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Antenatal care, or prenatal care, is the regular medical and nursing care recommended for women during pregnancy. It includes a series of check-ups and tests to monitor the health of the mother and the developing foetus, as well as counselling and education about pregnancy and childbirth.
Antenatal care aims to identify and treat potential problems early on, ensuring a healthy pregnancy and delivery.
Antenatal care is important because it:
During pregnancy, a woman can expect to experience a wide range of physical and emotional changes as her body adjusts to the growing foetus.
Some of the most common changes that women experience during pregnancy include:
Every pregnancy is different, and not all women will experience all of these symptoms. It is also essential to have regular antenatal check-ups with a doctor to ensure that both mother and the baby are healthy throughout the pregnancy.
To have a healthy pregnancy, it is essential to:
Consult with our doctors to determine which healthy habits will most benefit you during your pregnancy.
Pregnancy can be a joyful and exciting time, but it can also come with certain complications that can be dangerous for both the mother and the baby. Some possible pregnancy complications include:
Most pregnancies proceed without complications. It is crucial to have regular antenatal check-ups to detect any potential problems early on and to follow the doctor’s instructions to ensure a healthy pregnancy and delivery.
Antenatal care includes regular medical visits, screening tests, and diagnostic tests to help assess your health status and keep you and your baby healthy during pregnancy.
The routine visits to the doctor are scheduled so any problems present may be recognised and treated well in advance. These visits also educate you on handling various aspects of your pregnancy. Your doctor will discuss healthy eating, activity, screening tests necessary and what can be expected during labour and delivery.
There are several antenatal tests to assess the development of the baby in your womb. Antenatal tests are done at a stipulated time, from 8-10 weeks of gestation to 20 weeks. Before an examination, counselling will assist you in deciding the type of test based on the advantages and disadvantages of each.
Antenatal screening tests such as ultrasound and first-trimester and second-trimester screening are done to determine whether your baby is at risk of having a particular genetic condition such as Down's syndrome or other abnormalities. You should have antenatal screening done mainly if you have the following conditions:
However, it is always better to have antenatal screening tests done, irrespective of age or family history.
The first-trimester screening is done between 11 and 14 weeks of gestation, including blood tests and an ultrasound examination. It is done to detect the risk of abnormalities such as Down's syndrome and trisomy 18.
The blood tests determine the level of pregnancy-associated plasma protein-A and human chorionic gonadotropin in your blood.
The nuchal translucency screening test, ultrasound examination, measures the thickness of the back of the foetal neck. Ample space or increased space indicates Down's syndrome, trisomy 18 or other chromosomal abnormalities.
If first-trimester screening tests are positive, your doctor may suggest a more detailed examination at around 20 weeks of pregnancy.
During this period, multiple marker screening is done to screen for Down's syndrome, trisomy 18 and neural tube defects. The test measures the concentration of alpha-fetoprotein and hormones estriol, human chorionic gonadotropin, and inhibin-A in the mother's blood. These tests are done between 15 and 20 weeks of gestation.
The combined reports of the first and second trimesters may yield more helpful information about diagnosing Down syndrome.
Suppose the screening tests indicate a problem in the baby. Further diagnostic tests such as detailed ultrasound, amniocentesis, chorionic villus sampling and cordocentesis may be done to check whether the baby has a defect.
After the screening, genetic counselling will support you with other decisions if your baby is found to have an increased risk for developing a chromosomal abnormality or if a problem is detected with diagnostic testing. Genetic counselling provides you with the chance to discuss the following issues:
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