What Are Invasive Diagnostic Procedures?

Invasive diagnostic procedures are specialized prenatal tests that help detect genetic or chromosomal conditions in the developing baby. These tests involve collecting samples directly from the womb, such as amniotic fluid or placental tissue. They are performed when screening results show higher risk or when there’s a family history of genetic disorders.

Types of Invasive Diagnostic Procedures

The two most common procedures are Amniocentesis and Chorionic Villus Sampling (CVS).

• Amniocentesis is done after 15 weeks of pregnancy. It involves collecting a small amount of amniotic fluid to check for chromosomal or genetic abnormalities.

• Chorionic Villus Sampling (CVS) is performed earlier, between 11 and 14 weeks. It tests placental tissue to detect genetic conditions early in pregnancy.

Both methods offer valuable information to guide pregnancy care and future decisions.

Why Are These Procedures Important?

These procedures help doctors confirm if a baby has any genetic or chromosomal issues, such as Down syndrome or thalassemia. With accurate results, parents can make informed choices about treatment and care. Early diagnosis also allows specialists to plan for the safest possible delivery and newborn management.

How the Procedures Are Performed

At Isha IVF Centre in Palanpur, invasive diagnostic procedures are performed under high-resolution ultrasound guidance. The process is safe, sterile, and handled by experienced fetal medicine specialists. Local anesthesia and precise monitoring ensure maximum comfort and safety for the mother and baby.