Maternal Fetal Medicine

The Maternal Fetal Medicine (MFM) Service is a special part of obstetrics. It focuses on high-risk pregnancies and complex fetal conditions. Our expert team includes specialists in maternal-fetal medicine, fetal sonographers, genetic counselors, and neonatologists. We provide advanced care to ensure the best outcomes for both mother and baby.

We offer a comprehensive, multidisciplinary approach, working closely with referring obstetricians, pediatric specialists, and neonatal intensive care teams to deliver personalized, evidence-based care.

Our Expertise & Services

1. High-Risk Pregnancy Management

We specialize in managing pregnancies complicated by:

• Maternal medical conditions (e.g., diabetes, hypertension, autoimmune disorders, thyroid disease, obesity).
• Prior pregnancy complications (e.g., preterm birth, preeclampsia, recurrent pregnancy loss).
• Fetal growth abnormalities (IUGR, macrosomia).
• Placental disorders (placenta previa, accreta, abruption).
• Fetal genetic or structural anomalies.

Our team develops individualized care plans, including close monitoring, medical management, and delivery planning to optimize safety for both mother and baby.

2. Advanced Fetal Ultrasound & Imaging

We provide state-of-the-art diagnostic imaging, including:

• Detailed Fetal Anatomy Scans (Level II ultrasound) provide a complete check of fetal growth. This includes the brain, heart, spine, limbs, and organs.
• Fetal Echocardiography – Specialized imaging to diagnose congenital heart defects before birth, allowing for early intervention planning with pediatric cardiologists.
• Doppler Ultrasound – Assesses blood flow in the umbilical cord, fetal brain, and maternal uterine arteries to detect complications like placental insufficiency, fetal anemia, or growth restriction.

3. Twin & Multiple Pregnancy Care

Multiple pregnancies (twins, triplets) require specialized monitoring due to higher risks of complications such as:

• Twin-to-Twin Transfusion Syndrome (TTTS) – Managed with laser surgery or amnioreduction.
• Selective Intrauterine Growth Restriction (sIUGR) – Close tracking to optimize outcomes.
• Preterm labor prevention strategies.

We provide serial ultrasounds, Doppler studies, and coordinated care with neonatology teams to ensure the best possible outcomes for both babies.

4. Prenatal Diagnostic & Genetic Testing

For families at risk of genetic conditions or fetal anomalies, we offer:

• Chorionic Villus Sampling (CVS) – Performed between 10–13 weeks, this test analyzes placental tissue for chromosomal abnormalities (e.g., Down syndrome) or genetic disorders.
• Amniocentesis – Conducted after 15 weeks, this procedure tests amniotic fluid for genetic conditions, infections, or lung maturity in high-risk cases.
• Non-Invasive Prenatal Testing (NIPT) – A blood-based screening for chromosomal conditions with high accuracy.

Our genetic counselors provide pre- and post-test counseling, helping families understand results and make informed decisions.

5. Pregnancy Screening & Risk Assessment

• Preeclampsia Screening – Early first-trimester risk assessment (blood pressure, uterine artery Doppler, biomarkers) to identify high-risk women who may benefit from low-dose aspirin or closer monitoring.
• Fetal Anomaly Screening – Integrated first- and second-trimester screenings (including nuchal translucency, quad screen, and detailed anatomy scans) to detect structural or chromosomal abnormalities.
• Preterm Birth Risk Assessment – Cervical length monitoring and progesterone therapy for women at risk of early delivery.

Why Choose PRIME Hospital for Maternal-Fetal Medicine?

At PRIME Hospital, we combine world-class expertise, cutting-edge technology, and compassionate care to guide you through high-risk pregnancies with confidence. Here’s what sets us apart: