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Best TIFFA Scan Center In Hyderabad
A Triple Integrated Fetal Follicle Assessment TIFFA scan Center In Hyderabad – is an essential Prenatal screening test that is carried out between 18 and 23 weeks of gestation.
Beyond a basic visual assessment, this painless ultrasound test offers important clues about the health of your developing baby.
Trulife Diagnostics is steadfastly committed to empowering expectant mothers with the knowledge and support they need to make informed choices about their pregnancy journey.
We strive to create a positive and reassuring environment where all your questions and anxieties are addressed. Contact Trulife Diagnostics today to schedule your TIFFA scan and experience our unwavering dedication to exceptional patient care and cutting-edge technology.
Here’s a closer look at the components of a TIFFA scan:
- Nuchal Translucency (NT): During this process, the sonographer meticulously measures the fluid collection at the back of the baby’s neck. An increased nuchal translucency can be an indicator of a potential risk for chromosomal abnormalities.
- Maternal Serum AFP (Alpha-Fetoprotein): A separate blood test measures the levels of alpha-fetoprotein, a protein produced by the fetus. Abnormal AFP levels can suggest neural tube defects or other developmental concerns.
- Free b-HCG (Beta-human chorionic gonadotropin): This hormone is produced by the placenta. Fluctuations in its levels can also be a factor in calculating potential risks.
By meticulously combining these measurements, a comprehensive picture of fetal health emerges.
Armed with this information, doctors can assess the likelihood of chromosomal abnormalities like Down syndrome, Edwards syndrome, and Patau syndrome.
This knowledge empowers you, as parents, to make informed decisions regarding further prenatal testing, such as amniocentesis or chorionic villus sampling, and create a personalized pregnancy management plan tailored to your specific needs.
When Do We Need TIFFA Scan ?
A TIFFA scan can be useful in a number of scenarios even though it is not a diagnostic test:
- Identifying Potential Chromosomal Abnormalities: The combined information from the TIFFA scan can help assess the likelihood of chromosomal abnormalities like Down syndrome, Edwards syndrome, and Patau syndrome.
- Making Informed Decisions: Armed with the results of the TIFFA scan, along with your doctor’s guidance, you can make informed decisions regarding further prenatal testing, if necessary.
- Creating a Personalized Pregnancy Plan: The information gleaned from a TIFFA scan can be factored into your doctor’s approach to managing your pregnancy, potentially leading to a more personalized plan.
Pregnancy is an emotional roller coaster that includes excitement, expectation, and a healthy dose of worry for the health of your unborn child.
During this time, Trulife Diagnostics in Hyderabad may provide you with an invaluable tool a TIFFA scan, which can provide you vital information about your baby’s growth.
TIFFA Scan – What Is It?
Triple Integrated Fetal Follicle Assessment is referred to as TIFFA. It’s a screening test for pregnancies that’s usually done between 18 and 23 weeks.
This non-invasive ultrasound examination combines three essential metrics to provide a more complete picture of fetal health than a mere visual assessment alone.
The measurement of the fluid accumulation at the back of the baby’s neck is called nuchal translucency (NT). Elevated nuchal translucency may serve as a sign of possible problems related to the chromosomes.
Maternal Serum AFP (Alpha-Fetoprotein): The amounts of this fetus-produced protein are measured by a different blood test.
Anomalies related to the AFP level may indicate neural tube abnormalities or other developmental issues.
Free b-HCG: The placenta is the organ that produces beta-human chorionic gonadotropin.
Variations in its concentrations may also be taken into account when estimating possible hazards.
Is There Any Alternative Of TIFFA Scan?
Here are a few options to consider, that are alternative of prenatal screening tests available besides TIFFA scans.
Combined First-Trimester Screening (CFTS): This screening combines a nuchal translucency scan (similar to the one in a TIFFA) with a blood test to assess the risk of Down syndrome and Edwards syndrome.
It’s typically performed between 11 and 14 weeks of pregnancy.
Cell-Free Fetal DNA (cfDNA) Testing: This non-invasive prenatal test (NIPT) analyzes fetal DNA circulating in your blood to assess the risk of chromosomal abnormalities like Down syndrome, Edwards syndrome, Patau syndrome, and sex chromosome aneuploidies. While more expensive than a TIFFA scan, cfDNA testing offers a higher detection rate.
Amniocentesis or Chorionic Villus Sampling (CVS): These are Diagnostic tests that involve collecting a small sample of fetal cells for chromosomal analysis.
They are more invasive than TIFFA scans or cfDNA testing but offer a definitive diagnosis of chromosomal abnormalities.
