Consultation

Consultations are available for fetal conditions affecting development including birth defects such as cardiac defect, facial abnormalities, neural tube defects, and Down syndrome. In addition, consultations are available those pregnancies complicated by hypertension, diabetes, pre-term labor, pre-term delivery, recurrent pregnancy loss, blood abnormalities, and autoimmune diseases (e.g. Lupus) as well as gynoloagical concerns, addressed using ultrasound. Telephone consultations and collaborative management are also available.

Perinatal/Gyn Ultrasound

SeeBaby HearBaby, With every ultrasound we provide, we do our best to capture optimal images. With prenatal ultrasound, the reverberations converted into video or photographic images of your infant. The ultrasound used during pregnancy to show pictures of the baby, amniotic sac, placenta, and ovaries. Significant anatomical abnormalities or congenital disabilities are visible on an ultrasound.

3D/4D imaging can be impeded secondary, but not limited to, low amniotic fluid, late gestational age, unfavorable fetal lie (position) or maternal body habitus. Only one complimentary visit per patient will be scheduled, if deemed necessary by See Baby employed Sonographer. No refunds will be made on 3D/4D services.

*SeeBaby reserves the right to charge a $25 cancellation fee for visits not cancelled within 24 hours of appointment date.

*All 3D images on this site are actual See Baby pictures!
*The CD/DVD provided (if applicable) are guaranteed to work on a PC. Due to variations in manufacturer’s specs, there is no guarantee for discs to play on your DVD player, BluRay, Xbox, or other electronic disc player.

OB Ultrasound

Quality evaluation and visualization occurs with traditional diagnostic ultrasound examinations. Our patients can start the bonding experience with the highest quality ultrasound service in compliance with all professional and technical standards. Our OB ultrasound examinations provide reassurance and detailed information regarding the condition of your pregnancy. The most common way to image your baby is with 2D diagnostic ultrasound. Our facility also provides 3D/4D ultrasound giving a “special” look at the baby, as an option. This is the basis of our practice also allows it to be a site for innovative development in the field; training and education for physicians, technologists and nurses. We offer only state of the art technology and have always had early access to new advances participating in application and development. See Baby steadfastly collaborates with MindRay ultrasound technology and MedStreaming image archiving system to bring a cutting edge evaluation to pregnancy and care of the patient. Thereby allowing the patient to “Experience Excellence”.

Diabetes Management/Teaching

The term diabetes encompasses various metabolic disorders that all if left untreated, result in an abnormally large concentration of sugar (glucose) in the blood. Undermanaged diabetes during pregnancy, the baby is exposed to high blood sugar levels. Affecting the newborn and mother throughout gestation, Infants of diabetic mothers (IDM) are frequently more significant in size than other babies.

We at SeeBaby understand that you are the one who manages your diabetes day by day. Our goal through Diabetes Management/Teaching is to educate you on several strategies and personal educational plans that can better help you manage your diabetes, especially during your pregnancy.

Please call See Baby to discuss your individual Diabetes Management (404) 223-9306.

NON-Invasive Genetic Testing

(Verifi, MaterniT21, Harmony, etc.) This type of test is designed to help women who would like to know, as accurately as possible, with little or no risk to their pregnancy (a routine blood draw), if their baby has an extra chromosome (e.g., Down Syndrome, Trisomy 13, Trisomy 18 and Trisomy 21). Gender determination can also be provided by this type of testing. The test may be an option for you to consider if you fit into one of the following categories: Prenatal ultraosund showing specific changes to the baby’s growth and/or development Abnormal or “positive” first trimester or second trimester maternal serum screening Personal or family history of chromosomal condition AMA (Advanced Maternal Age > 35 y.o.)

Amniocentesis For Fetal Lung Maturity

Perinatal Services Amniocentesis For Fetal Lung Maturity (L/S, PG) This procedure is performed to assess fetal lung maturity. The information obtained from these results will help aid your doctors in deciding the best time to deliver your baby. An amniocentesis is performed to obtain a small amount of the amniotic fluid surrounding the fetus. An ultrasound is performed during the amniocentesis to check the position of your baby and to locate pockets of fluid. The doctor will insert a needle into the amniotic sac to remove a small amount of fluid for testing. After your amniocentesis, you may be placed on a fetal monitor for a non-stress test (see below).

DNA Paternity/Amniocentesis DNA

Paternity/Amniocentesis This procedure is often performed between 14 – 22 weeks EGA, to identify or exclude chromosomal abnormalities. Amniocentesis is often offered as an optional test when risks or concerns are suspected for genetic problems. This procedure is brief and usually requires 10 minutes to complete. Unfortunately, there is a 1/200 or 0.5% risk of miscarriage or fetal loss. This procedure can also be performed after 24 weeks EGA, however carries a risk of preterm delivery of 1/500. Results typically take 7-10 days. This is a simple medical procedure used to obtain a small amount of the amniotic fluid surrounding the fetus. An ultrasound is performed with the amniocentesis to check the position of your baby and to locate pockets of fluid. The doctor will insert a needle through the abdominal wall into the amniotic sac to remove a ~ 4 teaspoons (20 cc) of fluid for testing. The test usually takes ~ 1 minute, and most patients experience very little discomfort. The fluid that is withdrawn typically reaccumulates within 12 – 24 hours. Amniotic fluid contains cells from the fetus that can be tested to yield a diagnostic result.

Chorionic Villus Sampling

CVS can be performed earlier in pregnancy than a genetic amniocentesis. It is usually performed at 11 – 13 weeks EGA. This allows for earlier detection of chromosomal abnormalities. When CVS is performed, a small sample of cells is taken from the placenta where it attaches to the wall of the uterus. Chorionic villi are tiny parts of the placenta, formed from the fertilized egg. Therefore, they have the same genes as the fetus. An ultrasound is also performed with CVS to facilitate appropriate sampling and safety. There are 2 approaches or techniques used to collect the sample:

Transabdominal, which is similar to amniocentesis Transcervical, which is perform using a speculum as it would be for a Pap test. Then, a very thin, plastic tube is inserted through the vagina and into the cervix. With ultrasound, the tube is guided to the placenta and a small sample is removed. The sample is then sent to the lab for genetic testing.

This decision regarding which approach to use is typically made at the time of your appointment after ultrasound assessment of the placental location. This will be discussed with you before any procedure is performed. This procedure usually takes 20 minutes to complete.

First Trimester Genetic Screen

First Trimester Screening is a normal, reliable test used for early pregnancy evaluation. It consists of two components:

A blood test, drawn from either your arm or your finger
A detailed ultrasound examination of your baby

The first phase, or Part I of First Trimester Screening, allows an early risk assessment for Down syndrome (Trisomy 21), Trisomy 18, & Trisomy 13. By having your blood drawn between 11.3 – 13.3 weeks EGA couple with a limited fetal ultrasound assessment (nuchal translucency NT) a genetic risk result can be obtained with ~ 85% accuracy. Increasing the accuracy to approx. 93% a second phase, or Part II, can be completed. Also, MSAFP screening for neural tube defect (NTD) is perfomred. This occurs between 16 – 22 weeks EGA. The Perinatologist will conduct and interpret your ultrasound examination to provide you withWater a final calculation of your risk for Down syndrome, Trisomy 18 and Trisomy 13. In the event of an “at risk” result, we will provide you with additional consultation, genetic counseling and testing options as clinically indicated and per your desire.

NON-Stress Test (NST)/Biophysical Profile (BPP)

This procedure is performed in our office using a fetal monitor to listen to and evaluate your baby’s heart activity. An NST observes the baby’s heart rate while the baby moves. Fetal activity with a rise in the baby’s heart rate is a good indication of fetal well being. This test usually takes 30 minutes to complete. Two monitors are placed on your abdomen. One will record the baby’s movements and/or uterine contractions, while the other records the baby’s heart rate. The BPP (biophysical profile), the ultrasound component of the examination, involves assessment of fetal activity and amniotic fluid volume. Evaluation of these elements help determine fetal well being. A score for fetal well being is then given. The medical team at See Baby will interpret the test and let you know if further testing is needed.

Cerclage For Cervical Incompetence

Patients with a history of second trimester loss or currently diagnosed with significant cervical changes are candidates for cervical cerclage. Briefly, the procedure invloves securing and reinforcing the cervix wtih a suture under anesthesia. The cerclage is typically placed between 12 – 20 weeks EGA. It is also done as an outpatient procedure. Afer placement, patients are continuously monitored to ensure successful pregancy outcome!