Fetal Medicine

Fetal Medicine at Shubham Hospitals

Shubham Hospitals is excited to soon launch a dedicated Fetal Medicine Centre, focusing on the early detection, monitoring, and treatment of fetal conditions. Our new unit will bring the latest in advanced prenatal care to expecting parents, offering precise diagnostics and personalized care to ensure the healthiest outcomes for both mother and baby.

We are committed to providing comprehensive fetal care services that address every aspect of prenatal health, from early screenings to targeted treatments for fetal conditions.

Services

Detailed Anomaly Scans

Anomaly scans are an essential part of prenatal care, typically performed between 18-22 weeks of pregnancy. These detailed scans provide a comprehensive look at the baby’s development, checking for physical abnormalities in organs and structures such as the heart, brain, spine, and kidneys. Early detection of fetal anomalies helps guide medical interventions and provides critical information for parents.

First-Trimester Screening (NT, Double Marker, NIPT Guidance)

The first-trimester screening is crucial for assessing the risk of chromosomal abnormalities, including Down syndrome and Trisomy 18. Our center will offer NT (Nuchal Translucency) scans, double marker tests, and guidance on NIPT (Non-Invasive Prenatal Testing). These screenings provide valuable early insight into the pregnancy and help identify those at higher risk for genetic conditions, allowing for timely follow-up and intervention.

Targeted Doppler Studies

Doppler studies are a non-invasive technique used to assess blood flow in the umbilical cord, placenta, and fetal vessels. This is particularly useful for monitoring pregnancies at high risk or those with concerns about fetal growth. Targeted Doppler studies can detect potential problems, such as insufficient blood supply or fetal growth restriction, allowing for early intervention to ensure the baby’s well-being.

Invasive Diagnostic Procedures (CVS, Amniocentesis)

In certain cases, invasive diagnostic procedures such as Chorionic Villus Sampling (CVS) and amniocentesis may be recommended. These procedures provide genetic testing and are used to detect chromosomal abnormalities or genetic disorders in the fetus. Our experienced team ensures these procedures are performed safely, with the utmost care to minimize risk to both mother and baby.

Fetal Echocardiography

Fetal echocardiography is a specialized ultrasound technique used to evaluate the baby’s heart and detect potential congenital heart defects. It is typically performed if there is a family history of heart conditions, abnormal routine scans, or any signs of fetal heart issues. Early detection allows for timely interventions, which can significantly improve outcomes for babies with congenital heart conditions.

Fetal Therapy & Counseling

Our Fetal Medicine Centre will also provide fetal therapy and counseling to support parents facing complex prenatal diagnoses. This service will include expert guidance on managing fetal conditions and navigating treatment options, including in-utero therapies and early delivery plans if necessary. We aim to provide compassionate care and support throughout your journey, ensuring informed decision-making for the best possible outcome.

Benefits of Fetal Medicine

Early Detection: With advanced screening and diagnostic tools, we detect fetal conditions early, allowing for timely interventions and improved outcomes.
Comprehensive Care: From detailed anomaly scans to fetal therapy, our services cover every aspect of fetal health, ensuring your baby’s well-being at every stage of pregnancy.
Specialized Expertise: Our center will be staffed by experienced specialists in fetal medicine, providing personalized care tailored to your unique needs.
Advanced Technology: We use the latest in prenatal diagnostic tools and fetal monitoring technology to provide the most accurate results and care.
Emotional and Psychological Support: We understand the emotional toll of facing complex prenatal conditions. Our team offers supportive counseling to help parents make informed decisions and prepare for the journey ahead.

FAQ's

What is an anomaly scan, and why is it important?

An anomaly scan is an ultrasound performed between 18 and 22 weeks to check for any physical abnormalities in the fetus. It evaluates the development of vital organs such as the brain, heart, and kidneys. Early detection allows for timely medical intervention if any abnormalities are found.

When should I get the first-trimester screening?

The first-trimester screening is typically done between 11 and 14 weeks of pregnancy. It includes the NT scan, double marker test, and guidance on NIPT. This screening helps assess the risk of chromosomal abnormalities like Down syndrome.

What is the purpose of targeted Doppler studies?

Targeted Doppler studies assess the blood flow to the baby through the placenta, umbilical cord, and fetal vessels. They are used to monitor pregnancies at high risk or those with concerns about fetal growth or placental function.

Are invasive diagnostic procedures safe?

Invasive diagnostic procedures like CVS and amniocentesis carry some risks but are generally very safe when performed by experienced specialists. These tests provide definitive results on genetic disorders and are used when there is a higher risk of chromosomal abnormalities.

What is fetal echocardiography, and when is it needed?

Fetal echocardiography is a specialized ultrasound used to evaluate the baby’s heart and detect congenital heart defects. It is typically recommended if there is a family history of heart conditions or if there are concerns raised during routine scans.

What kind of counseling is available for complex prenatal conditions?

Our team provides fetal counseling for parents dealing with complex diagnoses. This includes discussing treatment options, in-utero therapies, and delivery plans. We are committed to offering emotional support and guidance to help parents make informed decisions.