FIRST TRIMESTER SCREENING (FTS)

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FIRST TRIMESTER SCREENING (FTS)
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FIRST TRIMESTER SCREENING (FTS), in Visit Clinic

Combines two maternal blood markers and an early ultrasound to estimate risk of fetal chromosomal problems in Visit Clinic.

centreCentre Visit
SAMPLE TYPE
Blood
FASTING REQUIRED
No
GENDER
Female
GET REPORTS IN
24 hours
TEST INCLUDED
3
Customers
20K+Customers
Labs
CertifiedLabs
Rating
4.5+Rating
Accuracy
ProvenAccuracy

What is a FIRST TRIMESTER SCREENING (FTS) Test in Visit Clinic?

First trimester screening measures specific substances in the mother's blood and an early ultrasound measurement. The blood tests look at PAPP-A and free beta hCG. The ultrasound measures nuchal translucency at about 11 to 13 weeks and 6 days. These results, combined with maternal age and pregnancy dating, estimate the chance of chromosomal conditions such as Down syndrome and Trisomy 18. It gives a risk estimate, not a diagnosis. Doctors use the result to guide counseling and decide if further testing like cell-free DNA screening or diagnostic testing is needed.

FIRST TRIMESTER SCREENING (FTS) Test Preparation in Visit Clinic

No special preparation is required.

FIRST TRIMESTER SCREENING (FTS) Test Parameters in Visit Clinic

The FIRST TRIMESTER SCREENING (FTS) test evaluates various parameters. Here are the main parameters checked:

  • PAPP-A
  • free beta hCG
  • and first-trimester nuchal translucency ultrasound measurement

Why Take a FIRST TRIMESTER SCREENING (FTS) Test in Visit Clinic?

FIRST TRIMESTER SCREENING (FTS) is typically done as a combined panel of maternal blood markers and an early ultrasound. Clinicians order it for routine prenatal risk assessment, for older maternal age, or after an abnormal scan. It helps identify increased risk for chromosomal conditions such as Down syndrome and Trisomy 18. Abnormal results can arise from dating errors, multiple pregnancy, maternal factors, or true fetal problems, and a family history of chromosomal conditions makes the test especially relevant.

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Frequently asked questions

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What is a FTS test in pregnancy in Visit Clinic?plus

The FTS (first‑trimester screening) is a noninvasive assessment performed at about 11–13+6 weeks' gestation combining maternal blood tests (PAPP‑A and free beta‑hCG) with an ultrasound measurement of fetal nuchal translucency. It estimates risk for chromosomal conditions like Down syndrome (trisomy 21) and trisomy 18. It’s a screening, not diagnostic; positive results lead to diagnostic testing (CVS or amniocentesis) and counseling.

What is the FTS screening for pregnancy in Visit Clinic?plus

FTS (first‑trimester screening) is a non‑diagnostic combined test at 11–13+6 weeks that estimates the risk of chromosomal abnormalities, chiefly Down syndrome (trisomy 21) and trisomy 18. It combines nuchal translucency ultrasound measurement with maternal blood markers (free β‑hCG and PAPP‑A) and maternal factors; the result gives a risk score — abnormal or high‑risk findings may be followed by diagnostic tests (CVS or amniocentesis).

Is FTS the same as NIPT in Visit Clinic?plus

FTS (first‑trimester screening) and NIPT (non‑invasive prenatal testing) are both prenatal screening tests but are not the same. FTS combines nuchal translucency ultrasound with maternal blood markers early in pregnancy. NIPT analyzes cell‑free fetal DNA in maternal blood and is far more sensitive and specific for trisomies. Neither is diagnostic; positive results should be confirmed by CVS or amniocentesis.

What is the FTS at 12 weeks in Visit Clinic?plus

FTS at 12 weeks is the first‑trimester combined screening that assesses risk of chromosomal abnormalities. It includes a nuchal translucency ultrasound plus maternal blood tests (PAPP‑A and free β‑hCG), sometimes with nasal‑bone assessment. The result gives a risk estimate for trisomies 21, 18 and 13 but is not diagnostic; high‑risk findings prompt NIPT or invasive diagnostic testing.

What if my first trimester screen is positive in Visit Clinic?plus

A positive first‑trimester screen means elevated risk, not a diagnosis. You’ll be offered genetic counseling and further testing: non‑invasive prenatal testing (cell‑free DNA) for higher accuracy or diagnostic tests (CVS around 10–13 weeks or amniocentesis after ~15 weeks). A detailed ultrasound and discussion of options, risks, and timelines help decide next steps. Many positive screens are false positives.

How to diagnose FTS in Visit Clinic?plus

Do you mean flexor tenosynovitis (flexor tendon sheath infection), frozen shoulder (frozen tendon syndrome), or another condition abbreviated FTS? Please specify which FTS you mean and I’ll provide a 50–75 word diagnostic summary based on trusted medical sources.