • Trisomy 18 (Edwards Syndrome) 
  • Trisomy 13 (Patau Syndrome)
  • Turner Syndrome (Monosomy X/XO)
  • Klinefelter Syndrome (XXY)
  • Triple X (XXX)
  • Jacob's Syndrome (XYY)

Sample Requried: Blood collected in Streak Tube - 10 ml.
Test Mode: At Home
Turn Around Time: 15 Days
Fasting Time: None
Other Instructions: We require Prescription, Ultra Sound report (USG), Dual and Quadruple Marker Report, Photo Identification Proof
Recommended for: At gestational age : 11 to 17 weeks.

 

About the Non Invasive Prenatal Screening Test - NIPT/NIPS

Non-invasive prenatal testing (NIPT) is a screening test that is used to assess the risk of certain chromosomal abnormalities in a developing fetus. NIPT is typically performed during the first or second trimester of pregnancy / gestational age 11 to 17 weeks, and is used to screen for conditions such as Down syndrome (trisomy 21), trisomy 13, and trisomy 18.

NIPT is a blood test that analyzes fetal DNA that is present in the mother's bloodstream. The test is considered to be non-invasive because it does not involve any risk to the fetus and does not require a procedure such as amniocentesis (a procedure in which a sample of amniotic fluid is taken for testing).

NIPT can provide valuable information about the risk of certain chromosomal abnormalities in a developing fetus. If the NIPT results indicate an increased risk of a chromosomal abnormality, the healthcare provider may recommend further testing to confirm the diagnosis.

NIPT test is offered in three variants - 

  • NIPT Basic
  • NIPT Advance 
  • NIPT Basic Twin

 NIPT does not test for the gender of the fetus

Whats the difference between NIPT Basic v/s NIPT Advanced

Basic screens for 5 Chromosomes

Advanced screens for 22 Chromosomes 

 

Pls ask for Sample report to confirm your requirements. 

Accuracy and Results of NIPT Test 

The accuracy of NIPT depends on several factors, including the stage of pregnancy, the specific condition being tested for, and the specific NIPT test being used.

Overall, NIPT has a high sensitivity (the ability to correctly identify individuals with the condition being tested for) and a high negative predictive value (the ability to correctly identify individuals without the condition). This means that NIPT is very good at identifying women who are at low risk of having a baby with a chromosomal abnormality.

There are several different NIPT tests available, and the specific test used will determine the results of the test. In general, NIPT results are reported as low risk or high risk for a specific chromosomal abnormality.

If the NIPT results indicate a low risk for a chromosomal abnormality, it means that the risk of the baby having the condition is very low. If the NIPT results indicate a high risk for a chromosomal abnormality, it means that the risk of the baby having the condition is higher than average

While not all tests are 100% accurate, the NIPT test will be able to provide critical insights on your pre-screening risk. You can get further testing done to determine whether your foetus is testing positive for a specific condition.


How is NIPT test performed   

The NIPT test is performed at a National Accreditation Board for Testing and Calibration Laboratories (NABL) certified laboratory. The sample collection is done at your residence, making it a highly convenient way of screening.

The blood sample is collected in a streak tube, about 10 ml, and your sample is then sent for quality testing and analysis. The technician will require basic details, such as Ultra Sound report (USG), Dual and Quadruple Marker Report, Photo Identification Proof, etc.    

Is NIPT recommended for all pregnant women?

NIPT is not recommended for all pregnant women, but it may be offered to women who are at increased risk of having a baby with a chromosomal abnormality due to their age or other risk factors. It is important to discuss the benefits and limitations of NIPT with a healthcare provider to determine if the test is right for you

 

  • The woman is above 30 years of age.
  • A high risk for abnormality is found through serum screening.
  • Certain abnormalities on ultrasound are identified.
  • There is a family history of chromosomal conditions or birth defects.
  • Couples have had a child with a chromosomal disorder.
  • A couple has a history of infertility or pregnancy loss (miscarriages or stillbirths)

 

 

About the Quality

Quality assurance is done at 3 levels 

  • Sample collection from home using one time sealed QR coded sterile kits and transportation to the lab including the temperature condition requirements 
  • Sample acceptance and QC at the lab 
  • Sample run at the NABL/CAP/ISO certified labs - Medgenome 

What is NIPT test?

NIPT or non-invasive prenatal screening is a comprehensive prenatal testing solution that is designed for screening of chromosomal abnormalities. The NIPT blood test checks for abnormalities in a developing foetus, and analyses fragments of foetal DNA in the mother's blood. You can check the risk factor for Down syndrome, trisomy 18, and trisomy 13, among other conditions, in a complete NIPT test in pregnancy health screening.

How accurate is the NIPT test for Down syndrome?

The accuracy level of an NIPT test is quite high, nearly 99% according to some estimates by researchers et al. The test analyses cell free DNA (cfDNA) from the placenta to measure the risk factor for the development of a range of chromosomal abnormalities by testing maternal blood. You can check for a NIPT test results example and understand what parameters are measured with the screening test.

However, it is important to keep in mind that NIPT is not a diagnostic test and a positive result on an NIPT test should be confirmed with a diagnostic test, such as chorionic villus sampling (CVS) or amniocentesis.

Is the NIPT test done in India?

Yes, you can order an NIPT test in India through our platform. You can also get the best NIPT test cost when you buy from MyDiagnostics directly. The NIPT testing cost is optimized for at home sample collection and ease of testing convenience.

You can also check for all the parameters within the NIPT test if you are looking for a specific type of check-up pre-screening. You can search for the correct genetic conditions screenings that you are seeking, and ensure that they are covered within the package.

How do I prepare for the NIPT test?

There are no special requirements for the NIPT test, and you need to follow all the instructions of the technician. Key information and documents will be required during the sample collection stage.

When is the NIPT test done?

The NIPT test pregnancy screening can be performed between the 10 to 14 weeks of pregnancy period. You can get the best NIPT blood test cost with MyDiagnostics. The NIPT test in India can be performed with ease when you opt for an at-home sample collection. The NIPS test or NIPT test results can be delivered directly via email.

What if NIPT test is positive?

If the results of an NIPT test are positive, it means that there is an increased risk of a specific chromosomal abnormality, such as Down syndrome, trisomy 18, or trisomy 13. However, it is important to keep in mind that NIPT is a screening test and not a diagnostic test, and a positive result does not necessarily mean that the fetus has the condition.

In the event of a positive result, a diagnostic test, such as chorionic villus sampling (CVS) or amniocentesis, is typically recommended to confirm the diagnosis. These tests can provide more accurate information and a definitive diagnosis. The genetic testing pregnancy screening package can be the best prenatal testing solution for all mothers.

Which week is best for NIPT test?

The NIPT test in India or chromosome test pregnancy screening package is ideal for mothers between 10 and 14 weeks of pregnancy. The NIPT blood test cost is also optimized when you procure the package from MyDiagnostics. You can get the best NIPS price when you opt for an at-home solution.

Is NIPT test necessary in pregnancy?

The decision to have an NIPT test during pregnancy is a personal one and depends on several factors, including the individual's medical history, family history, and personal preferences.

NIPT is a screening test, not a diagnostic test, and is used to assess the risk of certain chromosomal abnormalities in a developing fetus. While it can detect conditions such as Down syndrome, trisomy 18, and trisomy 13 with a high degree of accuracy, it is not required for all pregnancies.

For some women, the results of Non invasive prenatal testing can provide important information and peace of mind, while others may prefer not to have the test or to wait for a diagnostic test such as chorionic villus sampling (CVS) or amniocentesis if the results of NIPT are positive. The choice to have an NIPT test should be made in consultation with a healthcare provider, who can provide information on the benefits and limitations of the test and help the individual make an informed decision. 

What is the cost of NIPT test in India?

The noninvasive prenatal testing NIPT solution ranges from INR 12500 to 17500 based on the type of test opted for. The report for NIPT testing is generated within 15 days, giving you complete insights on your NIPL test result.

The NIPT test cost is also optimized for at home sample collection, and complete screening for a range of conditions. The NIPT test cost in India is also inclusive of critical screening parameters required for all expecting mothers.

Can we know the gender in an NIPT test?

The NIPT test is not designed to test for gender.

Does NIPT detect autism?

The NIPT test doesn't detect autism in foetuses. The NIPT test in India is designed to detect specific chromosome abnormalities, which are predefined within the testing package. You can get the best NIPT test price when you buy from MyDiagnostics.

Can NIPT detect birth defects?

The NIPT test is not designed for checking of birth defects, however if a birth defect is suspected further testing may be recommended. This may involve testing for genetic conditions, such as Down syndrome, Trisomy, etc.

Some non invasive prenatal tests may be done for conditions that may be related to some birth defects. In this case your healthcare specialist will be able to provide the right next steps for further action.

How do you read a NIPT test report?

There are multiple insights present in the NIPT test report, which is why knowing how to read them properly will be important. You can focus on the overall test results, which will contain details of the presence or absence of the abnormalities tested.

Your risk factor for Down syndrome, trisomy 18, trisomy 13, etc. will be mentioned within the report along with a risk assessment number. This value will be indicative of the risk of having that specific condition. For the conditions with a higher number, you should get further testing performed.

There will also be a confidence interval mentioned, which is a statistical metric to represent uncertainty. There may be significantly larger uncertainty for some tests, along with limitations mentioned of the NIPT test as a whole.

You will also be provided recommendations for next steps along with what actions you can take. This should help in making the report more focused on what you can do with the information from the test.

How do I buy an NIPT test in India?

You can get an NIPT test in India performed in an NABL certified laboratory when you purchase the test from MyDiagnostics. You can buy NIPT test at the best price when you add to cart through MyDiagnostics. The sample collection of the NIPT blood test is performed at home so that you don't have to travel to a clinic to get a check-up done.

The NIPT test is a comprehensive pregnancy screening examination designed to check for potential risk factors of chromosomal abnormalities and conditions. The test is vital for all women to determiner whether their foetus is at risk of developing these genetic conditions.

  • The test is ideal for women who are pregnant and are within 11 - 17 weeks.
  • The test is also ideal for anyone pregnant while managing a chronic condition such as kidney disease or diabetes.
  • You should get the test if you have a family history of genetic or chromosomal conditions.
  • You need to provide a blood sample to the technician in a 10ml collection tube.
  • You need to provide details on prescriptions, ultrasound, dual and quadruple marker report, etc.
  • No special preparations are required for the test.