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Prenatal testing, which includes screening and diagnostic tests, can provide important information about the health of the baby. Understand the risks and advantages.
Though welcoming a new life into the world can be a journey filled with joy, anticipation, and a multitude of decisions, it can also bring anxiety and stress about the health of the baby. However, the health and well-being of the baby for expecting mothers can be a paramount concern from the moment they learn of their pregnancy.
According to a study, 97 out of 100 babies are born healthy, whereas there is just about a 3 to 4 percent chance that the baby will have a birth defect. Yet it’s still important to understand options for obtaining details about a baby’s health.
Thanks to medical advancements, it has become easy to offer invaluable tools to ease anxieties and provide clarity to parents. One such advancement is noninvasive prenatal testing (NIPT), a revolutionary technology that has transformed prenatal care. In this blog, we delve into the myriad benefits that NIPT brings to expecting mothers, offering a glimpse into the peace of mind and empowerment it provides during this precious time. Join us as we explore the NIPT Test benefits, offering accurate insights and informed decisions for the healthiest start to parenthood.
Noninvasive prenatal testing (NIPT) is an advanced screening method used during pregnancy to assess the risk of certain chromosomal abnormalities, such as:
Unlike invasive procedures like amniocentesis or chorionic villus sampling (CVS), NIPT is performed using a simple blood test from the mother, analyzing cell-free fetal DNA circulating in her bloodstream. This allows for early detection of potential genetic abnormalities with minimal risk to both the mother and the fetus, offering expectant parents valuable information for informed decision-making regarding their pregnancy.
Prenatal testing is a personal decision influenced by various factors, including medical history, age, and personal beliefs. While these tests can provide valuable information about the health of the fetus, they also carry risks, such as false positives and the potential for unnecessary stress or interventions. Couples with a family history of genetic disorders may find prenatal testing essential for informed decision-making about the pregnancy. However, others may opt out due to concerns about the procedure’s invasiveness or ethical considerations regarding termination. Ultimately, the decision should be made after thorough consideration and consultation with healthcare providers to align with individual values and needs.
There are two types of prenatal tests available:
However, two routine tests, such as urine analysis tests and blood pressure checks, are administered at every checkup. But to check for genetic abnormalities, a series of screening tests are performed during certain trimesters of the pregnancy.
This testing indicates the possible presence of a genetic disorder, but it does not indicate which disorder is present or its severity. If the result is positive after the screening test, the next step advised by the doctor to the patient is to perform a diagnostic test to determine which genetic disorder is present. As some diagnostic tests do often carry a slight risk of miscarriage, such as:
Many screening tests are non-invasive. It just requires a blood sample from the mother, whereas some tests are offered as a series of tests in a single checkup. These include, but are not limited to:
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If you are planning to do prenatal screening tests, then they may include the following:
When a woman is in her first trimester, the healthcare provider will offer a blood test and an ultrasound. These tests will help in measuring the size of the clear space in the tissue at the back of the neck of the baby (nuchal translucency). Whether it be Down syndrome or any other condition, the nuchal translucency measurement will usually be larger.
When a woman is in her second trimester, the health care provider will offer another blood test called the quad screen to measure the levels of four substances in the blood. Results from the test will help to indicate the risk of carrying a baby if you have certain chromosomal conditions, such as Down syndrome. The test can not only help in detecting neural tube defects but also serious abnormalities of the brain or spinal cord.
This blood test helps in examining fetal DNA in the maternal bloodstream to screen for the increased chance of specific chromosome problems, such as Down syndrome. It can provide information about a baby’s sex and Rh blood type.
Certainly, here are the benefits of prenatal testing for expecting mothers outlined in points:
We hope the above information has guided and cleared all your doubts about prenatal testing. So whether to pursue prenatal testing is up to you. Additionally, you can also discuss the risks and benefits with your healthcare provider if you’re concerned about prenatal testing. You can also consider meeting with a genetic counselor for help choosing a test and understanding the results. To make the best decision for you and your baby, it is advised to take the time to evaluate your options wisely.
AIMS Healthcare offers safe and smooth NIPT services that utilize advanced genetic screening techniques, ensuring reliable and precise outcomes. Our expertise in prenatal diagnostics, coupled with a commitment to patient well-being, ensures a supportive and empathetic experience for expecting mothers. Our DHA-certified team is highly dedicated to providing comprehensive prenatal care, empowering you with valuable information to make informed decisions about your pregnancy while receiving the utmost care and support throughout the process. Whether to pursue prenatal care or not is a choice. To learn more about prenatal testing, we warmly invite you to contact us at 800 AIMS 2467 or WhatsApp +971 505 136 505. We will be happy to answer any questions you may have. We are available 24 hours a day, 365 days a year. We will reach your doorstep within 30 minutes.
Prenatal testing can help to indicate whether the baby might have a birth defect or not.
Yes, the information obtained from the test can shape your prenatal care, guiding decisions regarding medical interventions, treatment options, and preparations for the baby’s health needs.
NIPT results are highly accurate, with a reported accuracy rate of over 99% for detecting common chromosomal abnormalities such as Down syndrome.
The risks associated with testing are minimal, typically limited to the possibility of false positives. It may even necessitate further diagnostic procedures and potential emotional stress for expecting parents.
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