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Expert Amniocentesis at Sattva The Fetal Medicine Centre

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Amniocentesis Care at Sattva The Fetal Medicine Centre

Amniocentesis

Expert Amniocentesis at Sattva The Fetal Medicine Centre

Amniocentesis is a highly accurate prenatal diagnostic procedure used to identify chromosomal abnormalities, genetic disorders, and certain fetal conditions during pregnancy. It involves collecting a small sample of amniotic fluid under continuous ultrasound guidance for laboratory analysis. At Sattva The Fetal Medicine Centre, our experienced fetal medicine specialists perform amniocentesis using advanced technology and internationally accepted safety protocols, ensuring the highest level of care for both mother and baby.

What is Amniocentesis?

Amniocentesis is a diagnostic test usually performed between 15 and 20 weeks of pregnancy. The amniotic fluid surrounding the baby contains fetal cells that can be analysed to detect chromosomal conditions such as Down syndrome, inherited genetic disorders, and certain neural tube defects. The procedure provides highly reliable diagnostic information that helps parents and healthcare providers make informed pregnancy management decisions.

Advanced Prenatal Diagnosis

When is Amniocentesis Recommended?

Amniocentesis is recommended when there is an increased risk of genetic or chromosomal abnormalities during pregnancy. It provides accurate diagnostic information that helps parents and healthcare providers make informed decisions about pregnancy management and fetal care.

01

Abnormal Prenatal Screening Results

Abnormal first trimester screening results.
Abnormal second trimester screening results.
Positive non-invasive prenatal testing (NIPT) requiring confirmation.
02

Increased Risk of Genetic Disorders

Increased risk of chromosomal abnormalities due to advanced maternal age.
Family history of inherited genetic disorders.
Previous pregnancy affected by a genetic or chromosomal condition.
03

Further Evaluation of Fetal Health

Suspicious findings detected during the anomaly scan.
Suspected fetal infection or other specific fetal conditions.
Helps confirm the diagnosis and guides appropriate pregnancy management.

Frequently Asked Questions

Find answers to common questions about Amniocentesis, its purpose, safety, procedure, results, and recovery at Sattva The Fetal Medicine Centre.

Amniocentesis is a prenatal diagnostic procedure in which a small sample of amniotic fluid is collected from around the baby using ultrasound guidance. The sample is tested to detect chromosomal abnormalities, genetic disorders, and certain birth defects.

Amniocentesis is generally recommended between 15 and 20 weeks of pregnancy if screening tests indicate a higher risk of genetic conditions, ultrasound findings are abnormal, there is a family history of inherited disorders, or the mother is at an increased risk of chromosomal abnormalities.

Yes. When performed by experienced fetal medicine specialists under continuous ultrasound guidance, amniocentesis is considered a safe procedure. Although there is a small risk of complications, every precaution is taken to ensure the safety of both the mother and the baby.

The procedure itself usually takes only a few minutes. Depending on the type of laboratory tests performed, results are generally available within 7 to 14 days, while some rapid genetic tests may provide preliminary results sooner.

No. Amniocentesis is usually performed as an outpatient procedure, allowing you to return home the same day. Your doctor may recommend avoiding strenuous activities for 24 to 48 hours after the procedure and will provide detailed aftercare instructions.