Amniocentesis
When is Amniocentesis Recommended?
Amniocentesis is generally recommended in the following situations:
- Advanced Maternal Age: Women aged 35 or older have a higher risk of having a baby with chromosomal abnormalities. Amniocentesis is often suggested to assess the fetal chromosomes in such cases.
- Abnormal Screening Test Results: Abnormal results from non-invasive prenatal screening tests, such as the first-trimester screening or NIPT (cell free DNA), may warrant further diagnostic confirmation through amniocentesis.
- Previous Child with Genetic Disorders: If a previous child has been diagnosed with a chromosomal abnormality or a genetic disorder, amniocentesis may be recommended for subsequent pregnancies.
- Family History of Genetic Conditions: If there is a known family history of specific genetic conditions, amniocentesis can provide detailed genetic information to assess the risk to the current pregnancy.
- Abnormal Ultrasound Findings: Certain ultrasound findings, such as structural abnormalities or growth concerns in the fetus, may prompt the recommendation for amniocentesis.
Information Obtained from Amniocentesis
The primary objective of amniocentesis is to obtain a sample of amniotic fluid, which surrounds the fetus in the womb. This fluid contains fetal cells that can be analyzed to provide the following information:
- Chromosomal Abnormalities: Amniocentesis is highly effective in detecting chromosomal abnormalities, including Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).
- Diagnosing Genetic Disorders running in the Family: Genetic testing during amniocentesis can identify specific genetic disorders if they are known to be present in the family.
- Neural Tube Defects: Though less common, amniocentesis can provide information about neural tube defects, such as spina bifida, by measuring the levels of certain markers in the amniotic fluid.
Cradle Fertility's Approach to Amniocentesis
At Cradle Fertility, we understand the significance of amniocentesis in providing expectant parents with crucial information about the health of their yet-to-be born child. Our approach to amniocentesis is characterized by:
- Expertise and Precision: Our team of experienced fetal medicine Specialist is well-versed in performing amniocentesis with precision, minimizing any potential risks and ensuring accurate results.
- Comprehensive Genetic Counselling: Before the procedure, our expert genetic counsellors and fetal medicine specialist provide comprehensive counseling to guide parents through the decision-making process and explaining the benefits and potential risks associated with amniocentesis.
- State-of-the-Art Technology: Cradle Fertility is equipped with state-of-the-art technology to conduct amniocentesis with the highest level of accuracy, ensuring reliable results.
- Compassionate Care: We prioritize compassionate care, recognizing the emotional aspects of prenatal testing. Our team is dedicated to providing support and addressing any concerns throughout the entire process.
At Cradle Fertility, we approach amniocentesis with a commitment to excellence, ensuring the highest standard of care for expectant parents. With a commitment to excellence and a focus on comprehensive care, Cradle Fertility stands as a trusted partner in navigating the complexities of prenatal testing, ensuring each family receives the best care and support on their path to a healthy and thriving pregnancy.