These interventions, such as amniocentesis, fetal blood transfusions, or fetal reduction, are typically guided by high-resolution ultrasound to ensure precision and safety. They play a crucial role in managing high-risk pregnancies, improving outcomes, and offering timely solutions to complex fetal conditions, often giving babies a better chance at healthy development and delivery.
A prenatal test where a small amount of amniotic fluid is sampled from the womb.
Used to diagnose genetic conditions, infections, and fetal lung maturity.
Typically performed between 15-20 weeks of pregnancy under ultrasound guidance.
Involves taking a small tissue sample from the placenta to test for genetic disorders.
Can be done earlier than amniocentesis, usually between 10-13 weeks of pregnancy.
Provides rapid diagnosis for chromosomal abnormalities and inherited conditions.
A procedure to reduce the number of fetuses in a multiple pregnancy.
Performed to lower risks associated with high-order multiples, improving outcomes for remaining fetuses.
Carried out carefully under ultrasound guidance, typically in the first trimester.
A diagnostic test where fetal blood is taken directly from the umbilical cord.
Used to detect blood disorders, infections, or to perform genetic tests.
Usually performed after 18 weeks of gestation with ultrasound guidance.
A procedure to transfuse blood to the fetus in cases of severe anemia or blood disorders.
Helps treat fetal conditions like Rh disease before birth to improve survival.
Carried out through the umbilical vein under continuous ultrasound monitoring.
The removal of excess amniotic fluid in cases of polyhydramnios (too much fluid).
Relieves maternal discomfort and reduces risks like preterm labor.
Performed using a needle under ultrasound guidance to safely drain fluid.
