At my last prenatal appointment I had a combination of tests done to screen for birth defects such as Down syndrome and Trisomy 13 and 18. I was nervous going, but my husband was with me for support. My visit started with an ultrasound. The doctor rubbed a hand-held device (called a transducer) across my belly. The baby was face up and the doctor needed him/her to turn to the side in order to measure the thickness at the back of the neck (called nuchal translucency). We waited and waited, but he/she wouldn’t budge. I certainly didn’t mind because I was able to admire the beautiful image on the screen longer.
After several minutes, the doctor finally called for a nurse. She brought me a very sweet orange drink and the doctor said he would be back in less than 10 minutes. I was thinking, “yeah right, this isn’t going to work.” Well, wouldn’t you know it. When he came back and put the transducer on my belly, there it was — the most perfect profile. I guess the baby just needed a little energy. Using the mouse on the ultrasound machine, he was able to measure the back of the neck.
Then I was passed off to the nurse who took a blood sample. I don’t know if this is always the case with maternal blood screening, but she pricked my finger and placed about 5 or 6 drops of blood on a card. The office sent the blood sample to a lab and I would get the results back in about four days. The lab calculated my risk of chromosomal birth defects, using the combined results of my blood test and ultrasound exam.
I received a call a few days later. I was told that based on my age, blood work and ultrasound my risk for Down syndrome was 1 in 1, 610 and my risk for Trisomy 18/13 was 1 in > 10,000. I know that no test can gaurantee the birth of a healthy baby, but I was so relieved. It’s always nice to here reassuring news. Waiting for test results can be so stressful.