Prenatal Screening & Diagnosis

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Established in 1985, Parvathi Hospital has earned a reputation for providing high-quality, safe, and affordable healthcare.

We offer a comprehensive range of services, from routine checkups to diagnosis and treatment for a full spectrum of women’s and children’s health concerns.Our team of experienced doctors and healthcare professionals are dedicated to providing world-class care.We understand that each patient is unique. We work with you to develop a personalized treatment plan tailored to your specific needs.We continuously update our technology to deliver the latest and most effective treatments. Our passion for patient care has driven us to perform over 30,000 successful deliveries.

Parvathi Hospital is your trusted partner in healthcare, ensuring a healthy and comfortable journey for women and children.

Prenatal Screening & Diagnosis: Gaining Peace of Mind During Pregnancy

Pregnancy is a time of immense joy and anticipation. However, it’s natural to have concerns about your baby’s health. Prenatal screening and diagnosis tests offered at Parvathi Hospital can provide valuable information and peace of mind throughout your pregnancy journey.

What is Prenatal Screening & Diagnosis?

Prenatal screening and diagnosis are two distinct approaches to assessing fetal health.

Prenatal Screening: These tests are non-invasive or minimally invasive procedures that estimate the chance of your baby having certain birth defects, such as Down syndrome or trisomy 18. Screening tests cannot provide a definitive diagnosis, but they can indicate a need for further testing.
Prenatal Diagnosis: Diagnostic tests are more definitive and can confirm the presence or absence of a specific condition. These tests are typically performed when screening tests indicate an increased risk. While some diagnostic tests are minimally invasive, others may be more involved and require specialized training.

Types of Prenatal Screening & Diagnosis at Parvathi Hospital

Parvathi Hospital offers a comprehensive range of prenatal screening and diagnostic tests, including:

First-Trimester Screening

This combination of blood tests and an ultrasound nuchal translucency scan can assess the risk of Down syndrome and Edwards syndrome.

Second-Trimester Screening

This blood test, also known as the quad screen, measures the levels of certain substances in your blood to estimate the risk of chromosomal abnormalities.

Cell-Free DNA Screening (NIPT)

This advanced blood test analyzes fetal DNA fragments present in your bloodstream to assess the risk of chromosomal abnormalities.

Amniocentesis

A sample of amniotic fluid surrounding the baby is withdrawn for chromosomal analysis.

Chorionic Villus Sampling (CVS)

A small sample of placental tissue is collected for chromosomal analysis.

We Tailor Our Approach to Your Needs

Our team of experienced healthcare professionals will work closely with you to determine the most appropriate screening or diagnostic tests based on your individual risk factors, medical history, and pregnancy preferences. We understand the importance of clear communication and will explain each test option thoroughly, addressing any questions or concerns you may have.

Our Doctors

Meet Our Specialist

Dr. Priyadharshika

Obstetrician & Gynaecology

DR. SWATHI APSANI

Gynecology, Laparoscopic Surgeon & Infertility Specialist

Dr. Malleboyina Salomi

Fetel Medicine, Obstetrician & Gynaecology

Dr. Rajani Peethala

Fetel Medicine, Obstetrician & Gynaecology

Dr. Prasanna Gonuguntla

Obstetrics & Gynaecology

FAQ's

01. What are the benefits of prenatal screening and diagnosis?

Early detection of potential birth defects allows for informed decision-making regarding your pregnancy and helps prepare for the baby's needs. It can also alleviate anxiety and provide peace of mind for expectant parents.

02. Are prenatal screening and diagnosis tests compulsory?

No, these tests are entirely voluntary. We will discuss the pros and cons of each option and respect your decision.

03. What if a screening test indicates an increased risk?

This doesn't necessarily mean your baby has a birth defect. It simply suggests the need for further testing, such as amniocentesis or CVS, to confirm the diagnosis. Our team will guide you through every step of the process.

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